| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
adaptation percent (1 – first/last ISI) |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
51.3
± 14.5
(45)
|
51.3 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
adaptation percent (1 – first/last ISI) |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
46.6
± 13.6
(48)
|
46.6 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
31.8
± 7.7
(5)
|
31.8 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
58.0
± 15.7
(19)
|
58.0 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
39.5
± 11.6
(6)
|
39.5 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
58.9
± 20.5
(5)
|
58.9 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
46.8
± 19.8
(26)
|
46.8 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
45.4
± 11.2
(3)
|
45.4 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
adaptation percent (1 – first/last ISI) |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
41.9
± 17.2
(5)
|
41.9 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
adaptation percent (1 – first/last ISI) |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
36.3
± 9.8
(3)
|
36.3 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
adaptation ratio |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
1.03
± 0.04
(235)
|
1.03 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
adaptation ratio |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.69
± 0.02
(10)
|
0.69 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
adaptation ratio |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
218.0
± 6.0
(13)
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
adaptation ratio |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.82
± 0.04
(17)
|
0.82 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
adaptation ratio |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.61
± 0.03
(20)
|
0.61 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
adaptation ratio (last/first ISI) |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
5.48
± 0.91
(10)
|
5.48 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
adaptation ratio (last/first ISI) |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
0.99
± 0.08
(11)
|
0.99 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
adaptation ratio (last/first ISI) |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
8.92
± 0.86
(47)
|
8.92 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
adaptation ratio (last/first ISI) |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
2.63
± 0.4
(11)
|
2.63 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
adaptation ratio (other) |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.69
± 0.16
(19)
|
0.69 (None)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
adaptation ratio (other) |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.47
± 0.15
(21)
|
0.47 (None)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-6.6
± 1.9
(3)
|
6.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
AHP amplitude |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
-10.0
± 5.0
(10)
|
10.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
AHP amplitude |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
16.0
± 1.0
(17)
|
16.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-18.5
± 4.7
(5)
|
18.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
AHP amplitude |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
9.2
± 5.2
(11)
|
9.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-9.8
± 2.3
(18)
|
9.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
AHP amplitude |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
25.0
± 4.0
(19)
|
25.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
AHP amplitude |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
17.8
± 1.2
(16)
|
17.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
AHP amplitude |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
-11.3
(42)
|
11.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-14.2
± 2.3
(5)
|
14.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
AHP amplitude |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-15.3
± 3.3
(3)
|
15.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
AHP amplitude |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
13.5
± 0.5
|
13.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
AHP amplitude |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-19.3
± 5.2
(45)
|
19.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-11.1
± 3.1
(6)
|
11.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-15.1
± 4.1
(19)
|
15.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
AHP amplitude |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
-15.0
± 6.0
(48)
|
15.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-12.7
± 2.5
(5)
|
12.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
AHP amplitude |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
-14.1
(47)
|
14.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
AHP amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-17.1
± 4.7
(26)
|
17.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
AHP amplitude |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
-7.9
± 0.5
(38)
|
7.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
AHP amplitude |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
19.0
± 4.0
(30)
|
19.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
AHP amplitude |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
19.4
± 1.1
(10)
|
19.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex aspiny multipolar adapting firing pattern interneuron
|
AHP amplitude from resting |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
-9.4
± 2.6
|
9.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex round aspiny multipolar nonadapting firing pattern interneuron
|
AHP amplitude from resting |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
-13.0
± 1.8
|
13.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
AHP duration |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
55.8
± 5.2
|
55.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
AHP duration |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
14.1
± 9.8
(3)
|
14.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
AHP duration |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
23.1
± 4.8
(45)
|
23.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
AHP duration |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
166.0
± 37.0
(11)
|
166.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
AHP duration |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
54.5
± 4.5
(38)
|
54.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
AHP duration |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
21.2
(47)
|
21.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
AHP duration |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
42.4
± 12.6
(10)
|
42.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex aspiny multipolar adapting firing pattern interneuron
|
AHP duration |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
5.6
± 1.1
|
5.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex round aspiny multipolar nonadapting firing pattern interneuron
|
AHP duration |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
4.6
± 1.4
|
4.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
AHP duration |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
166.0
± 37.0
(11)
|
166.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
AHP duration |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
63.7
± 7.6
(16)
|
63.7 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
AHP duration |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
31.5
(42)
|
31.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
cell capacitance |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
61.6
± 5.8
(47)
|
61.6 (pF)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-9.5
(1)
|
9.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-10.2
± 2.4
(7)
|
10.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-9.9
± 2.0
(9)
|
9.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V GABAergic neurons
|
fast AHP amplitude |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
-13.6
± 0.8
|
13.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
fast AHP amplitude |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-10.0
± 1.6
(20)
|
10.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-11.9
± 4.3
(11)
|
11.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-13.4
± 2.7
(7)
|
13.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
fast AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-8.6
± 3.1
(34)
|
8.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
fast AHP amplitude |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-10.9
± 1.3
(10)
|
10.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
fast AHP amplitude |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
-6.4
± 0.6
|
6.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
