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Christopher J Ward

Showing results (61-70 of 71) with videos related to

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Radiology|January 28, 2017
Distinguishing between Hepatic Inflammation and Fibrosis with MR ElastographyMeng Yin, Kevin J Glaser, Armando Manduca, et al.
Kidney International|November 8, 2013
Subfractionation, characterization, and in-depth proteomic analysis of glomerular membrane vesicles in human urineMarie C Hogan, Kenneth L Johnson, Roman M Zenka, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 8, 2005
Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney diseaseMark B Consugar, Sarah A Anderson, Sandro Rossetti, et al.
Journal of the American Society of Nephrology : JASN|January 23, 2009
Characterization of PKD protein-positive exosome-like vesiclesMarie C Hogan, Luca Manganelli, John R Woollard, et al.
Human Genetics|January 29, 2011
Germline PKHD1 mutations are protective against colorectal cancerChristopher J Ward, Yanhong Wu, Ruth A Johnson, et al.
Frontiers in Molecular Biosciences|December 16, 2022
Caspase-1 and the inflammasome promote polycystic kidney disease progressionKatherine I Swenson-Fields, Christopher J Ward, Micaila E Lopez, et al.
Journal of the American Society of Nephrology : JASN|December 6, 2014
Identification of Biomarkers for PKD1 Using Urinary ExosomesMarie C Hogan, Jason L Bakeberg, Vladimir G Gainullin, et al.
BMC Nephrology|November 19, 2015
Strategy and rationale for urine collection protocols employed in the NEPTUNE studyMarie C Hogan, John C Lieske, Chrysta C Lienczewski, et al.
Signal Transduction and Targeted Therapy|April 9, 2026
Cortisol-resistant CAR-NK cells overcome steroid-induced immunosuppression in lung cancerSoura Chakraborty, Jhuma Pramanik, Gustavo Alviter-Raymundo, et al.
Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Radiology|January 28, 2017
Distinguishing between Hepatic Inflammation and Fibrosis with MR ElastographyMeng Yin, Kevin J Glaser, Armando Manduca, et al.
Kidney International|November 8, 2013
Subfractionation, characterization, and in-depth proteomic analysis of glomerular membrane vesicles in human urineMarie C Hogan, Kenneth L Johnson, Roman M Zenka, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 8, 2005
Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney diseaseMark B Consugar, Sarah A Anderson, Sandro Rossetti, et al.
Journal of the American Society of Nephrology : JASN|January 23, 2009
Characterization of PKD protein-positive exosome-like vesiclesMarie C Hogan, Luca Manganelli, John R Woollard, et al.
Human Genetics|January 29, 2011
Germline PKHD1 mutations are protective against colorectal cancerChristopher J Ward, Yanhong Wu, Ruth A Johnson, et al.
Frontiers in Molecular Biosciences|December 16, 2022
Caspase-1 and the inflammasome promote polycystic kidney disease progressionKatherine I Swenson-Fields, Christopher J Ward, Micaila E Lopez, et al.
Journal of the American Society of Nephrology : JASN|December 6, 2014
Identification of Biomarkers for PKD1 Using Urinary ExosomesMarie C Hogan, Jason L Bakeberg, Vladimir G Gainullin, et al.
BMC Nephrology|November 19, 2015
Strategy and rationale for urine collection protocols employed in the NEPTUNE studyMarie C Hogan, John C Lieske, Chrysta C Lienczewski, et al.
Signal Transduction and Targeted Therapy|April 9, 2026
Cortisol-resistant CAR-NK cells overcome steroid-induced immunosuppression in lung cancerSoura Chakraborty, Jhuma Pramanik, Gustavo Alviter-Raymundo, et al.
Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.
Pageof 8