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Franco Pagani

Showing results (21-30 of 55) with videos related to

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Blood|April 24, 2009
Rescue of coagulation factor VII function by the U1+5A snRNAMirko Pinotti, Dario Balestra, Lara Rizzotto, et al.
Nature Genetics|March 13, 2002
A new type of mutation causes a splicing defect in ATMFranco Pagani, Emanuele Buratti, Cristiana Stuani, et al.
Human Mutation|February 10, 2015
Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory ElementAndrea Dal Mas, Paola Fortugno, Irving Donadon, et al.
Human Mutation|September 16, 2020
Rescue of common exon-skipping mutations in cystic fibrosis with modified U1 snRNAsStefano Donegà, Malgorzata Ewa Rogalska, Giulia Pianigiani, et al.
Experimental Dermatology|March 8, 2018
Analysis of psoriasis-relevant gene expression and exon usage alterations after silencing of SR-rich splicing regulatorsEszter Szlavicz, Peter Olah, Kornélia Szabo, et al.
Plos Genetics|May 27, 2016
Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein FunctionMojca 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 MutantsDario Balestra, Daniela Scalet, Franco Pagani, et al.
Nature Communications|April 5, 2016
Therapeutic activity of modified U1 core spliceosomal particlesMalgorzata Ewa Rogalska, Mojca Tajnik, Danilo Licastro, et al.
Molecular Cancer|July 20, 2013
TMEM16A alternative splicing coordination in breast cancerIfeoma Ubby, Erica Bussani, Antonio Colonna, et al.
Human Mutation|October 7, 2008
Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNAGaby Tanner, Esther Glaus, Daniel Barthelmes, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Blood|April 24, 2009
Rescue of coagulation factor VII function by the U1+5A snRNAMirko Pinotti, Dario Balestra, Lara Rizzotto, et al.
Nature Genetics|March 13, 2002
A new type of mutation causes a splicing defect in ATMFranco Pagani, Emanuele Buratti, Cristiana Stuani, et al.
Human Mutation|February 10, 2015
Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory ElementAndrea Dal Mas, Paola Fortugno, Irving Donadon, et al.
Human Mutation|September 16, 2020
Rescue of common exon-skipping mutations in cystic fibrosis with modified U1 snRNAsStefano Donegà, Malgorzata Ewa Rogalska, Giulia Pianigiani, et al.
Experimental Dermatology|March 8, 2018
Analysis of psoriasis-relevant gene expression and exon usage alterations after silencing of SR-rich splicing regulatorsEszter Szlavicz, Peter Olah, Kornélia Szabo, et al.
Plos Genetics|May 27, 2016
Molecular Basis and Therapeutic Strategies to Rescue Factor IX Variants That Affect Splicing and Protein FunctionMojca 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 MutantsDario Balestra, Daniela Scalet, Franco Pagani, et al.
Nature Communications|April 5, 2016
Therapeutic activity of modified U1 core spliceosomal particlesMalgorzata Ewa Rogalska, Mojca Tajnik, Danilo Licastro, et al.
Molecular Cancer|July 20, 2013
TMEM16A alternative splicing coordination in breast cancerIfeoma Ubby, Erica Bussani, Antonio Colonna, et al.
Human Mutation|October 7, 2008
Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNAGaby Tanner, Esther Glaus, Daniel Barthelmes, et al.
Pageof 6