CNR Institutional Research Information System

MANNINI, LINDA

MANNINI, LINDA  

Istituto di Fisiologia Clinica - IFC  

Mostra records
Risultati 1 - 12 di 12 (tempo di esecuzione: 0.028 secondi).
Titolo Data di pubblicazione Autore(i) File
Association Between Physical Activity and the Risk of Burnout in Health Care Workers: Systematic Review 1-gen-2024 Mincarone, P.; Bodini, A.; Tumolo, M. R.; Sabina, S.; Colella, R.; Mannini, L.; Sabato, E.; Leo, C. G.
RFID-based Sensing and Reconstruction of Human Movements for Safety Monitoring of Workers 1-gen-2022 Colella, R; Mannini, L; Tumolo, Mr; Sabina, S; Molinaro, V; Ranavolo, A; Leo, Cg; Mincarone, P; Guarino, R; Catarinucci, L
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.
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance 1-gen-2014 Kaiser, F. J.; Ansari, M.; Braunholz, D.; Gil-Rodr('i)guez, M. C.; Decroos, C.; Wilde, J. J.; Fincher, C. T.; Kaur, M.; Bando, M.; Amor, D. J.; Atwal, P. S.; Bahlo, M.; Bowman, C. M.; Bradley, J. J.; Brunner, H. G.; Clark, D.; Campo, M. D.; Di Donato, N.; Diakumis, P.; Dubbs, H.; Dyment, D. A.; Eckhold, J.; Ernst, S.; Ferreira, J. C.; Francey, L. J.; Gehlken, U.; Guill('e)n-Navarro, E.; Gyftodimou, Y.; Hall, B. D.; Hennekam, R.; Hudgins, L.; Hullings, M.; Hunter, J. M.; Yntema, H.; Innes, A. M.; Kline, A. D.; Krumina, Z.; Lee, H.; Leppig, K.; Lynch, S. A.; Mallozzi, M. B.; Mannini, L.; Mckee, S.; Mehta, S. G.; Micule, I.; Consortium, C. C.; Mohammed, S.; Moran, E.; Mortier, G. R.; Moser, J. -A. S.; Noon, S. E.; Nozaki, N.; Nunes, L.; Pappas, J. G.; Penney, L. S.; P('e)rez-Ayt('e)s, A.; Petersen, M. B.; Puisac, B.; Revencu, N.; Roeder, E.; Saitta, S.; Scheuerle, A. E.; Schindeler, K. L.; Siu, V. M.; Stark, Z.; Strom, S. P.; Thiese, H.; Vater, I.; Willems, P.; Williamson, K.; Wilson, L. C.; Hakonarson, H.; Quintero-Rivera, F.; Wierzba, J.; Musio, A.; Gillessen-Kaesbach, G.; Ramos, F. J.; Jackson, L. G.; Shirahige, K.; Pi('e), J.; Christianson, D. W.; Krantz, I. D.; Fitzpatrick, D. R.; Deardorff, M. 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.