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Isolation and characterization of cholangiocyte primary ciliaHUANG, Bing Q; MASYUK, Tatyana V; MUFF, Melissa A et al.American journal of physiology. Gastrointestinal and liver physiology. 2006, Vol 54, Num 3, issn 0193-1857, G500-G509Article

Towards an understanding of the molecular pathogenesis of autosomal-recessive polycystic kidney disease (ARPKD): identification of a novel protein, fibrocystinYANAI, A.Clinical genetics. 2002, Vol 62, Num 1, pp 27-28, issn 0009-9163Article

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body areaSHIXUAN WANG; YING LUO; WILSON, Patricia D et al.Journal of the American Society of Nephrology. 2004, Vol 15, Num 3, pp 592-602, issn 1046-6673, 11 p.Article

Abnormalities in focal adhesion complex formation, regulation, and function in human autosomal recessive polycystic kidney disease epithelial cellsISRAELI, Sharon; AMSLER, Kurt; ZHELEZNOVA, Nadezhda et al.American journal of physiology. Cell physiology. 2010, Vol 67, Num 4, issn 0363-6143, C831-C846Article

Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasmMENEZES, Luis F. C; YIQIANG CAI; NAGASAWA, Yasuyuki et al.Kidney international. 2004, Vol 66, Num 4, pp 1345-1355, issn 0085-2538, 11 p.Article

A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatationWOOLLARD, J. R; PUNYASHTITI, R; LARUSSO, N. F et al.Kidney international. 2007, Vol 72, Num 3, pp 328-336, issn 0085-2538, 9 p.Article

Polycystic liver and kidney diseasesTAHVANAINEN, Esa; TAHVANAINEN, Pia; KÄÄRIÄINEN, Helena et al.Annals of medicine (Helsinki). 2005, Vol 37, Num 8, pp 546-555, issn 0785-3890, 10 p.Article

Maladies kystiques du foie : Génétique et biologie cellulaire = Cystic liver diseases. Genetics and cell biologyHOUSSET, Chantai.Gastroentérologie clinique et biologique. 2005, Vol 29, Num 8-9, pp 861-869, issn 0399-8320, 9 p.Article

Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)FISCHER, Dagmar-Christiane; JACOBY, Ulrike; BERGMANN, Carsten et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 6, pp 1819-1827, issn 0931-0509, 9 p.Article

Successful transplantation in a child with rapid progression of autosomal recessive polycystic kidney disease associated with a novel mutationPRELOG, Martina; BERGMANN, Carsten; BERND ZIMMERHACKL, Lothar et al.Pediatric transplantation. 2006, Vol 10, Num 3, pp 362-366, issn 1397-3142, 5 p.Article

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like proteinWARD, Christopher J; HOGAN, Marie C; MILLINER, Dawn S et al.Nature genetics. 2002, Vol 30, Num 3, pp 259-269, issn 1061-4036Article

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)BERGMANN, Carsten; SENDEREK, Jan; SEEMAN, Tomas et al.Kidney international. 2005, Vol 67, Num 3, pp 829-848, issn 0085-2538, 20 p.Article

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