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Animal Genetics|August 1, 1997
Characterization of the erythrocyte superoxide dismutase allozymes in the deer Cervus elaphusK He, S D Wilton, M L Tate, et al.The EMBO Journal|January 1, 1984
A comparison of genomic coding sequences for feather and scale keratins: structural and evolutionary implicationsK Gregg, S D Wilton, D A Parry, et al.International Journal of Molecular Sciences|June 19, 2024
Limb Girdle Muscular Dystrophy Type 2B (LGMD2B): Diagnosis and Therapeutic PossibilitiesBal Hari Poudel, Sue Fletcher, Steve D Wilton, et al.Inorganic Chemistry|November 13, 2001
Diversity in the structural chemistry of (phosphine)gold(I) 1,3,4-thiadiazole-2,5-dithiolates (bismuthiolates I)J D Wilton-Ely, A Schier, N W Mitzel, et al.Human Molecular Genetics|July 23, 2003
Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscleBianca L Gebski, Chrisopher J Mann, Susan Fletcher, et al.The Journal of Gene Medicine|June 11, 2003
Target selection for antisense oligonucleotide induced exon skipping in the dystrophin geneStephen J Errington, Christopher J Mann, Sue Fletcher, et al.Human Mutation|June 24, 2008
Characterization of a complex Duchenne muscular dystrophy-causing dystrophin gene inversion and restoration of the reading frame by induced exon skippingHeidi R Madden, Sue Fletcher, Mark R Davis, et al.Molecular Therapy. Nucleic Acids|June 4, 2026
Expanding the toolbox: Emerging antisense oligonucleotide mechanisms for modulating gene expressionIsabella Trew, Steve D Wilton, Jessica M Cale, et al.American Journal of Medical Genetics|June 15, 1993
Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutationS D Wilton, R D Johnsen, J R Pedretti, et al.Human Mutation|January 1, 1994
Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy familyS D Wilton, D C Chandler, B A Kakulas, et al.Pageof 19