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- W1881614320 endingPage "17975" @default.
- W1881614320 startingPage "17944" @default.
- W1881614320 abstract "The liver has become an increasingly interesting target for oligonucleotide therapy. Mutations of the gene encoding transthyretin (TTR), expressed in vast amounts by the liver, result in a complex degenerative disease, termed familial amyloid polyneuropathy (FAP). Misfolded variants of TTR are linked to the establishment of extracellular protein deposition in various tissues, including the heart and the peripheral nervous system. Recent progress in the chemistry and formulation of antisense (ASO) and small interfering RNA (siRNA) designed for a knockdown of TTR mRNA in the liver has allowed to address the issue of gene-specific molecular therapy in a clinical setting of FAP. The two therapeutic oligonucleotides bind to RNA in a sequence specific manner but exploit different mechanisms. Here we describe major developments that have led to the advent of therapeutic oligonucleotides for treatment of TTR-related disease." @default.
- W1881614320 created "2016-06-24" @default.
- W1881614320 creator A5040220251 @default.
- W1881614320 creator A5059204501 @default.
- W1881614320 creator A5089060660 @default.
- W1881614320 date "2015-09-30" @default.
- W1881614320 modified "2023-10-02" @default.
- W1881614320 title "Therapeutic Oligonucleotides Targeting Liver Disease: TTR Amyloidosis" @default.
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