Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.
Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder caused by mutations in the dystrophin gene that result in the absence of functional protein. Antisense-mediated exon-skipping is one of the most promising approaches for the treatment of DMD because of its capacity to correct the r...
Հիմնական հեղինակներ: | Goyenvalle, A, Babbs, A, Powell, D, Kole, R, Fletcher, S, Wilton, S, Davies, K |
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Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2010
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Նմանատիպ նյութեր
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Rescu of severely affected dystrophin/utrophin deficient mice by morpholino-oligomer mediated exon skipping
: Goyenvalle, A, և այլն
Հրապարակվել է: (2010) -
Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping
: Goyenvalle, A, և այլն
Հրապարակվել է: (2012) -
Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping.
: Goyenvalle, A, և այլն
Հրապարակվել է: (2012) -
Extensive and prolonged restoration of dystrophin expression with vivo-morpholino-mediated multiple exon skipping in dystrophic dogs.
: Yokota, T, և այլն
Հրապարակվել է: (2012) -
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse.
: Lu, Q, և այլն
Հրապարակվել է: (2003)