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Neuromuscular Disorders : NMD|September 7, 2010
Personalized exon skipping strategies to address clustered non-deletion dystrophin mutationsSarah Forrest, Penny L Meloni, Francesco Muntoni, et al.FEBS Letters|October 7, 2003
Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscleK E Wells, S Fletcher, C J Mann, et al.Genetic Vaccines and Therapy|May 25, 2006
Induction of revertant fibres in the mdx mouse using antisense oligonucleotidesAbbie M Fall, Russell Johnsen, Kaite Honeyman, et al.Experimental Neurology|June 26, 2001
The regrowth of axons within tissue defects in the CNS is promoted by implanted hydrogel matrices that contain BDNF and CNTF producing fibroblastsN K Loh, S Woerly, S M Bunt, et al.Neuromuscular Disorders : NMD|August 9, 2005
Terminal antisense oligonucleotide modifications can enhance induced exon skippingBijanka L Gebski, Stephen J Errington, Russell D Johnsen, et al.Plos One|January 5, 2012
Translational regulation of utrophin by miRNAsUtpal Basu, Olga Lozynska, Catherine Moorwood, et al.International Journal of Molecular Sciences|October 6, 2020
A Splice Intervention Therapy for Autosomal Recessive Juvenile Parkinson's Disease Arising from Parkin MutationsDunhui Li, May T Aung-Htut, Kristin A Ham, et al.American Journal of Veterinary Research|January 5, 2002
Evaluation of a short interspersed nucleotide element in the 3' untranslated region of the defective dystrophin gene of dogs with muscular dystrophyS Fletcher, K S Carville, J M Howell, et al.Current Oncology (Toronto, Ont.)|June 7, 2012
Effect of exercise in reducing breast and chest-wall pain in patients with breast cancer: a pilot studyP Wong, T Muanza, T Hijal, et al.Frontiers in Medicine|March 10, 2022
Primary Nasal Epithelial Cells as a Surrogate Cell Culture Model for Type-II Alveolar Cells to Study ABCA-3 DeficiencyNicole C Shaw, Anthony Kicic, Sue Fletcher, et al.Pageof 24