Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

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P1476

Kv1.2 Channels Promote Nonlinear Spiking Motoneurons for Powering Up Locomotion.

@en

P2093

Cécile Brocard

http://www.w3.org/2001/XMLSchema#string

Frédéric Brocard

http://www.w3.org/2001/XMLSchema#string

Liliia E Demianenko

http://www.w3.org/2001/XMLSchema#string

Marin Manuel

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Ronald M Harris-Warrick

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Sergiy M Korogod

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P2860

Subunit composition and novel localization of K+ channels in spinal cord

Tityustoxin-K alpha, a structurally novel and highly potent K+ channel peptide toxin, interacts with the alpha-dendrotoxin binding site on the cloned Kv1.2 K+ channel

The Inhibitory Effects of Ca2+ Channel Blocker Nifedipine on Rat Kv2.1 Potassium Channels

Focal aggregation of voltage-gated, Kv2.1 subunit-containing, potassium channels at synaptic sites in rat spinal motoneurones

Molecular diversity of K+ channels.

Characterization of the axon initial segment (AIS) of motor neurons and identification of a para-AIS and a juxtapara-AIS, organized by protein 4.1B.

Novel tarantula toxins for subtypes of voltage-dependent potassium channels in the Kv2 and Kv4 subfamilies.

A new Kv1.2 channelopathy underlying cerebellar ataxia.

Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

P304

3315-3327

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P31

scholarly article

P356

10.1016/J.CELREP.2018.02.093

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Daniel Zytnicki

Rémi Bos

P577

2018-03-01T00:00:00Z

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P698

29562186

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P932

5907934

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