Complex seizure disorder caused by Brunol4 deficiency in mice. - Wikidata - awgldk - TriplyDB

Complex seizure disorder caused by Brunol4 deficiency in mice.

Complex seizure disorder caused by Brunol4 deficiency in mice.

http://www.wikidata.org/entity/Q33293169

about

CELF family RNA-binding protein UNC-75 regulates two sets of mutually exclusive exons of the unc-32 gene in neuron-specific manners in Caenorhabditis elegans MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1 RNA-binding proteins, neural development and the addictions The importance of CELF control: molecular and biological roles of the CUG-BP, Elav-like family of RNA-binding proteins Complex network analysis of CA3 transcriptome reveals pathogenic and compensatory pathways in refractory temporal lobe epilepsy A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice Bruno Protein Contains an Expanded RNA Recognition Motif Etiology of a genetically complex seizure disorder in Celf4 mutant mice Szt2, a novel gene for seizure threshold in mice Elevated Id2 expression results in precocious neural stem cell depletion and abnormal brain development.Hidden in plain sight: spike-wave discharges in mouse inbred strains.Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function.Genome-wide prediction and analysis of human tissue-selective genes using microarray expression data The role of CELF proteins in neurological disorders.The relevance of individual genetic background and its role in animal models of epilepsy Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity.CELFish ways to modulate mRNA decay.CUG-BP, Elav-like family (CELF)-mediated alternative splicing regulation in the brain during health and disease.A targeted deleterious allele of the splicing factor SCNM1 in the mouse.CELF RNA binding proteins promote axon regeneration in C. elegans and mammals through alternative splicing of Syntaxins.Diverse molecular functions of Hu proteins.Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats.Epigenetic mechanisms underlying human epileptic disorders and the process of epileptogenesis.Position-dependent and neuron-specific splicing regulation by the CELF family RNA-binding protein UNC-75 in Caenorhabditis elegans.Models and detection of spontaneous recurrent seizures in laboratory rodents.Quantitative Nucleotide Level Analysis of Regulation of Translation in Response to Depolarization of Cultured Neural Cells.Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice.

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P2860

Complex seizure disorder caused by Brunol4 deficiency in mice.

http://www.wikidata.org/entity/Q33293169

description

2007 nî lūn-bûn

@nan

2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հուլիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

@zh-hant

2007年論文

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2007年論文

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2007年論文

@zh-tw

2007年论文

@wuu

name

Complex seizure disorder caused by Brunol4 deficiency in mice.

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Complex seizure disorder caused by Brunol4 deficiency in mice.

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type

label

Complex seizure disorder caused by Brunol4 deficiency in mice.

@ast

Complex seizure disorder caused by Brunol4 deficiency in mice.

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prefLabel

Complex seizure disorder caused by Brunol4 deficiency in mice.

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Complex seizure disorder caused by Brunol4 deficiency in mice.

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Complex seizure disorder caused by Brunol4 deficiency in mice.

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Connie L Mahaffey

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Gregory A Cox

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Nathalie Bérubé

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Terry P Maddatu

http://www.w3.org/2001/XMLSchema#string

Wayne N Frankel

http://www.w3.org/2001/XMLSchema#string

Yan Yang

http://www.w3.org/2001/XMLSchema#string

P2860

CELF6, a member of the CELF family of RNA-binding proteins, regulates muscle-specific splicing enhancer-dependent alternative splicing

ETR-3 and CELF4 protein domains required for RNA binding and splicing activity in vivo

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Genome-wide atlas of gene expression in the adult mouse brain

Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors

Novel role for RNA-binding protein CUGBP2 in mammalian RNA editing. CUGBP2 modulates C to U editing of apolipoprotein B mRNA by interacting with apobec-1 and ACF, the apobec-1 complementation factor

Coupled mRNA stabilization and translational silencing of cyclooxygenase-2 by a novel RNA binding protein, CUGBP2

Mutations in EFHC1 cause juvenile myoclonic epilepsy

A novel gene causing a mendelian audiogenic mouse epilepsy

Inactivation of CUG-BP1/CELF1 causes growth, viability, and spermatogenesis defects in mice

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10.1371/JOURNAL.PGEN.0030124

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7

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17677002

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1934399

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