BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 14574006)

  • 21. Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations.
    Thompson E; Meldrum CJ; Crooks R; McPhillips M; Thomas L; Spigelman AD; Scott RJ
    Clin Genet; 2004 Mar; 65(3):215-25. PubMed ID: 14756672
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
    Nakahara M; Yokozaki H; Yasui W; Dohi K; Tahara E
    Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):1057-64. PubMed ID: 9419403
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.
    Yuen ST; Chan TL; Ho JW; Chan AS; Chung LP; Lam PW; Tse CW; Wyllie AH; Leung SY
    Oncogene; 2002 Oct; 21(49):7585-92. PubMed ID: 12386821
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.
    Southey MC; Jenkins MA; Mead L; Whitty J; Trivett M; Tesoriero AA; Smith LD; Jennings K; Grubb G; Royce SG; Walsh MD; Barker MA; Young JP; Jass JR; St John DJ; Macrae FA; Giles GG; Hopper JL
    J Clin Oncol; 2005 Sep; 23(27):6524-32. PubMed ID: 16116158
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular basis of HNPCC: mutations of MMR genes.
    Papadopoulos N; Lindblom A
    Hum Mutat; 1997; 10(2):89-99. PubMed ID: 9259192
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer.
    Curia MC; Palmirotta R; Aceto G; Messerini L; Verì MC; Crognale S; Valanzano R; Ficari F; Fracasso P; Stigliano V; Tonelli F; Casale V; Guadagni F; Battista P; Mariani-Costantini R; Cama A
    Cancer Res; 1999 Aug; 59(15):3570-5. PubMed ID: 10446963
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
    Malander S; Rambech E; Kristoffersson U; Halvarsson B; Ridderheim M; Borg A; Nilbert M
    Gynecol Oncol; 2006 May; 101(2):238-43. PubMed ID: 16360201
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).
    Glasl S; Papatheodorou L; Baretton G; Jung C; Gross M
    Hum Mutat; 2000 Jul; 16(1):91-2. PubMed ID: 10874318
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotype and phenotype of a new 2-bp deletion of hMSH2 at codon 233.
    Müller A; Beyser K; Arps H; Bolander S; Becker H; Rüschhoff J
    Virchows Arch; 2001 Aug; 439(2):191-5. PubMed ID: 11561760
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications.
    Lynch HT; Lemon SJ; Karr B; Franklin B; Lynch JF; Watson P; Tinley S; Lerman C; Carter C
    Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):987-91. PubMed ID: 9419392
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinicopathologic and genetic features of nonfamilial colorectal carcinomas with DNA replication errors.
    Senba S; Konishi F; Okamoto T; Kashiwagi H; Kanazawa K; Miyaki M; Konishi M; Tsukamoto T
    Cancer; 1998 Jan; 82(2):279-85. PubMed ID: 9445183
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Microsatellite instability and expression of MLH1 and MSH2 in normal and malignant endometrial and ovarian epithelium in hereditary nonpolyposis colorectal cancer family members.
    Ichikawa Y; Lemon SJ; Wang S; Franklin B; Watson P; Knezetic JA; Bewtra C; Lynch HT
    Cancer Genet Cytogenet; 1999 Jul; 112(1):2-8. PubMed ID: 10432927
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Immunohistochemical detection of the hMLH1 and hMSH2 proteins in hereditary non-polyposis colon cancer and sporadic colon cancer.
    Plevová P; Krepelová A; Papezová M; Sedláková E; Curík R; Foretová L; Navrátilová M; Novotný J; Zapletalová J; Palas J; Nieslanik J; Horácek J; Dvorácková J; Kolár Z
    Neoplasma; 2004; 51(4):275-84. PubMed ID: 15254659
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?
    Müller-Koch Y; Kopp R; Lohse P; Baretton G; Stoetzer A; Aust D; Daum J; Kerker B; Gross M; Dietmeier W; Holinski-Feder E
    Eur J Med Res; 2001 Nov; 6(11):473-82. PubMed ID: 11726306
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients.
    Spaepen M; Vankeirsbilck B; Van Opstal S; Tejpar S; Van Cutsem E; Geboes K; Legius E; Matthijs G
    Fam Cancer; 2006; 5(2):179-89. PubMed ID: 16736289
    [TBL] [Abstract][Full Text] [Related]  

  • 36. HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions.
    Heinen CD; Wilson T; Mazurek A; Berardini M; Butz C; Fishel R
    Cancer Cell; 2002 Jun; 1(5):469-78. PubMed ID: 12124176
    [TBL] [Abstract][Full Text] [Related]  

  • 37. hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer.
    Kim JC; Kim HC; Roh SA; Koo KH; Lee DH; Yu CS; Lee JH; Kim TW; Lee HL; Beck NE; Bodmer WF
    Cancer Detect Prev; 2001; 25(6):503-10. PubMed ID: 12132870
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Loss or somatic mutations of hMSH2 occur in hereditary nonpolyposis colorectal cancers with hMSH2 germline mutations.
    Lu SL; Akiyama Y; Nagasaki H; Nomizu T; Ikeda E; Baba S; Ushio K; Iwama T; Maruyama K; Yuasa Y
    Jpn J Cancer Res; 1996 Mar; 87(3):279-87. PubMed ID: 8613431
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mismatch repair gene expression defects contribute to microsatellite instability in ovarian carcinoma.
    Geisler JP; Goodheart MJ; Sood AK; Holmes RJ; Hatterman-Zogg MA; Buller RE
    Cancer; 2003 Nov; 98(10):2199-206. PubMed ID: 14601090
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1.
    Wahlberg S; Liu T; Lindblom P; Lindblom A
    Genet Test; 1999; 3(3):259-64. PubMed ID: 10495924
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.