POC1B gene

Known as: POC1 centriolar protein B, TUWD12, FLJ14923 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2006-2018
012320062018

Papers overview

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2018
2018
PURPOSE To describe the clinical characteristics of a Chinese family with peripheral cone dystrophy (PCD) and identify the gene… (More)
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Review
2018
Review
2018
BACKGROUND Biallelic variants of POC1B were recently reported to cause autosomal recessive non-syndromic cone dystrophy. However… (More)
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2015
2015
Proteomic analysis of the mouse photoreceptor sensory cilium identified a set of cilia proteins, including Poc1 centriolar… (More)
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2015
2015
We aimed to analyze the mutation site and frequency of catechol-O-methyltransferase (COMT) gene, to explore the relationship… (More)
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2014
2014
We describe a consanguineous Iraqi family with Leber congenital amaurosis (LCA), Joubert syndrome (JBTS), and polycystic kidney… (More)
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2014
2014
IMPORTANCE A new form of cone-rod dystrophy (CORD) is described and the gene responsible for the disease is identified… (More)
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2014
2014
Exome sequencing revealed a homozygous missense mutation (c.317C>G [p.Arg106Pro]) in POC1B, encoding POC1 centriolar protein B… (More)
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2013
2013
Proteomic studies in unicellular eukaryotes identified a set of centriolar proteins that included proteome of centriole 1 (Poc1… (More)
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2008
2008
In many animals, the germ line develops from a distinct mitochondria-rich region of embryonic cytoplasm called the germ plasm… (More)
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Highly Cited
2006
Highly Cited
2006
Formation of the microtubule-based centriole is a poorly understood process that is crucial for duplication of the centrosome… (More)
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