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BARDET-BIEDL SYNDROME 5

Known as: BBS5 
 
National Institutes of Health

Papers overview

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2019
2019
Bardet-Biedl syndrome (BBS), an autosomal recessive disease, is associated with non-functional primary cilia. BBS5 is part of the… Expand
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2016
2016
The transcription factor PITX2 is implicated in glaucoma pathology. In an earlier study we had used microarray analysis to… Expand
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2016
2016
tics of the domains in the FABB proteome should be like known domains of CFB; (3) after deflagellation a certain amount of genes… Expand
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2013
2013
BackgroundBardet-Biedl syndrome (BBS) is an autosomal recessive ciliopathy disorder with 18 known causative genes (BBS1-18). The… Expand
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2013
2013
SINE-VNTR-Alu (SVA) elements are present in hominoid primates and are divided into 6 subfamilies (SVA-A to SVA-F) and active in… Expand
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Highly Cited
2006
Highly Cited
2006
PURPOSE To develop large-scale, high-throughput annotation of the human macula transcriptome and to identify and prioritize… Expand
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Highly Cited
2002
Highly Cited
2002
Bardet-Biedl syndrome (BBS, OMIM 209900) is a genetic disorder with the primary features of obesity, pigmentary retinopathy… Expand
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