Highly Efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin α2 chain-null congenital muscular dystrophy mice
Page 1 of 1
Highly Efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin α2 chain-null congenital muscular dystrophy mice
Jon Moulton Wed Jul 31, 2013 8:50 am
Aoki Y, Nagata T, Yokota T, Nakamura A, Wood MJ, Partridge T, Takeda S. Highly Efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin α2 chain-null congenital muscular dystrophy mice. Hum Mol Genet. 2013 Jul 23. [Epub ahead of print]
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 61
Location : Philomath, Oregon, USA -
Similar topics» Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
» Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
» Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan
» Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy
» Efficient in vivo manipulation of alternative pre-mRNA splicing events using antisense morpholinos in mice
» Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
» Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan
» Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy
» Efficient in vivo manipulation of alternative pre-mRNA splicing events using antisense morpholinos in mice
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum