Polycystins and Autosomal Polycystic Kidney Disease
Author:
Publisher
Springer Vienna
Link
http://link.springer.com/content/pdf/10.1007/978-3-7091-1065-2_45
Reference91 articles.
1. Adelsberg JV (2000) Polycystin-1 interacts with E-cadherin and the catenins—clues to the pathogenesis of cyst formation in ADPKD? Nephrol Dial Transplant 15:1–2
2. Aguiari G, Banzi M, Gessi S et al (2004) Deficiency of polycystin-2 reduces Ca2+ channel activity and cell proliferation in ADPKD lymphoblastoid cells. FASEB J 18:884–886
3. Anyatonwu GI, Estrada M, Tian X et al (2007) Regulation of ryanodine receptor-dependent calcium signaling by polycystin-2. Proc Natl Acad Sci USA 104:6454–6459
4. Babich V, Zeng WZ et al (2004) The N-terminal extracellular domain is required for polycystin-1-dependent channel activity. J Biol Chem 279:25582–25589
5. Basora N, Nomura H, Berger UV et al (2002) Tissue and cellular localization of a novel polycystic kidney disease-like gene product, polycystin-L. J Am Soc Nephrol 13:293–301
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