Homophilic and heterophilic polycystin 1 interactions regulate E-cadherin recruitment and junction assembly in MDCK cells

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited human renal disease and is caused by mutations in two genes, PKD1 (85%) and PKD2 (15%). Cyst epithelial cells are characterised by a complex cellular phenotype including changes in proliferation, apoptosis, basement me...

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Detaylı Bibliyografya
Asıl Yazarlar: Streets, Andrew J., Wagner, Bart E., Harris, Peter C., Ward, Christopher J., Ong, Albert C. M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Company of Biologists 2009
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2671929/
https://ncbi.nlm.nih.gov/pubmed/19351715
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.045021
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