(Q78757338)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

title

High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spot (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1

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16 December 2019

author name string

Michelle Trudeau

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

Alfred L George

3

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16 December 2019

Leslie K Sprunger

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

Miriam H Meisler

5

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16 December 2019

publication date

1 October 2003

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

volume

82

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

issue

4

1 reference

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16 December 2019

page(s)

452-459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

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

16 December 2019

cites work

1 reference

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7 January 2021

Ion channel mutations in mouse models of inherited neurological disease

1 reference

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7 January 2021

Evolution and diversity of mammalian sodium channel genes

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7 January 2021

Resurgence of sodium channel research

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7 January 2021

A novel, abundant sodium channel expressed in neurons and glia

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7 January 2021

Sodium channels and neurological disease: insights from Scn8a mutations in the mouse

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7 January 2021

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

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

D1/D5 dopamine receptor activation differentially modulates rapidly inactivating and persistent sodium currents in prefrontal cortex pyramidal neurons.

1 reference

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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

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7 January 2021

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

1 reference

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7 January 2021

VISTA : visualizing global DNA sequence alignments of arbitrary length

1 reference

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7 January 2021

A physical map of the mouse genome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

TSRC1, a widely expressed gene containing seven thrombospondin type I repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Initial sequencing and comparative analysis of the mouse genome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

The comprehensive mouse radiation hybrid map densely cross-referenced to the recombination map: a tool to support the sequence assemblies

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Meiotic recombination hot spots and cold spots

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Control of meiotic recombination initiation: a role for the environment?

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

The mosaic structure of variation in the laboratory mouse genome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

The human gene mutation database

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Splicing regulation as a potential genetic modifier

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Recombinational hotspot specific to female meiosis in the mouse major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

An initiation site for meiotic crossing-over and gene conversion in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Molecular characterization of the Pb recombination hotspot in the mouse major histocompatibility complex class II region

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900152-6

7 January 2021

10.1016/S0888-7543(03)00152-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13679025%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference