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Peter C Harris

Showing results (201-210 of 314) with videos related to

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Hypertension (Dallas, Tex. : 1979)|October 5, 2020
Impaired Hedgehog-Gli1 Pathway Activity Underlies the Vascular Phenotype of Polycystic Kidney DiseaseFederico Franchi, Karen M Peterson, Katherine Quandt, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 5, 2021
Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2Prince Singh, Jason K Viehman, Ramila A Mehta, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 2025
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40Stijn Wigerinck, Pieter Schellekens, Byron H Smith, et al.
Journal of the American Society of Nephrology : JASN|October 26, 2023
State of the Science and Ethical Considerations for Preimplantation Genetic Testing for Monogenic Cystic Kidney Diseases and CiliopathiesWhitney S Thompson, Samir N Babayev, Michelle L McGowan, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 4, 2018
The Value of Genetic Testing in Polycystic Kidney Diseases Illustrated by a Family With PKD2 and COL4A1 MutationsEmilie Cornec-Le Gall, Fouad T Chebib, Charles D Madsen, et al.
Kidney International Reports|December 23, 2017
Autosomal Dominant Polycystic Kidney Patients May Be Predisposed to Various CardiomyopathiesFouad T Chebib, Marie C Hogan, Ziad M El-Zoghby, et al.
Pediatric Nephrology (Berlin, Germany)|March 11, 2019
Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohortsLada Beara-Lasic, Andrea Cogal, Kristin Mara, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 6, 2004
Deficiency of polycystin-2 reduces Ca2+ channel activity and cell proliferation in ADPKD lymphoblastoid cellsGianluca Aguiari, Manuela Banzi, Stefania Gessi, et al.
European Radiology|February 27, 2019
Multiple unilateral subcapsular cortical hemorrhagic cystic disease of the kidney: CT and MRI findings and clinical characteristicKotaro Yoshida, Naoki Takahashi, Bernard F King, et al.
Journal of the American Society of Nephrology : JASN|October 25, 2011
Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystinJason L Bakeberg, Rachaneekorn Tammachote, John R Woollard, et al.
Pageof 32

Showing results (201-210 of 314) with videos related to

Sort By:
Pageof 32
Hypertension (Dallas, Tex. : 1979)|October 5, 2020
Impaired Hedgehog-Gli1 Pathway Activity Underlies the Vascular Phenotype of Polycystic Kidney DiseaseFederico Franchi, Karen M Peterson, Katherine Quandt, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 5, 2021
Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2Prince Singh, Jason K Viehman, Ramila A Mehta, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 2025
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40Stijn Wigerinck, Pieter Schellekens, Byron H Smith, et al.
Journal of the American Society of Nephrology : JASN|October 26, 2023
State of the Science and Ethical Considerations for Preimplantation Genetic Testing for Monogenic Cystic Kidney Diseases and CiliopathiesWhitney S Thompson, Samir N Babayev, Michelle L McGowan, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 4, 2018
The Value of Genetic Testing in Polycystic Kidney Diseases Illustrated by a Family With PKD2 and COL4A1 MutationsEmilie Cornec-Le Gall, Fouad T Chebib, Charles D Madsen, et al.
Kidney International Reports|December 23, 2017
Autosomal Dominant Polycystic Kidney Patients May Be Predisposed to Various CardiomyopathiesFouad T Chebib, Marie C Hogan, Ziad M El-Zoghby, et al.
Pediatric Nephrology (Berlin, Germany)|March 11, 2019
Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohortsLada Beara-Lasic, Andrea Cogal, Kristin Mara, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 6, 2004
Deficiency of polycystin-2 reduces Ca2+ channel activity and cell proliferation in ADPKD lymphoblastoid cellsGianluca Aguiari, Manuela Banzi, Stefania Gessi, et al.
European Radiology|February 27, 2019
Multiple unilateral subcapsular cortical hemorrhagic cystic disease of the kidney: CT and MRI findings and clinical characteristicKotaro Yoshida, Naoki Takahashi, Bernard F King, et al.
Journal of the American Society of Nephrology : JASN|October 25, 2011
Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystinJason L Bakeberg, Rachaneekorn Tammachote, John R Woollard, et al.
Pageof 32