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BMC Nephrology|April 19, 2018
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populationsCyril Cyrus, Samir Al-Mueilo, Chittibabu Vatte, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 21, 2007
Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosisNing He, Alireza Zahirieh, Yan Mei, et al.
American Journal of Human Genetics|February 3, 2009
A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systemsPiya Lahiry, Jian Wang, John F Robinson, et al.
Journal of Vascular and Interventional Radiology : JVIR|May 31, 2022
Safety of High-Dose 3% Sodium Tetradecyl Sulfate for Sclerotherapy of Renal Cysts in Patients with Autosomal Dominant Polycystic Kidney DiseaseNeeral R Patel, Steffan Frosi Stella, Mark Nasser, et al.
Cells|June 19, 2024
Myocardin-Related Transcription Factor Mediates Epithelial Fibrogenesis in Polycystic Kidney DiseaseZsuzsanna Lichner, Mei Ding, Tarang Khare, et al.
Journal of the American Society of Nephrology : JASN|July 20, 2007
Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36Andrew D Paterson, Xiao-Qing Liu, Kairong Wang, et al.
Journal of the American Society of Nephrology : JASN|January 29, 2005
Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney diseaseAndrew D Paterson, Riccardo Magistroni, Ning He, et al.
Journal of the American Society of Nephrology : JASN|February 24, 2022
Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney DiseaseCaitlyn Vlasschaert, Amy J M McNaughton, Michael Chong, et al.
Blood|January 18, 2023
A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic data setsCaitlyn Vlasschaert, Taralynn Mack, J Brett Heimlich, et al.
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