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VERRILLO, LUCIA

VERRILLO, LUCIA  

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Risultati 1 - 20 di 34 (tempo di esecuzione: 0.046 secondi).
Titolo Data di pubblicazione Autore(i) File
A novel promising therapeutic paradigm in a preclinical mouse model for developmental and epileptic encephalopathy 1-gen-2023 Di Palma, R; Verrillo, L; Mangano, E; Drongitis, D; Schiano Visconte, M; Barra, A; Terrone, G; Miano, Mg
Cell type-specific changes identified by single-cell transcriptomics in Arx mouse model of developmental and epileptic encephalopathy 1-gen-2023 Verrillo L; Mangano E; Drongitis D; Di Palma R; Schiano Visconte M; Barra A; Merelli I; Piccoli G; Flore G; Consolandi C; Bordoni R;Miano MG
Characterization of highly conserved molecular pathways involved in neurodevelopmental disorders (NDDs) 1-gen-2023 Verrillo, Lucia; Drongitis, Denise; Santonicola, Pamela; Schiano Visconte, Martina; Zampi, Giuseppina; DI SCHIAVI, Elia; Miano, MARIA GIUSEPPINA
Clinical and molecular characterization of FOXP1 variants in subjects with neurodevelopmental disorders. 1-gen-2023 Bettella, E; Drongitis, D; Polli, R; Verrillo, L; Leonardi, E; Cameran, M; Della Monica, M; Cernetti, R; Spitalier, C; Stanzial, F; Baldo, D; Turolla, L; Milani, D; Cossu, G; Miano, Mg; Murgia, A
Conserved functions of mouse ARX and Caenorhabditis elegans alr-1 in controlling pathways damaged in neurodevelopmental disorders (NDDs) 1-gen-2023 Drongitis, D; Verrillo, L; Santonicola, P; Di Palma, R; Poeta, L; Schiano Visconte, M; Lioi, Mb; Terrone, G; Di Schiavi, E; Miano, Mg
Deregulation of microtubule organization and RNA metabolism in Arx models for DEE 1-gen-2023 Drongitis, D; Caterino, M; Verrillo, L; Santonicola, P; Costanzo, M; Poeta, L; Attianese, B; Barra, A; Terrone, G; Lioi, Mb; Paladino, S; Di Schiavi, E; Costa, V; Ruoppolo, M; Miano, Mg
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants 1-gen-2023 Emanuela Leonardi ; Maria Cristina Aspromonte ; Denise Drongitis ; Elisa Bettella ; Lucia Verrillo ; Roberta Polli ; Meriel McEntagart ; Laura Licchetta ; Robertino Dilena ; Stefano D'Arrigo ; Claudia Ciaccio ; Silvia Esposito ; Vincenzo Leuzzi ; Annalaura Torella ; Demetrio Baldo ; Fortunato Lonardo ; Giulia Bonato ; Serena Pellegrin ; Franco Stanzial ; Renata Posmyk ; Ewa Kaczorowska ; Miryam Carecchio ; Monika Gos ; Sylwia RzocaNiewczas ; Maria Giuseppina Miano ; Alessandra Murgia
Exploitation of the Bio-MEMORY collection CNR-IBBR-CeLITABASE for the characterization of highly conserved molecular pathways involved in neurodevelopmental disorders (NDD). 1-gen-2023 Verrillo L; Drongitis D; Santonicola P; Di Palma R; Zampi G; Schiano Visconte M; Di Schiavi ;Miano M.G
Suberoylanilide Hydroxamic Acid (SAHA) Is a Driver Molecule of Neuroplasticity: Implication for Neurological Diseases 1-gen-2023 Verrillo, Lucia; Di Palma, Rosita; de Bellis, Alberto; Drongitis, Denise; Miano, MARIA GIUSEPPINA
A novel promising therapeutic paradigm for the treatment of drug-resistant seizures in a genetic mouse model of developmental and epileptic encephalopathy 1-gen-2022 Verrillo, L; Drongitis, D; Barra, A; Terrone, G; Miano, Mg
Analysis of the X-chromosome cancer driver gene Lysine-specific demethylase 5C (KDM5C) in Glioblastoma Multiforme (GBM) reveals novel molecular signatures 1-gen-2022 Drongitis, D; Verrillo, L; De Marinis, P; Orabona, P; Caiola, A; Turitto, G; Costa, V; Miano, Mg; Alberto de Bellis, A
Defective corticogenesis in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations 1-gen-2022 Verrillo, L; Mangano, E; Drongitis, D; Di Palma, R; Barra, A; Merelli, I; Piccoli, G; Flore, G; Consolandi, C; Bordoni, R; Miano, Mg
Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy 1-gen-2022 Drongitis, D; Caterino, M; Verrillo, L; Santonicola, P; Costanzo, M; Poeta, L; Attianese, B; Barra, A; Terrone, G; Lioi, Mb; Paladino, S; Di Schiavi, E; Costa, V; Ruoppolo, M; Miano, Mg
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants. 1-gen-2022 Leonardi E; Aspromonte MC; Drongitis D; Bettella E; Verrillo L; Polli R; McEntagart M; Licchetta L; Dilena R; D'Arrigo S; Ciaccio C; Esposito S; Leuzzi V; Torella A; Baldo D; Lonardo F; Bonato G; Pellegrin S; Stanzial F; Posmyk R; Kaczorowska E; Carecchio M; Gos M; RzocaNiewczas S; Miano MG; Murgia A.
Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. 1-gen-2022 Poeta, L; Malacarne, M; Padula, A; Drongitis, D; Verrillo, L; Lioi, Mb; Chiariello, Am; Bianco, S; Nicodemi, M; Piccione, M; Salzano, E; Coviello, D; Miano, Mg
Identification of a novel class of small molecules for the treatment of TREM2-related neurodegenerative dysfunctions 1-gen-2022 Gallo, C; Verrillo, L; Manzo, E; Miano, Mg; Fontana, A
Microtubule organization and splicing switches are altered in Arx animal models for neurodevelopmental disorders 1-gen-2022 Drongitis D; Caterino M; Verrillo L; Santonicola P; Costanzo M; Poeta L; Attianese B; Barra A; Terrone G; Lioi MB; Paladino S; Di Schiavi E; Costa V; Ruoppolo M; Miano MG
Particular musical aptitude in a female patient with speech disorders: analysis of a de novo FOXP1 truncating mutation and possible role in song-learning. 1-gen-2022 Maria G. Miano; Lucia Verrillo; Maria Oro; Rosita Di Palma; Denise Drongitis; Matteo Della Monica
Sulfavant A: a novel modulator of microglia activity 1-gen-2022 Franco, Cristina; Gallo, Carmela; Manzo, Emiliano; Verrillo, Lucia; Miano, MARIA GIUSEPPINA; Fontana, Angelo; Maria Teresa Canzoniero, Lorella
The Chromatin-Oxygen Sensor Gene KDM5C Associates with Novel Hypoxia-Related Signatures in Glioblastoma Multiforme. 1-gen-2022 Drongitis, D; Verrillo, L; De Marinis, P; Orabona, P; Caiola, A; Turitto, G; Alfieri, A; Bruscella, S; Gentile, M; Moriello, V; Sannino, E; Di Muccio, I; Costa, V; Miano, Mg; de Bellis, A.