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Matthew G Sampson

Showing results (31-40 of 94) with videos related to

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Glomerular Diseases|October 30, 2023
Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) InvestigatorsJennifer E Fishbein, Loryn Wilson Dass, Chrysta Lienczewski, et al.
Journal of the American Society of Nephrology : JASN|November 5, 2015
Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case CohortMatthew G Sampson, Christopher E Gillies, Catherine C Robertson, et al.
G3 (Bethesda, Md.)|December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination eventChristopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung diseaseMatthew G Sampson, Curtis R Coughlin, Paige Kaplan, et al.
The Journal of Biological Chemistry|June 2, 2019
The human nephrin Y<sup>1139</sup>RSL motif is essential for podocyte foot process organization and slit diaphragm formation during glomerular developmentEugenel B Espiritu, Huajun Jiang, Sophie Moreau-Marquis, et al.
Kidney International Reports|November 17, 2017
A Familial Infantile Renal FailureSidharth K Sethi, Nikita Wadhwani, Pranaw Jha, et al.
Pediatric Nephrology (Berlin, Germany)|January 17, 2024
Pediatric contributions and lessons learned from the NEPTUNE cohort studyZubin J Modi, Yan Zhai, Jennifer Yee, 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.
Kidney International Reports|July 11, 2026
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for HematuriaFrida Lona-Durazo, Ian R Dinsmore, Michelle T McNulty, et al.
The Journal of Biological Chemistry|May 11, 2019
Disruption of the exocyst induces podocyte loss and dysfunctionDeepak Nihalani, Ashish K Solanki, Ehtesham Arif, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
Glomerular Diseases|October 30, 2023
Assessment of the Needs of Nephrology Divisions to Implement Return of Clinically Significant Research Genetic Results: A Survey of Nephrotic Syndrome Study Network (NEPTUNE) InvestigatorsJennifer E Fishbein, Loryn Wilson Dass, Chrysta Lienczewski, et al.
Journal of the American Society of Nephrology : JASN|November 5, 2015
Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case CohortMatthew G Sampson, Christopher E Gillies, Catherine C Robertson, et al.
G3 (Bethesda, Md.)|December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination eventChristopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung diseaseMatthew G Sampson, Curtis R Coughlin, Paige Kaplan, et al.
The Journal of Biological Chemistry|June 2, 2019
The human nephrin Y<sup>1139</sup>RSL motif is essential for podocyte foot process organization and slit diaphragm formation during glomerular developmentEugenel B Espiritu, Huajun Jiang, Sophie Moreau-Marquis, et al.
Kidney International Reports|November 17, 2017
A Familial Infantile Renal FailureSidharth K Sethi, Nikita Wadhwani, Pranaw Jha, et al.
Pediatric Nephrology (Berlin, Germany)|January 17, 2024
Pediatric contributions and lessons learned from the NEPTUNE cohort studyZubin J Modi, Yan Zhai, Jennifer Yee, 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.
Kidney International Reports|July 11, 2026
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for HematuriaFrida Lona-Durazo, Ian R Dinsmore, Michelle T McNulty, et al.
The Journal of Biological Chemistry|May 11, 2019
Disruption of the exocyst induces podocyte loss and dysfunctionDeepak Nihalani, Ashish K Solanki, Ehtesham Arif, et al.
Pageof 10