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...
Κύριοι συγγραφείς: | 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 |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2011
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.
ανά: Goyenvalle, A, κ.ά.
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Upgrading U7snRNA To Complete Efficient Rescue of Dystrophin by Exon-Skipping in DMD Patients
ανά: Goyenvalle, A, κ.ά.
Έκδοση: (2009) -
Functional rescue of dystrophin-deficient mdx mice by a chimeric peptide-PMO
ανά: Yin, H, κ.ά.
Έκδοση: (2010) -
Rescu of severely affected dystrophin/utrophin deficient mice by morpholino-oligomer mediated exon skipping
ανά: Goyenvalle, A, κ.ά.
Έκδοση: (2010) -
Lipolysis and cyclic AMP response to isoproterenol in diaphragms from control and dystrophic mice.
ανά: N A Abumrad, κ.ά.
Έκδοση: (1980-02-01)