| Hippocampus CA1 basket cell |
Hippocampus CA1 fast spiking basket cell
|
adaptation percent (1 – first/last ISI) |
Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation.
(NeuroElectro data)
(PubMed)
|
20.0
± 2.0
(20)
|
20.0 (ratio)
|
Data Table |
| Hippocampus CA1 oriens lacunosum moleculare neuron |
Hippocampus CA1 oriens lacunosum moleculare non-fast-spiking neuron
|
adaptation percent (1 – first/last ISI) |
Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation.
(NeuroElectro data)
(PubMed)
|
26.0
± 3.0
(66)
|
26.0 (ratio)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
49.0
± 15.0
(6)
|
49.0 (ratio)
|
Data Table |
| Hippocampus CA1 pyramidal cell |
|
adaptation percent (1 – first/last ISI) |
Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation.
(NeuroElectro data)
(PubMed)
|
40.0
± 5.0
(53)
|
40.0 (ratio)
|
Data Table |
| Neocortex basket cell |
Neocortex medial ganglionic eminence fast spiking interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
17.6
(71)
|
17.6 (ratio)
|
Data Table |
| Neocortex basket cell |
Neocortex Layer 2-3 Fast-Spiking Interneuron
|
adaptation percent (1 – first/last ISI) |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
11.0
± 2.4
(9)
|
11.0 (ratio)
|
Data Table |
| Neocortex basket cell |
sensorimotor cortex fast spiking cell
|
adaptation percent (1 – first/last ISI) |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
15.3
± 15.0
(34)
|
15.3 (ratio)
|
Data Table |
| Neocortex basket cell |
Layer 5 somatosensory cortex Fast Spiking parvalbumin positive interneurons
|
adaptation percent (1 – first/last ISI) |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
9.1
± 5.9
(8)
|
9.1 (ratio)
|
Data Table |
| Neocortex bipolar neuron |
neocortex layer 2-3 cholinergic interneurons
|
adaptation percent (1 – first/last ISI) |
Functional characterization of intrinsic cholinergic interneurons in the cortex.
(NeuroElectro data)
(PubMed)
|
60.4
± 16.9
|
60.4 (ratio)
|
Data Table |
| Neocortex layer 4 stellate cell |
Layer 4 sensorimotor cortex spiny stellate neurons
|
adaptation percent (1 – first/last ISI) |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
65.8
± 18.3
(10)
|
65.8 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Layer 2/3 sensorimotor cortex pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
57.6
± 10.0
(28)
|
57.6 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
|
adaptation percent (1 – first/last ISI) |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
68.0
± 2.7
(13)
|
68.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
Somatosensory cortex layer 2/3 pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
52.0
± 4.0
(15)
|
52.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 2-3 |
somatosensory cortex layer 2/3 regular-spiking pyramidal neuron
|
adaptation percent (1 – first/last ISI) |
Threshold firing frequency-current relationships of neurons in rat somatosensory cortex: type 1 and type 2 dynamics.
(NeuroElectro data)
(PubMed)
|
71.4
± 4.2
(20)
|
71.4 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
sensorimotor cortex pyramidal cell
|
adaptation percent (1 – first/last ISI) |
Molecular and physiological diversity of cortical nonpyramidal cells.
(NeuroElectro data)
(PubMed)
|
66.2
± 7.1
(29)
|
66.2 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory cortex small amplitude pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
20.3
± 4.8
(10)
|
20.3 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 corticocortical pyramidal cell
|
adaptation percent (1 – first/last ISI) |
Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics.
(NeuroElectro data)
(PubMed)
|
40.2
± 3.9
(8)
|
40.2 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 5 sensorimotor cortex pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
59.5
± 9.4
(33)
|
59.5 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 thick tufted pyramidal cell projecting to superior colliculus
|
adaptation percent (1 – first/last ISI) |
Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics.
(NeuroElectro data)
(PubMed)
|
32.8
± 4.1
(8)
|
32.8 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 corticocortical pyramidal cell
|
adaptation percent (1 – first/last ISI) |
Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics.
(NeuroElectro data)
(PubMed)
|
77.3
± 2.2
(7)
|
77.3 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory barrel cortex pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Effect of common anesthetics on dendritic properties in layer 5 neocortical pyramidal neurons.
