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GPR143 gene

Known as: OA1 GENE, G protein-coupled receptor 143, GPR143 
National Institutes of Health

Related topics

Related topics

1 relation
Ocular albinism, type I

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A novel GPR143 mutation in a Chinese family with X-linked ocular albinism type 1
Ocular albinism type 1 (OA1) is a genetic disorder characterized by reduced eye pigmentation and nystagmus, which is often… 
2019
2019
Overexpression of the gene product of ocular albinism 1 (GPR143/OA1) but not its mutant forms inhibits neurite outgrowth in PC12 cells.
Highly Cited
2015
Highly Cited
2015
Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration
2015
2015
Expression of ocular albinism 1 (OA1), 3, 4- dihydroxy- L-phenylalanine (DOPA) receptor, in both neuronal and non-neuronal organs
Review
2014
Review
2014
Cardiovascular actions of DOPA mediated by the gene product of ocular albinism 1.
l-3,4-Dihydroxyphenylalanine (DOPA) is the metabolic precursor of dopamine, and the single most effective agent in the treatment… 
2014
2014
The protein Ocular albinism 1 is the orphan GPCR GPR143 and mediates depressor and bradycardic responses to DOPA in the nucleus tractus solitarii
L‐DOPA is generally considered to alleviate the symptoms of Parkinson's disease by its conversion to dopamine. We have proposed… 
2014
2014
Congenital nasal pyriform aperture stenosis and ocular albinism co‐occurring in a sibship with a maternally‐inherited 97 kb Xp22.2 microdeletion
Congenital Nasal Pyriform Aperture Stenosis (CNPAS) is a rare congenital malformation caused by overgrowth of the maxillary bone… 
2012
2012
Melanosomal Dynamics Assessed with a Live-Cell Fluorescent Melanosomal Marker
Melanocytes present in skin and other organs synthesize and store melanin pigment within membrane-delimited organelles called… 
2006
2006
Ocular albinism 1 protein: trafficking and function when expressed in Saccharomyces cerevisiae.
2006
2006
Scanning the Ocular Albinism 1 (OA1) Gene for Polymorphisms in Congenital Nystagmus by DHPLC
Background: Nystagmus is common to all types of albinism. Some subjects with nystagmus lack convincing signs of albinism, have no… 
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