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Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 1-gen-2015 Paraboschi, E; Cardamone, G; Rimoldi, V; Gemmati, D; Spreafico, M; Duga, S; Solda, G; Asselta, R
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
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 1-gen-2015 Nuzzo, F; Paraboschi, Em; Straniero, L; Pavlova, A; Duga, S; Castoldi, E.
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 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
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 1-gen-2017 Paraboschi, E; Cardamone, G; Rimoldi, V; Duga, S; Solda, G; 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
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.
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 1-gen-2018 Paraboschi, E; Cardamone, G; Solda', G; Duga, S; Asselta, R.
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 1-gen-2018 Todisco, M; Fraccia, Tp; Smith, Gp; Corno, A; Bethge, L; Klussmann, S; Paraboschi, Em; Asselta, R; Colombo, D; Zanchetta, G; Clark, Na; Bellini, T
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.
Newtonian to non-newtonian fluid transition of a model transient network 1-gen-2018 Nava, G; Yang, T; Vitali, V; Minzioni, P; Cristiani, I; Bragheri, F; Osellame, R; Bethge, L; Klussmann, S; Paraboschi, Em; Asselta, R; Bellini, T
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
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 1-gen-2018 Rimoldi, V; Paraboschi, E; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S; Asselta, R.
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 1-gen-2019 Cardamone, G; Paraboschi, E; Solda, G; Cantoni, C; Supino, D; Piccio, L; Duga, S; Asselta, R
Sighting acute myocardial infarction through platelet gene expression 1-gen-2019 Gobbi, G; Carubbi, C; Tagliazucchi, Gm; Masselli, E; Mirandola, P; Pigazzani, F; Crocamo, A; Notarangelo, Mf; Suma, S; Paraboschi, E; Maglietta, G; Nagalla, S; Pozzi, G; Galli, D; Vaccarezza, M; Fortina, P; Addya, S; Ertel, A; Bray, P; Duga, S; Berzuini, C; Vitale, M; Ardissino, D.
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 1-gen-2019 La Manna, Mp; Orlando, V; Paraboschi, Em; Tamburini, B; Di Carlo, P; Cascio, A; Asselta, R; Dieli, F; Caccamo, N
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 1-gen-2019 Paraboschi, Em; Menegatti, M; Peyvandi, F; Duga, S
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
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 1-gen-2020 Facchi, D; Rimoldi, V; Straniero, L; Paraboschi, Em; Soldà, G; Zecchinelli, Al; Cilia, R; Duga, S; Pezzoli, G; Asselta, R.
Mostrati risultati da 21 a 40 di 61
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