Length-dependent CTG{middle dot}CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/22/25/5276/1546860/ddt386.pdf
Reference71 articles.
1. Expandable DNA repeats and human disease
2. Features of trinucleotide repeat instability in vivo
3. Mechanisms of trinucleotide repeat instability during human development
4. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
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
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1. 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
2. High-Resolution NMR Structures of Intrastrand Hairpins Formed by CTG Trinucleotide Repeats;ACS Chemical Neuroscience;2024-02-06
3. All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency;2023-12-26
4. Tandem MutSβ binding to long extruded DNA trinucleotide repeats underpins pathogenic expansions;2023-12-13
5. Generation of induced pluripotent stem cell lines from pediatric patients with congenital myotonic dystrophy (CBRCULi012-A and CBRCULi013-A) and age-matched controls (CBRCULi010-A and CBRCULi011-A);Stem Cell Research;2023-10
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