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Peter C Harris

Showing results (41-50 of 314) with videos related to

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Neoreviews|March 1, 2022
Genetic Etiologies, Diagnosis, and Management of Neonatal Cystic Kidney DiseaseLeah S Heidenreich, Ellen M Bendel-Stenzel, Peter C Harris, et al.
Human Molecular Genetics|December 24, 2016
Autophagy activators suppress cystogenesis in an autosomal dominant polycystic kidney disease modelPing Zhu, Cynthia J Sieben, Xiaolei Xu, et al.
Clinical Nephrology. Case Studies|May 13, 2021
Bariatric surgery in a patient with cystinuriaMelissa R Nemati, Peter C Harris, Andrea G Cogal, et al.
BMC Nephrology|September 10, 2013
Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnosticsReza Vazifehmand, Sandro Rossetti, Sassan Saber, et al.
Journal of the American Society of Nephrology : JASN|November 23, 2007
Vasopressin directly regulates cyst growth in polycystic kidney diseaseXiaofang Wang, Yanhong Wu, Christopher J Ward, et al.
Journal of Nephrology|January 2, 2021
CYP24A1 deficiency causing persistent hypercalciuria in a stone formerJanina Paula T Sy-Go, Ladan Zand, Peter C Harris, et al.
American Journal of Physiology. Renal Physiology|June 11, 2025
Kidney organoid models of Polycystic Kidney Disease - challenges and future directionsHumayra Afrin, Usama Qamar, Jielu Hao Robichaud, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2006
Tuberous sclerosis complex and polycystic kidney disease together: an exception to the contiguous gene syndromeAudrey C Woerner, Kit-Sing Au, Aimee T Williams, et al.
Human Molecular Genetics|January 8, 2010
Pkd1 transgenic mice: adult model of polycystic kidney disease with extrarenal and renal phenotypesAlmira Kurbegovic, Olivier Côté, Martin Couillard, et al.
Nature Reviews. Nephrology|April 15, 2015
Vasopressin and disruption of calcium signalling in polycystic kidney diseaseFouad T Chebib, Caroline R Sussman, Xiaofang Wang, et al.
Pageof 32

Showing results (41-50 of 314) with videos related to

Sort By:
Pageof 32
Neoreviews|March 1, 2022
Genetic Etiologies, Diagnosis, and Management of Neonatal Cystic Kidney DiseaseLeah S Heidenreich, Ellen M Bendel-Stenzel, Peter C Harris, et al.
Human Molecular Genetics|December 24, 2016
Autophagy activators suppress cystogenesis in an autosomal dominant polycystic kidney disease modelPing Zhu, Cynthia J Sieben, Xiaolei Xu, et al.
Clinical Nephrology. Case Studies|May 13, 2021
Bariatric surgery in a patient with cystinuriaMelissa R Nemati, Peter C Harris, Andrea G Cogal, et al.
BMC Nephrology|September 10, 2013
Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnosticsReza Vazifehmand, Sandro Rossetti, Sassan Saber, et al.
Journal of the American Society of Nephrology : JASN|November 23, 2007
Vasopressin directly regulates cyst growth in polycystic kidney diseaseXiaofang Wang, Yanhong Wu, Christopher J Ward, et al.
Journal of Nephrology|January 2, 2021
CYP24A1 deficiency causing persistent hypercalciuria in a stone formerJanina Paula T Sy-Go, Ladan Zand, Peter C Harris, et al.
American Journal of Physiology. Renal Physiology|June 11, 2025
Kidney organoid models of Polycystic Kidney Disease - challenges and future directionsHumayra Afrin, Usama Qamar, Jielu Hao Robichaud, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2006
Tuberous sclerosis complex and polycystic kidney disease together: an exception to the contiguous gene syndromeAudrey C Woerner, Kit-Sing Au, Aimee T Williams, et al.
Human Molecular Genetics|January 8, 2010
Pkd1 transgenic mice: adult model of polycystic kidney disease with extrarenal and renal phenotypesAlmira Kurbegovic, Olivier Côté, Martin Couillard, et al.
Nature Reviews. Nephrology|April 15, 2015
Vasopressin and disruption of calcium signalling in polycystic kidney diseaseFouad T Chebib, Caroline R Sussman, Xiaofang Wang, et al.
Pageof 32