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Simone Sanna-Cherchi

Showing results (41-50 of 93) with videos related to

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Blood Advances|September 30, 2025
Population-scale Analysis Reveals Germline Loss of SERPING1 (C1-Inhibitor) is a Polyphenotypic Thrombotic DisorderAlfonso Rodriguez Espada, Amelia Haj, Sean Joseph Jurgens, et al.
American Journal of Human Genetics|February 3, 2007
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33Simone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, et al.
Acta Histochemica|May 4, 2019
Immunohistochemical expression pattern of RIP5, FGFR1, FGFR2 and HIP2 in the normal human kidney developmentAnita Racetin, Fila Raguž, Merica Glavina Durdov, et al.
The Journal of Clinical Investigation|September 2, 2017
Isolated polycystic liver disease genes define effectors of polycystin-1 functionWhitney Besse, Ke Dong, Jungmin Choi, et al.
The Journal of Clinical Investigation|April 5, 2017
Isolated polycystic liver disease genes define effectors of polycystin-1 functionWhitney Besse, Ke Dong, Jungmin Choi, et al.
Kidney International|September 10, 2015
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidneyRik Westland, Miguel Verbitsky, Katarina Vukojevic, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2009
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13Patricia L Weng, Simone Sanna-Cherchi, Terry Hensle, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Journal of the American Society of Nephrology : JASN|July 25, 2009
Urinary NGAL marks cystic disease in HIV-associated nephropathyNeal Paragas, Thomas L Nickolas, Christina Wyatt, et al.
JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Pageof 10

Showing results (41-50 of 93) with videos related to

Sort By:
Pageof 10
Blood Advances|September 30, 2025
Population-scale Analysis Reveals Germline Loss of SERPING1 (C1-Inhibitor) is a Polyphenotypic Thrombotic DisorderAlfonso Rodriguez Espada, Amelia Haj, Sean Joseph Jurgens, et al.
American Journal of Human Genetics|February 3, 2007
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33Simone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, et al.
Acta Histochemica|May 4, 2019
Immunohistochemical expression pattern of RIP5, FGFR1, FGFR2 and HIP2 in the normal human kidney developmentAnita Racetin, Fila Raguž, Merica Glavina Durdov, et al.
The Journal of Clinical Investigation|September 2, 2017
Isolated polycystic liver disease genes define effectors of polycystin-1 functionWhitney Besse, Ke Dong, Jungmin Choi, et al.
The Journal of Clinical Investigation|April 5, 2017
Isolated polycystic liver disease genes define effectors of polycystin-1 functionWhitney Besse, Ke Dong, Jungmin Choi, et al.
Kidney International|September 10, 2015
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidneyRik Westland, Miguel Verbitsky, Katarina Vukojevic, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2009
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13Patricia L Weng, Simone Sanna-Cherchi, Terry Hensle, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Journal of the American Society of Nephrology : JASN|July 25, 2009
Urinary NGAL marks cystic disease in HIV-associated nephropathyNeal Paragas, Thomas L Nickolas, Christina Wyatt, et al.
JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Pageof 10