Showing results (121-130 of 234) with videos related to

Sort By:
Pageof 24
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 22, 2009
Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skippingAurélie Goyenvalle, Arran Babbs, Dave Powell, et al.
The Journal of Gene Medicine|November 15, 2005
Dystrophin expression in the mdx mouse after localised and systemic administration of a morpholino antisense oligonucleotideSusan Fletcher, Kaite Honeyman, Abbie M Fall, et al.
Frontiers in Neuroscience|December 24, 2019
ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?Rita Mejzini, Loren L Flynn, Ianthe L Pitout, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationH Eyre, P A Akkari, S D Wilton, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 25, 2010
Dystrophin isoform induction in vivo by antisense-mediated alternative splicingSue Fletcher, Abbie M Adams, Russell D Johnsen, et al.
Molecular Therapy. Nucleic Acids|December 31, 2018
Antisense Oligonucleotides Targeting Angiogenic Factors as Potential Cancer TherapeuticsBao T Le, Prithi Raguraman, Tamer R Kosbar, et al.
International Journal of Molecular Sciences|August 29, 2024
Is Exon Skipping a Viable Therapeutic Approach for Vascular Ehlers-Danlos Syndrome with Mutations in COL3A1 Exon 10 or 15?Sasiwimon Utama, Jessica M Cale, Chalermchai Mitrpant, et al.
Medical Oncology (Northwood, London, England)|January 1, 2013
Perioperative DCF chemotherapy protocol for patients with gastroesophageal adenocarcinoma: correlation between response to treatment and outcomeT Alcindor, L E Ferri, V Marcus, et al.
Journal of Neuromuscular Diseases|September 5, 2017
Efficient Skipping of Single Exon Duplications in DMD Patient-Derived Cell Lines Using an Antisense Oligonucleotide ApproachNicolas Wein, Adeline Vulin, Andrew R Findlay, et al.
Neuromuscular Disorders : NMD|July 1, 1997
A splice-site mutation causing ovine McArdle's diseaseP Tan, J G Allen, S D Wilton, et al.
Pageof 24