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DRD5 gene

Known as: DOPAMINE RECEPTOR D5, DOPAMINE RECEPTOR D1B, DRD1B 
This gene plays a regulatory role in adenylate cyclase activity and intracellular cAMP store accumulation. The gene is thought to act as a stimulus… 
National Institutes of Health

Related topics

Related topics

6 relations
G Protein-Coupled Receptor SignalingLigand BindingReceptor SignalingSignal Transduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
PW01-54 - Correlation Of A Set Of Gene Variants, Life Events And Personality Features On Adult Adhd Severity
2009
2009
Association study of the gamma-aminobutyric acid type a receptor γ2 subunit gene with schizophrenia
Review
2007
Review
2007
ADHD genetics: 2007 update
Attention-deficit/hyperactivity disorder (ADHD) is highly heritable. Confirmed association has been reported for several… 
2004
2004
Polymorphisms in the dopamine D5 receptor (DRD5) gene and ADHD
There is considerable evidence to support a role of dopamine‐related genes in the molecular aetiology of attention‐deficit… 
Highly Cited
2003
Highly Cited
2003
Candidate gene studies in focal dystonia
Background: Genetic susceptibility factors for focal idiopathic torsion dystonia (F-ITD) are not established. Mutations in the… 
2003
2003
Association study between the phenotype migraine without aura-panic disorder and dopaminergic receptor genes.
Highly Cited
1999
Highly Cited
1999
Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5
The dopaminergic system has been implicated in the aetiology of mood disorders. We conducted family-based association studies for… 
1996
1996
A linkage study between bipolar disorder and genes involved in dopaminergic and GABAergic neurotransmission
Neurobiological studies indicate a dysregulation of the dopaminergic and GABAergic neurotransmission in bipolar disorder. We… 
Highly Cited
1996
Highly Cited
1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
Wolfram syndrome (DIDMOAD syndrome; MIM 222300) is an autosomal recessive neurodegenerative disorder characterized by juvenile… 
1991
1991
Human dopamine D5 receptor pseudogenes.
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