CAPUTO, VALERIO

CAPUTO, VALERIO  

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Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2020 Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications Strafella, C; Caputo, V; Termine, A; Barati, S; Gambardella, S; Borgiani, P; Caltagirone, C; Novelli, G; Giardina, E; Cascella, R Articolo su rivista
1-gen-2018 Application of precision medicine in neurodegenerative diseases Strafella, C; Caputo, V; Galota, Mr; Zampatti, S; Marella, G; Mauriello, S; Cascella, R; Giardina, E Articolo su rivista
4-giu-2019 Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E Articolo su rivista
1-giu-2021 Case report: Sars-CoV-2 infection in a vaccinated individual: evaluation of the immunological profile and virus transmission risk Strafella, C; Caputo, V; Guerrera, G; Termine, A; Fabrizio, C; Cascella, R; Picozza, M; Caltagirone, C; Rossini, A; Balice, Mp; Salvia, A; Battistini, L; Borsellino, G; Giardina, E Articolo su rivista
1-ago-2021 Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy Di Rita, A; Angelini, D; Maiorino, T; Caputo, V; Cascella, R; Kumar, M; Tiberti, M; Lambrughi, M; Wesch, N; Löhr, F; Dötsch, V; Carinci, M; D'Acunzo, P; Chiurchiù, V; Papaleo, E; Rogov, V; Giardina, E; Battistini, L; Strappazzon, F Articolo su rivista
1-lug-2021 Comparative analysis of antigen and molecular tests for the detection of Sars-CoV-2 and related variants: a study on 4266 samples Caputo, V; Bax, C; Colantoni, L; Peconi, C; Termine, A; Fabrizio, C; Calvino, G; Luzzi, L; Panunzi, G; Fusco, C; Strafella, C; Cascella, R; Battistini, L; Caltagirone, C; Salvia, A; Sancesario, G; Giardina, E Articolo su rivista
1-gen-2020 Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations Sbardella, D; Tundo, Gr; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, Am; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; Graziani, G; Marini, S Articolo su rivista
1-gen-2018 Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD Cascella, R; Strafella, C; Caputo, V; Galota, Rm; Errichiello, V; Scutifero, M; Petillo, R; Marella, Gl; Arcangeli, M; Colantoni, L; Zampatti, S; Ricci, E; Deidda, G; Politano, L; Giardina, E Articolo su rivista
1-gen-2018 Effects of micro-textured polystyrene substrates by compression molding on cell adhesion and proliferation Bellisario, D; Quadrini, F; Santolim, G; Tedde, Gm; Caputo, V; Spitalieri, P; Sangiuolo, F; Santo, L Articolo su rivista
1-gen-2021 Epigenomic signatures in age-related macular degeneration: Focus on their role as disease modifiers and therapeutic targets Caputo, V; Strafella, C; Termine, A; Fabrizio, C; Ruffo, P; Cusumano, A; Giardina, E; Ricci, F; Cascella, R Articolo su rivista
1-feb-2021 Evaluation of OpenArray™ as a genotyping method for forensic DNA phenotyping and human identification Ragazzo, M; Puleri, G; Errichiello, V; Manzo, L; Luzzi, L; Potenza, S; Strafella, C; Peconi, C; Nicastro, F; Caputo, V; Giardina, E Articolo su rivista
1-gen-2019 Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. Zampatti, S; Colantoni, L; Strafella, C; Galota, R; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E Articolo su rivista
1-gen-2019 Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis Musumeci, Ml; Fiorentini, F; Bianchi, L; Cascella, R; Giardina, E; Caputo, V; Micali, G Articolo su rivista
1-gen-2018 Gender and complex diseases: Insights into sex-specific epigenetic|Genere e malattie complesse: Meccanismi epigenetici sesso-specifici Caputo, V; Cascella, R; Strafella, C; Giardina, E; Novelli, G Articolo su rivista
1-gen-2020 Genetic counseling and NGS screening for recessive LGMD2A families Strafella, C; Caputo, V; Campoli, G; Galota, R; Mela, J; Zampatti, S; Minozzi, G; Sancricca, C; Servidei, S; Giardina, E; Cascella, R Articolo su rivista
1-gen-2021 Genetic counselling improves the molecular characterisation of dementing disorders Zampatti, S; Ragazzo, M; Peconi, C; Luciano, S; Gambardella, S; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E Articolo su rivista
1-mag-2021 Genetic determinants highlight the existence of shared etiopathogenetic mechanisms characterizing age-related macular degeneration and neurodegenerative disorders Strafella, C; Caputo, V; Termine, A; Fabrizio, C; Ruffo, P; Potenza, S; Cusumano, A; Ricci, F; Caltagirone, C; Giardina, E; Cascella, R Articolo su rivista
1-mar-2021 Genetic variants allegedly linked to antisocial behaviour are equally distributed across different populations Zampatti, S; Ragazzo, M; Fabrizio, C; Termine, A; Campoli, G; Caputo, V; Strafella, C; Cascella, R; Caltagirone, C; Giardina, E Articolo su rivista
1-gen-2021 Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions Strafella, C; Caputo, V; Termine, A; Assogna, F; Pellicano, C; Pontieri, Fe; Macchiusi, L; Minozzi, G; Gambardella, S; Centonze, D; Bossù, P; Spalletta, G; Caltagirone, C; Giardina, E; Cascella, R Articolo su rivista
1-gen-2020 Interpreting mixture profiles: comparison between precision ID GlobalFiler™ NGS STR panel v2 and traditional methods Ragazzo, M; Carboni, S; Caputo, V; Buttini, C; Manzo, L; Errichiello, V; Puleri, G; Giardina, E Articolo su rivista