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    Results: 1 to 20 of 48

    1.

    Demethylation of the region around exon 2 of MLH1 gene in gastrointestinal cancer.

    Tang Y, Liu C, Wang X, Liu D, Ingvarsson S, Chen H.

    Anticancer Res. 2012 Nov;32(11):4861-4.

    PMID:
    23155252
    [PubMed - indexed for MEDLINE]
    2.

    Expression of p27, COX-2, MLH1, and MSH2 in young patients with colon carcinoma and correlation with morphologic findings.

    Kenney B, Deng Y, Mitchell K.

    Hum Pathol. 2013 Apr;44(4):591-7. doi: 10.1016/j.humpath.2012.07.003. Epub 2012 Oct 16.

    PMID:
    23084580
    [PubMed - indexed for MEDLINE]
    3.

    Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndrome.

    Valentin MD, Da Silva FC, Santos EM, Da Silva SD, De Oliveira Ferreira F, Aguiar Junior S, Gomy I, Vaccaro C, Redal MA, Della Valle A, Sarroca C, Rasmussen LJ, Carraro DM, Rossi BM.

    Anticancer Res. 2012 Oct;32(10):4347-51.

    PMID:
    23060557
    [PubMed - indexed for MEDLINE]
    4.

    Evaluation of microsatellite instability, MLH1 expression and hMLH1 promoter hypermethylation in colorectal carcinomas among Tunisians patients.

    Kria Ben Mahmoud L, Arfaoui A, Khiari M, Chaar I, Lounis A, Sammoud S, Ben Hmida AM, Gharbi L, Mzabi SR, Bouraoui S.

    Tunis Med. 2012 Aug-Sep;90(8-9):646-53.

    PMID:
    22987381
    [PubMed - indexed for MEDLINE]
    5.

    Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.

    Talseth-Palmer BA, Wijnen JT, Brenne IS, Jagmohan-Changur S, Barker D, Ashton KA, Tops CM, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G; Dutch Cancer Genetics Group, Spigelman A, Møller P, Morreau HM, Van Wezel T, Lubinski J, Vasen HF, Scott RJ.

    Int J Cancer. 2013 Apr 1;132(7):1556-64. doi: 10.1002/ijc.27843. Epub 2012 Oct 11.

    PMID:
    22987364
    [PubMed - indexed for MEDLINE]
    6.

    MLH1-silenced and non-silenced subgroups of hypermutated colorectal carcinomas have distinct mutational landscapes.

    Donehower LA, Creighton CJ, Schultz N, Shinbrot E, Chang K, Gunaratne PH, Muzny D, Sander C, Hamilton SR, Gibbs RA, Wheeler D.

    J Pathol. 2013 Jan;229(1):99-110. doi: 10.1002/path.4087.

    PMID:
    22899370
    [PubMed - indexed for MEDLINE]
    7.

    Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations.

    Lindor NM, Smyrk TC, Buehler S, Gunawardena SR, Thomas BC, Limburg P, Kirmani S, Thibodeau SN.

    Fam Cancer. 2012 Dec;11(4):667-9. doi: 10.1007/s10689-012-9561-3.

    PMID:
    22886683
    [PubMed - indexed for MEDLINE]
    8.

    Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

    Therkildsen C, Isinger-Ekstrand A, Ladelund S, Nissen A, Rambech E, Bernstein I, Nilbert M.

    Fam Cancer. 2012 Dec;11(4):579-85. doi: 10.1007/s10689-012-9552-4.

    PMID:
    22864660
    [PubMed - indexed for MEDLINE]
    9.

    MLH1 and XRCC1 polymorphisms in Mexican patients with colorectal cancer.

    Muñiz-Mendoza R, Ayala-Madrigal ML, Partida-Pérez M, Peregrina-Sandoval J, Leal-Ugarte E, Macías-Gómez N, Peralta-Leal V, Meza-Espinoza JP, Moreno-Ortiz JM, Ramírez-Ramírez R, Suárez-Villanueva S, Gutiérrez-Angulo M.

    Genet Mol Res. 2012 Aug 13;11(3):2315-20. doi: 10.4238/2012.June.27.6.

    PMID:
    22843073
    [PubMed - indexed for MEDLINE]
    10.

    CpG island methylator phenotype-positive tumors in the absence of MLH1 methylation constitute a distinct subset of duodenal adenocarcinomas and are associated with poor prognosis.

    Fu T, Pappou EP, Guzzetta AA, Jeschke J, Kwak R, Dave P, Hooker CM, Morgan R, Baylin SB, Iacobuzio-Donahue CA, Wolfgang CL, Ahuja N.

    Clin Cancer Res. 2012 Sep 1;18(17):4743-52. doi: 10.1158/1078-0432.CCR-12-0707. Epub 2012 Jul 23.

    PMID:
    22825585
    [PubMed - indexed for MEDLINE]
    11.

    Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.

