GENTILE, GIULIA

GENTILE, GIULIA  

Istituto per la Ricerca e l'Innovazione Biomedica -IRIB  

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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 Giulia Gentile; Benedetta Perrone; Giovanna Morello; Isabella Laura Simone; Sebastiano Andò; Sebastiano Cavallaro; Francesca Luisa Conforti;
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 Giovanna Morello; Giulia Gentile; Rossella Spataro; Antonio Gianmaria Spampinato; Maria Guarnaccia; Salvatore Salomone; Vincenzo La Bella; Francesca Luisa Conforti; Sebastiano Cavallaro
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
Translational Medicine in Neurological Disorders: A Genomic Perspective 1-gen-2019 Giulia Gentile; Sebastiano Cavallaro
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
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease 1-gen-2016 LA COGNATA, Valentina; Morello, Giovanna; Gentile, Giulia; D'Agata, Velia; Criscuolo, Chiara; Cavalcanti, Francesca; Cavallaro, Sebastiano
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 1-gen-2016 Pavone, Piero; Praticò, Andrea Domenico; Gentile, Giulia; Falsaperla, Raffaele; Iemmolo, Rosario; Guarnaccia, Maria; Cavallaro, Sebastiano; Ruggieri, Martino
Functional Genomics Identifies Tis21-Dependent Mechanisms and Putative Cancer Drug Targets Underlying Medulloblastoma Shh-Type Development 1-gen-2016 Gentile, Giulia; Ceccarelli, Manuela; Micheli, Laura; Tirone, Felice; Cavallaro, Sebastiano
CXCL12 (chemokine (C-X-C motif) ligand 12) 1-gen-2015 Gentile, Giulia; Guarnaccia, Maria; Cavallaro, Sebastiano
Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndrome 1-gen-2015 Steel, D; Salpietro, V; Phadke, R; Pitt, M; Gentile, G; Massoud, A; Batten, L; Bashamboo, A; Mcelreavey, K; Saggar, A; Kinali, M
Biomarkers: Towards the Dream of Personalized Medicine 1-gen-2014 Morello, G; Gentile, G; Cavallaro, S
Is this the real time for genomics? 1-gen-2014 Guarnaccia, Maria; Gentile, Giulia; Alessi, Enrico; Schneider, Claudio; Petralia, Salvatore; Cavallaro, Sebastiano