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Stefano Duga

Showing results (21-30 of 141) with videos related to

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British Journal of Haematology|September 15, 2007
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemiaSilvia Spena, Rosanna Asselta, Manuela Platé, 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.
Blood|October 24, 2002
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sitesSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Haematologica|December 6, 2006
Coagulation factor V gene analysis in five Indian patients: identification of three novel small deletionsRosanna Asselta, Claudia Dall'Osso, Stefano Duga, 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.
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.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2012
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's diseaseIlaria Guella, Giulia Soldà, Roberto Cilia, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Pageof 15

Showing results (21-30 of 141) with videos related to

Sort By:
Pageof 15
British Journal of Haematology|September 15, 2007
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemiaSilvia Spena, Rosanna Asselta, Manuela Platé, 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.
Blood|October 24, 2002
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sitesSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Haematologica|December 6, 2006
Coagulation factor V gene analysis in five Indian patients: identification of three novel small deletionsRosanna Asselta, Claudia Dall'Osso, Stefano Duga, 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.
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.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2012
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's diseaseIlaria Guella, Giulia Soldà, Roberto Cilia, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Pageof 15