Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
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Molecular targets for antiepileptic drug developmentPotassium Channels and Human Epileptic Phenotypes: An Updated OverviewNew Insights on Astrocyte Ion Channels: Critical for Homeostasis and Neuron-Glia SignalingCommon variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsiesK(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.Mouse SNP Miner: an annotated database of mouse functional single nucleotide polymorphisms.Dissection of a QTL hotspot on mouse distal chromosome 1 that modulates neurobehavioral phenotypes and gene expression.The genetics of status epilepticus.Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice.Molecular mechanisms of EAST/SeSAME syndrome mutations in Kir4.1 (KCNJ10)Susceptibility to seizure-induced excitotoxic cell death is regulated by an epistatic interaction between Chr 18 (Sicd1) and Chr 15 (Sicd2) loci in mice.Systems genetics of the lateral septal nucleus in mouse: heritability, genetic control, and covariation with behavioral and morphological traits.Congenic strains provide evidence that a mapped locus on chromosome 15 influences excitotoxic cell deathChronic dysfunction of astrocytic inwardly rectifying K+ channels specific to the neocortical epileptic focus after fluid percussion injury in the ratA novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice.Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueductsFinding the molecular basis of complex genetic variation in humans and miceSegregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl modelMouse ERG K(+) channel clones reveal differences in protein trafficking and function.The relevance of individual genetic background and its role in animal models of epilepsyPotassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice.Strain differences in seizure-induced cell death following pilocarpine-induced status epilepticus.Regulation of magnesium balance: lessons learned from human genetic diseaseMapping a mouse limbic seizure susceptibility locus on chromosome 10Molecular genetic analysis of two loci (Ity2 and Ity3) involved in the host response to infection with Salmonella typhimurium using congenic mice and expression profilingThe role of astroglia in the epileptic brain.Sodium channel mutations in epilepsy and other neurological disorders.Challenges and opportunities in the application of pharmacogenetics to antiepileptic drug therapy.Gene profiling in temporal lobe epilepsy tissue and dysplastic lesions.Gene expression, genetics, and genomics in epilepsy: some answers, more questions.Chemoconvulsant-induced seizure susceptibility: toward a common genetic basis?Functional implications for Kir4.1 channels in glial biology: from K+ buffering to cell differentiationUse of chromosome substitution strains to identify seizure susceptibility loci in mice.Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesisLinkage and linkage disequilibrium scan for autism loci in an extended pedigree from FinlandEpilepsy in kcnj10 morphant zebrafish assessed with a novel method for long-term EEG recordings.Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats.A large QTL for fear and anxiety mapped using an F2 cross can be dissected into multiple smaller QTLs.A locus on mouse Ch10 influences susceptibility to limbic seizure severity: fine mapping and in silico candidate gene analysis.
P2860
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P2860
Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@en
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@nl
type
label
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@en
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@nl
prefLabel
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@en
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@nl
P2093
P1433
P1476
Fine mapping of a seizure susc ...... of Kcnj10 as a causative gene.
@en
P2093
Candice L Schwebel
Danielle M Press
Deborah Zamboni
Falk W Lohoff
George G Smith
Gregory T Golden
Hongyu Zhao
James F Martin
Russell J Buono
Stephanie O Kratzer
P2888
P304
P356
10.1007/S00335-003-2270-3
P577
2004-04-01T00:00:00Z