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Cristiano Simone

Showing results (61-70 of 87) with videos related to

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Cells|November 24, 2023
SMYD3 Modulates AMPK-mTOR Signaling Balance in Cancer Cell Response to DNA DamageMartina Lepore Signorile, Paola Sanese, Elisabetta Di Nicola, et al.
Cancers|July 29, 2025
An Integrated Clinical, Germline, Somatic, and In Silico Approach to Assess a Novel PMS2 Gene Variant Identified in Two Unrelated Lynch Syndrome FamiliesCandida Fasano, Antonia Lucia Buonadonna, Giovanna Forte, et al.
Plos One|April 4, 2015
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyCinzia Forleo, Monica Carmosino, Nicoletta Resta, et al.
BMC Cancer|September 12, 2014
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromesGiovanna Forte, Valentina Grossi, Valentina Celestini, et al.
Genes & Diseases|September 11, 2023
Corrigendum to 'Coinheritance of germline mutations in <i>APC</i> and <i>MUTYH</i> genes defines the clinical outcome of adenomatous polyposis syndromes' [Gene Dis (10) (2023), 1187-1189]Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, et al.
Cellular and Molecular Life Sciences : CMLS|January 4, 2013
A novel AMPK-dependent FoxO3A-SIRT3 intramitochondrial complex sensing glucose levelsAlessia Peserico, Fulvio Chiacchiera, Valentina Grossi, et al.
Cancers|September 28, 2021
Spectrum of Germline Pathogenic Variants in BRCA1/2 Genes in the Apulian Southern Italy Population: Geographic Distribution and Evidence for Targeted Genetic TestingMargherita Patruno, Simona De Summa, Nicoletta Resta, et al.
Clinical Genetics|November 25, 2020
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defectsMattia Gentile, Carlotta Ranieri, Daria C Loconte, et al.
International Journal of Molecular Sciences|December 23, 2023
Classic Galactosemia: Clinical and Computational Characterization of a Novel <i>GALT</i> Missense Variant (p.A303D) and a Literature ReviewGiovanna Forte, Antonia Lucia Buonadonna, Antonino Pantaleo, et al.
Cancers|October 28, 2023
Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer CohortAntonino Pantaleo, Giovanna Forte, Filomena Cariola, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Cells|November 24, 2023
SMYD3 Modulates AMPK-mTOR Signaling Balance in Cancer Cell Response to DNA DamageMartina Lepore Signorile, Paola Sanese, Elisabetta Di Nicola, et al.
Cancers|July 29, 2025
An Integrated Clinical, Germline, Somatic, and In Silico Approach to Assess a Novel PMS2 Gene Variant Identified in Two Unrelated Lynch Syndrome FamiliesCandida Fasano, Antonia Lucia Buonadonna, Giovanna Forte, et al.
Plos One|April 4, 2015
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyCinzia Forleo, Monica Carmosino, Nicoletta Resta, et al.
BMC Cancer|September 12, 2014
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromesGiovanna Forte, Valentina Grossi, Valentina Celestini, et al.
Genes & Diseases|September 11, 2023
Corrigendum to 'Coinheritance of germline mutations in <i>APC</i> and <i>MUTYH</i> genes defines the clinical outcome of adenomatous polyposis syndromes' [Gene Dis (10) (2023), 1187-1189]Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, et al.
Cellular and Molecular Life Sciences : CMLS|January 4, 2013
A novel AMPK-dependent FoxO3A-SIRT3 intramitochondrial complex sensing glucose levelsAlessia Peserico, Fulvio Chiacchiera, Valentina Grossi, et al.
Cancers|September 28, 2021
Spectrum of Germline Pathogenic Variants in BRCA1/2 Genes in the Apulian Southern Italy Population: Geographic Distribution and Evidence for Targeted Genetic TestingMargherita Patruno, Simona De Summa, Nicoletta Resta, et al.
Clinical Genetics|November 25, 2020
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defectsMattia Gentile, Carlotta Ranieri, Daria C Loconte, et al.
International Journal of Molecular Sciences|December 23, 2023
Classic Galactosemia: Clinical and Computational Characterization of a Novel <i>GALT</i> Missense Variant (p.A303D) and a Literature ReviewGiovanna Forte, Antonia Lucia Buonadonna, Antonino Pantaleo, et al.
Cancers|October 28, 2023
Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer CohortAntonino Pantaleo, Giovanna Forte, Filomena Cariola, et al.
Pageof 9