(Q34388928)

English

Multiple transcripts of sodium channel SCN8A (Na(V)1.6) with alternative 5'- and 3'-untranslated regions and initial characterization of the SCN8A promoter

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Multiple transcripts of sodium channel SCN8A (Na(V)1.6) with alternative 5'- and 3'-untranslated regions and initial characterization of the SCN8A promoter (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Valerie L Drews

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Andrew P Lieberman

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

Miriam H Meisler

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 February 2005

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Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

85

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Europe PubMed Central

PubMed publication ID

1 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

245-257

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

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De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

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

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

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Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3

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Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).

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SCNM1, a putative RNA splicing factor that modifies disease severity in mice

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Overview of the voltage-gated sodium channel family

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A novel, abundant sodium channel expressed in neurons and glia

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Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses

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

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Changes of sodium channel expression in experimental painful diabetic neuropathy

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Abnormal sodium channel distribution in optic nerve axons in a model of inflammatory demyelination

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

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Identifying the promoter region of the human brain sodium channel subtype II gene (SCN2A)

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Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus

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Isolation of the 5'-flanking region for human brain sodium channel subtype II alpha-subunit

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

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AVID: A global alignment program

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

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Molecular cloning, distribution and functional analysis of the NA(V)1.6. Voltage-gated sodium channel from human brain

1 reference

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Evolution and divergence of sodium channel genes in vertebrates.

1 reference

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Evolutionary parameters of the transcribed mammalian genome: an analysis of 2,820 orthologous rodent and human sequences

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Initial sequencing and comparative analysis of the mouse genome

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Generality of a functional initiator consensus sequence

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Transcriptional Activation of the Human Brain-derived Neurotrophic Factor Gene Promoter III by Dopamine Signaling in NT2/N Neurons

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Translational control by CPEB: a means to the end

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CPEB-mediated cytoplasmic polyadenylation and the regulation of experience-dependent translation of alpha-CaMKII mRNA at synapses

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Facilitation of dendritic mRNA transport by CPEB

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Identification of a Coordinate Regulator of Interleukins 4, 13, and 5 by Cross-Species Sequence Comparisons

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Human and mouse ABCA1 comparative sequencing and transgenesis studies revealing novel regulatory sequences

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A combinatorial network of evolutionarily conserved myelin basic protein regulatory sequences confers distinct glial-specific phenotypes

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REST: a mammalian silencer protein that restricts sodium channel gene expression to neurons

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10.1016/J.YGENO.2004.09.002

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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