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Peter C Harris

Showing results (121-130 of 314) with videos related to

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Apoptosis : an International Journal on Programmed Cell Death|November 28, 2009
NF-kappaB activation is required for apoptosis in fibrocystin/polyductin-depleted kidney epithelial cellsAlessandra Mangolini, Marco Bogo, Chiara Durante, et al.
Physiological Reports|April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patientsXiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Medical Physics|February 12, 2019
Development of a simple numerical model for trabecular bone structuresCarlos A Peña-Solórzano, David W Albrecht, David M Paganin, et al.
Scientific Reports|September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in EgyptNeveen A Soliman, Mohamed A Elmonem, Safaa M Abdelrahman, et al.
Expert Reviews in Molecular Medicine|November 27, 2019
The role of DNA damage as a therapeutic target in autosomal dominant polycystic kidney diseaseJennifer Q J Zhang, Sayanthooran Saravanabavan, Alexandra Munt, et al.
The Anatomical Record. Part A, Discoveries in Molecular, Cellular, and Evolutionary Biology|March 31, 2004
Development of multiorgan pathology in the wpk rat model of polycystic kidney diseaseVincent H Gattone, Benjamin A Tourkow, Chad M Trambaugh, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 29, 2010
Disease stage characterization of hepatorenal fibrocystic pathology in the PCK rat model of ARPKDStephen B Mason, Yun Liang, Rachel M Sinders, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.
American Journal of Physiology. Renal Physiology|February 27, 2009
Attenuated, flow-induced ATP release contributes to absence of flow-sensitive, purinergic Cai2+ signaling in human ADPKD cyst epithelial cellsChang Xu, Boris E Shmukler, Katherine Nishimura, et al.
Human Molecular Genetics|February 9, 2013
The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarityAmanda C Leightner, Cynthia J Hommerding, Ying Peng, et al.
Pageof 32

Showing results (121-130 of 314) with videos related to

Sort By:
Pageof 32
Apoptosis : an International Journal on Programmed Cell Death|November 28, 2009
NF-kappaB activation is required for apoptosis in fibrocystin/polyductin-depleted kidney epithelial cellsAlessandra Mangolini, Marco Bogo, Chiara Durante, et al.
Physiological Reports|April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patientsXiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Medical Physics|February 12, 2019
Development of a simple numerical model for trabecular bone structuresCarlos A Peña-Solórzano, David W Albrecht, David M Paganin, et al.
Scientific Reports|September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in EgyptNeveen A Soliman, Mohamed A Elmonem, Safaa M Abdelrahman, et al.
Expert Reviews in Molecular Medicine|November 27, 2019
The role of DNA damage as a therapeutic target in autosomal dominant polycystic kidney diseaseJennifer Q J Zhang, Sayanthooran Saravanabavan, Alexandra Munt, et al.
The Anatomical Record. Part A, Discoveries in Molecular, Cellular, and Evolutionary Biology|March 31, 2004
Development of multiorgan pathology in the wpk rat model of polycystic kidney diseaseVincent H Gattone, Benjamin A Tourkow, Chad M Trambaugh, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 29, 2010
Disease stage characterization of hepatorenal fibrocystic pathology in the PCK rat model of ARPKDStephen B Mason, Yun Liang, Rachel M Sinders, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.
American Journal of Physiology. Renal Physiology|February 27, 2009
Attenuated, flow-induced ATP release contributes to absence of flow-sensitive, purinergic Cai2+ signaling in human ADPKD cyst epithelial cellsChang Xu, Boris E Shmukler, Katherine Nishimura, et al.
Human Molecular Genetics|February 9, 2013
The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarityAmanda C Leightner, Cynthia J Hommerding, Ying Peng, et al.
Pageof 32