CNR Institutional Research Information System

GENTILE, GIULIA

GENTILE, GIULIA  

Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Catania  

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Risultati 1 - 20 di 32 (tempo di esecuzione: 0.045 secondi).
Titolo Data di pubblicazione Autore(i) File
Artificial Intelligence-Driven Multi-Omics Approaches in Glioblastoma 1-gen-2025 Morello, Giovanna; La Cognata, Valentina; Guarnaccia, Maria; Gentile, Giulia; Cavallaro, Sebastiano
Multi-Omics Integration for Advancing Glioma Precision Medicine 1-gen-2025 Guarnaccia, M.; La Cognata, V.; Gentile, G.; Morello, G.; Cavallaro, S.
Predicting amyotrophic lateral sclerosis in the pre-symptomatic phase: Insights from SOD1G93A mouse gene expression profiles 1-gen-2025 La Cognata, V.; Guarnaccia, M.; Morello, G.; Gentile, G.; Cavallaro, S.
Unraveling the missing heritability of amyotrophic lateral sclerosis: should we focus more on copy number variations? 1-gen-2025 Guarnaccia, Maria; LA COGNATA, Valentina; Gentile, Giulia; Morello, Giovanna; Cavallaro, Sebastiano
Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases 1-gen-2022 Gentile, Giulia; Morello, Giovanna; LA COGNATA, Valentina; Guarnaccia, Maria; Luisa Conforti, Francesca; Cavallaro, Sebastiano
Individual oligogenic background in P.D91A-SOD1 amyotrophic lateral sclerosis patients 1-gen-2021 Gentile, Giulia; Perrone, Benedetta; Morello, Giovanna; Laura Simone, Isabella; Andò, Sebastiano; Cavallaro, Sebastiano; Luisa Conforti, Francesca
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse Stria Vascularis 1-gen-2021 Gentile, Giulia; Paciello, Fabiola; Zorzi, Veronica; Spampinato, ANTONIO GIANMARIA; Guarnaccia, Maria; Crispino, Giulia; Tetteymatey, Abraham; Scavizzi, Ferdinando; Raspa, Marcello; Rita Fetoni, Anna; Cavallaro, Sebastiano; Mammano, Fabio
Transcriptional profiles of cell fate transitions reveal early drivers of neuronal apoptosis and survival 1-gen-2021 Morello, GIOVANNA MARIA ALESSANDRA; Villari, Ambra; Spampinato, ANTONIO GIANMARIA; LA COGNATA, Valentina; Guarnaccia, Maria; Gentile, Giulia; Ciotti, MARIA TERESA; Calissano, Pietro; D'Agata, Velia; Severini, Cinzia; Cavallaro, Sebastiano
Tumor Growth in the High Frequency Medulloblastoma Mouse Model Ptch1+/-/Tis21KO Has a Specific Activation Signature of the PI3K/AKT/mTOR Pathway and Is Counteracted by the PI3K Inhibitor MEN1611 1-gen-2021 Ceccarelli, Manuela; D'Andrea, Giorgio; Micheli, Laura; Gentile, Giulia; Cavallaro, Sebastiano; Merlino, Giuseppe; Papoff, Giuliana; Tirone, Felice
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family 1-gen-2020 Morello, Giovanna; Gentile, Giulia; Spataro, Rossella; Spampinato, ANTONIO GIANMARIA; Guarnaccia, Maria; Salomone, Salvatore; La Bella, Vincenzo; Luisa Conforti, Francesca; Cavallaro, Sebastiano
Splicing Players Are Differently Expressed in Sporadic Amyotrophic Lateral Sclerosis Molecular Clusters and Brain Regions 1-gen-2020 LA COGNATA, Valentina; Gentile, Giulia; Aronica, Eleonora; Cavallaro, Sebastiano
The contribution of CNVs to the most common aging-related neurodegenerative diseases 1-gen-2020 Gentile, Giulia; LA COGNATA, Valentina; Cavallaro, Sebastiano
A genomic screening platform highlighting differences and overlaps in neurodegenerative diseases 1-gen-2019 Gentile, Giulia; LA COGNATA, Valentina; Morello, Giovanna; Guarnaccia, Maria; Spampinato, ANTONIO GIANMARIA; Cavallaro, Sebastiano
Translational Medicine in Neurological Disorders: A Genomic Perspective 1-gen-2019 Gentile, Giulia; Cavallaro, Sebastiano
ALS and CHARGE syndrome: a clinical and genetic study 1-gen-2018 Ungaro, Carmine; Citrigno, Luigi; Trojsi, Francesca; Sprovieri, Teresa; Gentile, Giulia; Muglia, Maria; Monsurro Maria, Rosaria; Tedeschi, Gioacchino; Cavallaro, Sebastiano; Conforti, FRANCESCA LUISA
Copy Number Variants in Neurological Disorder 1-gen-2018 Giulia Gentile; Sebastiano Cavallaro
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 1-gen-2018 Fetoni, Anna Rita; Zorzi, Veronica; Paciello, Fabiola; Ziraldo, Gaia; Peres, Chiara; Raspa, Marcello; Scavizzi, Ferdinando; Salvatore, ANNA MARIA; Crispino, Giulia; Tognola, Gabriella; Gentile, Giulia; Spampinato, ANTONIO GIANMARIA; Cuccaro, Denis; Guarnaccia, Maria; Morello, Giovanna; Van Camp, Guy; Fransen, Erik; Brumat, Marco; Girotto, Giorgia; Paludetti, Gaetano; Gasparini, Paolo; Cavallaro, Sebastiano; Mammano, Fabio
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 1-gen-2018 La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 1-gen-2017 Citrigno L.; Gentile G. ; Praticò A. ; Conforti FL. ; Magariello A. ; Patitucci A. ; Cavallaro S. ; Ruggieri M. ;Muglia M.
A customized Comparative Genomic Hybridization array for the analysis of Copy Number Variations and exon-dosage anomalies in neurological disorders 1-gen-2016 LA COGNATA, Valentina; Morello, Giovanna; Gentile, Giulia; D'Agata, Velia; Cavallaro, Sebastiano