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Neuromuscular Disorders : NMD|July 1, 1997
Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?S D Wilton, D E Dye, L M Blechynden, et al.
FEBS Letters|December 21, 2018
YAPping about and not forgetting TAZBernard A Callus, Megan L Finch-Edmondson, Sue Fletcher, et al.
Journal of Clinical Microbiology|January 1, 1992
Use of polymerase chain reaction for rapid diagnosis of tuberculosisD V Cousins, S D Wilton, B R Francis, et al.
Journal of Cellular and Molecular Medicine|January 22, 2011
Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafishJoachim Berger, Silke Berger, Arie S Jacoby, et al.
The Clinical Biochemist. Reviews|September 14, 2011
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesNigel G Laing, Mark R Davis, Klair Bayley, et al.
Neuromuscular Disorders : NMD|April 12, 2001
Cryptic splicing involving the splice site mutation in the canine model of Duchenne muscular dystrophyS Fletcher, T Ly, R M Duff, et al.
Expert Opinion on Biological Therapy|November 3, 2016
Translational development of splice-modifying antisense oligomersS Fletcher, M I Bellgard, L Price, et al.
Molecular Therapy. Nucleic Acids|June 3, 2018
Antisense Oligonucleotide-Mediated Terminal Intron Retention of the SMN2 TranscriptLoren L Flynn, Chalermchai Mitrpant, Ianthe L Pitout, et al.
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