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Showing results (161-170 of 198) with videos related to

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American Journal of Physiology. Renal Physiology|March 7, 2002
Autocrine extracellular purinergic signaling in epithelial cells derived from polycystic kidneysErik M Schwiebert, Darren P Wallace, Gavin M Braunstein, et al.
Hepatology (Baltimore, Md.)|March 11, 2011
A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesisPeggy Raynaud, Joshua Tate, Céline Callens, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31M Vollmer, N Jeck, H H Lemmink, et al.
The Journal of Biological Chemistry|April 16, 1998
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchangerP Jarolim, C Shayakul, D Prabakaran, et al.
American Journal of Medical Genetics|March 25, 1998
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphologyK Zerres, G Mücher, J Becker, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 2, 2024
Evaluation for genetic disease in kidney transplant candidates: A practice resourceElizabeth G Ames, Prince M Anand, Mir Reza Bekheirnia, et al.
Scientific Reports|September 15, 2021
Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expressionChaozhe Yang, Naoe Harafuji, Amber K O'Connor, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 20, 2025
Polycystic Kidney Disease in Children: The Current Status and the Next HorizonMelissa A Cadnapaphornchai, Katherine M Dell, Charlotte Gimpel, et al.
Journal of the American Society of Nephrology : JASN|May 9, 2015
The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan AwardeesCorinne Antignac, James P Calvet, Gregory G Germino, et al.
Kidney International|September 12, 1998
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domainH H Lemmink, N V Knoers, L Károlyi, et al.
Pageof 20

Showing results (161-170 of 198) with videos related to

Sort By:
Pageof 20
American Journal of Physiology. Renal Physiology|March 7, 2002
Autocrine extracellular purinergic signaling in epithelial cells derived from polycystic kidneysErik M Schwiebert, Darren P Wallace, Gavin M Braunstein, et al.
Hepatology (Baltimore, Md.)|March 11, 2011
A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesisPeggy Raynaud, Joshua Tate, Céline Callens, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31M Vollmer, N Jeck, H H Lemmink, et al.
The Journal of Biological Chemistry|April 16, 1998
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchangerP Jarolim, C Shayakul, D Prabakaran, et al.
American Journal of Medical Genetics|March 25, 1998
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphologyK Zerres, G Mücher, J Becker, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 2, 2024
Evaluation for genetic disease in kidney transplant candidates: A practice resourceElizabeth G Ames, Prince M Anand, Mir Reza Bekheirnia, et al.
Scientific Reports|September 15, 2021
Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expressionChaozhe Yang, Naoe Harafuji, Amber K O'Connor, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 20, 2025
Polycystic Kidney Disease in Children: The Current Status and the Next HorizonMelissa A Cadnapaphornchai, Katherine M Dell, Charlotte Gimpel, et al.
Journal of the American Society of Nephrology : JASN|May 9, 2015
The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan AwardeesCorinne Antignac, James P Calvet, Gregory G Germino, et al.
Kidney International|September 12, 1998
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domainH H Lemmink, N V Knoers, L Károlyi, et al.
Pageof 20