Paraboschi, Elvezia Maria

Paraboschi, Elvezia Maria  

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A Frequent Oligogenic Involvement in Congenital Hypothyroidism 1-gen-2017 de Filippis, T; Gelmini, G; Paraboschi, E; Vigone, Mc; Di Frenna, M; Marelli, F; Bonomi, M; Cassio, A; Larizza, D; Moro, M; Radetti, G; Salerno, M; Ardissino, D; Weber, G; Gentilini, D; Guizzardi, F; Duga, S; Persani, L.
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 1-gen-2015 Fraccia, Tp; Smith, Gp; Zanchetta, G; Paraboschi, E; Yi, Y; Walba, Dm; Dieci, G; Clark, Na; Bellini, T
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 1-gen-2020 Asselta, Rosanna; Paraboschi, Elvezia Maria; Mantovani, Alberto; Duga, Stefano
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 1-gen-2017 Cardamone, G; Paraboschi, Em; Rimoldi, V; Duga, S; Solda, G; Asselta, R
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
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
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 1-gen-2021 Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 1-gen-2021 Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo
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
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 1-gen-2017 Asselta, R; Paraboschi, E; Rimoldi, V; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 1-gen-2017 Paraboschi, E; Duga, S; Asselta, R
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 1-gen-2020 Corrado, L; Pensato, V; Croce, R; Di Pierro, A; Mellone, S; Dalla Bella, E; Salsano, E; Paraboschi, E; Giordano, M; Saraceno, M; Mazzini, L; Gellera, C; D'Alfonso, S
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
Functional and clinical implications of genetic structure in 1686 Italian exomes 1-gen-2021 Birolo, Giovanni; Aneli, Serena; Di Gaetano, Cornelia; Cugliari, Giovanni; Russo, Alessia; Allione, Alessandra; Casalone, Elisabetta; Giorgio, Elisa; Paraboschi, Elvezia M; Ardissino, Diego; Duga, Stefano; Asselta, Rosanna; Matullo, Giuseppe
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
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.
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 1-gen-2018 Tisato, V; Zuliani, G; Vigliano, M; Longo, G; Franchini, E; Secchiero, P; Zauli, G; Paraboschi, Em; Vikram Singh, A; Serino, Ml; Ortolani, B; Zurlo, A; Bosi, C; Greco, A; Seripa, D; Asselta, R; Gemmati, D
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 1-gen-2018 Cardamone, G; Paraboschi, E; Solda', G; Duga, S; Saarela, J; Asselta, R.
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.
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.