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Renal Failure|September 7, 2019
Exome sequencing of Saudi Arabian patients with ADPKDFahad A Al-Muhanna, Abdullah M Al-Rubaish, Chittibabu Vatte, et al.
Lancet (London, England)|July 5, 2003
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotypeSandro Rossetti, Dominique Chauveau, Vickie Kubly, et al.
Molecular Genetics and Metabolism|June 19, 2007
Evaluating the clinical utility of a molecular genetic test for polycystic kidney diseaseMiguel A Garcia-Gonzalez, Jeffrey G Jones, Susan K Allen, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Nature Materials|October 3, 2017
Organoid cystogenesis reveals a critical role of microenvironment in human polycystic kidney diseaseNelly M Cruz, Xuewen Song, Stefan M Czerniecki, et al.
Iscience|November 29, 2023
Short salsalate administration affects cell proliferation, metabolism, and inflammation in polycystic kidney diseaseAnish A Kanhai, Elena Sánchez-López, Thomas B Kuipers, et al.
Kidney Diseases (Basel, Switzerland)|December 1, 2025
How to Enhance Kidney Donation around the World: A Summary of Expert Opinions from the 5th International Congress of Chinese NephrologistsPhilip K T Li, Lik Fung Sam Lau, Kai-Ming Chow, et al.
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