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Human Molecular Genetics|December 22, 2011
A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mousePaul N Porensky, Chalermchai Mitrpant, Vicki L McGovern, et al.American Journal of Human Genetics|February 1, 1995
Autosomal dominant distal myopathy: linkage to chromosome 14N G Laing, B A Laing, C Meredith, et al.Nature Medicine|July 9, 2003
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouseQi Long Lu, Christopher J Mann, Fang Lou, et al.Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.Journal of Neuroimmunology|September 27, 2012
Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositisArada Rojana-udomsart, Chalermchai Mitrpant, Ian James, et al.Studies in Health Technology and Informatics|July 27, 2015
A Registry Framework Enabling Patient-Centred CareMatthew I Bellgard, Kathryn Napier, Lee Render, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|June 21, 2007
Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouseSue Fletcher, Kaite Honeyman, Abbie M Fall, et al.Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationC C Hunt, H J Eyre, P A Akkari, et al.Biochemical Society Transactions|July 20, 2007
Cell-penetrating peptide-morpholino conjugates alter pre-mRNA splicing of DMD (Duchenne muscular dystrophy) and inhibit murine coronavirus replication in vivoH M Moulton, S Fletcher, B W Neuman, et al.Annals of Neurology|December 7, 2007
DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapyOlga L Gurvich, Therese M Tuohy, Michael T Howard, et al.Pageof 19