The origin of genetic instability in CCTG repeats
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/39/14/6260/18784684/gkr185.pdf
Reference38 articles.
1. Expandable DNA repeats and human disease;Mirkin;Nature,2007
2. Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat;Mankodi;Science,2000
3. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9;Liquori;Science,2001
4. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992
5. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
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1. Effects of interrupting residues on DNA dumbbell structures formed by CCTG tetranucleotide repeats associated with myotonic dystrophy type 2;FEBS Letters;2024-06-25
2. High-Resolution NMR Structures of Intrastrand Hairpins Formed by CTG Trinucleotide Repeats;ACS Chemical Neuroscience;2024-02-06
3. Massive contractions of myotonic dystrophy type 2-associated CCTG tetranucleotide repeats occur via double-strand break repair with distinct requirements for DNA helicases;G3: Genes, Genomes, Genetics;2023-11-10
4. Massive contractions of Myotonic Dystrophy Type 2-associated CCTG tetranucleotide repeats occur via double strand break repair with distinct requirements for helicases;2023-07-07
5. Structures and conformational dynamics of DNA minidumbbells in pyrimidine-rich repeats associated with neurodegenerative diseases;Computational and Structural Biotechnology Journal;2023
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