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Mirko Pinotti

Showing results (1-10 of 100) with videos related to

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Thrombosis Research|January 25, 2020
A recoded view on the F9 p.Cys178Ter pathogenic mechanismAlessio Branchini, Mirko Pinotti
Expert Review of Hematology|January 24, 2025
Could targeted gene insertion of factor 9 be a potential durable treatment for Hemophilia B?Giancarlo Castaman, Mirko Pinotti
Orphanet Journal of Rare Diseases|April 10, 2026
Prime editing of the common Familial Dysautonomia-causing c.2204 + 6T > C splicing mutationLaura Peretto, Mirko Pinotti, Dario Balestra
Advances in Protein Chemistry and Structural Biology|September 10, 2022
Translation termination codons in protein synthesis and diseaseSilvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
International Journal of Molecular Sciences|December 16, 2020
Molecular Insights into Determinants of Translational Readthrough and Implications for Nonsense Suppression ApproachesSilvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
Haematologica|March 4, 2008
Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiencyBarbara Lunghi, Mirko Pinotti, Iva Maestri, et al.
Haematologica|April 13, 2004
Molecular characterization of factor X deficiency associated with borderline plasma factor X levelMirko Pinotti, Monia Monti, Marcello Baroni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Gene Editing for Haemophilia-The Next FrontierMirko Pinotti, Gregory A Newby, Sundar Selvaraj, et al.
Molecular Medicine (Cambridge, Mass.)|November 8, 2006
Intracellular evaluation of ER targeting elucidates a mild form of inherited coagulation deficiencyLara Rizzotto, Mirko Pinotti, Paolo Pinton, et al.
Thrombosis Research|November 22, 2011
Functional geneticsGiovanna Marchetti, Mirko Pinotti, Barbara Lunghi, et al.
Pageof 10

Showing results (1-10 of 100) with videos related to

Sort By:
Pageof 10
Thrombosis Research|January 25, 2020
A recoded view on the F9 p.Cys178Ter pathogenic mechanismAlessio Branchini, Mirko Pinotti
Expert Review of Hematology|January 24, 2025
Could targeted gene insertion of factor 9 be a potential durable treatment for Hemophilia B?Giancarlo Castaman, Mirko Pinotti
Orphanet Journal of Rare Diseases|April 10, 2026
Prime editing of the common Familial Dysautonomia-causing c.2204 + 6T > C splicing mutationLaura Peretto, Mirko Pinotti, Dario Balestra
Advances in Protein Chemistry and Structural Biology|September 10, 2022
Translation termination codons in protein synthesis and diseaseSilvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
International Journal of Molecular Sciences|December 16, 2020
Molecular Insights into Determinants of Translational Readthrough and Implications for Nonsense Suppression ApproachesSilvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
Haematologica|March 4, 2008
Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiencyBarbara Lunghi, Mirko Pinotti, Iva Maestri, et al.
Haematologica|April 13, 2004
Molecular characterization of factor X deficiency associated with borderline plasma factor X levelMirko Pinotti, Monia Monti, Marcello Baroni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Gene Editing for Haemophilia-The Next FrontierMirko Pinotti, Gregory A Newby, Sundar Selvaraj, et al.
Molecular Medicine (Cambridge, Mass.)|November 8, 2006
Intracellular evaluation of ER targeting elucidates a mild form of inherited coagulation deficiencyLara Rizzotto, Mirko Pinotti, Paolo Pinton, et al.
Thrombosis Research|November 22, 2011
Functional geneticsGiovanna Marchetti, Mirko Pinotti, Barbara Lunghi, et al.
Pageof 10