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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
Familial glomerulopathy with giant fibrillar (fibronectin-positive) deposits: 15-year follow-up in a large kindredO Gemperle, J Neuweiler, F W Reutter, et al.
Archives of Biochemistry and Biophysics|February 1, 1984
Solubilization and characterization of vitamin K epoxide reductase from normal and warfarin-resistant rat liver microsomesE F Hildebrandt, P C Preusch, J L Patterson, et al.
Virology|May 31, 2002
Sequence-specific binding of poly(ADP-ribose) polymerase-1 to the human T cell leukemia virus type-I tax responsive elementZhan Zhang, Ellen F Hildebrandt, Cynthia M Simbulan-Rosenthal, et al.
Pediatric Radiology|February 7, 2001
Appearance of autosomal recessive polycystic kidney disease in magnetic resonance imaging and RARE-MR-urographyS Kern, L B Zimmerhackl, F Hildebrandt, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 9, 2001
Nephrocystin interacts with Pyk2, p130(Cas), and tensin and triggers phosphorylation of Pyk2T Benzing, P Gerke, K Höpker, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndromeM Vollmer, M Koehrer, R Topaloglu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 29, 2001
Evidence for further genetic heterogeneity in nephronophthisisH Omran, K Häffner, S Burth, et al.
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