264 related articles for article (PubMed ID: 22354993)
21. Replication-dependent instability at (CTG) x (CAG) repeat hairpins in human cells.
Liu G; Chen X; Bissler JJ; Sinden RR; Leffak M
Nat Chem Biol; 2010 Sep; 6(9):652-9. PubMed ID: 20676085
[TBL] [Abstract][Full Text] [Related]
22. Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome.
Freudenreich CH; Stavenhagen JB; Zakian VA
Mol Cell Biol; 1997 Apr; 17(4):2090-8. PubMed ID: 9121457
[TBL] [Abstract][Full Text] [Related]
23. Instability of (CTG)n•(CAG)n trinucleotide repeats and DNA synthesis.
Liu G; Leffak M
Cell Biosci; 2012 Feb; 2(1):7. PubMed ID: 22369689
[TBL] [Abstract][Full Text] [Related]
24. Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.
Winchester CL; Ferrier RK; Sermoni A; Clark BJ; Johnson KJ
Hum Mol Genet; 1999 Mar; 8(3):481-92. PubMed ID: 9949207
[TBL] [Abstract][Full Text] [Related]
25. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
Savić D; Rakocvic-Stojanovic V; Keckarevic D; Culjkovic B; Stojkovic O; Mladenovic J; Todorovic S; Apostolski S; Romac S
Hum Mutat; 2002 Feb; 19(2):131-9. PubMed ID: 11793472
[TBL] [Abstract][Full Text] [Related]
26. Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus.
Brouwer JR; Huguet A; Nicole A; Munnich A; Gourdon G
J Nucleic Acids; 2013; 2013():567435. PubMed ID: 24455202
[TBL] [Abstract][Full Text] [Related]
27. 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
PLoS Genet; 2009 May; 5(5):e1000482. PubMed ID: 19436705
[TBL] [Abstract][Full Text] [Related]
28. Myotonic dystrophy--a multigene disorder.
Larkin K; Fardaei M
Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):389-95. PubMed ID: 11719277
[TBL] [Abstract][Full Text] [Related]
29. Human FEN-1 can process the 5'-flap DNA of CTG/CAG triplet repeat derived from human genetic diseases by length and sequence dependent manner.
Lee S; Park MS
Exp Mol Med; 2002 Sep; 34(4):313-7. PubMed ID: 12515398
[TBL] [Abstract][Full Text] [Related]
30. Instability in the transmission of the myotonic dystrophy CTG repeat in human oocytes and preimplantation embryos.
Dean NL; Tan SL; Ao A
Fertil Steril; 2006 Jul; 86(1):98-105. PubMed ID: 16716318
[TBL] [Abstract][Full Text] [Related]
31. Replication restart: a pathway for (CTG).(CAG) repeat deletion in Escherichia coli.
Kim SH; Pytlos MJ; Sinden RR
Mutat Res; 2006 Mar; 595(1-2):5-22. PubMed ID: 16472829
[TBL] [Abstract][Full Text] [Related]
32. Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.
López Castel A; Nakamori M; Tomé S; Chitayat D; Gourdon G; Thornton CA; Pearson CE
Hum Mol Genet; 2011 Jan; 20(1):1-15. PubMed ID: 21044947
[TBL] [Abstract][Full Text] [Related]
33. Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodies.
Tam M; Erin Montgomery S; Kekis M; Stollar BD; Price GB; Pearson CE
J Mol Biol; 2003 Sep; 332(3):585-600. PubMed ID: 12963369
[TBL] [Abstract][Full Text] [Related]
34. Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1.
van den Broek WJ; Nelen MR; van der Heijden GW; Wansink DG; Wieringa B
FEBS Lett; 2006 Oct; 580(22):5208-14. PubMed ID: 16978612
[TBL] [Abstract][Full Text] [Related]
35. Identification of RTG2 as a modifier gene for CTG*CAG repeat instability in Saccharomyces cerevisiae.
Bhattacharyya S; Rolfsmeier ML; Dixon MJ; Wagoner K; Lahue RS
Genetics; 2002 Oct; 162(2):579-89. PubMed ID: 12399373
[TBL] [Abstract][Full Text] [Related]
36. Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model.
Amack JD; Paguio AP; Mahadevan MS
Hum Mol Genet; 1999 Oct; 8(11):1975-84. PubMed ID: 10484765
[TBL] [Abstract][Full Text] [Related]
37. Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.
Seznec H; Lia-Baldini AS; Duros C; Fouquet C; Lacroix C; Hofmann-Radvanyi H; Junien C; Gourdon G
Hum Mol Genet; 2000 May; 9(8):1185-94. PubMed ID: 10767343
[TBL] [Abstract][Full Text] [Related]
38. Changes in myotonic dystrophy protein kinase levels and muscle development in congenital myotonic dystrophy.
Furling D; Lam le T; Agbulut O; Butler-Browne GS; Morris GE
Am J Pathol; 2003 Mar; 162(3):1001-9. PubMed ID: 12598332
[TBL] [Abstract][Full Text] [Related]
39. Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism.
Tomé S; Dandelot E; Dogan C; Bertrand A; Geneviève D; Péréon Y; ; Simon M; Bonnefont JP; Bassez G; Gourdon G
Hum Mutat; 2018 Jul; 39(7):970-982. PubMed ID: 29664219
[TBL] [Abstract][Full Text] [Related]
40. Identification, molecular characterization and segregation analysis of a variant
Fontana L; Santoro M; D'Apice MR; Peluso F; Gori G; Morrone A; Novelli G; Dosa L; Botta A
Acta Myol; 2020 Mar; 39(1):13-18. PubMed ID: 32607474
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]