15.2
± 3.1
(6)
|
15.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
74.3
± 18.0
(5)
|
74.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
fast AHP duration |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
7.1
± 0.8
|
7.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
19.0
± 11.9
(18)
|
19.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
25.7
± 11.9
(19)
|
25.7 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
26.8
± 8.3
(5)
|
26.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
21.3
± 5.4
(26)
|
21.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
12.5
± 11.2
(5)
|
12.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
fast AHP duration |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
15.5
± 4.6
(3)
|
15.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
FI slope |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
0.16
± 0.03
(16)
|
160.0 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
FI slope |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.16
± 0.02
(17)
|
0.16 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
FI slope |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
108.7
± 13.7
(11)
|
108.7 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
FI slope |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.15
± 0.01
(20)
|
150.0 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
FI slope |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
338.5
± 15.5
(11)
|
338.5 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
FI slope |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
149.6
± 17.5
(10)
|
149.6 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
FI slope |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
344.8
± 15.2
(235)
|
344.8 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
FI slope |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.17
± 0.01
(10)
|
170.0 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
FI slope |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
0.25
± 0.05
(10)
|
250.0 (Hz/nA)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
192.4
± 127.7
(18)
|
192.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
174.8
± 117.7
(19)
|
174.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
90.5
± 58.9
(5)
|
90.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
348.6
± 104.6
(26)
|
348.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
286.4
± 137.5
(5)
|
286.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
first spike latency |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
59.0
± 36.0
(30)
|
59.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
245.8
± 103.0
(3)
|
245.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
303.8
± 71.6
(6)
|
303.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
first spike latency |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
208.7
± 141.9
(5)
|
208.7 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
first spike latency |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
209.0
± 122.0
(19)
|
209.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
first spike latency |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
14.1
± 9.8
(3)
|
14.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
first spike latency |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
376.3
± 79.8
(45)
|
376.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex round aspiny multipolar nonadapting firing pattern interneuron
|
input resistance |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
220.0
|
220.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
input resistance |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
196.0
± 13.0
(20)
|
196.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
input resistance |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
171.5
± 9.6
(235)
|
171.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
input resistance |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
39.6
± 2.1
(38)
|
39.6 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
input resistance |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
165.1
± 14.8
(11)
|
165.1 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
input resistance |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
142.5
± 11.8
(22)
|
142.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
insular cortex neuron
|
input resistance |
Selective changes in inhibition as determinants for limited hyperexcitability in the insular cortex of epileptic rats.
(NeuroElectro data)
(PubMed)
|
44.89
± 3.85
(24)
|
44.89 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
input resistance |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
179.9
± 20.6
(11)
|
179.9 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
884.1
(1)
|
884.1 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
763.0
± 263.4
(5)
|
763.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
input resistance |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
241.2
± 19.1
(10)
|
241.2 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
input resistance |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
94.3
± 8.7
(10)
|
94.3 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
input resistance |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
330.0
± 27.0
(31)
|
330.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
468.0
± 165.2
(6)
|
468.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
input resistance |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
334.9
± 62.6
(9)
|
334.9 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
|
input resistance |
Increased pyramidal excitability and NMDA conductance can explain posttraumatic epileptogenesis without disinhibition: a model.
(NeuroElectro data)
(PubMed)
|
45.0
|
45.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
341.5
± 153.1
(34)
|
341.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
input resistance |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
389.0
± 138.0
(48)
|
389.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
input resistance |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
281.4
± 31.5
(10)
|
281.4 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
input resistance |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
111.0
± 39.0
(11)
|
111.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
input resistance |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
127.7
± 7.2
|
127.7 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
input resistance |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
254.0
± 15.0
(15)
|
254.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
input resistance |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
285.0
± 36.0
(16)
|
285.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
input resistance |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
370.0
± 200.0
(30)
|
370.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
450.8
± 244.3
(7)
|
450.8 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Frontal cortex layer 2-3 and layer 5 α-actinin-2–positive late-spiking Venus-expressing GABAergic neurogliaform cell
|
input resistance |
Quantitative chemical composition of cortical GABAergic neurons revealed in transgenic venus-expressing rats.
(NeuroElectro data)
(PubMed)
|
126.0
± 26.0
(6)
|
126.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
input resistance |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
631.0
± 310.0
(3)
|
631.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V GABAergic neurons
|
input resistance |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
310.0
± 6.0
|
310.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
273.0
± 95.8
(19)
|
273.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
|
input resistance |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
295.0
± 26.0
|
295.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
input resistance |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
403.0
± 122.0
(10)
|
403.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
input resistance |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
357.9
± 21.4
(47)
|
357.9 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
input resistance |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
329.0
± 89.0
(45)
|
329.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
469.7
± 240.2
(11)
|
469.7 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
387.5
± 171.2
(5)
|
387.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
input resistance |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
111.0
± 39.0
(11)
|
111.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
355.1
± 149.5
(26)
|
355.1 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
input resistance |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
53.5
(47)
|
53.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Auditory Cortex neuron
|
input resistance |
An auditory colliculothalamocortical brain slice preparation in mouse.
