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GPR143 gene

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

Papers overview

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2019
2019
Ocular albinism type 1 (OA1) is a genetic disorder characterized by reduced eye pigmentation and nystagmus, which is often… 
2014
2014
L‐DOPA is generally considered to alleviate the symptoms of Parkinson's disease by its conversion to dopamine. We have proposed… 
Review
2014
Review
2014
l-3,4-Dihydroxyphenylalanine (DOPA) is the metabolic precursor of dopamine, and the single most effective agent in the treatment… 
2014
2014
Congenital Nasal Pyriform Aperture Stenosis (CNPAS) is a rare congenital malformation caused by overgrowth of the maxillary bone… 
2012
2012
Melanocytes present in skin and other organs synthesize and store melanin pigment within membrane-delimited organelles called… 
2006
2006
Background: Nystagmus is common to all types of albinism. Some subjects with nystagmus lack convincing signs of albinism, have no…