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Simone Sanna-Cherchi

Showing results (31-40 of 93) with videos related to

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JAMA|March 3, 2025
Population-Scale Studies of Protein S Abnormalities and ThrombosisSharjeel A Chaudhry, Amelia K Haj, Justine Ryu, et al.
Glomerular Diseases|February 24, 2025
RESOLVE: Recurrence Posttransplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change DiseaseEloise C Salmon, Ashley E Rahimi, Hailey E Desmond, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
Journal of the American Society of Nephrology : JASN|December 11, 2021
GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the <i>Ssbp2</i> LocusNicholas J Steers, Yask Gupta, Vivette D D'Agati, et al.
Kidney International|March 13, 2003
Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosisMaurizio Bruschi, Paolo Catarsi, Giovanni Candiano, et al.
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.
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.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
JAMA|March 3, 2025
Population-Scale Studies of Protein S Abnormalities and ThrombosisSharjeel A Chaudhry, Amelia K Haj, Justine Ryu, et al.
Glomerular Diseases|February 24, 2025
RESOLVE: Recurrence Posttransplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change DiseaseEloise C Salmon, Ashley E Rahimi, Hailey E Desmond, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
Journal of the American Society of Nephrology : JASN|December 11, 2021
GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the <i>Ssbp2</i> LocusNicholas J Steers, Yask Gupta, Vivette D D'Agati, et al.
Kidney International|March 13, 2003
Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosisMaurizio Bruschi, Paolo Catarsi, Giovanni Candiano, et al.
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.
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.
Pageof 10