(NeuroElectro data)
(PubMed)
|
152.6
± 73.0
(42)
|
152.6 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
348.2
± 113.9
(9)
|
348.2 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
input resistance |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
44.3
(42)
|
44.3 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
input resistance |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
125.0
± 11.0
|
125.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
587.0
± 305.9
(3)
|
587.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
571.7
± 339.1
(18)
|
571.7 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
input resistance |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
309.4
± 142.0
(7)
|
309.4 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
input resistance |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
238.0
± 80.0
(19)
|
238.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
|
input resistance |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
390.7
± 159.5
|
--
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
input resistance |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
558.0
± 170.0
(13)
|
558.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
input resistance |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
155.6
± 30.9
(9)
|
155.6 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
input resistance |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
453.5
± 251.3
(5)
|
453.5 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex aspiny multipolar adapting firing pattern interneuron
|
input resistance |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
287.0
± 41.0
|
287.0 (MΩ)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
66.6
± 20.7
(26)
|
66.6 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
82.0
± 28.3
(3)
|
82.0 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
maximum firing rate |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
26.0
± 11.0
(19)
|
26.0 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
maximum firing rate |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
95.7
± 19.0
(10)
|
95.7 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
63.2
± 40.0
(5)
|
63.2 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
maximum firing rate |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
81.3
± 21.4
(3)
|
81.3 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
76.6
± 26.6
(18)
|
76.6 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
maximum firing rate |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
79.3
± 30.1
(45)
|
79.3 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
48.4
± 16.6
(5)
|
48.4 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
maximum firing rate |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
77.5
± 12.1
(16)
|
77.5 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
maximum firing rate |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
50.0
± 28.0
(21)
|
50.0 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
78.4
± 19.9
(5)
|
78.4 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
maximum firing rate |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
204.5
± 18.3
(235)
|
204.5 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
77.7
± 22.5
(6)
|
77.7 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
maximum firing rate |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
42.0
± 14.0
(48)
|
42.0 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
maximum firing rate |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
54.4
± 21.3
(19)
|
54.4 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-13.9
± 1.6
(11)
|
13.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
medium AHP amplitude |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-4.8
± 0.6
(15)
|
4.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
medium AHP amplitude |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-4.6
± 0.38
(31)
|
4.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-12.1
± 2.3
(34)
|
12.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-13.1
± 2.5
(7)
|
13.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-13.4
± 1.4
(9)
|
13.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-15.5
(1)
|
15.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 visual cortex fast spiking interneurons
|
medium AHP amplitude |
GABAA receptor-mediated currents in interneurons and pyramidal cells of rat visual cortex.
(NeuroElectro data)
(PubMed)
|
200.0
± 46.0
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
medium AHP amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-13.2
± 3.2
(7)
|
13.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
membrane time constant |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
18.6
± 2.1
(10)
|
18.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
32.5
± 13.5
(5)
|
32.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
18.9
± 5.5
(5)
|
18.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
membrane time constant |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
9.2
± 0.5
(38)
|
9.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
19.2
± 4.0
(6)
|
19.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
membrane time constant |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
11.0
± 4.0
(30)
|
11.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
membrane time constant |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
15.3
± 1.9
(11)
|
15.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
19.4
± 6.6
(34)
|
19.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
membrane time constant |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
9.0
(47)
|
9.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
20.4
± 7.1
(7)
|
20.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
membrane time constant |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
7.3
(42)
|
7.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2/3 perirhinal cortex pyramidal cell projecting to L5 perirhinal cortex pyramidal cell
|
membrane time constant |
Specialized cortical subnetworks differentially connect frontal cortex to parahippocampal areas.
(NeuroElectro data)
(PubMed)
|
9.9
± 5.3
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
membrane time constant |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
15.8
± 1.3
(22)
|
15.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex aspiny multipolar adapting firing pattern interneuron
|
membrane time constant |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
24.0
± 1.0
|
24.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
18.3
± 6.2
(19)
|
18.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex round aspiny multipolar nonadapting firing pattern interneuron
|
membrane time constant |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
17.0
± 4.0
|
17.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
membrane time constant |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
10.0
± 4.0
(19)
|
10.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
18.6
± 7.6
(26)
|
18.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
membrane time constant |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
13.8
± 1.5
(11)
|
13.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
33.1
(1)
|
33.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
18.0
± 11.4
(3)
|
18.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
25.9
± 10.1
(18)
|
25.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
20.0
± 6.2
(7)
|
20.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
membrane time constant |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
13.9
± 0.9
(235)
|
13.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
membrane time constant |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
18.4
± 9.6
(5)
|
18.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
membrane time constant |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
27.7
± 12.3
(3)
|
27.7 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
22.3
± 8.7
(11)
|
22.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
membrane time constant |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
22.6
± 1.9
(47)
|
22.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
membrane time constant |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
12.2
± 1.0
|
12.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
membrane time constant |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
22.7
± 7.2
(11)
|
22.7 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
membrane time constant |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
17.3
± 6.5
(45)
|
17.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
membrane time constant |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
20.6
± 4.9
(9)
|
20.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 visual cortex fast spiking interneurons
|
membrane time constant |
GABAA receptor-mediated currents in interneurons and pyramidal cells of rat visual cortex.
