Similar articles for PMID: 11809728

Year	Number of Results
1992	2
1993	4
1994	4
1995	6
1996	14
1997	11
1998	10
1999	13
2000	10
2001	11
2002	14
2003	10
2004	8
2005	2
2006	6
2007	4
2008	2
2009	5
2010	11
2011	10
2012	16
2013	16
2014	5
2015	6
2016	8
2017	7
2018	10
2019	13
2020	19
2021	15
2022	10
2023	4
2024	0

1

Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.

van den Broek WJ, Nelen MR, Wansink DG, Coerwinkel MM, te Riele H, Groenen PJ, Wieringa B. van den Broek WJ, et al. Hum Mol Genet. 2002 Jan 15;11(2):191-8. doi: 10.1093/hmg/11.2.191. Hum Mol Genet. 2002. PMID: 11809728

2

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.

Foiry L, Dong L, Savouret C, Hubert L, te Riele H, Junien C, Gourdon G. Foiry L, et al. Hum Genet. 2006 Jun;119(5):520-6. doi: 10.1007/s00439-006-0164-7. Epub 2006 Mar 22. Hum Genet. 2006. PMID: 16552576

3

A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.

Morales F, Vásquez M, Santamaría C, Cuenca P, Corrales E, Monckton DG. Morales F, et al. DNA Repair (Amst). 2016 Apr;40:57-66. doi: 10.1016/j.dnarep.2016.01.001. Epub 2016 Mar 8. DNA Repair (Amst). 2016. PMID: 26994442

4

Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.

Du J, Campau E, Soragni E, Jespersen C, Gottesfeld JM. Du J, et al. Hum Mol Genet. 2013 Dec 20;22(25):5276-87. doi: 10.1093/hmg/ddt386. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933738 Free PMC article.

5

MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.

Tomé S, Holt I, Edelmann W, Morris GE, Munnich A, Pearson CE, Gourdon G. Tomé S, et al. PLoS Genet. 2009 May;5(5):e1000482. doi: 10.1371/journal.pgen.1000482. Epub 2009 May 15. PLoS Genet. 2009. PMID: 19436705 Free PMC article.

6

MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.

Tomé S, Manley K, Simard JP, Clark GW, Slean MM, Swami M, Shelbourne PF, Tillier ER, Monckton DG, Messer A, Pearson CE. Tomé S, et al. PLoS Genet. 2013;9(2):e1003280. doi: 10.1371/journal.pgen.1003280. Epub 2013 Feb 28. PLoS Genet. 2013. PMID: 23468640 Free PMC article.

7

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. Franck S, et al. Hum Mol Genet. 2021 Jan 6;29(21):3566-3577. doi: 10.1093/hmg/ddaa250. Hum Mol Genet. 2021. PMID: 33242073

8

Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.

Seriola A, Spits C, Simard JP, Hilven P, Haentjens P, Pearson CE, Sermon K. Seriola A, et al. Hum Mol Genet. 2011 Jan 1;20(1):176-85. doi: 10.1093/hmg/ddq456. Epub 2010 Oct 8. Hum Mol Genet. 2011. PMID: 20935170

9

Large expansion of CTG•CAG repeats is exacerbated by MutSβ in human cells.

Nakatani R, Nakamori M, Fujimura H, Mochizuki H, Takahashi MP. Nakatani R, et al. Sci Rep. 2015 Jun 5;5:11020. doi: 10.1038/srep11020. Sci Rep. 2015. PMID: 26047474 Free PMC article.

10

Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.

Ashizawa T, Monckton DG, Vaishnav S, Patel BJ, Voskova A, Caskey CT. Ashizawa T, et al. Genomics. 1996 Aug 15;36(1):47-53. doi: 10.1006/geno.1996.0424. Genomics. 1996. PMID: 8812415

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