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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
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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
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2014
2014
BACKGROUND AND PURPOSE L-DOPA is generally considered to alleviate the symptoms of Parkinson's disease by its conversion to… Expand
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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
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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
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2006
2006
Background: Nystagmus is common to all types of albinism. Some subjects with nystagmus lack convincing signs of albinism, have no… Expand
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