Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Graham McClorey

Showing results (1-10 of 36) with videos related to

Pageof 4
Sort By:
Biomedicines|May 9, 2018
Cell-Penetrating Peptides to Enhance Delivery of Oligonucleotide-Based TherapeuticsGraham McClorey, Subhashis Banerjee
Current Opinion in Pharmacology|August 17, 2015
An overview of the clinical application of antisense oligonucleotides for RNA-targeting therapiesGraham McClorey, Matthew J Wood
Plos Genetics|July 3, 2007
Modulating the expression of disease genes with RNA-based therapyMatthew Wood, Haifang Yin, Graham McClorey
Current Opinion in Pharmacology|August 9, 2005
Splicing intervention for Duchenne muscular dystrophyGraham McClorey, Susan Fletcher, Stephen Wilton
Genes|June 13, 2017
Splice-Switching Therapy for Spinal Muscular AtrophyKatharina E Meijboom, Matthew J A Wood, Graham McClorey
Gene|December 14, 2011
Antisense oligonucleotide corrects splice abnormality in hereditary myopathy with lactic acidosisPetter Schandl Sanaker, Marina Toompuu, Graham McClorey, et al.
The Journal of Gene Medicine|November 20, 2002
Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophyChristopher J Mann, Kaite Honeyman, Graham McClorey, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
Small RNA-Mediated Epigenetic Myostatin SilencingThomas C Roberts, Samir El Andaloussi, Kevin V Morris, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 8, 2007
Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcriptSteve D Wilton, Abbie M Fall, Penny L Harding, et al.
Nucleic Acids Research|December 4, 2014
Bi-specific splice-switching PMO oligonucleotides conjugated via a single peptide active in a mouse model of Duchenne muscular dystrophyFazel Shabanpoor, Graham McClorey, Amer F Saleh, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Biomedicines|May 9, 2018
Cell-Penetrating Peptides to Enhance Delivery of Oligonucleotide-Based TherapeuticsGraham McClorey, Subhashis Banerjee
Current Opinion in Pharmacology|August 17, 2015
An overview of the clinical application of antisense oligonucleotides for RNA-targeting therapiesGraham McClorey, Matthew J Wood
Plos Genetics|July 3, 2007
Modulating the expression of disease genes with RNA-based therapyMatthew Wood, Haifang Yin, Graham McClorey
Current Opinion in Pharmacology|August 9, 2005
Splicing intervention for Duchenne muscular dystrophyGraham McClorey, Susan Fletcher, Stephen Wilton
Genes|June 13, 2017
Splice-Switching Therapy for Spinal Muscular AtrophyKatharina E Meijboom, Matthew J A Wood, Graham McClorey
Gene|December 14, 2011
Antisense oligonucleotide corrects splice abnormality in hereditary myopathy with lactic acidosisPetter Schandl Sanaker, Marina Toompuu, Graham McClorey, et al.
The Journal of Gene Medicine|November 20, 2002
Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophyChristopher J Mann, Kaite Honeyman, Graham McClorey, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
Small RNA-Mediated Epigenetic Myostatin SilencingThomas C Roberts, Samir El Andaloussi, Kevin V Morris, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 8, 2007
Antisense oligonucleotide-induced exon skipping across the human dystrophin gene transcriptSteve D Wilton, Abbie M Fall, Penny L Harding, et al.
Nucleic Acids Research|December 4, 2014
Bi-specific splice-switching PMO oligonucleotides conjugated via a single peptide active in a mouse model of Duchenne muscular dystrophyFazel Shabanpoor, Graham McClorey, Amer F Saleh, et al.
Pageof 4