Diaphragm rescue alone prevents heart dysfunction in dystrophic mice.
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused, in most cases, by the complete absence of the 427 kDa cytoskeletal protein, dystrophin. There is no effective treatment, and affected individuals die from respiratory failure and cardiomyopathy by age 30. Here, we investigate...
主要な著者: | Crisp, A, Yin, H, Goyenvalle, A, Betts, C, Moulton, H, Seow, Y, Babbs, A, Merritt, T, Saleh, A, Gait, M, Stuckey, D, Clarke, K, Davies, K, Wood, M |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2011
|
類似資料
-
Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.
著者:: Goyenvalle, A, 等
出版事項: (2010) -
Upgrading U7snRNA To Complete Efficient Rescue of Dystrophin by Exon-Skipping in DMD Patients
著者:: Goyenvalle, A, 等
出版事項: (2009) -
Functional rescue of dystrophin-deficient mdx mice by a chimeric peptide-PMO
著者:: Yin, H, 等
出版事項: (2010) -
Rescu of severely affected dystrophin/utrophin deficient mice by morpholino-oligomer mediated exon skipping
著者:: Goyenvalle, A, 等
出版事項: (2010) -
Lipolysis and cyclic AMP response to isoproterenol in diaphragms from control and dystrophic mice.
著者:: N A Abumrad, 等
出版事項: (1980-02-01)