Du, 2010 - Google Patents
The mechanisms by which CUG repeats cause myotonic dystrophy type 1Du, 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 …
- 201000009340 myotonic dystrophy type 1 0 title abstract description 18
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- C12N15/1137—Non-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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