MURDOCCA, MICHELA

MURDOCCA, MICHELA  

Dipartimento di Biomedicina e Prevenzione  

Mostra records
Risultati 1 - 20 di 29 (tempo di esecuzione: 0.065 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2018 A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family Maroofian, R; Murdocca, M; Rezaei-Delui, H; Nekooei, A; Mojarad, M; Sangiuolo, F; Novelli, G; Superti-Furga, A; D'Apice, Mr Articolo su rivista
1-gen-2018 AFM nano-mechanical study of the beating profile of hiPSC-derived cardiomyocytes beating bodies WT and DM1 Dinarelli, S; Girasole, M; Spitalieri, P; Talarico, Rv; Murdocca, M; Botta, A; Novelli, G; Mango, R; Sangiuolo, F; Longo, G Articolo su rivista
1-gen-2020 Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery De Masi, C; Spitalieri, P; Murdocca, M; Novelli, G; Sangiuolo, F Articolo su rivista
1-gen-2024 Cell electrokinetic fingerprint: a novel approach based on optically induced dielectrophoresis (ODEP) for in-flow identification of single cells Filippi, J; Casti, P; Antonelli, G; Murdocca, M; Mencattini, A; Corsi, F; D'Orazio, M; Pecora, A; De Luca, M; Curci, G; Ghibelli, L; Sangiuolo, F; Neale, Sl; Martinelli, E Articolo su rivista
1-gen-2018 Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene Fiorillo, C; D'Apice, Mr; Trucco, F; Murdocca, M; Spitalieri, P; Assereto, S; Baratto, S; Morcaldi, G; Minetti, C; Sangiuolo, F; Novelli, G Articolo su rivista
1-gen-2021 Clinical features of LMNA-related cardiomyopathy in 18 patients and characterization of two novel variants Ferradini, V; Cosma, J; Romeo, F; De Masi, C; Murdocca, M; Spitalieri, P; Mannucci, S; Parlapiano, G; Di Lorenzo, F; Martino, A; Fedele, F; Calò, L; Novelli, G; Sangiuolo, Farm Articolo su rivista
1-giu-2023 COVID-19: S-Peptide RBD 484–508 Induces IFN-γ T-Cell Response in Naïve-to-Infection and Unvaccinated Subjects with Close Contact with SARS-CoV-2-Positive Patients Murdocca, M; Citro, G; Centanini, E; Giannini, R; Latini, A; Centofanti, F; Piano Mortari, E; Cocciadiferro, D; Novelli, A; Bernardini, S; Novelli, G; Sangiuolo, F Articolo su rivista
1-gen-2020 Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G Articolo su rivista
1-gen-2017 Early hippocampal i-LTP and LOX-1 overexpression induced by anoxia: A potential role in neurodegeneration in NPC mouse model Castro, Al; Murdocca, M; Pucci, S; Zaratti, A; Greggi, C; Sangiuolo, F; Tancredi, V; Frank, C; D'Arcangelo, G Articolo su rivista
1-gen-2021 Effects of simulated microgravity on wild type and Marfan hiPSCs-derived embryoid bodies Spitalieri, P; Marini, M; Scioli, M; Murdocca, M; Longo, G; Orlandi, A; Novelli, G; Sangiuolo, F Articolo su rivista
1-ott-2022 Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors Latini, A; Vancheri, C; Amati, F; Morini, E; Grelli, S; Matteucci, C; Petrone, V; Colona, Vl; Murdocca, M; Andreoni, M; Malagnino, V; Raponi, M; Cocciadiferro, D; Novelli, A; Borgiani, P; Novelli, G Articolo su rivista
1-ott-2022 Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors Latini, A; Vancheri, C; Amati, F; Morini, E; Grelli, S; Matteucci, C; Petrone, V; Colona, Vl; Murdocca, M; Andreoni, M; Malagnino, V; Raponi, M; Cocciadiferro, D; Novelli, A; Borgiani, P; Novelli, G Articolo su rivista
1-apr-2023 From cue to meaning: The involvement of POLD1 gene in DNA replication, repair and aging Murdocca, M; Spitalieri, P; D'Apice, Mr; Novelli, G; Sangiuolo, F Articolo su rivista
1-gen-2021 Functional analysis of POLD1 p.ser605del variant: the aging phenotype of MDPL syndrome is associated with an impaired DNA repair capacity Murdocca, M; Spitalieri, P; De Masi, C; Udroiu, I; Marinaccio, J; Sanchez, M; Talarico, R; Fiorillo, C; D'Adamo, M; Sbraccia, P; D'Apice, M; Novelli, G; Sgura, A; Sangiuolo, F Articolo su rivista
1-gen-2018 Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2 Spitalieri, P; Talarico, Rv; Murdocca, M; Fontana, L; Marcaurelio, M; Campione, E; Massa, R; Meola, G; Serafino, A; Novelli, G; Sangiuolo, F; Botta, A Articolo su rivista
1-gen-2019 Generation of patient-specific hiPSCs model to study POLD1-related MDPL syndrome Spitalieri, P; Talarico, R; Murdocca, M; De Masi, C; Campione, E; Serafino, A; D'Adamo, M; Sbraccia, P; D'Apice, M; Novelli, G; Sangiuolo, F Articolo su rivista
26-apr-2016 Human induced pluripotent stem cells for monogenic disease modelling and therapy Spitalieri, P; Talarico, V; Murdocca, M; Novelli, G; Sangiuolo, Fc Articolo su rivista
15-dic-2022 Indole-3-carbinol in vitro antiviral activity against SARS-Cov-2 virus and in vivo toxicity Centofanti, F; Alonzi, T; Latini, A; Spitalieri, P; Murdocca, M; Chen, X; Cui, W; Shang, Q; Goletti, D; Shi, Y; Duranti, A; Tomino, C; Biancolella, M; Sangiuolo, F; Capobianchi, Mr; Jain, S; Novelli, G; Pandolfi, Pp Articolo su rivista
1-gen-2021 LOX-1 and cancer: an indissoluble liaison Murdocca, M; De Masi, C; Pucci, S; Mango, R; Novelli, G; Di Natale, C; Sangiuolo, F Articolo su rivista
1-gen-2017 Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies Rizzacasa, B; Morini, E; Pucci, S; Murdocca, M; Novelli, G; Amati, F Articolo su rivista