Structural Studies of a Trinucleotide Repeat Sequence Using 2-Aminopurine

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| The underlying genetic mutations for many inherited neurodegenerative disorders have been identified in recent years. One frequent type of mutation is trinucleotide repeat expansion. Depending on the location of the repeat expansion, the mutation might result in a loss of function of the disease gene, a toxic gain of function or both. Disease gene identification has led to the development of ...

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Trinucleotide repeat (TNR) expansions are present in a wide range of genes involved in several neurological disorders, being directly involved in the molecular mechanisms underlying pathogenesis through modulation of gene expression and/or the function of the RNA or protein it encodes. Structural and functional information on the role of TNR sequences in RNA and protein is crucial to understand...

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ژورنال

عنوان ژورنال: Biochemistry

سال: 2009

ISSN: 0006-2960,1520-4995

DOI: 10.1021/bi802225y