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Showing results (141-150 of 198) with videos related to

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Human Molecular Genetics|June 19, 2007
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathwayMiguel A Garcia-Gonzalez, Luis F Menezes, Klaus B Piontek, et al.
Journal of the American Society of Nephrology : JASN|November 30, 2000
New rat model that phenotypically resembles autosomal recessive polycystic kidney diseaseJeroen Nauta, Miriam A Goedbloed, Harry VAN Herck, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 31, 2023
Tolvaptan for Children and Adolescents with Autosomal Dominant Polycystic Kidney Disease: Randomized Controlled TrialDjalila Mekahli, Lisa M Guay-Woodford, Melissa A Cadnapaphornchai, et al.
Journal of the American Society of Nephrology : JASN|July 29, 2025
Structured Application of Genetic Testing in a Pediatric Kidney ClinicJordy Salcedo-Giraldo, Krista R Wink, Nicholas Dadzie, et al.
American Journal of Physiology. Renal Physiology|January 7, 2006
Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cellsBrian J Siroky, William B Ferguson, Amanda L Fuson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 14, 1999
Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate geneL F Onuchic, M Mrug, A L Lakings, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 16, 2023
Pkhd1<sup>cyli/cyli</sup> mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver diseaseChaozhe Yang, Naoe Harafuji, Ljubica Caldovic, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 3, 2009
MRI-based kidney volume measurements in ADPKD: reliability and effect of gadolinium enhancementKyongtae T Bae, Cheng Tao, Fang Zhu, et al.
American Journal of Medical Genetics|July 13, 2002
Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate geneLuiz F Onuchic, Michal Mrug, Xiaoying Hou, et al.
Pageof 20

Showing results (141-150 of 198) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|June 19, 2007
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathwayMiguel A Garcia-Gonzalez, Luis F Menezes, Klaus B Piontek, et al.
Journal of the American Society of Nephrology : JASN|November 30, 2000
New rat model that phenotypically resembles autosomal recessive polycystic kidney diseaseJeroen Nauta, Miriam A Goedbloed, Harry VAN Herck, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 31, 2023
Tolvaptan for Children and Adolescents with Autosomal Dominant Polycystic Kidney Disease: Randomized Controlled TrialDjalila Mekahli, Lisa M Guay-Woodford, Melissa A Cadnapaphornchai, et al.
Journal of the American Society of Nephrology : JASN|July 29, 2025
Structured Application of Genetic Testing in a Pediatric Kidney ClinicJordy Salcedo-Giraldo, Krista R Wink, Nicholas Dadzie, et al.
American Journal of Physiology. Renal Physiology|January 7, 2006
Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cellsBrian J Siroky, William B Ferguson, Amanda L Fuson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 14, 1999
Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate geneL F Onuchic, M Mrug, A L Lakings, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 16, 2023
Pkhd1<sup>cyli/cyli</sup> mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver diseaseChaozhe Yang, Naoe Harafuji, Ljubica Caldovic, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 3, 2009
MRI-based kidney volume measurements in ADPKD: reliability and effect of gadolinium enhancementKyongtae T Bae, Cheng Tao, Fang Zhu, et al.
American Journal of Medical Genetics|July 13, 2002
Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate geneLuiz F Onuchic, Michal Mrug, Xiaoying Hou, et al.
Pageof 20