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R Pollak

Showing results (261-270 of 326) with videos related to

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Nature Genetics|December 22, 2009
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisElizabeth J Brown, Johannes S Schlöndorff, Daniel J Becker, et al.
Plos One|May 2, 2015
Copy Number Variation at the APOL1 LocusRupam Ruchi, Giulio Genovese, Jessica Lee, et al.
American Journal of Human Genetics|May 1, 1995
Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemiaY H Chou, M R Pollak, M L Brandi, et al.
Kidney International|December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosisMichelle T McNulty, Damian Fermin, Felix Eichinger, et al.
The Journal of Urology|December 22, 2020
Mutations in <i>HOGA1</i> do Not Confer a Dominant Phenotype Manifesting as Kidney Stone DiseaseRoi Bar, Efrat Ben-Shalom, Mordechai Duvdevani, et al.
Journal of the American Society of Nephrology : JASN|April 10, 2010
Metabolite profiling identifies markers of uremiaEugene P Rhee, Amanda Souza, Laurie Farrell, et al.
Kidney International|August 8, 2014
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1Brendan Nichols, Prachi Jog, Jessica H Lee, et al.
Journal of the American Society of Nephrology : JASN|July 17, 2019
Contributions of Rare Gene Variants to Familial and Sporadic FSGSMinxian Wang, Justin Chun, Giulio Genovese, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 28, 2006
Calcium receptor stimulates chemotaxis and secretion of MCP-1 in GnRH neurons in vitro: potential impact on reduced GnRH neuron population in CaR-null miceNaibedya Chattopadhyay, Kyeong-Hoon Jeong, Shozo Yano, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 14, 2020
Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantationMargaret Berrigan, Jasmine Austrie, Aaron Fleishman, et al.
Pageof 33

Showing results (261-270 of 326) with videos related to

Sort By:
Pageof 33
Nature Genetics|December 22, 2009
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisElizabeth J Brown, Johannes S Schlöndorff, Daniel J Becker, et al.
Plos One|May 2, 2015
Copy Number Variation at the APOL1 LocusRupam Ruchi, Giulio Genovese, Jessica Lee, et al.
American Journal of Human Genetics|May 1, 1995
Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemiaY H Chou, M R Pollak, M L Brandi, et al.
Kidney International|December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosisMichelle T McNulty, Damian Fermin, Felix Eichinger, et al.
The Journal of Urology|December 22, 2020
Mutations in <i>HOGA1</i> do Not Confer a Dominant Phenotype Manifesting as Kidney Stone DiseaseRoi Bar, Efrat Ben-Shalom, Mordechai Duvdevani, et al.
Journal of the American Society of Nephrology : JASN|April 10, 2010
Metabolite profiling identifies markers of uremiaEugene P Rhee, Amanda Souza, Laurie Farrell, et al.
Kidney International|August 8, 2014
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1Brendan Nichols, Prachi Jog, Jessica H Lee, et al.
Journal of the American Society of Nephrology : JASN|July 17, 2019
Contributions of Rare Gene Variants to Familial and Sporadic FSGSMinxian Wang, Justin Chun, Giulio Genovese, et al.
American Journal of Physiology. Endocrinology and Metabolism|September 28, 2006
Calcium receptor stimulates chemotaxis and secretion of MCP-1 in GnRH neurons in vitro: potential impact on reduced GnRH neuron population in CaR-null miceNaibedya Chattopadhyay, Kyeong-Hoon Jeong, Shozo Yano, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 14, 2020
Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantationMargaret Berrigan, Jasmine Austrie, Aaron Fleishman, et al.
Pageof 33