GPR143 gene

Known as: OA1 GENE, G PROTEIN-COUPLED RECEPTOR 143, GPR143 
 

Topic mentions per year

Topic mentions per year

2007-2017
0246820072017

Papers overview

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2014
2014
Albinism is an autosomal recessive genetic disorder due to low secretion of melanin. The oculocutaneous albinism (OCA) and ocular… (More)
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2013
2013
Previous studies in cell lines have suggested a role for melanosomes and related protein trafficking pathways in melanoma drug… (More)
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2012
2012
BACKGROUND The purpose of this study was to elucidate the molecular basis of ocular albinism type I in a Chinese pedigree… (More)
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2011
2011
BACKGROUND A broad spectrum of pigmentation of the skin and hair is found among patients diagnosed with ocular albinism (OA) and… (More)
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2011
2011
PURPOSE The purpose of the current research was to detect the underlying genetic defect in a Chinese family with X-linked… (More)
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2009
2009
X-linked ocular albinism (OA1) is the most common form of ocular albinism. Affected males are characterized by nystagmus… (More)
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2009
2009
PURPOSE To elucidate the molecular genetic defect of X-linked congenital nystagmus in a Chinese family. METHODS Genomic DNA was… (More)
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2009
2009
The pseudoautosomal region (PAR) is a small region of sequence homology between mammalian X and Y chromosomes and is needed for… (More)
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2008
2008
PURPOSE To map and identify the genetic mutation underlying X-linked congenital nystagmus in a Chinese family. METHODS Genomic… (More)
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2008
2008
PURPOSE There are few genetic studies and clinical descriptions of Asian patients with X-linked ocular albinism (OA1). In the… (More)
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