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Items: 1 to 20 of 108

1.

In vitro studies of DNA mismatch repair proteins.

Geng H, Du C, Chen S, Salerno V, Manfredi C, Hsieh P.

Anal Biochem. 2011 Jun 15;413(2):179-84. doi: 10.1016/j.ab.2011.02.017. Epub 2011 Feb 15.

2.

Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair.

Tomer G, Buermeyer AB, Nguyen MM, Liskay RM.

J Biol Chem. 2002 Jun 14;277(24):21801-9. Epub 2002 Mar 15.

3.

Analysis of the excision step in human DNA mismatch repair.

Genschel J, Modrich P.

Methods Enzymol. 2006;408:273-84.

PMID:
16793375
4.

Conservation of functional asymmetry in the mammalian MutLα ATPase.

Johnson JR, Erdeniz N, Nguyen M, Dudley S, Liskay RM.

DNA Repair (Amst). 2010 Nov 10;9(11):1209-13. doi: 10.1016/j.dnarep.2010.08.006.

5.

Efficient repair of A/C mismatches in mouse cells deficient in long-patch mismatch repair.

Oda S, Humbert O, Fiumicino S, Bignami M, Karran P.

EMBO J. 2000 Apr 3;19(7):1711-8.

6.

Interactions of human mismatch repair proteins MutSalpha and MutLalpha with proteins of the ATR-Chk1 pathway.

Liu Y, Fang Y, Shao H, Lindsey-Boltz L, Sancar A, Modrich P.

J Biol Chem. 2010 Feb 19;285(8):5974-82. doi: 10.1074/jbc.M109.076109. Epub 2009 Dec 22.

7.

Nuclear import of human MLH1, PMS2, and MutLalpha: redundancy is the key.

Leong V, Lorenowicz J, Kozij N, Guarné A.

Mol Carcinog. 2009 Aug;48(8):742-50. doi: 10.1002/mc.20514.

PMID:
19148896
8.

Human DNA mismatch repair: coupling of mismatch recognition to strand-specific excision.

Wang H, Hays JB.

Nucleic Acids Res. 2007;35(20):6727-39. Epub 2007 Oct 4.

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Mutations in the MutSalpha interaction interface of MLH1 can abolish DNA mismatch repair.

Plotz G, Welsch C, Giron-Monzon L, Friedhoff P, Albrecht M, Piiper A, Biondi RM, Lengauer T, Zeuzem S, Raedle J.

Nucleic Acids Res. 2006;34(22):6574-86. Epub 2006 Nov 28.

13.

A novel interaction between human DNA polymerase eta and MutLalpha.

Kanao R, Hanaoka F, Masutani C.

Biochem Biophys Res Commun. 2009 Nov 6;389(1):40-5. doi: 10.1016/j.bbrc.2009.08.090. Epub 2009 Aug 22.

PMID:
19703417
14.

Mismatch repair genes expression defects & association with clinicopathological characteristics in colorectal carcinoma.

Kaur G, Masoud A, Raihan N, Radzi M, Khamizar W, Kam LS.

Indian J Med Res. 2011 Aug;134:186-92.

15.

Role of MutSalpha in the recognition of iododeoxyuridine in DNA.

Berry SE, Loh T, Yan T, Kinsella TJ.

Cancer Res. 2003 Sep 1;63(17):5490-5.

16.

Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel.

Shia J, Tang LH, Vakiani E, Guillem JG, Stadler ZK, Soslow RA, Katabi N, Weiser MR, Paty PB, Temple LK, Nash GM, Wong WD, Offit K, Klimstra DS.

Am J Surg Pathol. 2009 Nov;33(11):1639-45. doi: 10.1097/PAS.0b013e3181b15aa2. Erratum in: Am J Surg Pathol. 2010 Mar;34(3):432.

PMID:
19701074
17.

Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates.

Hombauer H, Campbell CS, Smith CE, Desai A, Kolodner RD.

Cell. 2011 Nov 23;147(5):1040-53. doi: 10.1016/j.cell.2011.10.025.

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PCNA-MutSalpha-mediated binding of MutLalpha to replicative DNA with mismatched bases to induce apoptosis in human cells.

Hidaka M, Takagi Y, Takano TY, Sekiguchi M.

Nucleic Acids Res. 2005 Oct 4;33(17):5703-12. Print 2005.

20.

Reconstitution of 5'-directed human mismatch repair in a purified system.

Zhang Y, Yuan F, Presnell SR, Tian K, Gao Y, Tomkinson AE, Gu L, Li GM.

Cell. 2005 Sep 9;122(5):693-705.

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