Cystic diseases of the kidney: role of adhesion molecules in normal and abnormal tubulogenesis

PD Wilson, CR Burrow - Experimental nephrology, 1999 - karger.com
This short review summarizes some information concerning what is known about matrix
adhesion molecules, focal adhesion proteins, and cell-cell adhesion molecules in normal …

Functional analysis of PKD1 transgenic lines reveals a direct role for polycystin-1 in mediating cell-cell adhesion

AJ Streets, LJ Newby, MJ O'Hare… - Journal of the …, 2003 - journals.lww.com
The PKD1 protein, polycystin-1, is a large transmembrane protein of uncertain function and
topology. To study the putative functions of polycystin-1, conditionally immortalized kidney …

Abnormalities in focal adhesion complex formation, regulation, and function in human autosomal recessive polycystic kidney disease epithelial cells

S Israeli, K Amsler, N Zheleznova… - American Journal of …, 2010 - journals.physiology.org
Integrin-associated focal adhesion complex formation and turnover plays an essential role in
directing interactions between epithelial cells and the extracellular matrix during …

[HTML][HTML] Polycystin-1, the PKD1 gene product, is in a complex containing E-cadherin and the catenins

Y Huan, J van Adelsberg - The Journal of clinical …, 1999 - Am Soc Clin Investig
Autosomal dominant polycystic kidney disease (ADPKD) is a common human genetic
disease characterized by cyst formation in kidney tubules and other ductular epithelia. Cells …

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

O Ibraghimov-Beskrovnaya, NO Bukanov… - Human molecular …, 2000 - academic.oup.com
The 14 kb mRNA of the polycystic kidney disease gene PKD1 encodes a novel large (~ 460
kDa) protein, polycystin-1, of unknown function that is responsible for autosomal dominant …

Polycystin: new aspects of structure, function, and regulation

PD Wilson - Journal of the American Society of Nephrology, 2001 - journals.lww.com
Polycystin-1 is a modular membrane protein with a long extracellular N-terminal portion that
bears several ligand-binding domains, 11 transmembrane domains, and a≥ 200 amino …

A polycystin-1 multiprotein complex is disrupted in polycystic kidney disease cells

T Roitbak, CJ Ward, PC Harris, R Bacallao… - Molecular biology of …, 2004 - Am Soc Cell Biol
Autosomal dominant polycystic kidney disease (ADPKD) is typified by the accumulation of
fluid-filled cysts and abnormalities in renal epithelial cell function. The disease is principally …

Polycystin expression is temporally and spatially regulated during renal development

J Van Adelsberg, S Chamberlain… - American Journal of …, 1997 - journals.physiology.org
Mutations in PKD1 cause autosomal dominant polycystic kidney disease (ADPKD), a
common genetic disease in which cysts form from kidney tubules. The predicted product of …

[HTML][HTML] Polycystins, focal adhesions and extracellular matrix interactions

IA Drummond - Biochimica et Biophysica Acta (BBA)-Molecular Basis …, 2011 - Elsevier
Polycystic kidney disease is the most common heritable disease in humans. In addition to
epithelial cysts in the kidney, liver and pancreas, patients with autosomal dominant …

[HTML][HTML] The polycystin 1-C-terminal fragment stimulates ERK-dependent spreading of renal epithelial cells

D Joly, S Ishibe, C Nickel, Z Yu, S Somlo… - Journal of biological …, 2006 - ASBMB
Polycystin 1, the product of the PKD1 gene, is mutated in autosomal dominant polycystic
kidney disease, a disease characterized by renal cyst formation and progressive renal …