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BBSome

Known as: Bardet-Biedl syndrome complex, Bardet-Biedl syndrome complex location 
A protein complex that associates with the primary cilium and is involved in cilium biogenesis; consists of seven conserved proteins: BBS1, BBS2… 
National Institutes of Health

Papers overview

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2020
2020
Cilia both receive and send information, the latter in the form of extracellular vesicles (EVs). EVs are nano-communication… 
Review
2018
Review
2018
Cilia and flagella of eukaryotic cells are evolutionarily conserved organelles with a microtubule-based axoneme as a scaffold. To… 
Highly Cited
2013
Highly Cited
2013
The BBSome, a regulator of ciliary membrane protein composition, is required only for the export phase of a process that… 
Highly Cited
2013
Highly Cited
2013
Summary Bardet-Biedl Syndrome (BBS) is a pleiotropic and genetically heterozygous disorder caused independently by numerous genes… 
Highly Cited
2012
Highly Cited
2012
The bidirectional movement of intraflagellar transport (IFT) particles, which are composed of motors, IFT-A and IFT-B… 
Highly Cited
2012
Highly Cited
2012
Background Bardet–Biedl Syndrome (BBS) is an emblematic recessive genetically highly heterogeneous ciliopathy characterised… 
Highly Cited
2011
Highly Cited
2011
Many signaling proteins including G protein-coupled receptors localize to primary cilia, regulating cellular processes including… 
Highly Cited
2010
Highly Cited
2010
Bardet-Biedl syndrome (BBS) is a human genetic disorder resulting in obesity, retinal degeneration, polydactyly, and nephropathy…