(NeuroElectro data)
(PubMed)
|
13.0
± 2.0
|
--
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
membrane time constant |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
45.8
± 14.3
(13)
|
45.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
membrane time constant |
Increased pyramidal excitability and NMDA conductance can explain posttraumatic epileptogenesis without disinhibition: a model.
(NeuroElectro data)
(PubMed)
|
20.0
|
20.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
other |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
23.0
± 25.0
(10)
|
23.0 (None)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
other |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
21.4
± 30.6
(48)
|
21.4 (None)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
other |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
26.0
± 11.0
(10)
|
26.0 (None)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
other |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
13.1
± 11.1
(48)
|
13.1 (None)
|
Data Table |
| Neocortex uncharacterized cell |
|
resting membrane potential |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-55.0
± 0.98
|
-55.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
resting membrane potential |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
-60.0
± 3.0
(11)
|
-60.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
resting membrane potential |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
-85.8
± 4.2
(9)
|
-85.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
resting membrane potential |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
-78.4
(47)
|
-78.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
resting membrane potential |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-74.2
± 1.5
(11)
|
-74.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Frontal cortex layer 2-3 and layer 5 α-actinin-2–positive late-spiking Venus-expressing GABAergic neurogliaform cell
|
resting membrane potential |
Quantitative chemical composition of cortical GABAergic neurons revealed in transgenic venus-expressing rats.
(NeuroElectro data)
(PubMed)
|
-68.0
± 2.0
(6)
|
-68.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
resting membrane potential |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
-69.0
± 2.0
|
-69.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-64.5
± 6.7
(19)
|
-64.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-58.1
(1)
|
-58.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
resting membrane potential |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-65.0
± 6.3
(3)
|
-65.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
resting membrane potential |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
-65.2
± 0.9
(235)
|
-65.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-70.7
± 6.5
(11)
|
-70.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-61.5
± 4.4
(5)
|
-61.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-67.7
± 4.2
(7)
|
-67.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-64.5
± 6.0
(26)
|
-64.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
resting membrane potential |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-61.2
± 5.8
(45)
|
-61.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
resting membrane potential |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
-66.0
± 4.0
(19)
|
-66.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
resting membrane potential |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
-64.0
± 3.0
(13)
|
-64.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
resting membrane potential |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
-73.5
(42)
|
-73.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex Pyramidal Neuron
|
resting membrane potential |
Cortical synaptic integration in vivo is disrupted by amyloid-beta plaques.
(NeuroElectro data)
(PubMed)
|
-63.2
± 4.6
(8)
|
-63.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
resting membrane potential |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-73.7
± 1.4
(11)
|
-73.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-72.2
± 4.1
(9)
|
-72.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-68.8
± 5.8
(3)
|
-68.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
resting membrane potential |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
-70.0
± 7.0
(10)
|
-70.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
resting membrane potential |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
-60.0
± 3.0
(11)
|
-60.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
resting membrane potential |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
-57.8
± 1.1
(38)
|
-57.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex Pyramidal Neuron
|
resting membrane potential |
Cortical synaptic integration in vivo is disrupted by amyloid-beta plaques.
(NeuroElectro data)
(PubMed)
|
-61.8
± 4.2
(10)
|
-61.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-61.8
± 8.7
(5)
|
-61.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
resting membrane potential |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
-80.3
± 2.2
(9)
|
-80.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
resting membrane potential |
Increased pyramidal excitability and NMDA conductance can explain posttraumatic epileptogenesis without disinhibition: a model.
(NeuroElectro data)
(PubMed)
|
-60.0
|
-60.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
insular cortex neuron
|
resting membrane potential |
Selective changes in inhibition as determinants for limited hyperexcitability in the insular cortex of epileptic rats.
(NeuroElectro data)
(PubMed)
|
-75.91
± 1.64
(24)
|
-75.91 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
resting membrane potential |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-71.1
± 1.5
(10)
|
-71.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
resting membrane potential |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-66.1
± 3.3
(20)
|
-66.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
resting membrane potential |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
-73.2
± 2.2
(10)
|
-73.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
resting membrane potential |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-53.0
± 0.76
(31)
|
-53.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
resting membrane potential |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-60.0
± 1.0
(15)
|
-60.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-69.1
± 5.0
(7)
|
-69.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
resting membrane potential |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
-66.0
± 7.0
(48)
|
-66.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
resting membrane potential |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
69.2
± 1.4
(22)
|
-69.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-63.7
± 5.9
(5)
|
-63.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
resting membrane potential |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-76.0
± 2.1
(10)
|
-76.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-57.7
± 8.5
(18)
|
-57.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Auditory Cortex neuron
|
resting membrane potential |
An auditory colliculothalamocortical brain slice preparation in mouse.
