Receptor protein tyrosine phosphatases are novel components of a polycystin complex

Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutation of PKD1 and PKD2 that encode polycystin-1 and polycystin-2. Polycystin-1 is tyrosine phosphorylated and modulates multiple signaling pathways including AP-1, but the identity of the phosphatases regulating polycystin-1 are pr...

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Detalhes bibliográficos
Main Authors: Boucher, Catherine A., Ward, Heather H., Case, Ruth L., Thurston, Katie S., Li, Xiaohong, Needham, Andrew, Romero, Elsa, Hyink, Deborah, Qamar, Seema, Roitbak, Tamara, Powell, Samantha, Ward, Christopher, Wilson, Patricia D., Wandinger-Ness, Angela, Sandford, Richard N.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3156852/
https://ncbi.nlm.nih.gov/pubmed/21126580
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2010.11.006
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