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MANNINI, LINDA

MANNINI, LINDA  

Istituto di Fisiologia Clinica - IFC  

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Risultati 1 - 11 di 11 (tempo di esecuzione: 0.012 secondi).
Titolo Data di pubblicazione Autore(i) File
Association between physical activity and the risk of burnout in healthcare workers: systematic review 1-gen-2023 Mincarone, Pierpaolo; Bodini, Antonella; Rosaria Tumolo, Maria; Sabina, Saverio; Colella, Riccardo; Mannini, Linda; Sabato, Eugenio; Leo, CARLO GIACOMO
RFID-based Sensing and Reconstruction of Human Movements for Safety Monitoring of Workers 1-gen-2022 R. Colella; L. Mannini; M.R. Tumolo; S. Sabina; V. Molinaro; A. Ranavolo; C.G. Leo; P. Mincarone; R. Guarino; L. Catarinucci
CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome. 1-gen-2014 Pinson L; Mannini L; Willems M; Cucco F; Sirvent N; Frebourg T; Quarantotti V; Collet C; Schneider A; Sarda P; Geneviève D; Puechberty J; Lefort G; Musio A.
Mutant cohesin drives chromosomal instability in early colorectal adenomas. 1-gen-2014 Cucco, F; Servadio, A; Gatti, V; Bianchi, P; Mannini, L; Prodosmo, A; De Vitis, E; Basso, G; Friuli, A; Laghi, L; Soddu, S; Fontanini, G; Musio, A
Mutation spectrum and genotype-phenotype correlation in Cornelia de Lange syndrome. 1-gen-2013 Mannini, L; Cucco, F; Quarantotti, V; Krantz, Id; Musio, A
Proteomic Profile Identifies Dysregulated Pathways in Cornelia de Lange Syndrome Cells with Distinct Mutations in SMC1A and SMC3 Genes. 1-gen-2012 Gimigliano, A; Mannini, L; Bianchi, L; Puglia, M; Deardorff, Ma; Menga, S; Krantz, Id; Musio, A; Bini, L
Coesina e sue funzioni: un mondo in espansione 1-gen-2010 Mannini, L; Musio, A
A conserved role for the mitochondrial citrate transporter Sea/SLC25A1 in the maintenance of chromosome integrity 1-gen-2009 Morciano, P; Carrisi, C; Capobianco, L; Mannini, L; Burgio, G; Cestra, G; De Benedetto, Ge; Corona, Dfv; Musio, A; Cenci, G
Claspin inhibition leads to fragile site expression. 1-gen-2009 Focarelli ML; Soza S; Mannini L; Paulis M; Montecucco A; Musio A.
Coesina e coesinopatie 1-gen-2009 Mannini, L; Musio, A
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA. 1-gen-2009 Revenkova E; Focarelli ML; Susani L; Paulis M; Bassi MT; Mannini L; Frattini A; Delia D; Krantz I; Vezzoni P; Jessberger R; Musio A.