These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 8940269)

  • 1. Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.
    Moisio AL; Sistonen P; Weissenbach J; de la Chapelle A; Peltomäki P
    Am J Hum Genet; 1996 Dec; 59(6):1243-51. PubMed ID: 8940269
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.
    Nyström-Lahti M; Sistonen P; Mecklin JP; Pylkkänen L; Aaltonen LA; Järvinen H; Weissenbach J; de la Chapelle A; Peltomäki P
    Proc Natl Acad Sci U S A; 1994 Jun; 91(13):6054-8. PubMed ID: 8016114
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.
    Nyström-Lahti M; Parsons R; Sistonen P; Pylkkänen L; Aaltonen LA; Leach FS; Hamilton SR; Watson P; Bronson E; Fusaro R
    Am J Hum Genet; 1994 Oct; 55(4):659-65. PubMed ID: 7942843
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online.
    Holmberg M; Kristo P; Chadwicks RB; Mecklin JP; Järvinen H; de la Chapelle A; Nyström-Lahti M; Peltomäki P
    Hum Mutat; 1998; 11(6):482. PubMed ID: 10200055
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.
    von Salomé J; Liu T; Keihäs M; Morak M; Holinski-Feder E; Berry IR; Moilanen JS; Baert-Desurmont S; Lindblom A; Lagerstedt-Robinson K
    Fam Cancer; 2018 Oct; 17(4):531-537. PubMed ID: 29288294
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations.
    Peltomäki P; Gao X; Mecklin JP
    Fam Cancer; 2001; 1(1):9-15. PubMed ID: 14574010
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.
    Wijnen JT; Vasen HF; Khan PM; Zwinderman AH; van der Klift H; Mulder A; Tops C; Møller P; Fodde R
    N Engl J Med; 1998 Aug; 339(8):511-8. PubMed ID: 9709044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families.
    Thiffault I; Foulkes WD; Marcus VA; Farber D; Kasprzak L; MacNamara E; Wong N; Hutter P; Radice P; Bertario L; Chong G
    Clin Genet; 2004 Aug; 66(2):137-43. PubMed ID: 15253764
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microsatellite instability in early onset and familial colorectal cancer.
    Brassett C; Joyce JA; Froggatt NJ; Williams G; Furniss D; Walsh S; Miller R; Evans DG; Maher ER
    J Med Genet; 1996 Dec; 33(12):981-5. PubMed ID: 9004127
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.
    Nyström-Lahti M; Wu Y; Moisio AL; Hofstra RM; Osinga J; Mecklin JP; Järvinen HJ; Leisti J; Buys CH; de la Chapelle A; Peltomäki P
    Hum Mol Genet; 1996 Jun; 5(6):763-9. PubMed ID: 8776590
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Founding mutations and Alu-mediated recombination in hereditary colon cancer.
    Nyström-Lahti M; Kristo P; Nicolaides NC; Chang SY; Aaltonen LA; Moisio AL; Järvinen HJ; Mecklin JP; Kinzler KW; Vogelstein B
    Nat Med; 1995 Nov; 1(11):1203-6. PubMed ID: 7584997
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Colorectal and extracolonic cancer variations in MLH1/MSH2 hereditary nonpolyposis colorectal cancer kindreds and the general population.
    Lin KM; Shashidharan M; Ternent CA; Thorson AG; Blatchford GJ; Christensen MA; Lanspa SJ; Lemon SJ; Watson P; Lynch HT
    Dis Colon Rectum; 1998 Apr; 41(4):428-33. PubMed ID: 9559626
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.
    Wagner A; Hendriks Y; Meijers-Heijboer EJ; de Leeuw WJ; Morreau H; Hofstra R; Tops C; Bik E; Bröcker-Vriends AH; van Der Meer C; Lindhout D; Vasen HF; Breuning MH; Cornelisse CJ; van Krimpen C; Niermeijer MF; Zwinderman AH; Wijnen J; Fodde R
    J Med Genet; 2001 May; 38(5):318-22. PubMed ID: 11333868
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome.
    Froggatt NJ; Brassett C; Koch DJ; Evans DG; Hodgson SV; Ponder BA; Maher ER
    J Med Genet; 1996 Sep; 33(9):726-30. PubMed ID: 8880570
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.
    Schiemann U; Müller-Koch Y; Gross M; Daum J; Lohse P; Baretton G; Muders M; Mussack T; Kopp R; Holinski-Feder E
    Digestion; 2004; 69(3):166-76. PubMed ID: 15118395
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis.
    de Leon MP; Pedroni M; Benatti P; Percesepe A; Di Gregorio C; Foroni M; Rossi G; Genuardi M; Neri G; Leonardi F; Viel A; Capozzi E; Boiocchi M; Roncucci L
    Gut; 1999 Jul; 45(1):32-8. PubMed ID: 10369701
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.
    Froggatt NJ; Green J; Brassett C; Evans DG; Bishop DT; Kolodner R; Maher ER
    J Med Genet; 1999 Feb; 36(2):97-102. PubMed ID: 10051005
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Histologic comparison of hereditary nonpolyposis colorectal cancer associated with MSH2 and MLH1 and colorectal cancer from the general population.
    Shashidharan M; Smyrk T; Lin KM; Ternent CA; Thorson AG; Blatchford GJ; Christensen MA; Lynch HT
    Dis Colon Rectum; 1999 Jun; 42(6):722-6. PubMed ID: 10378595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
    Liu B; Parsons RE; Hamilton SR; Petersen GM; Lynch HT; Watson P; Markowitz S; Willson JK; Green J; de la Chapelle A
    Cancer Res; 1994 Sep; 54(17):4590-4. PubMed ID: 8062247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic testing for hereditary nonpolyposis colorectal cancer.
    Hoedema R; Monroe T; Bos C; Palmer S; Kim D; Marvin M; Luchtefeld M
    Am Surg; 2003 May; 69(5):387-91; discussion 391-2. PubMed ID: 12769209
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.