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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 cells
Alessandra Mangolini, Marco Bogo, Chiara Durante, et al.
Physiological Reports
|
April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients
Xiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Medical Physics
|
February 12, 2019
Development of a simple numerical model for trabecular bone structures
Carlos A Peña-Solórzano, David W Albrecht, David M Paganin, et al.
Scientific Reports
|
September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in Egypt
Neveen 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 disease
Jennifer 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 disease
Vincent 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 ARPKD
Stephen 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 diagnosis
Carla 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 cells
Chang 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 polarity
Amanda C Leightner, Cynthia J Hommerding, Ying Peng, et al.
Page
of 32
Search research articles
Search
Showing results (121-130 of 314) with videos related to
Sort By:
Page
of 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 cells
Alessandra Mangolini, Marco Bogo, Chiara Durante, et al.
Physiological Reports
|
April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients
Xiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Medical Physics
|
February 12, 2019
Development of a simple numerical model for trabecular bone structures
Carlos A Peña-Solórzano, David W Albrecht, David M Paganin, et al.
Scientific Reports
|
September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in Egypt
Neveen 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 disease
Jennifer 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 disease
Vincent 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 ARPKD
Stephen 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 diagnosis
Carla 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 cells
Chang 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 polarity
Amanda C Leightner, Cynthia J Hommerding, Ying Peng, et al.
Page
of 32