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European Journal of Pediatrics|April 12, 2011
Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafnessPierre Robitaille, Aicha Merouani, Ning He, et al.
Kidney International|October 12, 2025
Inactivation of Pkd2 in adult mice results in delayed cyst formation and identifies sex as a major modifier of disease severityPatricia Outeda, Perry Summers, Denis Basquin, et al.
Expert Review of Molecular Diagnostics|July 21, 2017
Molecular diagnosis of autosomal dominant polycystic kidney diseaseXuewen Song, Amirreza Haghighi, Ioan-Andrei Iliuta, et al.
Cellular Signalling|July 5, 2020
Targeting AMP-activated protein kinase (AMPK) for treatment of autosomal dominant polycystic kidney diseaseXuewen Song, Evelyn Tsakiridis, Gregory R Steinberg, et al.
Genomics|December 7, 2007
Analysis of PKD1 for genomic deletion by multiplex ligation-dependent probe assay: absence of hot spotsPiotr Kozlowski, John Bissler, York Pei, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 20, 2019
Alterations of Proximal Tubular Secretion in Autosomal Dominant Polycystic Kidney DiseaseKe Wang, Leila R Zelnick, Yan Chen, et al.
World Journal of Nephrology|July 27, 2016
Constitutive renal Rel/nuclear factor-κB expression in Lewis polycystic kidney disease ratsMichelle H T Ta, Kristina G Schwensen, David Liuwantara, et al.
Human Molecular Genetics|October 11, 2008
The tuberous sclerosis proteins regulate formation of the primary cilium via a rapamycin-insensitive and polycystin 1-independent pathwayTiffiney R Hartman, Dongyan Liu, Jack T Zilfou, et al.
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