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Giulia Gentile

Showing results (31-40 of 38) with videos related to

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Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Journal of Genetics|December 23, 2015
Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndromeDora Steel, Vincenzo Salpietro, Rahul Phadke, et al.
Cells|November 27, 2021
Transcriptional Profiles of Cell Fate Transitions Reveal Early Drivers of Neuronal Apoptosis and SurvivalGiovanna Morello, Ambra Villari, Antonio Gianmaria Spampinato, et al.
Frontiers in Cell and Developmental Biology|February 11, 2021
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse <i>Stria Vascularis</i>Giulia Gentile, Fabiola Paciello, Veronica Zorzi, et al.
Journal of Translational Medicine|November 28, 2025
Extracellular vesicles in multiple myeloma-bone marrow niche crosstalk: from cellular dialogue to clinical perspectivesMartina Forestiero, Anna Maria Zimbo, Giulia Gentile, et al.
Current Genomics|September 28, 2018
<i>NeuroArray</i>: A Customized aCGH for the Analysis of Copy Number Variations in Neurological DisordersValentina La Cognata, Giovanna Morello, Giulia Gentile, et al.
Journal of Experimental & Clinical Cancer Research : CR|January 8, 2026
PROTAC-mediated degradation of Bcl-xL potentiates target therapy in preclinical melanoma modelsElisabetta Valentini, Giulia Gentile, Marta Di Martile, et al.
Redox Biology|September 11, 2018
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathwayAnna Rita Fetoni, Veronica Zorzi, Fabiola Paciello, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Journal of Genetics|December 23, 2015
Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndromeDora Steel, Vincenzo Salpietro, Rahul Phadke, et al.
Cells|November 27, 2021
Transcriptional Profiles of Cell Fate Transitions Reveal Early Drivers of Neuronal Apoptosis and SurvivalGiovanna Morello, Ambra Villari, Antonio Gianmaria Spampinato, et al.
Frontiers in Cell and Developmental Biology|February 11, 2021
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse <i>Stria Vascularis</i>Giulia Gentile, Fabiola Paciello, Veronica Zorzi, et al.
Journal of Translational Medicine|November 28, 2025
Extracellular vesicles in multiple myeloma-bone marrow niche crosstalk: from cellular dialogue to clinical perspectivesMartina Forestiero, Anna Maria Zimbo, Giulia Gentile, et al.
Current Genomics|September 28, 2018
<i>NeuroArray</i>: A Customized aCGH for the Analysis of Copy Number Variations in Neurological DisordersValentina La Cognata, Giovanna Morello, Giulia Gentile, et al.
Journal of Experimental & Clinical Cancer Research : CR|January 8, 2026
PROTAC-mediated degradation of Bcl-xL potentiates target therapy in preclinical melanoma modelsElisabetta Valentini, Giulia Gentile, Marta Di Martile, et al.
Redox Biology|September 11, 2018
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathwayAnna Rita Fetoni, Veronica Zorzi, Fabiola Paciello, et al.
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