(NeuroElectro data)
(PubMed)
|
-64.0
± 11.4
(42)
|
-64.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
resting membrane potential |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-54.0
± 4.6
(6)
|
-54.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
resting membrane potential |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
-74.2
± 1.6
(16)
|
-74.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
resting membrane potential |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
-67.0
± 5.0
(30)
|
-67.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V GABAergic neurons
|
resting membrane potential |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
-66.0
± 1.0
|
-66.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
resting membrane potential |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-66.3
± 4.8
(34)
|
-66.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
71.2
± 26.8
(7)
|
71.2 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
rheobase |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
81.5
± 21.0
(10)
|
81.5 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
|
rheobase |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
102.0
± 8.5
|
102.0 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
34.8
± 20.7
(11)
|
34.8 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
rheobase |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
78.1
± 11.0
(16)
|
78.1 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
58.5
± 35.8
(34)
|
58.5 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
53.6
± 36.7
(9)
|
53.6 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
rheobase |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
94.0
± 12.0
(15)
|
94.0 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
9.9
(1)
|
9.9 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
rheobase |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
103.0
± 10.0
(31)
|
103.0 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
rheobase |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
53.2
± 33.5
(7)
|
53.2 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
Frontal cortex layer 2-3 and layer 5 α-actinin-2–positive late-spiking Venus-expressing GABAergic neurogliaform cell
|
rheobase |
Quantitative chemical composition of cortical GABAergic neurons revealed in transgenic venus-expressing rats.
(NeuroElectro data)
(PubMed)
|
178.0
± 39.0
(6)
|
178.0 (pA)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.3
± 1.8
(19)
|
2.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
3.8
± 3.8
(5)
|
3.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.1
± 1.5
(26)
|
2.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
2.7
± 1.5
(3)
|
2.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.3
± 1.5
(5)
|
1.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
0.7
± 0.9
(5)
|
0.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
6.8
± 3.8
(18)
|
6.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
sag amplitude |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
13.8
± 5.6
|
--
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
sag amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
4.4
± 3.6
(6)
|
4.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
sag amplitude |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
1.17
± 0.12
(31)
|
1.17 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
9.0
± 4.6
(11)
|
0.09 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
10.9
± 8.2
(9)
|
0.109 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
15.7
± 6.2
(7)
|
0.157 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
sag ratio |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-0.9
± 0.4
(10)
|
-0.009 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
11.0
± 6.7
(34)
|
0.11 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
11.4
(1)
|
0.114 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
sag ratio |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
6.3
± 1.4
(20)
|
0.063 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
sag ratio |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
10.4
± 4.2
(7)
|
0.104 (ratio)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
slow AHP amplitude |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-2.8
± 0.4
(15)
|
2.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
slow AHP amplitude |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-1.9
± 0.26
(31)
|
1.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
slow AHP amplitude |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
-0.7
± 0.1
|
0.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
slow AHP amplitude |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-1.9
± 0.23
|
1.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
spike amplitude |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
80.6
± 9.0
(11)
|
80.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
spike amplitude |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
68.0
± 3.4
(10)
|
68.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike amplitude |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
102.7
(47)
|
102.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike amplitude |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
76.9
± 7.6
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
spike amplitude |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
63.7
± 1.1
(235)
|
63.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
spike amplitude |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
69.8
± 12.9
(9)
|
69.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
spike amplitude |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
56.0
± 3.8
(16)
|
56.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
67.0
± 9.5
(7)
|
67.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike amplitude |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
97.5
(42)
|
97.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike amplitude |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
58.0
± 9.0
(30)
|
58.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2/3 perirhinal cortex pyramidal cell projecting to L5 perirhinal cortex pyramidal cell
|
spike amplitude |
Specialized cortical subnetworks differentially connect frontal cortex to parahippocampal areas.
(NeuroElectro data)
(PubMed)
|
22.9
± 34.9
|
--
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
68.1
± 13.4
(5)
|
68.1 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
64.2
± 9.7
(34)
|
64.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
spike amplitude |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
56.9
± 1.7
(10)
|
56.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
65.4
± 10.1
(11)
|
65.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
spike amplitude |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
63.9
± 2.8
(20)
|
63.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
62.7
± 7.5
(18)
|
62.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
spike amplitude |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
88.0
± 10.0
(10)
|
88.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
62.9
± 7.1
(7)
|
62.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
spike amplitude |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
40.5
± 1.4
(47)
|
40.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
62.6
± 5.7
(6)
|
62.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Auditory Cortex neuron
|
spike amplitude |
An auditory colliculothalamocortical brain slice preparation in mouse.
(NeuroElectro data)
(PubMed)
|
62.9
± 10.6
(42)
|
62.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
spike amplitude |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
88.0
± 10.0
(48)
|
88.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
69.7
± 7.8
(19)
|
69.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
66.5
(1)
|
66.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
58.9
± 5.2
(5)
|
58.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
65.5
± 7.9
(26)
|
65.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike amplitude |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
60.0
± 7.0
(19)
|
60.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike amplitude |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
82.9
± 7.0
|
--
|
Data Table |
| Neocortex uncharacterized cell |
|
spike amplitude |
Sub- and suprathreshold receptive field properties of pyramidal neurones in layers 5A and 5B of rat somatosensory barrel cortex.
(NeuroElectro data)
(PubMed)
|
4.9
± 0.6
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
spike amplitude |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
67.0
± 2.0
|
67.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
spike amplitude |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
77.6
± 9.9
(22)
|
77.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
61.4
± 4.8
(3)
|
61.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
spike amplitude |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
81.0
± 9.0
(11)
|
81.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
spike amplitude |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
81.0
± 10.3
(9)
|
81.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
spike amplitude |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
74.0
± 5.0
(13)
|
74.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
spike amplitude |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
59.9
± 8.4
(5)
|
59.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2/3 perirhinal cortex pyramidal cell projecting to L5 perirhinal cortex pyramidal cell
|
spike amplitude |
Specialized cortical subnetworks differentially connect frontal cortex to parahippocampal areas.
