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GABRB3 gene

Known as: GABRB3, GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-3, GABA(A) receptor, beta 3 
National Institutes of Health

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Related topics

1 relation
GABRE gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
The GABRB3 Polymorphism and its Association with Schizophrenia
The aim of this study was to explore whether schizophrenia occurrence is associated with polymorphisms in the 5′ regulatory… 
2017
2017
Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent pattern
2014
2014
Genetic analysis of GABRB3 at 15q12 as a candidate gene of schizophrenia
Objective Copy number variations encompassing the chromosome 15q11-q13 region have been implicated in the pathogenesis of several… 
Review
2014
Review
2014
Epilepsy in 2013: Progress across the spectrum of epilepsy research
Over the past year, we have witnessed major advances in several areas of epilepsy research, including genetics and disease… 
2005
2005
An association analysis of microsatellite markers across the Prader–Willi/Angelman critical region on chromosome 15 (q11‐13) and autism spectrum disorder
Autism (OMIM 209850) is a neurodevelopmental disorder with a significant genetic component of a complex nature. Cytogenetic… 
2004
2004
Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.
BACKGROUND Childhood absence epilepsy (CAE) is one of the most frequently recognized syndromes among the idiopathic generalized… 
2002
2002
Prader Willi/Angelman and DiGeorge/velocardiofacial syndrome deletions: diagnosis by primed in situ labeling (PRINS).
A recently developed methodology-primed in situ labeling (PRINS)-can be used in place of fluorescence in situ hybridization (FISH… 
2000
2000
Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder.
OBJECTIVE To test for genetic linkage and association with GABAergic candidate genes in lithium-responsive bipolar disorder… 
1995
1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
We have studied a patient with Angelman syndrome (AS) and a 47,XY,+inv dup(15) (pter-->q11::q11-->pter) karyotype. Molecular… 
1993
1993
Linkage analysis in familial Angelman syndrome.
Familial Angelman syndrome (AS) can result from mutations in chromosome 15q11q13 that, when transmitted from father to child… 
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