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Showing results (131-140 of 198) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 15, 2023
Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells: A mechanistic connection between the kidney defects in cpk mice and human ARPKDYiming J Zhang, Chaozhe Yang, Wei Wang, et al.
Kidney International|October 26, 2007
Determinants of renal volume in autosomal-dominant polycystic kidney diseaseJ J Grantham, L T Cook, V E Torres, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney diseaseY Hofmann, J Becker, F Wright, et al.
Kidney Medicine|November 10, 2025
Qualitative Analysis and Comparison of Externally Led Patient-Focused Drug Development Concepts for Autosomal Recessive Polycystic Kidney Disease Against SONG InitiativesBelle Soyfer, Sorin Fedeles, Wendy Ruyle, et al.
Journal of the American Society of Nephrology : JASN|November 14, 1997
A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: evidence for a founder effectC L Kurtz, L Karolyi, H W Seyberth, et al.
Human Molecular Genetics|May 2, 2007
Polyductin undergoes notch-like processing and regulated release from primary ciliaJun-ya Kaimori, Yasuyuki Nagasawa, Luis F Menezes, et al.
American Journal of Medical Genetics. Part A|January 31, 2025
Elucidating the Molecular Landscape of Cystic Kidney Disease: Old Friends, New Friends and Some SurprisesDeborah Watson, Frank Mentch, Jonathan Billings, et al.
American Journal of Human Genetics|May 1, 1995
The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counselingL M Guay-Woodford, G Muecher, S D Hopkins, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2014
Neurocognition in children with autosomal recessive polycystic kidney disease in the CKiD cohort studyErum A Hartung, Matthew Matheson, Marc B Lande, et al.
Pageof 20

Showing results (131-140 of 198) with videos related to

Sort By:
Pageof 20
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 15, 2023
Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells: A mechanistic connection between the kidney defects in cpk mice and human ARPKDYiming J Zhang, Chaozhe Yang, Wei Wang, et al.
Kidney International|October 26, 2007
Determinants of renal volume in autosomal-dominant polycystic kidney diseaseJ J Grantham, L T Cook, V E Torres, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney diseaseY Hofmann, J Becker, F Wright, et al.
Kidney Medicine|November 10, 2025
Qualitative Analysis and Comparison of Externally Led Patient-Focused Drug Development Concepts for Autosomal Recessive Polycystic Kidney Disease Against SONG InitiativesBelle Soyfer, Sorin Fedeles, Wendy Ruyle, et al.
Journal of the American Society of Nephrology : JASN|November 14, 1997
A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: evidence for a founder effectC L Kurtz, L Karolyi, H W Seyberth, et al.
Human Molecular Genetics|May 2, 2007
Polyductin undergoes notch-like processing and regulated release from primary ciliaJun-ya Kaimori, Yasuyuki Nagasawa, Luis F Menezes, et al.
American Journal of Medical Genetics. Part A|January 31, 2025
Elucidating the Molecular Landscape of Cystic Kidney Disease: Old Friends, New Friends and Some SurprisesDeborah Watson, Frank Mentch, Jonathan Billings, et al.
American Journal of Human Genetics|May 1, 1995
The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counselingL M Guay-Woodford, G Muecher, S D Hopkins, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2014
Neurocognition in children with autosomal recessive polycystic kidney disease in the CKiD cohort studyErum A Hartung, Matthew Matheson, Marc B Lande, et al.
Pageof 20