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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… Expand
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2019
2019
Neurite outgrowth is a complex differentiation process regulated by external and/or internal mechanisms. Among external… Expand
2016
2016
BACKGROUND Age-related macular degeneration (AMD) is a leading cause of visual loss among the elderly. A key cell type involved… Expand
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2015
2015
Oa1 is the casual gene for ocular albinism-1 in humans. The gene product OA1, alternatively designated as GPR143, belongs to G… Expand
2014
2014
L‐DOPA is generally considered to alleviate the symptoms of Parkinson's disease by its conversion to dopamine. We have proposed… Expand
Review
2014
Review
2014
l-3,4-Dihydroxyphenylalanine (DOPA) is the metabolic precursor of dopamine, and the single most effective agent in the treatment… Expand
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2014
2014
Congenital Nasal Pyriform Aperture Stenosis (CNPAS) is a rare congenital malformation caused by overgrowth of the maxillary bone… Expand
2012
2012
Melanocytes present in skin and other organs synthesize and store melanin pigment within membrane-delimited organelles called… Expand
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2006
2006
The ocular albinism 1 (Oa1) protein is believed to be involved in the biogenesis of melanosomes, but its cellular localization is… Expand
2006
2006
Background: Nystagmus is common to all types of albinism. Some subjects with nystagmus lack convincing signs of albinism, have no… Expand