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Showing results (121-130 of 166) with videos related to

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The Journal of Clinical Investigation|February 23, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosisHaiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
The Journal of Pediatrics|June 23, 2019
Damaging Variants in Proangiogenic Genes Impair Growth in Fetuses with Cardiac DefectsMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.
Data in Brief|August 28, 2019
Effect of parental origin of damaging variants in pro-angiogenic genes on fetal growth in patients with congenital heart defects: Data and analysesMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 21, 2023
The Significance of Hematuria in PodocytopathiesDorota Marchel, Howard Trachtman, Maria Larkina, et al.
Journal of the American Society of Nephrology : JASN|February 15, 2019
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study LociKarsten B Sieber, Anna Batorsky, Kyle Siebenthall, et al.
Journal of the American Society of Nephrology : JASN|June 16, 2018
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic SyndromeHanna Debiec, Claire Dossier, Eric Letouzé, et al.
Kidney International Reports|March 11, 2020
Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI)Luciana S Feltran, Andreia Watanabe, Mara S Guaragna, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.
Journal of the American Society of Nephrology : JASN|May 21, 2017
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase <i>ε</i>Karolis Azukaitis, Eva Simkova, Mohammad Abdul Majid, et al.
Journal of the American Society of Nephrology : JASN|November 4, 2021
Discovery of Autoantibodies Targeting Nephrin in Minimal Change Disease Supports a Novel Autoimmune EtiologyAndrew J B Watts, Keith H Keller, Gabriel Lerner, et al.
Pageof 17

Showing results (121-130 of 166) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Investigation|February 23, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosisHaiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
The Journal of Pediatrics|June 23, 2019
Damaging Variants in Proangiogenic Genes Impair Growth in Fetuses with Cardiac DefectsMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.
Data in Brief|August 28, 2019
Effect of parental origin of damaging variants in pro-angiogenic genes on fetal growth in patients with congenital heart defects: Data and analysesMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.
Clinical Journal of the American Society of Nephrology : CJASN|September 21, 2023
The Significance of Hematuria in PodocytopathiesDorota Marchel, Howard Trachtman, Maria Larkina, et al.
Journal of the American Society of Nephrology : JASN|February 15, 2019
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study LociKarsten B Sieber, Anna Batorsky, Kyle Siebenthall, et al.
Journal of the American Society of Nephrology : JASN|June 16, 2018
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic SyndromeHanna Debiec, Claire Dossier, Eric Letouzé, et al.
Kidney International Reports|March 11, 2020
Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI)Luciana S Feltran, Andreia Watanabe, Mara S Guaragna, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.
Journal of the American Society of Nephrology : JASN|May 21, 2017
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase <i>ε</i>Karolis Azukaitis, Eva Simkova, Mohammad Abdul Majid, et al.
Journal of the American Society of Nephrology : JASN|November 4, 2021
Discovery of Autoantibodies Targeting Nephrin in Minimal Change Disease Supports a Novel Autoimmune EtiologyAndrew J B Watts, Keith H Keller, Gabriel Lerner, et al.
Pageof 17