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Mismatch repair enhances convergent transcription-induced cell death at trinucleotide repeats by activating ATR.

Chatterjee N, Lin Y, Wilson JH.

DNA Repair (Amst). 2016 Jun;42:26-32. doi: 10.1016/j.dnarep.2016.03.016. Epub 2016 Apr 16.


Impact of DNA mismatch repair system alterations on human fertility and related treatments.

Hu MH, Liu SY, Wang N, Wu Y, Jin F.

J Zhejiang Univ Sci B. 2016 Jan;17(1):10-20. doi: 10.1631/jzus.B1500162. Review.


Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.

Zhao XN, Kumari D, Gupta S, Wu D, Evanitsky M, Yang W, Usdin K.

Hum Mol Genet. 2015 Dec 15;24(24):7087-96. doi: 10.1093/hmg/ddv408. Epub 2015 Sep 29.


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

Nakatani R, Nakamori M, Fujimura H, Mochizuki H, Takahashi MP.

Sci Rep. 2015 Jun 5;5:11020. doi: 10.1038/srep11020.


Proteomic-coupled-network analysis of T877A-androgen receptor interactomes can predict clinical prostate cancer outcomes between White (non-Hispanic) and African-American groups.

Zaman N, Giannopoulos PN, Chowdhury S, Bonneil E, Thibault P, Wang E, Trifiro M, Paliouras M.

PLoS One. 2014 Nov 19;9(11):e113190. doi: 10.1371/journal.pone.0113190. eCollection 2014.


The dual nature of mismatch repair as antimutator and mutator: for better or for worse.

Bak ST, Sakellariou D, Pena-Diaz J.

Front Genet. 2014 Aug 21;5:287. doi: 10.3389/fgene.2014.00287. eCollection 2014. Review.


Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instability.

Reddy K, Schmidt MH, Geist JM, Thakkar NP, Panigrahi GB, Wang YH, Pearson CE.

Nucleic Acids Res. 2014;42(16):10473-87. doi: 10.1093/nar/gku658. Epub 2014 Aug 21.


X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion.

Adihe Lokanga R, Zhao XN, Entezam A, Usdin K.

Hum Mol Genet. 2014 Sep 15;23(18):4985-94. doi: 10.1093/hmg/ddu213. Epub 2014 May 8.


Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.

Pinto RM, Dragileva E, Kirby A, Lloret A, Lopez E, St Claire J, Panigrahi GB, Hou C, Holloway K, Gillis T, Guide JR, Cohen PE, Li GM, Pearson CE, Daly MJ, Wheeler VC.

PLoS Genet. 2013 Oct;9(10):e1003930. doi: 10.1371/journal.pgen.1003930. Epub 2013 Oct 31.


DNA mismatch repair system: repercussions in cellular homeostasis and relationship with aging.

Conde-Pérezprina JC, León-Galván MÁ, Konigsberg M.

Oxid Med Cell Longev. 2012;2012:728430. doi: 10.1155/2012/728430. Epub 2012 Nov 8. Review.


Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats.

Panigrahi GB, Slean MM, Simard JP, Pearson CE.

J Biol Chem. 2012 Dec 7;287(50):41844-50. doi: 10.1074/jbc.M112.420398. Epub 2012 Oct 18.


Nucleotide excision repair, mismatch repair, and R-loops modulate convergent transcription-induced cell death and repeat instability.

Lin Y, Wilson JH.

PLoS One. 2012;7(10):e46807. doi: 10.1371/journal.pone.0046807. Epub 2012 Oct 3.


DNA methyltransferases, DNA damage repair, and cancer.

Jin B, Robertson KD.

Adv Exp Med Biol. 2013;754:3-29. doi: 10.1007/978-1-4419-9967-2_1. Review.


A DNA repair pathway-focused score for prediction of outcomes in ovarian cancer treated with platinum-based chemotherapy.

Kang J, D'Andrea AD, Kozono D.

J Natl Cancer Inst. 2012 May 2;104(9):670-81. doi: 10.1093/jnci/djs177. Epub 2012 Apr 13.


DNA MMR systems, microsatellite instability and antioxidant activity variations in two species of wild bats: Myotis velifer and Desmodus rotundus, as possible factors associated with longevity.

Conde-Pérezprina JC, Luna-López A, González-Puertos VY, Zenteno-Savín T, León-Galván MA, Königsberg M.

Age (Dordr). 2012 Dec;34(6):1473-92. doi: 10.1007/s11357-012-9399-5. Epub 2012 Mar 28.


Instability of (CTG)n•(CAG)n trinucleotide repeats and DNA synthesis.

Liu G, Leffak M.

Cell Biosci. 2012 Feb 27;2(1):7. doi: 10.1186/2045-3701-2-7.


Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.

Hubert L Jr, Lin Y, Dion V, Wilson JH.

Hum Mol Genet. 2011 Dec 15;20(24):4822-30. doi: 10.1093/hmg/ddr421. Epub 2011 Sep 15.


Topoisomerase 1 and single-strand break repair modulate transcription-induced CAG repeat contraction in human cells.

Hubert L Jr, Lin Y, Dion V, Wilson JH.

Mol Cell Biol. 2011 Aug;31(15):3105-12. doi: 10.1128/MCB.05158-11. Epub 2011 May 31.


Transcription-induced DNA toxicity at trinucleotide repeats: double bubble is trouble.

Lin Y, Wilson JH.

Cell Cycle. 2011 Feb 15;10(4):611-8. Epub 2011 Feb 15.

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