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.
102 related articles for article (PubMed ID: 32628834)
21. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. Burman RW; Popovich BW; Jacky PB; Turker MS Hum Mol Genet; 1999 Nov; 8(12):2293-302. PubMed ID: 10545610 [TBL] [Abstract][Full Text] [Related]
22. [Tissue heterogeneity analysis of CGG-repeat mutation in two fragile X affected male fetuses]. Huang W; Luo SY; Du Q; Yang P; Tan H; Wu LQ; Duan RH Zhonghua Er Ke Za Zhi; 2016 Apr; 54(4):287-9. PubMed ID: 27055429 [TBL] [Abstract][Full Text] [Related]
23. Small-molecule ligand induces nucleotide flipping in (CAG)n trinucleotide repeats. Nakatani K; Hagihara S; Goto Y; Kobori A; Hagihara M; Hayashi G; Kyo M; Nomura M; Mishima M; Kojima C Nat Chem Biol; 2005 Jun; 1(1):39-43. PubMed ID: 16407992 [TBL] [Abstract][Full Text] [Related]
24. Binding of naphthyridine carbamate dimer to the (CGG)n repeat results in the disruption of the G-C base pairing. Peng T; Nakatani K Angew Chem Int Ed Engl; 2005 Nov; 44(44):7280-3. PubMed ID: 16229032 [No Abstract] [Full Text] [Related]
25. [Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome]. Duan R; Luo S; Huang W; Li H; Peng Y; Du Q; Wu L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):606-9. PubMed ID: 27577204 [TBL] [Abstract][Full Text] [Related]
26. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein. Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; Baker E; Kokkinaki M; Talley P; Maltby EL; French L; Harder L; Hinzmann B; Nobile C; Richkind K; Finnis M; Deloukas P; Sutherland GR; Kutsche K; Moschonas NK; Siebert R; Gécz J; Genomics; 2004 Jul; 84(1):69-81. PubMed ID: 15203205 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. Inhibition of DNA replication by a d(CAG) repeat binding ligand. Hagihara M; Nakatani K Nucleic Acids Symp Ser (Oxf); 2006; (50):147-8. PubMed ID: 17150860 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. A cytosine methyltransferase converts 5-methylcytosine in DNA to thymine. Yebra MJ; Bhagwat AS Biochemistry; 1995 Nov; 34(45):14752-7. PubMed ID: 7578083 [TBL] [Abstract][Full Text] [Related]
31. Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes. Gurling HM; Bolton PF; Vincent J; Melmer G; Rutter M Hum Hered; 1997; 47(5):254-62. PubMed ID: 9358013 [TBL] [Abstract][Full Text] [Related]
32. Electrochemical detection of DNA triplet repeat expansion. Fojta M; Havran L; Vojtiskova M; Palecek E J Am Chem Soc; 2004 Jun; 126(21):6532-3. PubMed ID: 15161263 [TBL] [Abstract][Full Text] [Related]
33. Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells. Nichol Edamura K; Leonard MR; Pearson CE Am J Hum Genet; 2005 Feb; 76(2):302-11. PubMed ID: 15625623 [TBL] [Abstract][Full Text] [Related]
35. Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat. Igarashi S; Takiyama Y; Cancel G; Rogaeva EA; Sasaki H; Wakisaka A; Zhou YX; Takano H; Endo K; Sanpei K; Oyake M; Tanaka H; Stevanin G; Abbas N; Dürr A; Rogaev EI; Sherrington R; Tsuda T; Ikeda M; Cassa E; Nishizawa M; Benomar A; Julien J; Weissenbach J; Wang GX; Agid Y; St George-Hyslop PH; Brice A; Tsuji S Hum Mol Genet; 1996 Jul; 5(7):923-32. PubMed ID: 8817326 [TBL] [Abstract][Full Text] [Related]
36. Ligand-inducible formation of RNA pseudoknot. Matsumoto S; Hong C; Otabe T; Murata A; Nakatani K Bioorg Med Chem Lett; 2013 Jun; 23(12):3539-41. PubMed ID: 23664873 [TBL] [Abstract][Full Text] [Related]
37. Cytosine deamination and base excision repair cause R-loop-induced CAG repeat fragility and instability in Su XA; Freudenreich CH Proc Natl Acad Sci U S A; 2017 Oct; 114(40):E8392-E8401. PubMed ID: 28923949 [TBL] [Abstract][Full Text] [Related]
38. Instability of a (CGG)98 repeat in the Fmr1 promoter. Bontekoe CJ; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; de Lange D; Hirst MC; Oostra BA Hum Mol Genet; 2001 Aug; 10(16):1693-9. PubMed ID: 11487573 [TBL] [Abstract][Full Text] [Related]
39. Use of human-derived stem cells to create a novel, in vitro model designed to explore FMR1 CGG repeat instability amongst female premutation carriers. Gustin SLF; Wang G; Baker VM; Latham G; Sebastiano V J Assist Reprod Genet; 2018 Aug; 35(8):1443-1455. PubMed ID: 29926373 [TBL] [Abstract][Full Text] [Related]
40. Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect. Burman RW; Yates PA; Green LD; Jacky PB; Turker MS; Popovich BW Am J Hum Genet; 1999 Nov; 65(5):1375-86. PubMed ID: 10521303 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]