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Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, 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.
Clinical Journal of the American Society of Nephrology : CJASN|January 17, 2019
Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGSTony Yao, Khalil Udwan, Rohan John, et al.
Kidney Medicine|April 14, 2021
Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic VariantsCole Shulman, Emerald Liang, Misato Kamura, et al.
JCI Insight|December 22, 2025
Inhibition of cell surface GRP78 and activated α2M interaction attenuates kidney fibrosisJackie Trink, Ifeanyi Kennedy Nmecha, Katrine Pilely, et al.
Journal of the American Society of Nephrology : JASN|October 11, 2015
Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney DiseaseYoung-Hwan Hwang, John Conklin, Winnie Chan, et al.
Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder VariantMoumita Barua, Rohan John, Lorenzo Stella, et al.
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