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Edgar A Otto

Showing results (11-20 of 118) with videos related to

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Kidney International Reports|December 23, 2017
A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 PathwayJoseph Wang, Beth Vogt, Sidharth Kumar Sethi, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
Plos One|June 25, 2015
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic RicketsSara L Ma, Virginia Vega-Warner, Christopher Gillies, et al.
American Journal of Physiology. Renal Physiology|October 6, 2025
Decreased parietal epithelial cell density is linked to podocyte depletion and predictors of kidney disease progression in human kidneysJenna T Ference-Salo, Christopher L O'Connor, Rajasree Menon, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2005
Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndromeBoris Utsch, John A Sayer, Massimo Attanasio, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Pediatric Nephrology (Berlin, Germany)|March 29, 2017
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Kidney International|August 26, 2011
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathiesMoumita Chaki, Julia Hoefele, Susan J Allen, 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.
BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.
Pageof 12

Showing results (11-20 of 118) with videos related to

Sort By:
Pageof 12
Kidney International Reports|December 23, 2017
A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 PathwayJoseph Wang, Beth Vogt, Sidharth Kumar Sethi, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
Plos One|June 25, 2015
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic RicketsSara L Ma, Virginia Vega-Warner, Christopher Gillies, et al.
American Journal of Physiology. Renal Physiology|October 6, 2025
Decreased parietal epithelial cell density is linked to podocyte depletion and predictors of kidney disease progression in human kidneysJenna T Ference-Salo, Christopher L O'Connor, Rajasree Menon, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2005
Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndromeBoris Utsch, John A Sayer, Massimo Attanasio, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Pediatric Nephrology (Berlin, Germany)|March 29, 2017
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.
Kidney International|August 26, 2011
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathiesMoumita Chaki, Julia Hoefele, Susan J Allen, 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.
BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.
Pageof 12