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Edgar A Otto

Showing results (21-30 of 118) with videos related to

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American Journal of Physiology. Renal Physiology|April 1, 2020
Hypertension induces glomerulosclerosis in phospholipase C-ε1 deficiencyDouglas K Atchison, Christopher L O'Connor, Rajasree Menon, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
Evidence of oligogenic inheritance in nephronophthisisJulia Hoefele, Matthias T F Wolf, John F O'Toole, et al.
Kidney International Reports|November 17, 2017
A Familial Infantile Renal FailureSidharth K Sethi, Nikita Wadhwani, Pranaw Jha, et al.
Development (Cambridge, England)|September 1, 2018
Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidneyRajasree Menon, Edgar A Otto, Austin Kokoruda, et al.
Human Genetics|April 6, 2013
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathyJan Halbritter, Jonathan D Porath, Katrina A Diaz, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 18, 2012
Clinical characterization and NPHP1 mutations in nephronophthisis and associated ciliopathies: a single center experienceNeveen A Soliman, Friedhelm Hildebrandt, Edgar A Otto, et al.
American Journal of Physiology. Renal Physiology|December 2, 2024
Pax proteins mediate segment-specific functions in proximal tubule survival and response to ischemic injuryMadison C McElliott, Asha C Telang, Jenna T Ference-Salo, et al.
Human Mutation|December 14, 2007
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencingEdgar A Otto, Juliana Helou, Susan J Allen, et al.
Kidney International|September 9, 2011
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesisPawaree Saisawat, Velibor Tasic, Virginia Vega-Warner, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 17, 2009
Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24Shazia Ashraf, Bethan E Hoskins, Hassan Chaib, et al.
Pageof 12

Showing results (21-30 of 118) with videos related to

Sort By:
Pageof 12
American Journal of Physiology. Renal Physiology|April 1, 2020
Hypertension induces glomerulosclerosis in phospholipase C-ε1 deficiencyDouglas K Atchison, Christopher L O'Connor, Rajasree Menon, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
Evidence of oligogenic inheritance in nephronophthisisJulia Hoefele, Matthias T F Wolf, John F O'Toole, et al.
Kidney International Reports|November 17, 2017
A Familial Infantile Renal FailureSidharth K Sethi, Nikita Wadhwani, Pranaw Jha, et al.
Development (Cambridge, England)|September 1, 2018
Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidneyRajasree Menon, Edgar A Otto, Austin Kokoruda, et al.
Human Genetics|April 6, 2013
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathyJan Halbritter, Jonathan D Porath, Katrina A Diaz, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 18, 2012
Clinical characterization and NPHP1 mutations in nephronophthisis and associated ciliopathies: a single center experienceNeveen A Soliman, Friedhelm Hildebrandt, Edgar A Otto, et al.
American Journal of Physiology. Renal Physiology|December 2, 2024
Pax proteins mediate segment-specific functions in proximal tubule survival and response to ischemic injuryMadison C McElliott, Asha C Telang, Jenna T Ference-Salo, et al.
Human Mutation|December 14, 2007
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencingEdgar A Otto, Juliana Helou, Susan J Allen, et al.
Kidney International|September 9, 2011
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesisPawaree Saisawat, Velibor Tasic, Virginia Vega-Warner, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 17, 2009
Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24Shazia Ashraf, Bethan E Hoskins, Hassan Chaib, et al.
Pageof 12