GUARNACCIA, MARIA
GUARNACCIA, MARIA
Istituto per la Ricerca e l'Innovazione Biomedica -IRIB
A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis
2023 Morello G.; La Cognata V.; Guarnaccia M.; La Bella V.; Conforti FL.; Cavallaro S.
A genomic screening platform highlighting differences and overlaps in neurodegenerative diseases
2019 Giulia Gentile; Valentina La Cognata; Giovanna Morello; Maria Guarnaccia; Antonio Gianmaria Spampinato; Sebastiano Cavallaro;
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
A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy
2019 Giuseppina Daniela Naimo; Maria Guarnaccia; Teresa Sprovieri; Carmine Ungaro; Francesca Luisa Conforti; Sebastiano Andò; Sebastiano Cavallaro
A systems biology approach to interpret the pharmacogenomic role of copy number variations in a patient with refractory epilepsy and intellectual disability
2020 Guarnaccia, Maria; Daniela Naimo, Giuseppina; Luisa Conforti, Francesca; Cavallaro, Sebastiano
A Targeted Next-Generation Sequencing Panel to Genotype Gliomas
2022 Guarnaccia, Maria; Guarnaccia, Laura; LA COGNATA, Valentina; Elena Navone, Stefania; Campanella, Rolando; Ampollini, Antonella; Locatelli, Marco; Miozzo, Monica; Marfia, Giovanni; Cavallaro, Sebastiano
Allele frequencies for STR loci in a Sicilian population: Genetic prevalence and disequilibrium
2006 Ciuna, Ignazio; Guarnaccia, Maria; Ginestra, ; Agodi, Antonella; Dpiscitello, ; Sspitaleria, ; Marcì, Giovanni; Paravizzini, Gianluca; Ctrapani, ; Travali, Salvatore; Lsaravo,
ATTUALI E FUTURE APPLICAZIONI DELLE BIOTECNOLOGIE PER LA DIAGNOSI E IL MONITORAGGIO CLINICO DELLE MALATTIE RARE
2019 Guarnaccia Maria
Constituting a Y chromosome short tandem repeats loci database in Sicily
2006 E. Ginestra; I. Ciuna; Maria Guarnaccia; Antonella Agodi; D. Piscitello; C. Trapani; G. Marcí; G. Paravizzini; C. Romano; Salvatore Travali; L. Saravo
Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach
2018 Morello, Giovanna; Guarnaccia, Maria; Spampinato, ANTONIO GIANMARIA; LA COGNATA, Valentina; D'Agata, Velia; Cavallaro, Sebastiano
Cracking the Code of Neuronal Cell Fate
2023 Morello G.; La Cognata V.; Guarnaccia M.; D'Agata V.; Cavallaro S.
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
CXCL12 (chemokine (C-X-C motif) ligand 12)
2015 Gentile, Giulia; Guarnaccia, Maria; Cavallaro, Sebastiano
CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93A
2023 La Cognata, V; D'Amico, A G; Maugeri, G; Morello, G; Guarnaccia, M; Magrì, B; Aronica, E; D'Agata, V; Cavallaro, S
Deletion of Voltage-Dependent Anion Channel 1 knocks mitochondria down triggering metabolic rewiring in yeast
2019 Magri, Andrea; Carmela Di Rosa, Maria; Orlandi, Ivan; Guarino, Francesca; Reina, Simona; Guarnaccia, Maria; Morello, Giovanna; Spampinato, Antonio; Cavallaro, Sebastiano; Messina, Angela; Vai, Marina; De Pinto, Vito
Design and validation of a custom ngs panel targeting a set of lysosomal storage diseases candidate for nbs applications
2021 Valentina La Cognata; Maria Guarnaccia; Giovanna Morello; Martino Ruggieri; Agata Polizzi; Sebastiano Cavallaro;
Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing
2023 Tendi, Ea; Morello, G; Guarnaccia, M; La Cognata, V; Petralia, S; Messina, Ma; Meli, C; Fiumara, A; Ruggieri, M; Cavallaro, S
Development of a Pharmacogenetic Lab-on-Chip Assay Based on the In-Check Technology to Screen for Genetic Variations Associated to Adverse Drug Reactions to Common Chemotherapeutic Agents
2020 Iemmolo, Rosario; LA COGNATA, Valentina; Morello, Giovanna; Guarnaccia, Maria; Arbitrio, Mariamena; Alessi, Enrico; Cavallaro, Sebastiano
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
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family
2020 Giovanna Morello; Giulia Gentile; Rossella Spataro; Antonio Gianmaria Spampinato; Maria Guarnaccia; Salvatore Salomone; Vincenzo La Bella; Francesca Luisa Conforti; Sebastiano Cavallaro
