Showing results (241-250 of 302) with videos related to
Sort By:
Pageof 31
Journal of Public Health (Oxford, England)|November 27, 2013
Food for thought: pilot randomized controlled trial of lay health trainers supporting dietary change to reduce cardiovascular disease in deprived communitiesM Goodall, G R Barton, P Bower, 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.Human Molecular Genetics|December 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defectsIrene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, et al.The American Journal of Pathology|December 7, 2006
Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney diseaseMiliyun G Chiu, Tanya M Johnson, Adrian S Woolf, et al.European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.Pageof 31