GENTILE, GIULIA
GENTILE, GIULIA
Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Catania
Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases
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
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
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
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
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
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
2020 LA COGNATA, Valentina; Gentile, Giulia; Aronica, Eleonora; Cavallaro, Sebastiano
The contribution of CNVs to the most common aging-related neurodegenerative diseases
2020 Gentile, Giulia; LA COGNATA, Valentina; Cavallaro, Sebastiano
A genomic screening platform highlighting differences and overlaps in neurodegenerative diseases
2019 Gentile, Giulia; LA COGNATA, Valentina; Morello, Giovanna; Guarnaccia, Maria; Spampinato, ANTONIO GIANMARIA; Cavallaro, Sebastiano
Translational Medicine in Neurological Disorders: A Genomic Perspective
2019 Gentile, Giulia; Cavallaro, Sebastiano
ALS and CHARGE syndrome: a clinical and genetic study
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
2018 Giulia Gentile; Sebastiano Cavallaro
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway
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
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.
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
2016 LA COGNATA, Valentina; Morello, Giovanna; Gentile, Giulia; D'Agata, Velia; Cavallaro, Sebastiano
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease
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
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
2016 Gentile, Giulia; Ceccarelli, Manuela; Micheli, Laura; Tirone, Felice; Cavallaro, Sebastiano
La genomica funzionale nell'identificazione di bersagli terapeutici in un modello murino preneoplastico di medulloblastoma
2016 Gentile, Giulia; Ceccarelli, Manuela; Micheli, Laura; Tirone, Felice; Cavallaro, Sebastiano
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| 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 | |
| La genomica funzionale nell'identificazione di bersagli terapeutici in un modello murino preneoplastico di medulloblastoma | 1-gen-2016 | Gentile, Giulia; Ceccarelli, Manuela; Micheli, Laura; Tirone, Felice; Cavallaro, Sebastiano |