MKKS Is a Centrosome-shuttling Protein Degraded by Disease-causing Mutations via CHIP-mediated Ubiquitination

McKusick–Kaufman syndrome (MKKS) is a recessively inherited human genetic disease characterized by several developmental anomalies. Mutations in the MKKS gene also cause Bardet–Biedl syndrome (BBS), a genetically heterogeneous disorder with pleiotropic symptoms. However, little is known about how MK...

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Hoofdauteurs: Hirayama, Shoshiro, Yamazaki, Yuji, Kitamura, Akira, Oda, Yukako, Morito, Daisuke, Okawa, Katsuya, Kimura, Hiroshi, Cyr, Douglas M., Kubota, Hiroshi, Nagata, Kazuhiro
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The American Society for Cell Biology 2008
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2262992/
https://ncbi.nlm.nih.gov/pubmed/18094050
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E07-07-0631
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