Sfoglia per Autore
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform
2007 I. Guella, R. Asselta, V. Rimoldi, M.L. Tenchini, S. Duga
The Proprotein Convertase Subtilisin-Kexin Type 9 (PCSK9) R46L variant is associated with reduced serum low-density lipoprotein cholesterol in the Italian population
2007 I. Guella, R. Asselta, V. Rimoldi, F. Peyvandi, R. Fetiveau, P.A. Merlini, S. Kathiresan, D. Ardissino, P.M. Mannucci, S. Duga, A. Thrombosis, V. Biology Italian Study Group
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
2007 C. Bozzao, V. Rimoldi, R. Asselta, M. Landau, R. Ghiotto, M.L. Tenchini, R. De Cristofaro, G. Castaman, S. Duga
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
2008 I. Guella, V. Rimoldi, P.A. Merlini, R. Asselta, E.M. Paraboschi, M. Francolini, F. Peyvandi, D. Ardissino, P.M. Mannucci, S. Duga
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation FXI isoform
2008 V. Rimoldi, I. Guella, R. Asselta, R. De Cristofaro, F. Peyvandi, P.M. Mannucci, S. Duga
Characterization of the genetic basis of FXI deficiency in fourteen unrelated patients
2009 V. Rimoldi, I. Guella, S. Spena, N. Ciavarella, F. Peyvandi, R. Asselta, P.M. Mannucci, S. Duga
Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease
2009 I. Guella, V. Rimoldi, R. Asselta, D. Ardissino, M. Francolini, N. Martinelli, D. Girelli, F. Peyvandi, M. Tubaro, P.A. Merlini, P.M. Mannucci, S. Duga
Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema)
2009 M. Cicardi, A. Zanichelli, E. Bonanni, C. Suffritti, L. Maggioni, S. Caccia, R. Russo, Y. Zhi, S. Duga, R. Asselta, V. Rimoldi, G. Castellano
Mutational screening and functional analyses in the zebrafish model of GIGYF2 as a candidate gene for Parkinson disease
2009 I. Guella, L. Del Giacco, R. Asselta, A. Pistocchi, V. Rimoldi, F. Sironi, P. Primignani, M. Zini, G. Pezzoli, S. Duga, S. Goldwurm
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency
2009 S. Spena, R. Asselta, S. Caccia, V. Rimoldi, S.H. Giacomelli, A. Tagliaferri, F. Peyvandi, G. Castaman, S. Duga
Mutational screening and functional analyses in the zebrafish model of GIGYF2 as a candidate gene for Parkinson disease
2009 I. Guella, A.S. Pistocchi, R. Asselta, V. Rimoldi, F. Sironi, L.C. Trotta, P. Primignani, M. Zini, A. Zecchinelli, D. Coviello, G. Pezzoli, L.P.C. Del Giacco, S. Duga, S. Goldwurm
Mutational screening and Zebrafish functional analysis of Gigyf2 as a Parkinson-disease gene
2009 I. Guella, A. Pistocchi, R. Asselta, V. Rimoldi, A. Ghilardi, F. Sironi, L. Trotta, P. Primignani, M. Zini, A. Zecchinelli, D. Coviello, G. Pezzoli, L. Del Giacco, S. Duga, S. Goldwurm
Characterization of the genetic basis of FXI deficiency in two Turkish patients
2010 E. Berber, V. Rimoldi, S. Usluer, S. Aksu, Y. Pekçelen, S.H. Çağlayan, S. Duga
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA
2010 R. Asselta, V. Rimoldi, I. Guella, G.Soldà, R. De Cristofaro, F. Peyvandi, S. Duga
The double-faced association of the PRKCA gene with multiple sclerosis
2010 E.M. Paraboschi, G. Soldà, V. Rimoldi, C. Dall’Osso, G.M. Anelli, D. Gemmati, P. Zamboni, A. Salviati, M. Benedetti, S. D’Alfonso, S. Duga, R. Asselta
Hupf1 and hupf2 knockdown by RNA interference in HEPG2 cells as a model to study nonsense-mediated mRNA decay modulation of coagulation-gene expression
2010 M. Platè, V. Rimoldi, S. Duga, R. Asselta
Response: Further thoughts on the "phantom" delta6/7 FXI isoform
2010 R. Asselta, V. Rimoldi, I. Guella, G.M. Soldà, R. De Cristofaro, F. Peyvandi, S. Duga
Oxytocin-induced cell growth proliferation in human mymetrial cells and leiomyomas
2010 M. Busnelli, V. Rimoldi, P. Viganò, L. Persani, A.M. Di Blasio, B. Chini
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema)
2011 S. Caccia, V. Rimoldi, R. Asselta, G.M. Soldà, E. Bonanni, R. Russo, S. Duga, M. Cicardi
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript
2013 V. Rimoldi, G. Soldà, R. Asselta, S. Spena, C. Stuani, E. Buratti, S. Duga
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