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Human Molecular Genetics|July 18, 2008
Polycystin-1 C-terminal tail associates with beta-catenin and inhibits canonical Wnt signalingMark Lal, Xuewen Song, Jennifer L Pluznick, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 22, 2008
Presence of de novo mutations in autosomal dominant polycystic kidney disease patients without family historyBerenice Reed, Kim McFann, William J Kimberling, et al.Genetics in Medicine Open|September 22, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in OntarioAngela Du, Kaitlyn Lemay, Amit Bagga, et al.European Urology|February 14, 2016
Natural History of Renal Angiomyolipoma (AML): Most Patients with Large AMLs >4cm Can Be Offered Active Surveillance as an Initial Management StrategyJaimin R Bhatt, Patrick O Richard, Nicole S Kim, et al.Kidney International|March 3, 2017
Murine recombinant angiotensin-converting enzyme 2 attenuates kidney injury in experimental Alport syndromeEun Hui Bae, Fei Fang, Vanessa R Williams, et al.Journal of the American Society of Nephrology : JASN|February 8, 2008
IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathyXiao-Qing Liu, Andrew D Paterson, Ning He, et al.Nature Medicine|March 26, 2013
Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategyIsaline Rowe, Marco Chiaravalli, Valeria Mannella, et al.Genomics|June 25, 2002
A novel gene encoding a TIG multiple domain protein is a positional candidate for autosomal recessive polycystic kidney diseaseHuaqi Xiong, Yongxiong Chen, Yajun Yi, et al.The American Journal of Pathology|March 18, 2015
Characterization of the intrarenal renin-angiotensin system in experimental alport syndromeEun Hui Bae, Ana Konvalinka, Fei Fang, et al.Journal of Lipid Research|July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentrationMatthew B Lanktree, Clara C Elbers, Yun Li, et al.Pageof 19