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GABBR2 gene

Known as: G PROTEIN-COUPLED RECEPTOR 51, GPR51, GABA-B RECEPTOR, R2 SUBUNIT 
This gene plays a role in signaling.
National Institutes of Health

Related topics

Related topics

8 relations
G Protein-Coupled Receptor SignalingGABBR1 geneGamma-Aminobutyric Acid Type B Receptor Subunit 2Ligand Binding

Narrower (1)

GABBR2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Physiological Expression of Ion Channel Receptors in Human Periodontal Ligament Stem Cells
The etiopathogenesis of neurodegenerative diseases is characterized by the death of neurons. Human periodontal ligament stem… 
2018
2018
Validation and bioinformatic analysis of propofol-induced differentially expressed microRNAs in primary cultured neural stem cells.
2018
2018
Exploring different impaired speed of genetic-related brain function and structures in schizophrenic progress using multimodal analysis*
Schizophrenia (SZ) is a highly heritable disease exhibiting substantial structural and functional brain impairments. The duration… 
2018
2018
Reply to “a novel mutation in the transmembrane 6 domain of GABBR2 leads to a rett‐like phenotype”
We read the letter by Vuillaume et al with great interest because it provided a beautiful extension of our analyses of GABBR2 de… 
2017
2017
Motor neuron degeneration following glycine-mediated excitotoxicity induces spastic paralysis after spinal cord ischemia/reperfusion injury in rabbit.
Spinal cord ischemia and reperfusion (SCIR) injury is the major cause of a wide range of complications, including neural… 
2016
2016
A GABBR2 gene variant modifies pathophysiology in Huntington’s disease
2014
2014
Investigation of parental transmission of GABBR2 Single Nucleotide Polymorphisms and its association with nonsyndromic cleft lip with or without cleft palate
2013
2013
PP124—Pharmacokinetics of tolperisone in relation to CYP2C19 genotypes
2013
2013
PP126—In-vitro reactivity of drug-specific t-cells from a HLA-A*31:01 positive carbamazepine hypersensitive patient
2008
2008
Association between the γ-aminobutyric acid type B receptor 1 and 2 gene polymorphisms and mesial temporal lobe epilepsy in a Han Chinese population
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