A Pkd1-Fbn1 Genetic Interaction Implicates TGF-β Signaling in the Pathogenesis of Vascular Complications in Autosomal Dominant Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of renal failure that is due to mutations in two genes, PKD1 and PKD2. Vascular complications, including aneurysms, are a well recognized feature of ADPKD, and a subgroup of families exhibits traits reminiscent of Marfan syndrome...

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Detalhes bibliográficos
Main Authors: Liu, Dongyan, Wang, Connie J., Judge, Daniel P., Halushka, Marc K., Ni, Jie, Habashi, Jennifer P., Moslehi, Javid, Bedja, Djahida, Gabrielson, Kathleen L., Xu, Hangxue, Qian, Feng, Huso, David, Dietz, Harry C., Germino, Gregory G., Watnick, Terry
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2014
Assuntos:
Basic Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3871766/
https://ncbi.nlm.nih.gov/pubmed/24071006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2012050486
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