Pms2 is a genetic enhancer of trinucleotide CAG{middle dot}CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/13/16/1815/1960429/ddh186.pdf
Cited by 173 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. PMS2 has both pro-mutagenic and anti-mutagenic effects on repeat instability in the Repeat Expansion Diseases;2024-08-13
2. A single CAA interrupt in a DNA three-way junction containing a CAG repeat hairpin results in parity-dependent trapping;Nucleic Acids Research;2024-07-23
3. All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency;Scientific Reports;2024-06-14
4. Identification of genetic modifiers of Huntington’s disease somatic CAG repeat instability by in vivo CRISPR-Cas9 genome editing;2024-06-09
5. Therapeutic validation of MMR-associated genetic modifiers in a human ex vivo model of Huntington disease;The American Journal of Human Genetics;2024-06
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