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Items: 1 to 20 of 51

1.

Coexistence of MLH3 germline variants in colon cancer patients belonging to families with Lynch syndrome-associated brain tumors.

Duraturo F, Liccardo R, Izzo P.

J Neurooncol. 2016 Sep;129(3):577-578. doi: 10.1007/s11060-016-2203-0. Epub 2016 Jul 11. No abstract available.

PMID:
27401157
2.

Single-nucleotide polymorphism rs 175080 in the MLH3 gene and its relation to male infertility.

Markandona O, Dafopoulos K, Anifandis G, Messini CI, Dimitraki M, Tsezou A, Georgoulias P, Messinis IE.

J Assist Reprod Genet. 2015 Dec;32(12):1795-9. doi: 10.1007/s10815-015-0594-z. Epub 2015 Oct 31.

3.

Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene.

Lhotska H, Zemanova Z, Cechova H, Ransdorfova S, Lizcova L, Kramar F, Krejcik Z, Svobodova K, Bystricka D, Hrabal P, Dohnalova A, Michalova K.

Genes Chromosomes Cancer. 2015 Nov;54(11):655-67. doi: 10.1002/gcc.22266. Epub 2015 Aug 25.

PMID:
26303387
4.

Mismatch repair gene MLH3 Pro844Leu and Thr942Ile polymorphisms and the susceptibility to cervical carcinoma and HPV infection: a case-control study in a Chinese population.

Ye F, Cheng Q, Shen J, Zhou C, Chen H.

PLoS One. 2014 Apr 23;9(4):e96224. doi: 10.1371/journal.pone.0096224. eCollection 2014.

5.

Stable expression of MutLγ in human cells reveals no specific response to mismatched DNA, but distinct recruitment to damage sites.

Roesner LM, Mielke C, Fähnrich S, Merkhoffer Y, Dittmar KE, Drexler HG, Dirks WG.

J Cell Biochem. 2013 Oct;114(10):2405-14. doi: 10.1002/jcb.24591.

PMID:
23696135
6.

Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair.

Charbonneau N, Amunugama R, Schmutte C, Yoder K, Fishel R.

Cancer Biol Ther. 2009 Jul;8(14):1411-20. Epub 2009 Jul 30.

7.

Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.

Ou J, Rasmussen M, Westers H, Andersen SD, Jager PO, Kooi KA, Niessen RC, Eggen BJ, Nielsen FC, Kleibeuker JH, Sijmons RH, Rasmussen LJ, Hofstra RM.

Genes Chromosomes Cancer. 2009 Apr;48(4):340-50. doi: 10.1002/gcc.20644.

PMID:
19156873
8.

The first functional study of MLH3 mutations found in cancer patients.

Korhonen MK, Vuorenmaa E, Nyström M.

Genes Chromosomes Cancer. 2008 Sep;47(9):803-9. doi: 10.1002/gcc.20581.

PMID:
18521850
9.

Mutations affecting a putative MutLalpha endonuclease motif impact multiple mismatch repair functions.

Erdeniz N, Nguyen M, Deschênes SM, Liskay RM.

DNA Repair (Amst). 2007 Oct 1;6(10):1463-70. Epub 2007 Jun 12.

10.

DNA mismatch repair gene hMLH3 variants in meiotic arrest.

Ferrás C, Zhou XL, Sousa M, Lindblom A, Barros A.

Fertil Steril. 2007 Dec;88(6):1681-4. Epub 2007 May 7.

PMID:
17482610
11.
12.

Mutation screening of mismatch repair gene Mlh3 in familial esophageal cancer.

Liu HX, Li Y, Jiang XD, Yin HN, Zhang L, Wang Y, Yang J.

World J Gastroenterol. 2006 Sep 7;12(33):5281-6.

13.

MLH3 mutation in endometrial cancer.

Taylor NP, Powell MA, Gibb RK, Rader JS, Huettner PC, Thibodeau SN, Mutch DG, Goodfellow PJ.

Cancer Res. 2006 Aug 1;66(15):7502-8.

14.

Expression of the MutL homologue hMLH3 in human cells and its role in DNA mismatch repair.

Cannavo E, Marra G, Sabates-Bellver J, Menigatti M, Lipkin SM, Fischer F, Cejka P, Jiricny J.

Cancer Res. 2005 Dec 1;65(23):10759-66.

15.

No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk.

de Jong MM, Hofstra RM, Kooi KA, Westra JL, Berends MJ, Wu Y, Hollema H, van der Sluis T, van der Graaf WT, de Vries EG, Schaapveld M, Sijmons RH, te Meerman GJ, Kleibeuker JH.

Cancer Genet Cytogenet. 2004 Jul 1;152(1):70-1.

PMID:
15193445
16.

Little evidence for involvement of MLH3 in colorectal cancer predisposition.

Hienonen T, Laiho P, Salovaara R, Mecklin JP, Järvinen H, Sistonen P, Peltomäki P, Lehtonen R, Nupponen NN, Launonen V, Karhu A, Aaltonen LA.

Int J Cancer. 2003 Aug 20;106(2):292-6.

17.

Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers.

Lipkin SM, Wang V, Stoler DL, Anderson GR, Kirsch I, Hadley D, Lynch HT, Collins FS.

Hum Mutat. 2001 May;17(5):389-96.

PMID:
11317354
18.

The role of MSH5 C85T and MLH3 C2531T polymorphisms in the risk of male infertility with azoospermia or severe oligozoospermia.

Xu K, Lu T, Zhou H, Bai L, Xiang Y.

Clin Chim Acta. 2010 Jan;411(1-2):49-52. doi: 10.1016/j.cca.2009.09.038. Epub 2009 Oct 3.

PMID:
19808033
19.

MLH3 and EXO1 alterations in familial colorectal cancer patients not fulfilling Amsterdam criteria.

Kim JC, Roh SA, Yoon YS, Kim HC, Park IJ.

Cancer Genet Cytogenet. 2007 Jul 15;176(2):172-4. No abstract available.

PMID:
17656264
20.

Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes.

Lenzi ML, Smith J, Snowden T, Kim M, Fishel R, Poulos BK, Cohen PE.

Am J Hum Genet. 2005 Jan;76(1):112-27. Epub 2004 Nov 22.

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