BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

58 related articles for article (PubMed ID: 8640829)

  • 1. Genetic heterogeneity and unmapped genes for colorectal cancer.
    Lewis CM; Neuhausen SL; Daley D; Black FJ; Swensen J; Burt RW; Cannon-Albright LA; Skolnick MH
    Cancer Res; 1996 Mar; 56(6):1382-8. PubMed ID: 8640829
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.
    Baudi F; Fersini G; Lavecchia A; Terracciano R; Leone F; Quaresima B; Faniello MC; De Paola L; Doldo P; Cuda G; Costanzo F; Venuta S
    Cancer Lett; 2005 Jun; 223(2):285-91. PubMed ID: 15896463
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair.
    Boardman LA; Schmidt S; Lindor NM; Burgart LJ; Cunningham JM; Price-Troska T; Snow K; Ahlquist DA; Thibodeau SN
    Genes Chromosomes Cancer; 2001 Feb; 30(2):181-6. PubMed ID: 11135435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees.
    Weber TK; Conlon W; Petrelli NJ; Rodriguez-Bigas M; Keitz B; Pazik J; Farrell C; O'Malley L; Oshalim M; Abdo M; Anderson G; Stoler D; Yandell D
    Cancer Res; 1997 Sep; 57(17):3798-803. PubMed ID: 9288790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.
    Peltomäki P; Sistonen P; Mecklin JP; Pylkkänen L; Aaltonen L; Nordling S; Kere J; Järvinen H; Hamilton SR; Petersen G
    Cancer Res; 1992 Aug; 52(16):4530-3. PubMed ID: 1643645
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Diagnosis by directed mutagenesis of a mutation at the hMSH2 gene associated with hereditary nonpolyposis colorectal cancer].
    Roqué M; Pusiol E; Giribet G; Perinetti H; Mayorga LS
    Medicina (B Aires); 2000; 60(2):188-94. PubMed ID: 10962807
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
    Plasilova M; Russell AM; Wanner A; Wolf A; Dobbie Z; Müller HJ; Heinimann K
    Eur J Hum Genet; 2004 May; 12(5):365-71. PubMed ID: 14735163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes.
    Losi L; Di Gregorio C; Pedroni M; Ponti G; Roncucci L; Scarselli A; Genuardi M; Baglioni S; Marino M; Rossi G; Benatti P; Maffei S; Menigatti M; Roncari B; Ponz de Leon M
    Am J Gastroenterol; 2005 Oct; 100(10):2280-7. PubMed ID: 16181381
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer.
    Middeldorp A; Jagmohan-Changur SC; van der Klift HM; van Puijenbroek M; Houwing-Duistermaat JJ; Webb E; Houlston R; Tops C; Vasen HF; Devilee P; Morreau H; van Wezel T; Wijnen J
    Genes Chromosomes Cancer; 2010 Jun; 49(6):539-48. PubMed ID: 20222047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindreds.
    Peltomäki P; Sistonen P; Mecklin JP; Pylkkänen L; Järvinen H; Simons JW; Cho KR; Vogelstein B; de la Chapelle A
    Cancer Res; 1991 Aug; 51(16):4135-40. PubMed ID: 1868434
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HMSH6 alterations in patients with microsatellite instability-low colorectal cancer.
    Parc YR; Halling KC; Wang L; Christensen ER; Cunningham JM; French AJ; Burgart LJ; Price-Troska TL; Roche PC; Thibodeau SN
    Cancer Res; 2000 Apr; 60(8):2225-31. PubMed ID: 10786688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis].
    Doré MX; Dieumegard B; Grandjouan S; Avril MF; Martinet C; Ducreux M; Lasser P; Bressac-de Paillerets B
    Ann Dermatol Venereol; 1999; 126(8-9):582-6. PubMed ID: 10530344
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis of the APC gene regions involved in attenuated APC phenotype in Israeli patients with early onset and familial colorectal cancer.
    Figer A; Irmin L; Geva R; Flex D; Sulkes A; Friedman E
    Br J Cancer; 2001 Aug; 85(4):523-6. PubMed ID: 11506490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: a two-stage case-control study.
    Fernández-Rozadilla C; Tarrío R; Clofent J; de Castro L; Brea-Fernández A; Bessa X; Abulí A; Andreu M; Jover R; Xicola R; Llor X; Castells A; Castellví-Bel S; Carracedo A; Ruiz-Ponte C;
    Cancer Epidemiol Biomarkers Prev; 2010 Feb; 19(2):619-23. PubMed ID: 20142256
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosome 17q linkage studies of 18 Utah breast cancer kindreds.
    Goldgar DE; Cannon-Albright LA; Oliphant A; Ward JH; Linker G; Swensen J; Tran TD; Fields P; Uharriet P; Skolnick MH
    Am J Hum Genet; 1993 Apr; 52(4):743-8. PubMed ID: 8460640
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Colorectal cancer and the relationship between genes and the environment.
    Heavey PM; McKenna D; Rowland IR
    Nutr Cancer; 2004; 48(2):124-41. PubMed ID: 15231447
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Common familial colorectal cancer linked to chromosome 7q31: a genome-wide analysis.
    Neklason DW; Kerber RA; Nilson DB; Anton-Culver H; Schwartz AG; Griffin CA; Lowery JT; Schildkraut JM; Evans JP; Tomlinson GE; Strong LC; Miller AR; Stopfer JE; Finkelstein DM; Nadkarni PM; Kasten CH; Mineau GP; Burt RW
    Cancer Res; 2008 Nov; 68(21):8993-7. PubMed ID: 18974144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.
    Mary JL; Bishop T; Kolodner R; Lipford JR; Kane M; Weber W; Torhorst J; Müller H; Spycher M; Scott RJ
    Hum Mol Genet; 1994 Nov; 3(11):2067-9. PubMed ID: 7874129
    [No Abstract]   [Full Text] [Related]  

  • 19. A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2.
    Wiesner GL; Daley D; Lewis S; Ticknor C; Platzer P; Lutterbaugh J; MacMillen M; Baliner B; Willis J; Elston RC; Markowitz SD
    Proc Natl Acad Sci U S A; 2003 Oct; 100(22):12961-5. PubMed ID: 14566058
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic mapping of a locus predisposing to human colorectal cancer.
    Peltomäki P; Aaltonen LA; Sistonen P; Pylkkänen L; Mecklin JP; Järvinen H; Green JS; Jass JR; Weber JL; Leach FS
    Science; 1993 May; 260(5109):810-2. PubMed ID: 8484120
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.