(NeuroElectro data)
(PubMed)
|
0.29
± 0.1
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike amplitude |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
66.7
± 8.8
(9)
|
66.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
spike amplitude |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
56.2
± 4.3
(10)
|
56.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
insular cortex neuron
|
spike amplitude |
Selective changes in inhibition as determinants for limited hyperexcitability in the insular cortex of epileptic rats.
(NeuroElectro data)
(PubMed)
|
91.59
± 2.52
(24)
|
91.59 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
spike amplitude |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
70.7
± 1.6
(11)
|
70.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V GABAergic neurons
|
spike amplitude |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
61.0
± 2.0
|
61.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
spike amplitude |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
67.4
± 1.9
|
67.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
spike amplitude |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
82.2
± 2.0
(17)
|
82.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
spike amplitude |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
72.4
± 1.3
(11)
|
72.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike decay time |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.54
± 0.09
(30)
|
0.54 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike decay time |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.57
± 0.06
(19)
|
0.57 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.87
± 0.2
(34)
|
0.87 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
spike half-width |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.3
(3)
|
1.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.81
± 0.08
(7)
|
0.81 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.5
± 0.3
(5)
|
1.5 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
spike half-width |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
0.9
± 0.3
(11)
|
0.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.3
(26)
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
spike half-width |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.5
(45)
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike half-width |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.67
± 0.07
(19)
|
0.67 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike half-width |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
0.39
± 0.07
(45)
|
0.39 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 visual cortex fast spiking interneurons
|
spike half-width |
GABAA receptor-mediated currents in interneurons and pyramidal cells of rat visual cortex.
(NeuroElectro data)
(PubMed)
|
24.0
± 2.0
|
--
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.5
(3)
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex upper layer 2-3 Cck-containing CB1-expressing irregular spiking large cell
|
spike half-width |
Electrical coupling among irregular-spiking GABAergic interneurons expressing cannabinoid receptors.
(NeuroElectro data)
(PubMed)
|
0.8
± 0.05
|
0.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
spike half-width |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.62
± 0.03
(10)
|
0.62 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.3
(5)
|
1.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Frontal cortex layer 2-3 and layer 5 α-actinin-2–positive late-spiking Venus-expressing GABAergic neurogliaform cell
|
spike half-width |
Quantitative chemical composition of cortical GABAergic neurons revealed in transgenic venus-expressing rats.
(NeuroElectro data)
(PubMed)
|
0.69
± 0.06
(6)
|
0.69 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic regular spiking VGAT-expressing interneurons
|
spike half-width |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
0.8
(10)
|
0.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.0
± 0.1
(5)
|
1.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
1.16
(1)
|
1.16 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.0
± 0.2
(18)
|
1.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
spike half-width |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
1.1
± 0.03
(31)
|
1.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
spike half-width |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
0.42
± 0.02
(235)
|
0.42 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
0.9
± 0.2
(6)
|
0.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
spike half-width |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
1.8
± 0.1
(17)
|
1.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
spike half-width |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.2
(13)
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex regular spiking non-pyramidal cell
|
spike half-width |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
1.06
± 0.28
(48)
|
1.06 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.98
± 0.3
(11)
|
0.98 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
spike half-width |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
0.67
± 0.03
(20)
|
0.67 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
spike half-width |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
0.9
± 0.3
(11)
|
0.9 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.93
± 0.12
(7)
|
0.93 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
spike half-width |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
1.1
± 0.05
(38)
|
1.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Insular cortex Layer 5 Gabaergic late spiking VGAT-expressing interneurons
|
spike half-width |
Postsynaptic cell type-dependent cholinergic regulation of GABAergic synaptic transmission in rat insular cortex.
(NeuroElectro data)
(PubMed)
|
1.1
± 0.1
(16)
|
1.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
spike half-width |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
0.43
± 0.05
(11)
|
0.43 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike half-width |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.63
± 0.12
(30)
|
0.63 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex aspiny multipolar adapting firing pattern interneuron
|
spike half-width |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.13
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike half-width |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
1.2
± 0.04
|
1.2 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex round aspiny multipolar nonadapting firing pattern interneuron
|
spike half-width |
Synaptic alpha 5 subunit-containing GABAA receptors mediate IPSPs elicited by dendrite-preferring cells in rat neocortex.
