(Q48404454)

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20 December 2019

title

Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures (English)

1 reference

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20 December 2019

1

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20 December 2019

Massimo Mantegazza

7

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20 December 2019

Federico Zara

4

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20 December 2019

author name string

Raffaella Rusconi

2

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20 December 2019

Elena Armatura

3

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20 December 2019

Giuliano Avanzini

5

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20 December 2019

Silvana Franceschetti

6

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20 December 2019

language of work or name

English

0 references

publication date

1 October 2006

1 reference

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20 December 2019

published in

Journal of Neuroscience

1 reference

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20 December 2019

volume

26

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20 December 2019

issue

40

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20 December 2019

page(s)

10100-10109

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The Na channel voltage sensor associated with inactivation is localized to the external charged residues of domain IV, S4.

20 December 2019

cites work

1 reference

12 December 2020

Type I and type II Na(+) channel alpha-subunit polypeptides exhibit distinct spatial and temporal patterning, and association with auxiliary subunits in rat brain.

1 reference

12 December 2020

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

1 reference

12 December 2020

The voltage sensor in voltage-dependent ion channels

1 reference

12 December 2020

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

1 reference

12 December 2020

Classification of fusiform neocortical interneurons based on unsupervised clustering

1 reference

12 December 2020

Cloning, distribution and functional analysis of the type III sodium channel from human brain

1 reference

12 December 2020

Resurgence of sodium channel research

1 reference

12 December 2020

Comparative distribution of voltage-gated sodium channel proteins in human brain

1 reference

12 December 2020

Differential control of clustering of the sodium channels Na(v)1.2 and Na(v)1.6 at developing CNS nodes of Ranvier

1 reference

12 December 2020

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

1 reference

12 December 2020

Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons.

1 reference

12 December 2020

Neutralization of gating charges in domain II of the sodium channel alpha subunit enhances voltage-sensor trapping by a beta-scorpion toxin

1 reference

12 December 2020

Movement and crevices around a sodium channel S3 segment

1 reference

12 December 2020

Sodium-channel defects in benign familial neonatal-infantile seizures

1 reference

12 December 2020

Cellular biology of epileptogenesis

1 reference

12 December 2020

The biology of epilepsy genes

1 reference

12 December 2020

Coupling interactions between voltage sensors of the sodium channel as revealed by site-specific measurements

1 reference

12 December 2020

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline

1 reference

12 December 2020

A study of spike-density on EEG in West syndrome

1 reference

12 December 2020

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy

1 reference

12 December 2020

Seizure phenotypes of a family with missense mutations in SCN2A

1 reference

12 December 2020

Molecular determinants for modulation of persistent sodium current by G-protein betagamma subunits.

1 reference

12 December 2020

Voltage sensor of Kv1.2: structural basis of electromechanical coupling

1 reference

12 December 2020

Beta-scorpion toxin effects suggest electrostatic interactions in domain II of voltage-dependent sodium channels.

1 reference

12 December 2020

Inherited disorders of voltage-gated sodium channels

1 reference

12 December 2020

Sodium channel mutations in epilepsy and other neurological disorders

1 reference

12 December 2020

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

1 reference

12 December 2020

International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels

1 reference

12 December 2020

A novel SCN2A mutation in family with benign familial infantile seizures

1 reference

12 December 2020

GABA: an excitatory transmitter in early postnatal life

1 reference

12 December 2020

Structural parts involved in activation and inactivation of the sodium channel

1 reference

12 December 2020

Differential subcellular localization of the RI and RII Na+ channel subtypes in central neurons

1 reference

12 December 2020

Benign familial neonatal-infantile seizures

1 reference

12 December 2020

Mutation of conserved negatively charged residues in the S2 and S3 transmembrane segments of a mammalian K+ channel selectively modulates channel gating

1 reference

12 December 2020

Electrostatic interactions of S4 voltage sensor in Shaker K+ channel

1 reference

12 December 2020

Evidence of a third locus for benign familial convulsions

1 reference

12 December 2020

A unique role for the S4 segment of domain 4 in the inactivation of sodium channels

1 reference

12 December 2020

Interaction between the sodium channel inactivation linker and domain III S4-S5.

1 reference

12 December 2020

Sodium channel activation gating is affected by substitutions of voltage sensor positive charges in all four domains

1 reference

12 December 2020

Sodium channel inactivation is altered by substitution of voltage sensor positive charges

1 reference

12 December 2020

Anemone toxin (ATX II)-induced increase in persistent sodium current: effects on the firing properties of rat neocortical pyramidal neurones.

1 reference

12 December 2020

10.1523/JNEUROSCI.2476-06.2006

Identifiers

DOI

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20 December 2019

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20 December 2019

1 reference