Arl13b and the exocyst interact synergistically in ciliogenesis

Arl13b belongs to the ADP-ribosylation factor family within the Ras superfamily of regulatory GTPases. Mutations in Arl13b cause Joubert syndrome, which is characterized by congenital cerebellar ataxia, hypotonia, oculomotor apraxia, and mental retardation. Arl13b is highly enriched in cilia and is...

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Bibliografiska uppgifter
I publikationen:Mol Biol Cell
Huvudupphovsmän: Seixas, Cecília, Choi, Soo Young, Polgar, Noemi, Umberger, Nicole L., East, Michael P., Zuo, Xiaofeng, Moreiras, Hugo, Ghossoub, Rania, Benmerah, Alexandre, Kahn, Richard A., Fogelgren, Ben, Caspary, Tamara, Lipschutz, Joshua H., Barral, Duarte C.
Materialtyp: Artigo
Språk:Inglês
Publicerad: The American Society for Cell Biology 2016
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Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4713133/
https://ncbi.nlm.nih.gov/pubmed/26582389
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E15-02-0061
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