(NeuroElectro data)
(PubMed)
|
24.2
± 5.6
(27)
|
24.2 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
visual cortex layer 5 thick tufted pyramidal cell projecting to superior colliculus
|
adaptation percent (1 – first/last ISI) |
Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics.
(NeuroElectro data)
(PubMed)
|
76.7
± 1.6
(8)
|
76.7 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
somatosensory cortex layer 5a corticostriatal Etv1-expressing slender-tufted pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
76.0
± 2.0
(21)
|
76.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Somatosensory cortex layer 5b Glt25d2-expressing thick-tufted pyramidal neurons
|
adaptation percent (1 – first/last ISI) |
Electrophysiological properties of genetically identified subtypes of layer 5 neocortical pyramidal neurons: Ca²⁺ dependence and differential modulation by norepinephrine.
(NeuroElectro data)
(PubMed)
|
17.0
± 2.0
(27)
|
17.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Motor cortex layer 5 glutamatergic excitatory pyramidal neurons synapsing onto motor cortex layer 5 fast-spiking interneurons
|
adaptation percent (1 – first/last ISI) |
Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection.
(NeuroElectro data)
(PubMed)
|
15.0
± 15.0
(36)
|
15.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 5 somatosensory cortex large amplitude pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Differential effects of Na+-K+ ATPase blockade on cortical layer V neurons.
(NeuroElectro data)
(PubMed)
|
18.5
± 3.1
(9)
|
18.5 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Motor cortex layer 5 glutamatergic excitatory pyramidal neurons synapsing onto motor cortex layer 5 fast-spiking interneurons
|
adaptation percent (1 – first/last ISI) |
Developmental synaptic changes increase the range of integrative capabilities of an identified excitatory neocortical connection.
(NeuroElectro data)
(PubMed)
|
12.0
± 13.0
(20)
|
12.0 (ratio)
|
Data Table |
| Neocortex pyramidal cell layer 5-6 |
Layer 6 sensorimotor cortex nonpyramidal VGluT1 expressing neurons
|
adaptation percent (1 – first/last ISI) |
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons.
(NeuroElectro data)
(PubMed)
|
48.7
± 12.6
(71)
|
48.7 (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 |
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 |
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 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 |
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 |
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 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 |
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 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 |
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 |
| Nucleus of the solitary tract principal cell |
Ventrolateral Nucleus Tractus Solitarii 4-AP-/TEA-responsive cell
|
adaptation percent (1 – first/last ISI) |
Localization and function of the Kv3.1b subunit in the rat medulla oblongata: focus on the nucleus tractus solitarii.
(NeuroElectro data)
(PubMed)
|
32.4
± 3.3
(81)
|
32.4 (ratio)
|
Data Table |
| Nucleus of the solitary tract principal cell |
Comissural Nucleus Tractus Solitarii 4-AP-/TEA-unresponsive commissural cell
|
adaptation percent (1 – first/last ISI) |
Localization and function of the Kv3.1b subunit in the rat medulla oblongata: focus on the nucleus tractus solitarii.
(NeuroElectro data)
(PubMed)
|
39.0
± 5.3
(16)
|
39.0 (ratio)
|
Data Table |
| Other |
Corpus callosum white matter interstitial non-adapting interneurons projecting to lower subcortical layers
|
adaptation percent (1 – first/last ISI) |
5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks.
(NeuroElectro data)
(PubMed)
|
30.0
± 7.0
(7)
|
30.0 (ratio)
|
Data Table |
| Other |
medial septal/diagonal band complex type I burst-firing neurons
|
adaptation percent (1 – first/last ISI) |
Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex.
(NeuroElectro data)
(PubMed)
|
54.8
± 39.1
(7)
|
54.8 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus large round-ovoid polymorphic cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
15.4
± 4.4
(7)
|
15.4 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence deep and superficial layer irregular intrinsic bursting interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
41.7
(9)
|
41.7 (ratio)
|
Data Table |
| Other |
corpus callosum white matter interstitial non-adapting bursting interneuron projecting to lower subcortical layers
|
adaptation percent (1 – first/last ISI) |
5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks.
