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Du, 2010 - Google Patents

The mechanisms by which CUG repeats cause myotonic dystrophy type 1

Du, 2010

Document ID
14725228260582405264
Author
Du H
Publication year

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Abstract Myotonic dystrophy type 1 (DM1) is caused by CUG expansion (CUG exp) at the 3'UTR of the dystrophia myotonica-protein kinase gene (DMPK), leading to charateristic myotonia, progressive muscle wasting and insulin resistance. To test whether MBNL1 …
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    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
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