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American Journal of Human Genetics|November 22, 2000
Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney diseaseC Bingham, M P Bulman, S Ellard, et al.
Elife|July 11, 2024
Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2012
A paradoxical teratogenic mechanism for retinoic acidLeo M Y Lee, Chun-Yin Leung, Walfred W C Tang, et al.
Kidney International|November 21, 2025
Molecular pathways of kidney development and their applications to clinical researchFriederike Ehrhart, Helge Martens, Norman D Rosenblum, et al.
Journal of the American Society of Nephrology : JASN|June 4, 2015
Vascular Endothelial Growth Factor C for Polycystic Kidney DiseasesJennifer L Huang, Adrian S Woolf, Maria Kolatsi-Joannou, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 3, 2006
Mutation analyses of Uroplakin II in children with renal tract malformationsDagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, et al.
American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.
Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.
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