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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 afibrinogenaemia
Silvia 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 PRKCA
Elvezia 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 Sclerosis
Giulia 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 deficiency
Giulia 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 sites
Silvia 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 deletions
Rosanna 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 transcript
Valeria 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 Features
Letizia 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 disease
Ilaria 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 defects
Luca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Page
of 15
Search research articles
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Showing results (21-30 of 141) with videos related to
Sort By:
Page
of 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 afibrinogenaemia
Silvia 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 PRKCA
Elvezia 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 Sclerosis
Giulia 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 deficiency
Giulia 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 sites
Silvia 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 deletions
Rosanna 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 transcript
Valeria 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 Features
Letizia 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 disease
Ilaria 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 defects
Luca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Page
of 15