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Mostrati risultati da 1 a 20 di 59
Titolo Data di pubblicazione Autore(i) File
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 1-gen-2008 Guella, I; Paraboschi, E; Duga, S; Asselta, R
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction 1-gen-2008 Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S
Molecular characterization of six novel mutations causing factor V deficiency 1-gen-2008 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Song, J.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 1-gen-2008 Guella, I; Paraboschi, Em; Duga, S; Asselta, R
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 1-gen-2008 Dall'Osso, C.; Guella, I.; Duga, S.; Locatelli, N.; Paraboschi, E. M.; Spreafico, M.; Afrasiabi, A.; Pechlaner, C.; Peyvandi, F.; Tenchini, M. L.; Asselta, R.; Paraboschi, Elvezia Maria
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 1-gen-2009 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 1-gen-2009 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
Mutational screening of 25 unrelated FV-deficient patients from six countries 1-gen-2009 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Gemmati, D.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
The double-faced association of the PRKCA gene with multiple sclerosis 1-gen-2010 Paraboschi, E; Solda', G; Rimoldi, V; Dall’Osso, C; Anelli, G; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S; Asselta, R
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
MiR-634: a new player in the pathogenesis of multiple sclerosis? 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 1-gen-2011 Paraboschi, E.; Solda', G.; Gemmati, D.; Orioli, E.; Zeri, G.; Benedetti, D.; Salviati, A.; Barizzone, N.; Leone, M.; Duga, S.; Asselta, R.
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 1-gen-2011 Guella, I; Paraboschi, Em; van Schalkwyk, Wa; Asselta, R; Duga, S.
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 1-gen-2012 Cagliani, R; Fumagalli, M; Guerini, Fr; Riva, S; Galimberti, D; Comi, Gp; Agliardi, C; Scarpini, E; Pozzoli, U; Forni, D; Caputo, D; Asselta, R; Biasin, M; Paraboschi, Em; Bresolin, N; Clerici, M; Sironi, M.
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 1-gen-2012 Mirandola, L; Chiriva-Internati, M; Montagna, D; Locatelli, F; Zecca, M; Ranzani, M; Basile, A; Locati, M; Cobos, E; Kast, Wm; Asselta, R; Paraboschi, Em; Comi, P; Chiaramonte, R
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 1-gen-2012 Paraboschi, E; Kayıran, Sm; Özbek, N; Gürakan, B; Guella, I; Duga, S; Asselta, R
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 1-gen-2013 Biffi, S.; Cerbino, R.; Bomboi, F.; Paraboschi, E. M.; Asselta, R.; Sciortino, F.; Bellini, T.; Paraboschi, Elvezia Maria
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 1-gen-2014 Paraboschi, E; Rimoldi, V; Soldà, G; Tabaglio, T; Dall'Osso, C; Saba, E; Vigliano, M; Salviati, A; Leone, M; Benedetti, Md; Fornasari, D; Saarela, J; De Jager, Pl; Patsopoulos, Na; D'Alfonso, S; Gemmati, D; Duga, S; Asselta, R.
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 1-gen-2014 Biguzzi, E; Franchi, F; Acaia, B; Ossola, W; Nava, U; Paraboschi, Em; Asselta, R; Peyvandi, F.
Mostrati risultati da 1 a 20 di 59
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