BEST1 - bestrophin 1 - Genetics Home Reference
The BEST1 gene provides instructions for making a protein called bestrophin. Although the exact function of this protein is unknown, it appears to play a ...
http://ghr.nlm.nih.gov/gene=best1...
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OMIM - BESTROPHIN 1; BEST1
MIM *607854 · Description · Cloning · Gene Function · Molecular Genetics · Genotype/Phenotype Correlations · Animal Model · Allelic Variants ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=607854...
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Bestrophin 1 - Wikipedia, the free encyclopedia
BEST1 belongs to the bestrophin family of anion channels, which includes BEST2, BEST3, and BEST4. Bestrophins are transmembrane (TM) proteins that share a ...
http://en.wikipedia.org/wiki/Bestrophin_1...
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BEST1 expression in the retinal pigment epithelium is modulated by ...
BEST1 expression in the retinal pigment epithelium is modulated by OTX family ... we have been studying the mechanisms that control BEST1 expression, ...
http://www.ncbi.nlm.nih.gov/pubmed/18849347...
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Maki Goto Premium Best 1 - Wikipedia, the free encyclopedia
Goto Maki Premium Best 1 (後藤真希 プレミアムベスト①, Gotō Maki Puremiamu Besuto Ichi) is the first compilation album by solo singer and former Morning ...
http://en.wikipedia.org/wiki/Maki_Goto_Premium_Best_1...
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Biallelic mutation of BEST1 causes a distinct retinopathy in humans.
Biallelic mutation of BEST1 causes a distinct retinopathy in humans. ... Heterozygous mutations in BEST1 have previously been found to cause the two ...
http://www.ncbi.nlm.nih.gov/pubmed/18179881...
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Matsuura Aya Best 1 - Wikipedia, the free encyclopedia
Matsuura Aya Best 1 (松浦亜弥ベスト1) is Aya Matsuura's 'best of' album. It was released on March 24, 2005, and has sold 110367 copies. ...
http://en.wikipedia.org/wiki/Matsuura_Aya_Best_1...
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Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans
We describe a distinct retinal disorder, autosomal-recessive bestrophinopathy ( ARB), that is consequent upon biallelic mutation in BEST1 and is associated ...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253971/...
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AJHG - Biallelic Mutation of BEST1 Causes a Distinct Retinopathy ...
Mutations in the BEST1 gene cause the retinal dystrophies vitelliform macular dystrophy, autosomal-dominant vitreochoroidopathy, and autosomal-recessive ...
http://www.cell.com/AJHG/abstract/S0002-9297(07)00005-5...
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The spectrum of ocular phenotypes caused by mutations in the BEST1 ...
Bestrophin-1 is an integral membrane protein, encoded by the BEST1 gene, which is located in the basolateral membrane of the retinal pigment epithelium. ...
http://www.ncbi.nlm.nih.gov/pubmed/19375515...
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