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Terry Watnick

Showing results (31-40 of 56) with videos related to

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Transplantation|January 13, 2009
DNA testing for live kidney donors at risk for autosomal dominant polycystic kidney diseaseEdmund Huang, Millie Samaniego-Picota, Thomas McCune, et al.
Kidney360|March 26, 2021
Baseline Characteristics and Patient-Reported Outcomes of ADPKD Patients in the Multicenter TAME-PKD Clinical TrialStephen L Seliger, Terry Watnick, Andrew D Althouse, et al.
American Journal of Nephrology|January 8, 2026
Feasibility study of empagliflozin in patients with autosomal dominant polycystic kidney disease: Design and baseline characteristicsStephen L Seliger, Wei Wang, Terry Watnick, et al.
Physiological Genomics|September 18, 2023
Polycystin-2-dependent transcriptome reveals early response of autosomal dominant polycystic kidney diseaseHyun Jun Jung, Eryn E Dixon, Richard Coleman, et al.
Plos One|May 20, 2016
Hair-Cell Mechanotransduction Persists in TRP Channel Knockout MiceXudong Wu, Artur A Indzhykulian, Paul D Niksch, et al.
Kidney International|July 22, 2017
A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanismPatricia Outeda, Luis Menezes, Erum A Hartung, et al.
Plos One|September 24, 2010
Pkd1 and Pkd2 are required for normal placental developmentMiguel A Garcia-Gonzalez, Patricia Outeda, Qin Zhou, et al.
Kidney International|July 7, 2023
A novel ARPKD mouse model with near-complete deletion of the Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus presents with multiple phenotypes but not renal cystsYu Ishimoto, Luis F Menezes, Fang Zhou, et al.
Human Molecular Genetics|June 19, 2007
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathwayMiguel A Garcia-Gonzalez, Luis F Menezes, Klaus B Piontek, et al.
Nature Communications|October 16, 2023
Fibrocystin/Polyductin releases a C-terminal fragment that translocates into mitochondria and suppresses cystogenesisRebecca V Walker, Qin Yao, Hangxue Xu, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Transplantation|January 13, 2009
DNA testing for live kidney donors at risk for autosomal dominant polycystic kidney diseaseEdmund Huang, Millie Samaniego-Picota, Thomas McCune, et al.
Kidney360|March 26, 2021
Baseline Characteristics and Patient-Reported Outcomes of ADPKD Patients in the Multicenter TAME-PKD Clinical TrialStephen L Seliger, Terry Watnick, Andrew D Althouse, et al.
American Journal of Nephrology|January 8, 2026
Feasibility study of empagliflozin in patients with autosomal dominant polycystic kidney disease: Design and baseline characteristicsStephen L Seliger, Wei Wang, Terry Watnick, et al.
Physiological Genomics|September 18, 2023
Polycystin-2-dependent transcriptome reveals early response of autosomal dominant polycystic kidney diseaseHyun Jun Jung, Eryn E Dixon, Richard Coleman, et al.
Plos One|May 20, 2016
Hair-Cell Mechanotransduction Persists in TRP Channel Knockout MiceXudong Wu, Artur A Indzhykulian, Paul D Niksch, et al.
Kidney International|July 22, 2017
A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanismPatricia Outeda, Luis Menezes, Erum A Hartung, et al.
Plos One|September 24, 2010
Pkd1 and Pkd2 are required for normal placental developmentMiguel A Garcia-Gonzalez, Patricia Outeda, Qin Zhou, et al.
Kidney International|July 7, 2023
A novel ARPKD mouse model with near-complete deletion of the Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus presents with multiple phenotypes but not renal cystsYu Ishimoto, Luis F Menezes, Fang Zhou, et al.
Human Molecular Genetics|June 19, 2007
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathwayMiguel A Garcia-Gonzalez, Luis F Menezes, Klaus B Piontek, et al.
Nature Communications|October 16, 2023
Fibrocystin/Polyductin releases a C-terminal fragment that translocates into mitochondria and suppresses cystogenesisRebecca V Walker, Qin Yao, Hangxue Xu, et al.
Pageof 6