(NeuroElectro data)
(PubMed)
|
1.0
± 0.25
|
1.0 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
spike half-width |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
0.81
± 0.12
(10)
|
0.81 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
spike half-width |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
0.83
± 0.07
(47)
|
0.83 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
sensorimotor cortex irregular spiking cell
|
spike half-width |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
0.95
± 0.17
(10)
|
0.95 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
spike half-width |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
1.4
± 0.2
(19)
|
1.4 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike half-width |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.86
± 0.17
(9)
|
0.86 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
spike half-width |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
0.62
± 0.06
(11)
|
0.62 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
spike half-width |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
1.3
± 0.4
(22)
|
1.3 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max decay slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
95.0
± 25.0
(30)
|
95.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike max decay slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
56.3
(47)
|
56.3 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike max decay slope |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
0.55
± 0.33
(45)
|
0.55 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max decay slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
93.0
± 13.0
(19)
|
93.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike max decay slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
87.5
(42)
|
87.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
112.6
± 35.9
(11)
|
112.6 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max rise slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
180.0
± 25.0
(19)
|
180.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
124.5
± 31.8
(9)
|
124.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
92.1
(1)
|
92.1 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
119.5
± 25.0
(7)
|
119.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike max rise slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
175.4
(47)
|
175.4 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike max rise slope |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
0.49
± 0.46
(45)
|
0.49 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
124.8
± 34.5
(34)
|
124.8 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike max rise slope |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
116.5
± 28.2
(7)
|
116.5 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike max rise slope |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
217.4
(42)
|
217.4 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike max rise slope |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
184.0
± 45.0
(30)
|
184.0 (mV/ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike peak |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
36.0
± 1.4
|
36.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
spike peak |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
49.0
± 0.82
(31)
|
49.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.95
(1)
|
0.95 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.72
± 0.13
(9)
|
0.72 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.76
± 0.11
(7)
|
0.76 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike rise time |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.28
± 0.05
(30)
|
0.28 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 visual cortex fast spiking interneurons
|
spike rise time |
GABAA receptor-mediated currents in interneurons and pyramidal cells of rat visual cortex.
(NeuroElectro data)
(PubMed)
|
1.8
± 0.2
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.71
± 0.16
(34)
|
0.71 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike rise time |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
0.29
± 0.04
(19)
|
0.29 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.69
± 0.07
(7)
|
0.69 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike rise time |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
0.81
± 0.19
(11)
|
0.81 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex multipolar bursting GABAergic cell
|
spike threshold |
A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex.
(NeuroElectro data)
(PubMed)
|
-43.0
± 2.7
(11)
|
-43.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 3/5 pyramidal neuron projecting to basolateral amygdala
|
spike threshold |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-32.5
± 2.1
(20)
|
-32.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived sigmoid intrinsic bursting interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-43.3
± 5.2
(3)
|
-43.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived fast-adapting interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-36.4
± 4.6
(18)
|
-36.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 2-3 and 5 medial prefrontal cortex prelimibic and infralimbic pyramidal neurons
|
spike threshold |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-38.0
± 0.79
(31)
|
-38.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived irregular spiking interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-38.4
± 5.3
(6)
|
-38.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2-3 multipolar round bodied calretinin-expressing GABAergic interneuron
|
spike threshold |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
-41.0
± 3.0
(13)
|
-41.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed intrinsic bursting interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-36.9
± 4.1
(5)
|
-36.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5a vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-37.9
± 2.9
(7)
|
-37.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex GABAergic layer 4 calretinin-immunoreactive interneuron
|
spike threshold |
Altered firing rates and patterns in interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
-47.8
± 1.4
(47)
|
-47.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 5 medial prefrontal cortex infralimbic non-fast spiking interneurons
|
spike threshold |
Flexible spike timing of layer 5 neurons during dynamic beta oscillation shifts in rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
-36.9
± 1.2
(17)
|
-36.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 2/3 vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-38.3
± 3.6
(34)
|
-38.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike threshold |
Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-39.0
± 0.81
|
-39.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Layer 4 barrel cortex pyramidal cell
|
spike threshold |
High serotonin levels during brain development alter the structural input-output connectivity of neural networks in the rat somatosensory layer IV.
(NeuroElectro data)
(PubMed)
|
-37.4
± 1.3
(22)
|
-37.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex calretinin-expressing GABAergic inhibitory interneurons
|
spike threshold |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-49.8
± 1.5
(10)
|
-49.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic delayed non-fast-spiking Htr3a-expressing interneuron
|
spike threshold |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-42.2
± 6.1
(3)
|
-42.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 4 vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-38.8
± 2.9
(7)
|
-38.8 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 1-2 large oval or round multipolar bursting parvalbumin-positive GABAergic interneuron
|
spike threshold |
Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition.
(NeuroElectro data)
(PubMed)
|
-43.0
± 3.0
(11)
|
-43.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Infralimbic cortex layer 2 pyramidal neuron projecting to basolateral amygdala
|
spike threshold |
Highly differentiated cellular and circuit properties of infralimbic pyramidal neurons projecting to the periaqueductal gray and amygdala.
(NeuroElectro data)
(PubMed)
|
-38.4
± 2.3
(10)
|
-38.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike threshold |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
41.5
(47)
|
-41.5 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
neocortex layer 2/3 GABAergic late-spiking subtype 1 Htr3a-expressing interneuron
|
spike threshold |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
-38.2
± 5.4
(45)
|
-38.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 5b vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-38.4
± 1.9
(9)
|
-38.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
spike threshold |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
-51.3
± 2.7
(9)
|
-51.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike threshold |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
-41.0
± 4.0
(30)
|
-41.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex somatostatin-expressing GABAergic inhibitory interneurons
|
spike threshold |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-48.3
± 1.2
(11)
|
-48.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 6 vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-39.0
± 1.9
(11)
|
-39.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Somatosensory cortex layer 4 unidentified excitatory cell projecting to layer 2/3
|
spike threshold |
Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex.
