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Materials (Basel, Switzerland)
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March 29, 2023
Clinically Relevant Properties of 3D Printable Materials for Intraoral Use in Orthodontics: A Critical Review of the Literature
Cecilia Goracci, Jovana Juloski, Claudio D'Amico, et al.
Molecular Biology of the Cell
|
November 6, 2015
Mcl-1 involvement in mitochondrial dynamics is associated with apoptotic cell death
Giampaolo Morciano, Carlotta Giorgi, Dario Balestra, et al.
Thrombosis Research
|
November 20, 2018
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies
Mattia Ferrarese, Silvia Pignani, Silvia Lombardi, et al.
Molecular Medicine (Cambridge, Mass.)
|
June 29, 2026
Immunogenic implications of translational readthrough modulate the association of F8 nonsense mutations with inhibitors in Hemophilia A
Maria Francesca Testa, Mirko Pinotti, Alessio Branchini, et al.
Plos Genetics
|
May 27, 2016
Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein Function
Mojca Tajnik, Malgorzata Ewa Rogalska, Erica Bussani, et al.
Molecular Therapy. Nucleic Acids
|
October 5, 2016
An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants
Dario Balestra, Daniela Scalet, Franco Pagani, et al.
Materials (Basel, Switzerland)
|
March 28, 2024
3D Printed Materials for Permanent Restorations in Indirect Restorative and Prosthetic Dentistry: A Critical Review of the Literature
Dario Balestra, Morgan Lowther, Cecilia Goracci, et al.
Journal of Human Genetics
|
March 3, 2018
The somatic FAH C.1061C>A change counteracts the frequent FAH c.1062+5G>A mutation and permits U1snRNA-based splicing correction
Daniela Scalet, Claudia Sacchetto, Francesco Bernardi, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Counteracting the Common Shwachman-Diamond Syndrome-Causing <i>SBDS</i> c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing
Laura Peretto, Elena Tonetto, Iva Maestri, et al.
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 oligonucleotides
Dario Balestra, Elena Barbon, Daniela Scalet, et al.
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Search research articles
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Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Materials (Basel, Switzerland)
|
March 29, 2023
Clinically Relevant Properties of 3D Printable Materials for Intraoral Use in Orthodontics: A Critical Review of the Literature
Cecilia Goracci, Jovana Juloski, Claudio D'Amico, et al.
Molecular Biology of the Cell
|
November 6, 2015
Mcl-1 involvement in mitochondrial dynamics is associated with apoptotic cell death
Giampaolo Morciano, Carlotta Giorgi, Dario Balestra, et al.
Thrombosis Research
|
November 20, 2018
The carboxyl-terminal region of human coagulation factor X as a natural linker for fusion strategies
Mattia Ferrarese, Silvia Pignani, Silvia Lombardi, et al.
Molecular Medicine (Cambridge, Mass.)
|
June 29, 2026
Immunogenic implications of translational readthrough modulate the association of F8 nonsense mutations with inhibitors in Hemophilia A
Maria Francesca Testa, Mirko Pinotti, Alessio Branchini, et al.
Plos Genetics
|
May 27, 2016
Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein Function
Mojca Tajnik, Malgorzata Ewa Rogalska, Erica Bussani, et al.
Molecular Therapy. Nucleic Acids
|
October 5, 2016
An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants
Dario Balestra, Daniela Scalet, Franco Pagani, et al.
Materials (Basel, Switzerland)
|
March 28, 2024
3D Printed Materials for Permanent Restorations in Indirect Restorative and Prosthetic Dentistry: A Critical Review of the Literature
Dario Balestra, Morgan Lowther, Cecilia Goracci, et al.
Journal of Human Genetics
|
March 3, 2018
The somatic FAH C.1061C>A change counteracts the frequent FAH c.1062+5G>A mutation and permits U1snRNA-based splicing correction
Daniela Scalet, Claudia Sacchetto, Francesco Bernardi, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Counteracting the Common Shwachman-Diamond Syndrome-Causing <i>SBDS</i> c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing
Laura Peretto, Elena Tonetto, Iva Maestri, et al.
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 oligonucleotides
Dario Balestra, Elena Barbon, Daniela Scalet, et al.
Page
of 4