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747 related items for PubMed ID: 16728433

  • 1. Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6.
    Hegan DC, Narayanan L, Jirik FR, Edelmann W, Liskay RM, Glazer PM.
    Carcinogenesis; 2006 Dec; 27(12):2402-8. PubMed ID: 16728433
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  • 2. Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse.
    Chen PC, Dudley S, Hagen W, Dizon D, Paxton L, Reichow D, Yoon SR, Yang K, Arnheim N, Liskay RM, Lipkin SM.
    Cancer Res; 2005 Oct 01; 65(19):8662-70. PubMed ID: 16204034
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  • 3. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
    van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R.
    Genes Chromosomes Cancer; 2005 Oct 01; 44(2):123-38. PubMed ID: 15942939
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  • 4. Risk of secondary malignancy (including breast) in patients with mismatch-repair protein deficiency.
    Clay MR, Allison KH, Folkins AK, Longacre TA.
    Am J Surg Pathol; 2014 Nov 01; 38(11):1494-500. PubMed ID: 24921635
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  • 5. Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
    Haraldsdottir S, Hampel H, Tomsic J, Frankel WL, Pearlman R, de la Chapelle A, Pritchard CC.
    Gastroenterology; 2014 Dec 01; 147(6):1308-1316.e1. PubMed ID: 25194673
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  • 6. MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.
    Ezzatizadeh V, Sandi C, Sandi M, Anjomani-Virmouni S, Al-Mahdawi S, Pook MA.
    PLoS One; 2014 Dec 01; 9(6):e100523. PubMed ID: 24971578
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  • 9. Importance of universal mismatch repair protein immunohistochemistry in patients with sebaceous neoplasia as an initial screening tool for Muir-Torre syndrome.
    Jessup CJ, Redston M, Tilton E, Reimann JD.
    Hum Pathol; 2016 Mar 01; 49():1-9. PubMed ID: 26826402
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  • 11. Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.
    Buchanan DD, Tan YY, Walsh MD, Clendenning M, Metcalf AM, Ferguson K, Arnold ST, Thompson BA, Lose FA, Parsons MT, Walters RJ, Pearson SA, Cummings M, Oehler MK, Blomfield PB, Quinn MA, Kirk JA, Stewart CJ, Obermair A, Young JP, Webb PM, Spurdle AB.
    J Clin Oncol; 2014 Jan 10; 32(2):90-100. PubMed ID: 24323032
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  • 14. Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer.
    Sheng JQ, Chan TL, Chan YW, Huang JS, Chen JG, Zhang MZ, Guo XL, Mu H, Chan AS, Li SR, Yuen ST, Leung SY.
    Chin J Dig Dis; 2006 Jan 10; 7(4):197-205. PubMed ID: 17054581
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  • 16. Role for mismatch repair proteins Msh2, Mlh1, and Pms2 in immunoglobulin class switching shown by sequence analysis of recombination junctions.
    Schrader CE, Vardo J, Stavnezer J.
    J Exp Med; 2002 Feb 04; 195(3):367-73. PubMed ID: 11828012
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  • 20. Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.
    Pistorius S, Görgens H, Plaschke J, Hoehl R, Krüger S, Engel C, Saeger HD, Schackert HK.
    Cancer Lett; 2007 Apr 08; 248(1):89-95. PubMed ID: 16837128
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