Sfoglia per Autore
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
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
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
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009 G. Solda’, E.M. Paraboschi, D. Gemmati, P. Zamboni, S. Duga, R. Asselta
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population
2009 R. Asselta, E.M. Paraboschi, G. Soldà, C. Dall’Osso, D. Gemmati, P. Zamboni, M.D. Benedetti, S. D’Alfonso, S. Duga
Differential expression of microRNAs in peripheral blood mononuclear cells of multiple sclerosis patients
2009 E.M. Paraboschi, G. Soldà, D. Gemmati, G. Zeri, E. Orioli, P. Zamboni, S. Duga, R. Asselta
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
Identification of the first alu-mediated large deletion involving the f5 gene in a compound heterozygous patient with severe factor v deficiency
2011 I. Guella, E.M. Paraboschi, W.A. van Schalkwyk, R. Asselta, S. Duga
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
2011 E.M. Paraboschi, G. Soldà, D. Gemmati, E. Orioli, G. Zeri, D. Benedetti, A. Salviati, N. Barizzone, M. Leone, S. Duga, R. Asselta
ROLE OF THE PRKCA GENE AND OF MICRORNAS IN THE SUSCEPTIBILITY TO MULTIPLE SCLEROSIS
2012 E.M. Paraboschi
Phase behavior and critical activated dynamics of limited-valence DNA nanostars
2013 S. Biffi, R. Cerbino, F. Bomboi, E.M. Paraboschi, R. Asselta, F. Sciortino, T. Bellini
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
2014 E.M. Paraboschi, V. Rimoldi, G. Soldà, T. Tabaglio, C. Dall'Osso, E. Saba, M. Vigliano, A. Salviati, M. Leone, M.D. Benedetti, D. Fornasari, J. Saarela, P.L. De Jager, N.A. Patsopoulos, S. D'Alfonso, D. Gemmati, S. Duga, R. Asselta
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay
2015 F. Nuzzo, E.M. Paraboschi, L. Straniero, A. Pavlova, S. Duga, E. Castoldi
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering
2015 T.P. Fraccia, G.P. Smith, G. Zanchetta, E. Paraboschi, Y. Yi, D.M. Walba, G. Dieci, N.A. Clark, T. Bellini
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
2017 R. Asselta, E.M. Paraboschi, V. Rimoldi, M. Menegatti, F. Peyvandi, O. Salomon, S. Duga
Newtonian to non-newtonian fluid transition of a model transient network
2018 G. Nava, T. Yang, V. Vitali, P. Minzioni, I. Cristiani, F. Bragheri, R. Osellame, L. Bethge, S. Klussmann, E.M. Paraboschi, R. Asselta, T. Bellini
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency.
2019 E. Paraboschi, M. Menegatti, F. Payvandi, S. Duga, R. Asselta
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
2020 D. Ellinghaus, F. Degenhardt, L. Bujanda, M. Buti, A. Albillos, P. Invernizzi, J. Fernández, D. Prati, G. Baselli, R. Asselta, M.M. Grimsrud, C. Milani, F. Aziz, J. Kässens, S. May, M. Wendorff, L. Wienbrandt, F. Uellendahl-Werth, T. Zheng, X. Yi, R. de Pablo, A.G. Chercoles, A. Palom, A. Garcia-Fernandez, F. Rodriguez-Frias, A. Zanella, A. Bandera, A. Protti, A. Aghemo, A. Lleo, A. Biondi, A. Caballero-Garralda, A. Gori, A. Tanck, A. Carreras Nolla, A. Latiano, A.L. Fracanzani, A. Peschuck, A. Julià, A. Pesenti, A. Voza, D. Jiménez, B. Mateos, B. Nafria Jimenez, C. Quereda, C. Paccapelo, C. Gassner, C. Angelini, C. Cea, A. Solier, D. Pestaña, E. Muñiz-Diaz, E. Sandoval, E.M. Paraboschi, E. Navas, F. García Sánchez, F. Ceriotti, F. Martinelli-Boneschi, F. Peyvandi, F. Blasi, L. Téllez, A. Blanco-Grau, G. Hemmrich-Stanisak, G. Grasselli, G. Costantino, G. Cardamone, G. Foti, S. Aneli, H. Kurihara, H. ElAbd, I. My, I. Galván-Femenia, J. Martín, J. Erdmann, J. Ferrusquía-Acosta, K. Garcia-Etxebarria, L. Izquierdo-Sanchez, L.R. Bettini, L. Sumoy, L. Terranova, L. Moreira, L. Santoro, L. Scudeller, F. Mesonero, L. Roade, M.C. Rühlemann, M. Schaefer, M. Carrabba, M. Riveiro-Barciela, M.E. Figuera Basso, M.G. Valsecchi, M. Hernandez-Tejero, M. Acosta-Herrera, M. D’Angiò, M. Baldini, M. Cazzaniga, M. Schulzky, M. Cecconi, M. Wittig, M. Ciccarelli, M. Rodríguez-Gandía, M. Bocciolone, M. Miozzo, N. Montano, N. Braun, N. Sacchi, N. Martínez, O. Özer, O. Palmieri, P. Faverio, P. Preatoni, P. Bonfanti, P. Omodei, P. Tentorio, P. Castro, P.M. Rodrigues, A. Blandino Ortiz, R. de Cid, R. Ferrer, R. Gualtierotti, R. Nieto, S. Goerg, S. Badalamenti, S. Marsal, G. Matullo, S. Pelusi, S. Juzenas, S. Aliberti, V. Monzani, V. Moreno, T. Wesse, T.L. Lenz, T. Pumarola, V. Rimoldi, S. Bosari, W. Albrecht, W. Peter, M. Romero-Gómez, M. D’Amato, S. Duga, J.M. Banales, J.R. Hov, T. Folseraas, L. Valenti, A. Franke, T.H. Karlsen
Profiling the mutational landscape of coagulation factor V deficiency
2020 E.M. Paraboschi, M. Menegatti, V. Rimoldi, M. Borhany, M. Abdelwahab, D. Gemmati, F. Peyvandi, S. Duga, R. Asselta
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease
2020 E.M. Paraboschi, A.V. Khera, P.A. Merlini, L. Gigante, F. Peyvandi, M. Chaffin, M. Menegatti, F. Busti, D. Girelli, N. Martinelli, O. Olivieri, S. Kathiresan, D. Ardissino, R. Asselta, S. Duga
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