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A Diagnostic Gene-Expression Signature in Fibroblasts of Amyotrophic Lateral Sclerosis | 1-gen-2023 | Morello G.; La Cognata V.; Guarnaccia M.; La Bella V.; Conforti FL.; Cavallaro S. | |
A genomic screening platform highlighting differences and overlaps in neurodegenerative diseases | 1-gen-2019 | Giulia Gentile; Valentina La Cognata; Giovanna Morello; Maria Guarnaccia; Antonio Gianmaria Spampinato; Sebastiano Cavallaro; | |
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 | |
A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy | 1-gen-2019 | Giuseppina Daniela Naimo; Maria Guarnaccia; Teresa Sprovieri; Carmine Ungaro; Francesca Luisa Conforti; Sebastiano Andò; Sebastiano Cavallaro | |
A systems biology approach to interpret the pharmacogenomic role of copy number variations in a patient with refractory epilepsy and intellectual disability | 1-gen-2020 | Guarnaccia, Maria; Daniela Naimo, Giuseppina; Luisa Conforti, Francesca; Cavallaro, Sebastiano | |
A Targeted Next-Generation Sequencing Panel to Genotype Gliomas | 1-gen-2022 | Guarnaccia, Maria; Guarnaccia, Laura; LA COGNATA, Valentina; Elena Navone, Stefania; Campanella, Rolando; Ampollini, Antonella; Locatelli, Marco; Miozzo, Monica; Marfia, Giovanni; Cavallaro, Sebastiano | |
Allele frequencies for STR loci in a Sicilian population: Genetic prevalence and disequilibrium | 1-gen-2006 | Ciuna, Ignazio; Guarnaccia, Maria; Ginestra, ; Agodi, Antonella; Dpiscitello, ; Sspitaleria, ; Marcì, Giovanni; Paravizzini, Gianluca; Ctrapani, ; Travali, Salvatore; Lsaravo, | |
ATTUALI E FUTURE APPLICAZIONI DELLE BIOTECNOLOGIE PER LA DIAGNOSI E IL MONITORAGGIO CLINICO DELLE MALATTIE RARE | 1-gen-2019 | Guarnaccia Maria | |
Constituting a Y chromosome short tandem repeats loci database in Sicily | 1-gen-2006 | E. Ginestra; I. Ciuna; Maria Guarnaccia; Antonella Agodi; D. Piscitello; C. Trapani; G. Marcí; G. Paravizzini; C. Romano; Salvatore Travali; L. Saravo | |
Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach | 1-gen-2018 | Morello, Giovanna; Guarnaccia, Maria; Spampinato, ANTONIO GIANMARIA; LA COGNATA, Valentina; D'Agata, Velia; Cavallaro, Sebastiano | |
Cracking the Code of Neuronal Cell Fate | 1-gen-2023 | Morello G.; La Cognata V.; Guarnaccia M.; D'Agata V.; Cavallaro S. | |
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 | |
CXCL12 (chemokine (C-X-C motif) ligand 12) | 1-gen-2015 | Gentile, Giulia; Guarnaccia, Maria; Cavallaro, Sebastiano | |
CXCR2 Is Deregulated in ALS Spinal Cord and Its Activation Triggers Apoptosis in Motor Neuron-Like Cells Overexpressing hSOD1-G93A | 1-gen-2023 | La Cognata, V; D'Amico, A G; Maugeri, G; Morello, G; Guarnaccia, M; Magrì, B; Aronica, E; D'Agata, V; Cavallaro, S | |
Deletion of Voltage-Dependent Anion Channel 1 knocks mitochondria down triggering metabolic rewiring in yeast | 1-gen-2019 | Magri, Andrea; Carmela Di Rosa, Maria; Orlandi, Ivan; Guarino, Francesca; Reina, Simona; Guarnaccia, Maria; Morello, Giovanna; Spampinato, Antonio; Cavallaro, Sebastiano; Messina, Angela; Vai, Marina; De Pinto, Vito | |
Design and validation of a custom ngs panel targeting a set of lysosomal storage diseases candidate for nbs applications | 1-gen-2021 | Valentina La Cognata; Maria Guarnaccia; Giovanna Morello; Martino Ruggieri; Agata Polizzi; Sebastiano Cavallaro; | |
Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing | 1-gen-2023 | Tendi, Ea; Morello, G; Guarnaccia, M; La Cognata, V; Petralia, S; Messina, Ma; Meli, C; Fiumara, A; Ruggieri, M; Cavallaro, S | |
Development of a Pharmacogenetic Lab-on-Chip Assay Based on the In-Check Technology to Screen for Genetic Variations Associated to Adverse Drug Reactions to Common Chemotherapeutic Agents | 1-gen-2020 | Iemmolo, Rosario; LA COGNATA, Valentina; Morello, Giovanna; Guarnaccia, Maria; Arbitrio, Mariamena; Alessi, Enrico; 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 | |
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 |