These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination. Libby RT; Hagerman KA; Pineda VV; Lau R; Cho DH; Baccam SL; Axford MM; Cleary JD; Moore JM; Sopher BL; Tapscott SJ; Filippova GN; Pearson CE; La Spada AR PLoS Genet; 2008 Nov; 4(11):e1000257. PubMed ID: 19008940 [TBL] [Abstract][Full Text] [Related]
9. Trinucleotide repeat expansions and human genetic disease. Bates G; Lehrach H Bioessays; 1994 Apr; 16(4):277-84. PubMed ID: 8031305 [TBL] [Abstract][Full Text] [Related]
10. Stable DNA methylation boundaries and expanded trinucleotide repeats: role of DNA insertions. Naumann A; Kraus C; Hoogeveen A; Ramirez CM; Doerfler W J Mol Biol; 2014 Jul; 426(14):2554-66. PubMed ID: 24816393 [TBL] [Abstract][Full Text] [Related]
11. Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications. Laffita-Mesa JM; Bauer PO; Kourí V; Peña Serrano L; Roskams J; Almaguer Gotay D; Montes Brown JC; Martínez Rodríguez PA; González-Zaldívar Y; Almaguer Mederos L; Cuello-Almarales D; Aguiar Santiago J Hum Genet; 2012 Apr; 131(4):625-38. PubMed ID: 22037902 [TBL] [Abstract][Full Text] [Related]
12. The unstable trinucleotide repeat story of major psychosis. Vincent JB; Paterson AD; Strong E; Petronis A; Kennedy JL Am J Med Genet; 2000; 97(1):77-97. PubMed ID: 10813808 [TBL] [Abstract][Full Text] [Related]
13. MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells. Franck S; Barbé L; Ardui S; De Vlaeminck Y; Allemeersch J; Dziedzicka D; Spits C; Vanroye F; Hilven P; Duqué G; Vermeesch JR; Gheldof A; Sermon K Hum Mol Genet; 2021 Jan; 29(21):3566-3577. PubMed ID: 33242073 [TBL] [Abstract][Full Text] [Related]
14. DNA repair in the trinucleotide repeat disorders. Jones L; Houlden H; Tabrizi SJ Lancet Neurol; 2017 Jan; 16(1):88-96. PubMed ID: 27979358 [TBL] [Abstract][Full Text] [Related]
16. Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease. Zhao X; Kumari D; Miller CJ; Kim GY; Hayward B; Vitalo AG; Pinto RM; Usdin K J Huntingtons Dis; 2021; 10(1):149-163. PubMed ID: 33579860 [TBL] [Abstract][Full Text] [Related]
17. The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues. Al-Mahdawi S; Pinto RM; Ismail O; Varshney D; Lymperi S; Sandi C; Trabzuni D; Pook M Hum Mol Genet; 2008 Mar; 17(5):735-46. PubMed ID: 18045775 [TBL] [Abstract][Full Text] [Related]
18. Overview of the Complex Relationship between Epigenetics Markers, CTG Repeat Instability and Symptoms in Myotonic Dystrophy Type 1. de Pontual L; Tomé S Int J Mol Sci; 2022 Mar; 23(7):. PubMed ID: 35408837 [TBL] [Abstract][Full Text] [Related]
19. Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome. Mulvihill DJ; Nichol Edamura K; Hagerman KA; Pearson CE; Wang YH J Biol Chem; 2005 Feb; 280(6):4498-503. PubMed ID: 15574425 [TBL] [Abstract][Full Text] [Related]