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Journal of the American Society of Nephrology : JASN|April 25, 2009
HNF1B mutations associate with hypomagnesemia and renal magnesium wastingShazia Adalat, Adrian S Woolf, Karen A Johnstone, et al.
Annals of Neurology|June 3, 2010
Longitudinal study of vision and retinal nerve fiber layer thickness in multiple sclerosisLauren S Talman, Esther R Bisker, David J Sackel, et al.
Cell Reports|June 19, 2026
Osr1-expressing mesoderm contributes to lymphatic vessel assembly and complexity in the mammalian kidneyDaniyal J Jafree, Lauren G Russell, Athanasia Stathopoulou, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
A cross model spatial and single-cell atlas reveals the conserved involvement of osteopontin in polycystic kidney diseaseSarah J Miller, Hua Zhong, Weidong Wu, et al.
Disease Models & Mechanisms|March 21, 2025
Microvascular aberrations found in human polycystic kidneys are an early feature in a Pkd1 mutant mouse modelDaniyal J Jafree, Charith Perera, Mary Ball, et al.
The Journal of Clinical Investigation|July 15, 2025
Organ-specific features of human kidney lymphatics are disrupted in chronic transplant rejectionDaniyal J Jafree, Benjamin J Stewart, Karen L Price, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 20, 2020
Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitisEszter Balogh, Jennifer C Chandler, Máté Varga, et al.
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