BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 30136313)

  • 21. The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer.
    Halvarsson B; Lindblom A; Rambech E; Lagerstedt K; Nilbert M
    Fam Cancer; 2006; 5(4):353-8. PubMed ID: 16817031
    [TBL] [Abstract][Full Text] [Related]  

  • 22. SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cells.
    Takeishi Y; Fujikane R; Rikitake M; Obayashi Y; Sekiguchi M; Hidaka M
    J Biol Chem; 2020 Jan; 295(4):1056-1065. PubMed ID: 31843968
    [TBL] [Abstract][Full Text] [Related]  

  • 23. DNA mismatch repair deficiency in breast carcinoma: a pilot study of triple-negative and non-triple-negative tumors.
    Wen YH; Brogi E; Zeng Z; Akram M; Catalano J; Paty PB; Norton L; Shia J
    Am J Surg Pathol; 2012 Nov; 36(11):1700-8. PubMed ID: 22992699
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Human MutLγ, the MLH1-MLH3 heterodimer, is an endonuclease that promotes DNA expansion.
    Kadyrova LY; Gujar V; Burdett V; Modrich PL; Kadyrov FA
    Proc Natl Acad Sci U S A; 2020 Feb; 117(7):3535-3542. PubMed ID: 32015124
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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. PubMed ID: 23696135
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel interaction between human DNA polymerase eta and MutLalpha.
    Kanao R; Hanaoka F; Masutani C
    Biochem Biophys Res Commun; 2009 Nov; 389(1):40-5. PubMed ID: 19703417
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of tumor morphology with mismatch-repair protein status in older endometrial cancer patients: implications for universal versus selective screening strategies for Lynch syndrome.
    Rabban JT; Calkins SM; Karnezis AN; Grenert JP; Blanco A; Crawford B; Chen LM
    Am J Surg Pathol; 2014 Jun; 38(6):793-800. PubMed ID: 24503759
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer.
    Nyström-Lahti M; Perrera C; Räschle M; Panyushkina-Seiler E; Marra G; Curci A; Quaresima B; Costanzo F; D'Urso M; Venuta S; Jiricny J
    Genes Chromosomes Cancer; 2002 Feb; 33(2):160-7. PubMed ID: 11793442
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mismatch repair deficiency screening in colorectal carcinoma by a four-antibody immunohistochemical panel in Pakistani population and its correlation with histopathological parameters.
    Hashmi AA; Ali R; Hussain ZF; Faridi N; Khan EY; Bakar SMA; Edhi MM; Khan M
    World J Surg Oncol; 2017 Jun; 15(1):116. PubMed ID: 28651545
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Frequent Mismatch Repair Protein Deficiency in Mixed Endometrioid and Clear Cell Carcinoma of the Endometrium.
    Köbel M; Tessier-Cloutier B; Leo J; Hoang LN; Gilks CB; Soslow RA; Delair D; Stewart CJR; Lee CH
    Int J Gynecol Pathol; 2017 Nov; 36(6):555-561. PubMed ID: 28114191
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The PMS2 subunit of human MutLalpha contains a metal ion binding domain of the iron-dependent repressor protein family.
    Kosinski J; Plotz G; Guarné A; Bujnicki JM; Friedhoff P
    J Mol Biol; 2008 Oct; 382(3):610-27. PubMed ID: 18619468
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Alterations in PMS2, MSH2 and MLH1 expression in human prostate cancer.
    Chen Y; Wang J; Fraig MM; Henderson K; Bissada NK; Watson DK; Schweinfest CW
    Int J Oncol; 2003 May; 22(5):1033-43. PubMed ID: 12684669
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dynamic human MutSα-MutLα complexes compact mismatched DNA.
    Bradford KC; Wilkins H; Hao P; Li ZM; Wang B; Burke D; Wu D; Smith AE; Spaller L; Du C; Gauer JW; Chan E; Hsieh P; Weninger KR; Erie DA
    Proc Natl Acad Sci U S A; 2020 Jul; 117(28):16302-16312. PubMed ID: 32586954
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment.
    Rigter LS; Snaebjornsson P; Rosenberg EH; Atmodimedjo PN; Aleman BM; Ten Hoeve J; Geurts-Giele WR; ; van Ravesteyn TW; Hoeksel J; Meijer GA; Te Riele H; van Leeuwen FE; Dinjens WN; van Leerdam ME
    Gut; 2018 Mar; 67(3):447-455. PubMed ID: 29439113
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mismatch repair pathway: molecules, functions, and role in colorectal carcinogenesis.
    Sameer AS; Nissar S; Fatima K
    Eur J Cancer Prev; 2014 Jul; 23(4):246-57. PubMed ID: 24614649
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Different mutator phenotypes in Mlh1- versus Pms2-deficient mice.
    Yao X; Buermeyer AB; Narayanan L; Tran D; Baker SM; Prolla TA; Glazer PM; Liskay RM; Arnheim N
    Proc Natl Acad Sci U S A; 1999 Jun; 96(12):6850-5. PubMed ID: 10359802
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mismatch repair deficiency in Lynch syndrome-associated colorectal adenomas is more prevalent in older patients.
    Tanaka M; Nakajima T; Sugano K; Yoshida T; Taniguchi H; Kanemitsu Y; Nagino M; Sekine S
    Histopathology; 2016 Aug; 69(2):322-8. PubMed ID: 26826556
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Elevated levels of the mismatch repair protein PMS2 are associated with prostate cancer.
    Norris AM; Woodruff RD; D'Agostino RB; Clodfelter JE; Scarpinato KD
    Prostate; 2007 Feb; 67(2):214-25. PubMed ID: 17044039
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 49():1-9. PubMed ID: 26826402
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Validation of an in Vitro Mismatch Repair Assay Used in the Functional Characterization of Mismatch Repair Variants.
    González-Acosta M; Hinrichsen I; Fernández A; Lázaro C; Pineda M; Plotz G; Capellá G
    J Mol Diagn; 2020 Mar; 22(3):376-385. PubMed ID: 31881334
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.