    Farrell MP, Hughes DJ, Berry IR, Gallagher DJ, Glogowski EA, Payne SJ, Kennedy MJ, Clarke RM, White SA, Muldoon CB, Macdonald F, Rehal P, Crompton D, Roring S, Duke ST, McDevitt T, Barton DE, Hodgson SV, Green AJ, Daly PA.

    Fam Cancer. 2012 Sep;11(3):509-18. doi: 10.1007/s10689-012-9544-4. Review.

    PMID:
    22773173
    [PubMed - indexed for MEDLINE]
    12.

    Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome.

    Takahashi M, Furukawa Y, Shimodaira H, Sakayori M, Moriya T, Moriya Y, Nakamura Y, Ishioka C.

    Fam Cancer. 2012 Dec;11(4):559-64. doi: 10.1007/s10689-012-9547-1.

    PMID:
    22766992
    [PubMed - indexed for MEDLINE]
    13.

    MLH1 methylation screening is effective in identifying epimutation carriers.

    Pineda M, Mur P, Iniesta MD, Borràs E, Campos O, Vargas G, Iglesias S, Fernández A, Gruber SB, Lázaro C, Brunet J, Navarro M, Blanco I, Capellá G.

    Eur J Hum Genet. 2012 Dec;20(12):1256-64. doi: 10.1038/ejhg.2012.136. Epub 2012 Jul 4.

    PMID:
    22763379
    [PubMed - indexed for MEDLINE]
    14.

    Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.

    Andersen SD, Liberti SE, Lützen A, Drost M, Bernstein I, Nilbert M, Dominguez M, Nyström M, Hansen TV, Christoffersen JW, Jäger AC, de Wind N, Nielsen FC, Tørring PM, Rasmussen LJ.

    Hum Mutat. 2012 Dec;33(12):1647-55. doi: 10.1002/humu.22153. Epub 2012 Jul 23.

    PMID:
    22753075
    [PubMed - indexed for MEDLINE]
    15.

    Humans accumulate microsatellite instability with acquired loss of MLH1 protein in hematopoietic stem and progenitor cells as a function of age.

    Kenyon J, Fu P, Lingas K, Thomas E, Saurastri A, Santos Guasch G, Wald D, Gerson SL.

    Blood. 2012 Oct 18;120(16):3229-36. doi: 10.1182/blood-2011-12-401950. Epub 2012 Jun 26.

    PMID:
    22740444
    [PubMed - indexed for MEDLINE]
    16.

    Comprehensive functional assessment of MLH1 variants of unknown significance.

    Borràs E, Pineda M, Brieger A, Hinrichsen I, Gómez C, Navarro M, Balmaña J, Ramón y Cajal T, Torres A, Brunet J, Blanco I, Plotz G, Lázaro C, Capellá G.

    Hum Mutat. 2012 Nov;33(11):1576-88. doi: 10.1002/humu.22142. Epub 2012 Jul 12. Erratum in: Hum Mutat. 2013 Jan;34(1):274.

    PMID:
    22736432
    [PubMed - indexed for MEDLINE]
    17.

    Missense mutations in MLH1, MSH2, KRAS, and APC genes in colorectal cancer patients in Malaysia.

    Abdul Murad NA, Othman Z, Khalid M, Abdul Razak Z, Hussain R, Nadesan S, Sagap I, Mohamed Rose I, Wan Ngah WZ, Jamal R.

    Dig Dis Sci. 2012 Nov;57(11):2863-72. doi: 10.1007/s10620-012-2240-2. Epub 2012 Jun 6.

    PMID:
    22669205
    [PubMed - indexed for MEDLINE]
    18.

    MLH1 polymorphisms and cancer risk: a meta-analysis based on 33 case-control studies.

    Xu JL, Yin ZQ, Huang MD, Wang XF, Gao W, Liu LX, Wang RS, Huang PW, Yin YM, Liu P, Shu YQ.

    Asian Pac J Cancer Prev. 2012;13(3):901-7.

    PMID:
    22631669
    [PubMed - indexed for MEDLINE]
    Free Article
    19.

    FANCJ expression predicts the response to 5-fluorouracil-based chemotherapy in MLH1-proficient colorectal cancer.

    Nakanishi R, Kitao H, Fujinaka Y, Yamashita N, Iimori M, Tokunaga E, Yamashita N, Morita M, Kakeji Y, Maehara Y.

    Ann Surg Oncol. 2012 Oct;19(11):3627-35. doi: 10.1245/s10434-012-2349-8. Epub 2012 Apr 12.

    PMID:
    22526901
    [PubMed - indexed for MEDLINE]
    20.

    Molecular characterization of endometrial cancer: a correlative study assessing microsatellite instability, MLH1 hypermethylation, DNA mismatch repair protein expression, and PTEN, PIK3CA, KRAS, and BRAF mutation analysis.

    Peterson LM, Kipp BR, Halling KC, Kerr SE, Smith DI, Distad TJ, Clayton AC, Medeiros F.

    Int J Gynecol Pathol. 2012 May;31(3):195-205. doi: 10.1097/PGP.0b013e318231fc51.

    PMID:
    22498935
    [PubMed - indexed for MEDLINE]

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