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BBS9 gene

Known as: PARATHYROID HORMONE-RESPONSIVE B1 GENE, Bardet-Biedl syndrome 9, PTH-RESPONSIVE B1 GENE 
This gene plays a role in ciliogenesis.
National Institutes of Health

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BARDET-BIEDL SYNDROME 9BBS9 protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome
Bardet-Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized by retinal dystrophy, polydactyly, obesity… 
2016
2016
Structural and biophysical characterization of membrane-coating proteins from the nuclear pore and the primary cilium
A hallmark of eukaryotes is an endomembrane system that spatially separates cellular processes into discrete compartments… 
2014
2014
Genetics: Causative genes identified in rare renal ciliopathies
Further reading Renal Genes. A web site coordinating mutational analysis in selected monogenic renal disorders [online], www… 
2011
2011
A genome-wide association study using a DNA pooling strategy identifies BBS9 and GLIS3 as novel loci influencing patient’s outcome after stroke
This work was supported by the grant PTDC/SAU-GMG/64426/2006, Fundacao para a Ciencia e Tecnologia (FCT). Helena Manso and Tiago… 
2011
2011
GENETICS/RETINOBLASTOMA ADDENDUM: LATE-BREAKING NEW ARTICLES
  • 2011
  • Corpus ID: 195215
DESIGN: Single-arm, prospective registry from May 30, 2006, to May 30, 2010, at an ophthalmic oncology referral center with… 
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