(NeuroElectro data)
(PubMed)
|
70.0
± 11.0
(18)
|
70.0 (ratio)
|
Data Table |
| Other |
medial septal/diagonal band complex fast spiking GABAergic neurons projecting to fornix
|
adaptation percent (1 – first/last ISI) |
Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex.
(NeuroElectro data)
(PubMed)
|
52.3
± 20.4
(20)
|
52.3 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus silent cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
22.9
± 4.3
(31)
|
22.9 (ratio)
|
Data Table |
| Other |
Stratum radiatum fast-spiking interneurons
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
26.0
± 10.0
(5)
|
26.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence non-fast spiking 1 interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
36.2
(16)
|
36.2 (ratio)
|
Data Table |
| Other |
Corpus callosum white matter interstitial adapting interneurons projecting to lower subcortical layers
|
adaptation percent (1 – first/last ISI) |
5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks.
(NeuroElectro data)
(PubMed)
|
47.0
± 5.0
(4)
|
47.0 (ratio)
|
Data Table |
| Other |
neocortex layer 2/3 GABAergic late-spiking subtype 2 Htr3a-expressing interneuron
|
adaptation percent (1 – first/last ISI) |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
53.9
± 16.3
(15)
|
53.9 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus thick spiny bipolar vertical cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
21.5
± 3.3
(7)
|
21.5 (ratio)
|
Data Table |
| Other |
medial septal/diagonal band complex type II burst-firing neurons projecting to fornix
|
adaptation percent (1 – first/last ISI) |
Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex.
(NeuroElectro data)
(PubMed)
|
66.1
± 16.2
(8)
|
66.1 (ratio)
|
Data Table |
| Other |
somatosensory cortex CGE-derived burst non-adapting 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)
|
72.2
± 10.6
(6)
|
72.2 (ratio)
|
Data Table |
| Other |
Stratum radiatum non-pyramidal regular-spiking non-rebounding cells
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
41.0
± 11.0
|
41.0 (ratio)
|
Data Table |
| Other |
neocortex layer 2/3 GABAergic burst non-adapting 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)
|
63.7
± 18.2
(18)
|
63.7 (ratio)
|
Data Table |
| Other |
Stratum radiatum non-pyramidal regular-spiking rapidly adapting cells
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
71.0
± 13.0
|
71.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence superficial layer delayed-fast spiking Interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
15.5
(25)
|
15.5 (ratio)
|
Data Table |
| Other |
medial septum diagonal band of Broca fast firing large sag VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
15.4
± 6.2
(12)
|
15.4 (ratio)
|
Data Table |
| Other |
neocortex layer 2/3 GABAergic burst non-adapting subtype 2 Htr3a-expressing interneuron
|
adaptation percent (1 – first/last ISI) |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
59.4
± 21.4
(5)
|
59.4 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus dense arbor neurogliaform cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
21.8
± 8.1
(3)
|
21.8 (ratio)
|
Data Table |
| Other |
Neocortex Layer 2-3 Regular-Spiking Non-Pyramidal Interneuron
|
adaptation percent (1 – first/last ISI) |
Lack of depolarization-induced suppression of inhibition (DSI) in layer 2/3 interneurons that receive cannabinoid-sensitive inhibitory inputs.
(NeuroElectro data)
(PubMed)
|
55.0
± 5.8
(14)
|
55.0 (ratio)
|
Data Table |
| Other |
Stratum radiatum delayed spiking interneurons
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
34.0
± 13.0
|
34.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence deep and superficial layer regular intrinsic bursting Interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
44.4
(17)
|
44.4 (ratio)
|
Data Table |
| Other |
medial septum diagonal band of Broca fast firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
13.4
± 3.8
(19)
|
13.4 (ratio)
|
Data Table |
| Other |
neocortex layer 2/3 GABAergic irregular spiking bipolar Htr3a-expressing interneuron
|
adaptation percent (1 – first/last ISI) |
The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors.
