Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A (Q22008052)

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6 December 2019

title

Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A (English)

1 reference

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Sodium voltage-gated channel alpha subunit 8

6 December 2019

main subject

1 reference

Sodium channel, voltage-gated, type VIII, alpha

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1

N W Plummer

N W

Plummer

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6 December 2019

Galt J

2

J

Galt

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6 December 2019

Jones JM

3

J M

Jones

1 reference

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6 December 2019

Burgess DL

4

D L

Burgess

1 reference

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6 December 2019

Sprunger LK

5

L K

Sprunger

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6 December 2019

Kohrman DC

6

D C

Kohrman

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6 December 2019

Meisler MH

7

M H

Meisler

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6 December 2019

language of work or name

English

0 references

publication date

1 December 1998

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6 December 2019

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6 December 2019

volume

54

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6 December 2019

issue

2

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6 December 2019

page(s)

287-296

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The neuronal voltage-gated sodium channel, Scn8a, is essential for postnatal maturation of spinal, but not oculomotor, motor units

6 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Genomic organization of the human skeletal muscle sodium channel gene

1 reference

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7 January 2021

Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse

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7 January 2021

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Cloning and characterization of a mouse sensory neuron tetrodotoxin-resistant voltage-gated sodium channel gene, Scn10a

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic

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7 January 2021

Interpreting cDNA sequences: some insights from studies on translation

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7 January 2021

Neuromuscular transmission in the murine mutants "motor end-plate disease" and "jolting"

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7 January 2021

Cerebellar structure and function in the murine mutant "jolting".

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7 January 2021

Three new developments in P1 cloning. Increased cloning efficiency, improved clone recovery, and a new P1 mouse library

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Classification of introns: U2-type or U12-type

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Ataxia, arrhythmia and ion-channel gene defects

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7 January 2021

Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): different expression patterns in developing rat nervous system.

1 reference

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7 January 2021

Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice.

1 reference

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7 January 2021

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Terminal intron dinucleotide sequences do not distinguish between U2- and U12-dependent introns

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Functional analysis of a voltage-gated sodium channel and its splice variant from rat dorsal root ganglia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Cloning of a sodium channel alpha subunit from rabbit Schwann cells.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

cAMP-dependent phosphorylation of two sites in the alpha subunit of the cardiac sodium channel.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Marshall syndrome associated with a splicing defect at the COL11A1 locus

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

The genomic structure of the human skeletal muscle sodium channel gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Phenotype variation and newcomers in ion channel disorders

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Developmentally regulated alternative RNA splicing of rat brain sodium channel mRNAs

1 reference

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7 January 2021

The long QT syndrome. A review of recent molecular genetic and physiologic discoveries

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7 January 2021

Electrophysiological and morphological studies of a motor nerve in 'motor endplate disease' of the mouse

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Electrophysiological studies of neuromuscular transmission in hereditary 'motor end-plate disease' of the mouse.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Modulation of the human cardiac sodium channel alpha-subunit by cAMP-dependent protein kinase and the responsible sequence domain.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Structure and function of voltage-sensitive ion channels

1 reference

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7 January 2021

Structure and function of voltage-gated ion channels

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Expression of diverse Na+ channel messenger RNAs in rat myocardium. Evidence for a cardiac-specific Na+ channel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

A novel, abundant sodium channel expressed in neurons and glia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Phosphorylation of brain sodium channels in the I--II linker modulates channel function in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Functional analysis of the mouse Scn8a sodium channel.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Ion channel mutations in mouse models of inherited neurological disease

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5550

7 January 2021

Identifiers

DOI

10.1006/GENO.1998.5550

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9828131%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference