Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
about
Alterations of GABAergic signaling in autism spectrum disordersIdentification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13General anaesthetic actions on ligand-gated ion channelsGabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorderSox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal deathDynamic expression of a glutamate decarboxylase gene in multiple non-neural tissues during mouse developmentHomozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disordersClinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.Molecular basis of cleft palates in miceBehavioral and Neuroanatomical Phenotypes in Mouse Models of AutismAltered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.Epileptic encephalopathy de novo GABRB mutations impair GABAA receptor functionIncreased expression of GABA(A) receptor beta-subunits in the hippocampus of patients with temporal lobe epilepsyImmunologic and neurodevelopmental susceptibilities of autismLetting a typical mouse judge whether mouse social interactions are atypicalUsing mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsTranslational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Functional role of GABAergic innervation of the cochlea: phenotypic analysis of mice lacking GABA(A) receptor subunits alpha 1, alpha 2, alpha 5, alpha 6, beta 2, beta 3, or delta.Targeted disruption of the GABA(A) receptor delta subunit gene leads to an up-regulation of gamma 2 subunit-containing receptors in cerebellar granule cellsColocalization of multiple GABA(A) receptor subtypes with gephyrin at postsynaptic sitesGABAergic neurons regulate lateral ventricular development via transcription factor Pax5Altered GABAA,slow inhibition and network oscillations in mice lacking the GABAA receptor beta3 subunitPrioritizing the development of mouse models for childhood brain disordersStem cells and modeling of autism spectrum disorders.Somatosensory and sensorimotor consequences associated with the heterozygous disruption of the autism candidate gene, Gabrb3.Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.GABAB receptors role in cell migration and positioning within the ventromedial nucleus of the hypothalamus.Reduced conditioned fear response in mice that lack Dlx1 and show subtype-specific loss of interneuronsStress-hyperresponsive WKY rats demonstrate depressed dorsal raphe neuronal excitability and dysregulated CRF-mediated responses.New insight into the role of the beta3 subunit of the GABAA-R in development, behavior, body weight regulation, and anesthesia revealed by conditional gene knockout.Ion channels and the genetic contribution to epilepsy.Cleft palate is caused by CNS dysfunction in Gad1 and Viaat knockout mice.Adenosine-to-inosine RNA editing affects trafficking of the gamma-aminobutyric acid type A (GABA(A)) receptorEpilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase.Recent advances in the genetics of epilepsy: insights from human and animal studies.A deficit of functional GABA(A) receptors in neurons of beta 3 subunit knockout miceLow dose acute alcohol effects on GABA A receptor subtypesRole of GABA receptors in fetal lung development in rats.Alcohol-induced motor impairment caused by increased extrasynaptic GABA(A) receptor activity.
P2860
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P2860
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
description
1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1997
@ast
im April 1997 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1997/04/15)
@sk
vědecký článek publikovaný v roce 1997
@cs
wetenschappelijk artikel (gepubliceerd op 1997/04/15)
@nl
наукова стаття, опублікована у квітні 1997
@uk
name
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@ast
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@en
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@nl
type
label
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@ast
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@en
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@nl
prefLabel
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@ast
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@en
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@nl
P2093
P2860
P3181
P356
P1476
Mice devoid of gamma-aminobuty ...... e, and hypersensitive behavior
@en
P2093
A. Handforth
C. E. Rick
C. Ferguson
E. R. Korpi
G. E. Homanics
J. J. Quinlan
L. L. Firestone
M. D. Krasowski
M. H. Brilliant
P2860
P304
P3181
P356
10.1073/PNAS.94.8.4143
P407
P577
1997-04-15T00:00:00Z