(NeuroElectro data)
(PubMed)
|
41.5
± 11.6
(30)
|
41.5 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus bursting cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
32.2
± 4.3
(3)
|
32.2 (ratio)
|
Data Table |
| Other |
Stratum radiatum non-pyramidal regular-spiking rebounding cells
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
41.0
± 27.0
|
41.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence non-fast spiking 2 interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
33.1
(6)
|
33.1 (ratio)
|
Data Table |
| Other |
medial septum diagonal band of Broca burst firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
37.3
± 9.1
(11)
|
37.3 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus aspiny spherical cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
23.5
± 4.9
(31)
|
23.5 (ratio)
|
Data Table |
| Other |
Stratum radiatum irregularly spiking interneurons
|
adaptation percent (1 – first/last ISI) |
NMDA receptor-dependent long-term potentiation in mouse hippocampal interneurons shows a unique dependence on Ca(2+)/calmodulin-dependent kinases.
(NeuroElectro data)
(PubMed)
|
80.0
|
80.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence delayed non-fast spiking 1 interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
29.5
(11)
|
29.5 (ratio)
|
Data Table |
| Other |
medial septum diagonal band of Broca cluster firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
51.8
± 10.4
(13)
|
51.8 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus aspiny spindle-shaped horizontal fusiform cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
30.4
± 4.5
(17)
|
30.4 (ratio)
|
Data Table |
| Other |
somatosensory cortex layer 2/3 fast-spiking inhibitory interneuron
|
adaptation percent (1 – first/last ISI) |
Threshold firing frequency-current relationships of neurons in rat somatosensory cortex: type 1 and type 2 dynamics.
(NeuroElectro data)
(PubMed)
|
56.2
± 6.7
(23)
|
56.2 (ratio)
|
Data Table |
| Other |
Hippocampus CA1 trilaminar fast spiking interneuron
|
adaptation percent (1 – first/last ISI) |
Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation.
(NeuroElectro data)
(PubMed)
|
18.0
± 4.0
(21)
|
18.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence non-fast spiking 2 interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
32.1
(17)
|
32.1 (ratio)
|
Data Table |
| Other |
medial septum diagonal band of Broca slow firing VGLUT2-expressing neurons projecting to CA3 Hippocampal pyramidal cells
|
adaptation percent (1 – first/last ISI) |
Glutamatergic neurons of the mouse medial septum and diagonal band of Broca synaptically drive hippocampal pyramidal cells: relevance for hippocampal theta rhythm.
(NeuroElectro data)
(PubMed)
|
27.3
± 12.4
(11)
|
27.3 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus tonic irregular-spiking
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
18.7
± 4.1
(8)
|
18.7 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence initial adapting interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
45.1
(7)
|
45.1 (ratio)
|
Data Table |
| Other |
medial septal/diagonal band complex slow firing cholinergic neurons projecting to fornix
|
adaptation percent (1 – first/last ISI) |
Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex.
(NeuroElectro data)
(PubMed)
|
64.2
± 30.0
(10)
|
64.2 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus aspiny spindle-shaped vertical fusiform cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
24.7
± 4.8
(9)
|
24.7 (ratio)
|
Data Table |
| Other |
Corpus callosum white matter interstitial adapting bursting interneurons projecting to lower subcortical layers
|
adaptation percent (1 – first/last ISI) |
5-HT(3A) receptor-bearing white matter interstitial GABAergic interneurons are functionally integrated into cortical and subcortical networks.
(NeuroElectro data)
(PubMed)
|
77.0
± 11.0
(5)
|
77.0 (ratio)
|
Data Table |
| Other |
Neocortex medial ganglionic eminence superficial layer late spiking interneuron
|
adaptation percent (1 – first/last ISI) |
Physiologically distinct temporal cohorts of cortical interneurons arise from telencephalic Olig2-expressing precursors.
(NeuroElectro data)
(PubMed)
|
33.4
(17)
|
33.4 (ratio)
|
Data Table |
| Other |
medial septal/diagonal band complex regular spiking neurons projecting to fornix
|
adaptation percent (1 – first/last ISI) |
Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex.
(NeuroElectro data)
(PubMed)
|
68.9
± 18.42
(24)
|
68.9 (ratio)
|
Data Table |
| Other |
lateral habenular nucleus tonic regular-spiking cell
|
adaptation percent (1 – first/last ISI) |
Morphological and electrophysiological characteristics of neurons within identified subnuclei of the lateral habenula in rat brain slices.
(NeuroElectro data)
(PubMed)
|
24.4
± 3.3
(32)
|
24.4 (ratio)
|
Data Table |
