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Giulia Soldà

Showing results (1-10 of 69) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|January 11, 2025
Applying artificial intelligence to uncover the genetic landscape of coagulation factorsGiulia Soldà, Rosanna Asselta
Frontiers in Genetics|January 9, 2019
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated RegionsElvezia Maria Paraboschi, Giulia Cardamone, Giulia Soldà, et al.
Biomedicines|December 21, 2018
Genetic Association and Altered Gene Expression of <i>CYBB</i> in Multiple Sclerosis PatientsGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Biochimica Et Biophysica Acta. General Subjects|February 19, 2017
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCAElvezia Maria Paraboschi, Giulia Cardamone, Valeria Rimoldi, et al.
International Journal of Molecular Sciences|March 9, 2017
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple SclerosisGiulia Cardamone, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
Haematologica|December 7, 2005
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiencyGiulia Soldà, Rosanna Asselta, Rossella Ghiotto, et al.
Plos One|March 28, 2013
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcriptValeria Rimoldi, Giulia Soldà, Rosanna Asselta, et al.
Plos One|October 7, 2014
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesisVeronica Colangelo, Stéphanie François, Giulia Soldà, et al.
Briefings in Bioinformatics|April 23, 2009
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotesGiulia Soldà, Igor V Makunin, Osman U Sezerman, et al.
Frontiers in Genetics|October 27, 2018
First Replication of the Involvement of <i>OTUD6B</i> in Intellectual Disability Syndrome With Seizures and Dysmorphic FeaturesLetizia Straniero, Valeria Rimoldi, Giulia Soldà, et al.
Pageof 7

Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
Journal of Thrombosis and Haemostasis : JTH|January 11, 2025
Applying artificial intelligence to uncover the genetic landscape of coagulation factorsGiulia Soldà, Rosanna Asselta
Frontiers in Genetics|January 9, 2019
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated RegionsElvezia Maria Paraboschi, Giulia Cardamone, Giulia Soldà, et al.
Biomedicines|December 21, 2018
Genetic Association and Altered Gene Expression of <i>CYBB</i> in Multiple Sclerosis PatientsGiulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, et al.
Biochimica Et Biophysica Acta. General Subjects|February 19, 2017
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCAElvezia Maria Paraboschi, Giulia Cardamone, Valeria Rimoldi, et al.
International Journal of Molecular Sciences|March 9, 2017
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple SclerosisGiulia Cardamone, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
Haematologica|December 7, 2005
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiencyGiulia Soldà, Rosanna Asselta, Rossella Ghiotto, et al.
Plos One|March 28, 2013
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcriptValeria Rimoldi, Giulia Soldà, Rosanna Asselta, et al.
Plos One|October 7, 2014
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesisVeronica Colangelo, Stéphanie François, Giulia Soldà, et al.
Briefings in Bioinformatics|April 23, 2009
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotesGiulia Soldà, Igor V Makunin, Osman U Sezerman, et al.
Frontiers in Genetics|October 27, 2018
First Replication of the Involvement of <i>OTUD6B</i> in Intellectual Disability Syndrome With Seizures and Dysmorphic FeaturesLetizia Straniero, Valeria Rimoldi, Giulia Soldà, et al.
Pageof 7