Restoration of dystrophin expression in mdx muscle cells by chimeraplast-mediated exon skipping

By Bertoni Carmen   Lau Catherine   Rando Thomas A.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1087-1099

Oxford University Press

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A frameshifting mutation in CHRNE unmasks skipping of the preceding exon

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Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3055-3066

Oxford University Press

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Nonsense mutation in exon 4 of human complement C9 gene is the major cause of Japanese complement C9 deficiency

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Human Genetics, Vol. 102, Iss. 6, 1998-07 ,pp. : 605-610

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A fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice

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Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4405-4414

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Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays

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