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Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

Meckel syndrome (MKS) is a ciliopathy characterized by encephalocele, cystic renal disease, liver fibrosis and polydactyly. An identifying feature of MKS1, one of six MKS-associated proteins, is the presence of a B9 domain of unknown function. Using phylogenetic analyses, we show that this domain oc...

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Detalhes bibliográficos
Main Authors: Bialas, Nathan J., Inglis, Peter N., Li, Chunmei, Robinson, Jon F., Parker, Jeremy D. K., Healey, Michael P., Davis, Erica E., Inglis, Chrystal D., Toivonen, Tiina, Cottell, David C., Blacque, Oliver E., Quarmby, Lynne M., Katsanis, Nicholas, Leroux, Michel R.
Formato: Artigo
Idioma:Inglês
Publicado em: Company of Biologists 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2720918/
https://ncbi.nlm.nih.gov/pubmed/19208769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.028621
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