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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.
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.
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 the American Society of Nephrology : JASN|July 31, 2014
Imaging-based diagnosis of autosomal dominant polycystic kidney diseaseYork Pei, Young-Hwan Hwang, John Conklin, et al.
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