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A novel gene causing a mendelian audiogenic mouse epilepsy
scientific journal article
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scholarly article
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stated in
PubMed
PubMed ID
11545713
retrieved
24 January 2017
title
A novel gene causing a mendelian audiogenic mouse epilepsy
(English)
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stated in
PubMed
PubMed ID
11545713
retrieved
24 January 2017
main subject
Adhesion G protein-coupled receptor V1
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GOA release 2020-03-11
author name string
S. L. Skradski
series ordinal
1
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PubMed
PubMed ID
11545713
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24 January 2017
A. M. Clark
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2
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PubMed
PubMed ID
11545713
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24 January 2017
H. Jiang
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3
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PubMed
PubMed ID
11545713
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24 January 2017
H. S. White
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4
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PubMed
PubMed ID
11545713
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24 January 2017
Y. H. Fu
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5
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PubMed
PubMed ID
11545713
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24 January 2017
L. J. Ptácek
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6
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PubMed
PubMed ID
11545713
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24 January 2017
language of work or name
English
0 references
publication date
30 August 2001
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PubMed
PubMed ID
11545713
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24 January 2017
published in
Neuron
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stated in
PubMed
PubMed ID
11545713
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24 January 2017
volume
31
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PubMed
PubMed ID
11545713
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24 January 2017
page(s)
537–544
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PubMed
PubMed ID
11545713
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24 January 2017
issue
4
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PubMed
PubMed ID
11545713
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24 January 2017
cites work
The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake
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A potassium channel mutation in neonatal human epilepsy
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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7 January 2021
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Sound-induced seizures in serotonin 5-HT2c receptor mutant mice
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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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Aggression in mice selectively bred for brain weight
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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
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Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia
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Absence epilepsy in tottering mutant mice is associated with calcium channel defects
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Aceruloplasminemia: molecular characterization of this disorder of iron metabolism
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Audiogenic Seizure Susceptibility Induced in C57B1/6J Mice by Prior Auditory Exposure
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.
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The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
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Regulation of the cardiac Na(+)-Ca2+ exchanger by Ca2+. Mutational analysis of the Ca(2+)-binding domain
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Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.
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Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.
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Genetic dissection of susceptibility to audiogenic seizures in inbred mice
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Mutagenesis studies of the cardiac Na(+)-Ca2+ exchanger
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Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain
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7 January 2021
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Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24
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Identification of a mutation in the gene causing hyperkalemic periodic paralysis
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Anatomical and behavioral analyses of the inheritance of audiogenic seizures in the progeny of genetically epilepsy-prone and Sprague-Dawley rats.
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7 January 2021
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Development of susceptibility to audiogenic seizures in DBA/2J and Rb mice: toward a systematic nomenclature of audiogenic seizure levels.
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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7 January 2021
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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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7 January 2021
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Genetic mapping of a locus (mass1) causing audiogenic seizures in mice
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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7 January 2021
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Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies
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Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors
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Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
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Radicals r'aging
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An X-ray crystallographic study of the binding sites of the azide inhibitor and organic substrates to ceruloplasmin, a multi-copper oxidase in the plasma
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7 January 2021
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Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses
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https://api.crossref.org/works/10.1016%2FS0896-6273%2801%2900397-X
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7 January 2021
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Identifiers
DOI
10.1016/S0896-6273(01)00397-X
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PubMed ID
11545713
1 reference
stated in
PubMed
PubMed ID
11545713
retrieved
24 January 2017
ResearchGate publication ID
11800997
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