MURDOCCA, MICHELA
MURDOCCA, MICHELA
Dipartimento di Biomedicina e Prevenzione
A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family
2018-01-01 Maroofian, R; Murdocca, M; Rezaei-Delui, H; Nekooei, A; Mojarad, M; Sangiuolo, F; Novelli, G; Superti-Furga, A; D'Apice, Mr
A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of spinal muscular atrophy (SMA)
2015-01-01 Luchetti, A; Ciafre', Sa; Murdocca, M; Malgieri, A; Masotti, A; Sanchez, M; Farace, Mg; Novelli, G; Sangiuolo, Fc
A surge of late-occurring meiotic double-strand breaks rescues synapsis abnormalities in spermatocytes of mice with hypomorphic expression of SPO11
2015-10-06 Faieta, M; Di Cecca, S; de Rooij, D; Luchetti, A; Murdocca, M; Di Giacomo, M; Di Siena, S; Pellegrini, M; Rossi, P; Barchi, M
Adenosine Triphosphate stimulates differentiation and mineralization in human osteoblast-like Saos-2 cells
2016-01-01 Cutarelli, A; Marini, M; Tancredi, V; D'Arcangelo, G; Murdocca, M; Frank, C; Tarantino, U
AFM nano-mechanical study of the beating profile of hiPSC-derived cardiomyocytes beating bodies WT and DM1
2018-01-01 Dinarelli, S; Girasole, M; Spitalieri, P; Talarico, Rv; Murdocca, M; Botta, A; Novelli, G; Mango, R; Sangiuolo, F; Longo, G
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery
2020-01-01 De Masi, C; Spitalieri, P; Murdocca, M; Novelli, G; Sangiuolo, F
BASELINE LABORATORY PARAMETER MODIFICATIONS ARE ASSOCIATED TO THE TRAINING RATE IN AMATEUR AND ELITE ATHLETES
2012-01-01 Verna, R; Zenobi, R; Murdocca, M; Giganti, Mg
Cell electrokinetic fingerprint: a novel approach based on optically induced dielectrophoresis (ODEP) for in-flow identification of single cells
2024-01-01 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
Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene
2018-01-01 Fiorillo, C; D'Apice, Mr; Trucco, F; Murdocca, M; Spitalieri, P; Assereto, S; Baratto, S; Morcaldi, G; Minetti, C; Sangiuolo, F; Novelli, G
Clinical features of LMNA-related cardiomyopathy in 18 patients and characterization of two novel variants
2021-01-01 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
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
2023-06-01 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
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
2020-01-01 D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G
Doping genetico
2009-01-01 Minella, D; Murdocca, M; Novelli, G; Giganti, Mg
Early hippocampal i-LTP and LOX-1 overexpression induced by anoxia: A potential role in neurodegeneration in NPC mouse model
2017-01-01 Castro, Al; Murdocca, M; Pucci, S; Zaratti, A; Greggi, C; Sangiuolo, F; Tancredi, V; Frank, C; D'Arcangelo, G
Effects of simulated microgravity on wild type and Marfan hiPSCs-derived embryoid bodies
2021-01-01 Spitalieri, P; Marini, M; Scioli, M; Murdocca, M; Longo, G; Orlandi, A; Novelli, G; Sangiuolo, F
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors
2022-10-01 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
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors
2022-10-01 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
From cue to meaning: The involvement of POLD1 gene in DNA replication, repair and aging
2023-04-01 Murdocca, M; Spitalieri, P; D'Apice, Mr; Novelli, G; Sangiuolo, F
Functional analysis of POLD1 p.ser605del variant: the aging phenotype of MDPL syndrome is associated with an impaired DNA repair capacity
2021-01-01 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
Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2
2018-01-01 Spitalieri, P; Talarico, Rv; Murdocca, M; Fontana, L; Marcaurelio, M; Campione, E; Massa, R; Meola, G; Serafino, A; Novelli, G; Sangiuolo, F; Botta, A
| 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-2015 | A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of spinal muscular atrophy (SMA) | Luchetti, A; Ciafre', Sa; Murdocca, M; Malgieri, A; Masotti, A; Sanchez, M; Farace, Mg; Novelli, G; Sangiuolo, Fc | Articolo su rivista | |
| 6-ott-2015 | A surge of late-occurring meiotic double-strand breaks rescues synapsis abnormalities in spermatocytes of mice with hypomorphic expression of SPO11 | Faieta, M; Di Cecca, S; de Rooij, D; Luchetti, A; Murdocca, M; Di Giacomo, M; Di Siena, S; Pellegrini, M; Rossi, P; Barchi, M | Articolo su rivista | |
| 1-gen-2016 | Adenosine Triphosphate stimulates differentiation and mineralization in human osteoblast-like Saos-2 cells | Cutarelli, A; Marini, M; Tancredi, V; D'Arcangelo, G; Murdocca, M; Frank, C; Tarantino, U | 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-2012 | BASELINE LABORATORY PARAMETER MODIFICATIONS ARE ASSOCIATED TO THE TRAINING RATE IN AMATEUR AND ELITE ATHLETES | Verna, R; Zenobi, R; Murdocca, M; Giganti, Mg | Intervento a convegno | |
| 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-2009 | Doping genetico | Minella, D; Murdocca, M; Novelli, G; Giganti, Mg | 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 |