Sfoglia per Autore
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform
2006 R. Asselta, I. Guella, V. Rimoldi, M. Malcovati, M.L. Tenchini, S. Duga
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione
2006 R. Asselta, V. Rimoldi, I. Guella, M. Malcovati, M.L. Tenchini, S. Duga
The role of the Myocyte Enhancer Factor 2A (MEF2A) gene in the pathogenesis of myocardial infarction
2007 V. Rimoldi, I. Guella, R. Asselta, C. Ruggiero, M. Francolini, F. Peyvandi, D. Ardissino, M.L. Tenchini, P.M. Mannucci, S. Duga
The Proprotein Convertase Subtilisin-Kexin type 9 (PCSK9) R46L variant is associated with reduced serum low-density lipoprotein cholesterol (LDL-C) in the Italian population
2007 S. Duga, I. Guella, V. Rimoldi, R. Asselta, F. Peyvandi, R. Fetiveau, P.A. Merlini, D. Ardissino, P.M. Mannucci, A. Thrombosis, V. Biology Italian Study Group
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
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
Identification and characterization of 6 novel genetic defects leading to factor V deficiency
2008 I. Guella, E.M. Paraboschi, S. Duga, R. Asselta
Molecular characterization of six novel mutations causing factor V deficiency
2008 I. Guella, E.M. Paraboschi, S. Duga, F. Peyvandi, J. Song, N. Ciavarella, P.M. Mannucci, R. Asselta
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
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect
2008 I. Guella, G. Soldà, S. Spena, R. Asselta, R. Ghiotto, M.L. Tenchini, G. Castaman, S. Duga
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern
2008 C. Dall'Osso, I. Guella, S. Duga, N. Locatelli, E.M. Paraboschi, M. Spreafico, A. Afrasiabi, C. Pechlaner, F. Peyvandi, M.L. Tenchini, R. Asselta
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
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
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
2009 J. Song, I. Guella, K.Y. Kwon, H. Cho, R. Park, R. Asselta, J.R. Choi
Factor XI deficiency in Southern Iran: identification of a novel missense mutation
2009 M. Karimi, H. Jafari, S. Lahsaeizadeh, A. Afrasiabi, A. Akbari, J. Dehbozorgian, R. Ardeshiri, I. Guella, R. Asselta, F. Peyvandi
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
Molecular characterization of 9 genetic defects responsible for FV deficiency
2009 E.M. Paraboschi, I. Guella, S. Duga, F. Peyvandi, P.M. Mannucci, R. Asselta
Mutational screening of 25 unrelated FV-deficient patients from six countries
2009 I. Guella, E.M. Paraboschi, S. Duga, F. Peyvandi, D. Gemmati, N. Ciavarella, P.M. Mannucci, R. Asselta
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
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