(NeuroElectro data)
(PubMed)
|
-50.2
± 6.6
(9)
|
-50.2 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike threshold |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
30.9
(42)
|
-30.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 2 interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-37.4
± 4.1
(19)
|
-37.4 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex fast-spiking parvalbumin-immunoreactive interneurons
|
spike threshold |
Reduced chemical and electrical connections of fast-spiking interneurons in experimental cortical dysplasia.
(NeuroElectro data)
(PubMed)
|
-41.6
± 0.8
(235)
|
-41.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived burst non-adapting 2 interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-33.9
± 6.3
(5)
|
-33.9 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
prefrontal cortex neurogliaform Inhibitory Neuron
|
spike threshold |
Electrophysiological differences between neurogliaform cells from monkey and rat prefrontal cortex.
(NeuroElectro data)
(PubMed)
|
-35.0
± 3.0
(19)
|
-35.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
medial prefrontal cortex infralimbic layer II,III, and V pyramidal neurons
|
spike threshold |
Spontaneous recovery of fear reverses extinction-induced excitability of infralimbic neurons.
(NeuroElectro data)
(PubMed)
|
-37.0
± 1.0
(15)
|
-37.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived late spiking 1 interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-35.3
± 4.0
(26)
|
-35.3 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike threshold |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
0.27
± 0.14
(45)
|
--
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex parvalbumin-expressing GABAergic inhibitory interneurons
|
spike threshold |
Functional integration of human neural precursor cells in mouse cortex.
(NeuroElectro data)
(PubMed)
|
-47.6
± 1.1
(11)
|
-47.6 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
Barrel cortex layer 1 vasoactive intestinal polypeptide expressing neurons
|
spike threshold |
Characterizing VIP Neurons in the Barrel Cortex of VIPcre/tdTomato Mice Reveals Layer-Specific Differences.
(NeuroElectro data)
(PubMed)
|
-38.7
(1)
|
-38.7 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex CGE-derived delayed non-fast spiking 3 interneuron
|
spike threshold |
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons.
(NeuroElectro data)
(PubMed)
|
-44.0
± 3.9
(5)
|
-44.0 (mV)
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-positive Pyramidal Cell
|
spike width |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
0.8
(42)
|
0.8 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike width |
Altered information processing in the prefrontal cortex of Huntington's disease mouse models.
(NeuroElectro data)
(PubMed)
|
1.283
|
1.283 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V pyramidal neurons
|
spike width |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
2.6
± 0.2
|
2.6 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike width |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
1.5
± 0.3
|
--
|
Data Table |
| Neocortex uncharacterized cell |
insular cortex neuron
|
spike width |
Selective changes in inhibition as determinants for limited hyperexcitability in the insular cortex of epileptic rats.
(NeuroElectro data)
(PubMed)
|
1.45
± 0.06
(24)
|
1.45 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Prelimbic medial prefrontal cortex layer II/III or layer V GABAergic neurons
|
spike width |
Neurobiological dissociation of retrieval and reconsolidation of cocaine-associated memory.
(NeuroElectro data)
(PubMed)
|
2.1
± 0.1
|
2.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spike width |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
10.38
± 2.46
(45)
|
10.38 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike width |
Altered information processing in the prefrontal cortex of Huntington's disease mouse models.
(NeuroElectro data)
(PubMed)
|
0.832
|
0.832 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
|
spike width |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
1.9
± 0.5
|
--
|
Data Table |
| Neocortex uncharacterized cell |
somatosensory cortex Layers II/III/V ADP-negative Pyramidal Cell
|
spike width |
Spike sequences and mean firing rate in rat neocortical neurons in vitro.
(NeuroElectro data)
(PubMed)
|
1.1
(47)
|
1.1 (ms)
|
Data Table |
| Neocortex uncharacterized cell |
Primary auditory cortex pyramidal neurons
|
spontaneous firing rate |
The synaptic representation of sound source location in auditory cortex.
(NeuroElectro data)
(PubMed)
|
0.54
± 0.08
(38)
|
0.54 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex Pyramidal Neuron
|
spontaneous firing rate |
Cortical synaptic integration in vivo is disrupted by amyloid-beta plaques.
(NeuroElectro data)
(PubMed)
|
14.0
± 6.7
(8)
|
14.0 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Neocortex Pyramidal Neuron
|
spontaneous firing rate |
Cortical synaptic integration in vivo is disrupted by amyloid-beta plaques.
(NeuroElectro data)
(PubMed)
|
12.8
± 6.0
(10)
|
12.8 (Hz)
|
Data Table |
| Neocortex uncharacterized cell |
Parietal cortex pyramidal cells
|
spontaneous firing rate |
Maturation of "neocortex isole" in vivo in mice.
(NeuroElectro data)
(PubMed)
|
9.0
± 9.1
(45)
|
9.0 (Hz)
|
Data Table |
