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Simone Sanna

Showing results (81-90 of 149) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 31, 2003
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocinRoberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, et al.
Small (Weinheim an Der Bergstrasse, Germany)|March 12, 2026
Hole Polaronic Confinement in (111) Yttria-Stabilised ZirconiaMilica Vasiljevic, Victor Buratto Tinti, Javier Zamudio-García, et al.
Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.
Developmental Cell|January 22, 2009
Scara5 is a ferritin receptor mediating non-transferrin iron deliveryJau Yi Li, Neal Paragas, Renee M Ned, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
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.
Kidney International Reports|October 11, 2022
Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple MalignanciesNamrata G Jain, Dina F Ahram, Maddalena Marasa, et al.
Pageof 15

Showing results (81-90 of 149) with videos related to

Sort By:
Pageof 15
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 31, 2003
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocinRoberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, et al.
Small (Weinheim an Der Bergstrasse, Germany)|March 12, 2026
Hole Polaronic Confinement in (111) Yttria-Stabilised ZirconiaMilica Vasiljevic, Victor Buratto Tinti, Javier Zamudio-García, et al.
Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.
Developmental Cell|January 22, 2009
Scara5 is a ferritin receptor mediating non-transferrin iron deliveryJau Yi Li, Neal Paragas, Renee M Ned, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
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.
Kidney International Reports|October 11, 2022
Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple MalignanciesNamrata G Jain, Dina F Ahram, Maddalena Marasa, et al.
Pageof 15