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Mirko Pinotti

Showing results (41-50 of 100) with videos related to

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Human Molecular Genetics|June 12, 2015
Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotidesDario Balestra, Elena Barbon, Daniela Scalet, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 19, 2016
Exploring Splicing-Switching Molecules For Seckel Syndrome TherapyDaniela Scalet, Dario Balestra, Sara Rohban, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 20, 2009
Temporal and genotype-driven variation of factor VII levels in patients with acute myocardial infarctionPaolo Ferraresi, Gianluca Campo, Giovanna Marchetti, et al.
Haematologica|November 25, 2017
Clustered <i>F8</i> missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activityIrving Donadon, John H McVey, Isabella Garagiola, et al.
International Journal of Molecular Sciences|August 28, 2019
Splicing Mutations Impairing CDKL5 Expression and Activity Can be Efficiently Rescued by U1snRNA-Based TherapyDario Balestra, Domenico Giorgio, Matteo Bizzotto, et al.
Blood|December 25, 2007
U1-snRNA-mediated rescue of mRNA processing in severe factor VII deficiencyMirko Pinotti, Lara Rizzotto, Dario Balestra, et al.
International Journal of Pharmaceutics|July 2, 2021
An advanced method for the small-scale production of high-quality minicircle DNAHardy Mitdank, Simko Sama, Meike Tröger, et al.
Cell & Bioscience|August 31, 2019
The effect of the chemical chaperone 4-phenylbutyrate on secretion and activity of the p.Q160R missense variant of coagulation factor FVIIElisabeth Andersen, Maria Eugenia Chollet, Marcello Baroni, et al.
FEBS Letters|September 3, 2013
Replacement of the Y450 (c234) phenyl ring in the carboxyl-terminal region of coagulation factor IX causes pleiotropic effects on secretion and enzyme activityAlessio Branchini, Matteo Campioni, Maria Gabriella Mazzucconi, et al.
Human Mutation|May 24, 2012
Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutationsMirko Pinotti, Pierpaolo Caruso, Alessandro Canella, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|June 12, 2015
Regulation of a strong F9 cryptic 5'ss by intrinsic elements and by combination of tailored U1snRNAs with antisense oligonucleotidesDario Balestra, Elena Barbon, Daniela Scalet, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 19, 2016
Exploring Splicing-Switching Molecules For Seckel Syndrome TherapyDaniela Scalet, Dario Balestra, Sara Rohban, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 20, 2009
Temporal and genotype-driven variation of factor VII levels in patients with acute myocardial infarctionPaolo Ferraresi, Gianluca Campo, Giovanna Marchetti, et al.
Haematologica|November 25, 2017
Clustered <i>F8</i> missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activityIrving Donadon, John H McVey, Isabella Garagiola, et al.
International Journal of Molecular Sciences|August 28, 2019
Splicing Mutations Impairing CDKL5 Expression and Activity Can be Efficiently Rescued by U1snRNA-Based TherapyDario Balestra, Domenico Giorgio, Matteo Bizzotto, et al.
Blood|December 25, 2007
U1-snRNA-mediated rescue of mRNA processing in severe factor VII deficiencyMirko Pinotti, Lara Rizzotto, Dario Balestra, et al.
International Journal of Pharmaceutics|July 2, 2021
An advanced method for the small-scale production of high-quality minicircle DNAHardy Mitdank, Simko Sama, Meike Tröger, et al.
Cell & Bioscience|August 31, 2019
The effect of the chemical chaperone 4-phenylbutyrate on secretion and activity of the p.Q160R missense variant of coagulation factor FVIIElisabeth Andersen, Maria Eugenia Chollet, Marcello Baroni, et al.
FEBS Letters|September 3, 2013
Replacement of the Y450 (c234) phenyl ring in the carboxyl-terminal region of coagulation factor IX causes pleiotropic effects on secretion and enzyme activityAlessio Branchini, Matteo Campioni, Maria Gabriella Mazzucconi, et al.
Human Mutation|May 24, 2012
Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutationsMirko Pinotti, Pierpaolo Caruso, Alessandro Canella, et al.
Pageof 10