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 *

145 related articles for article (PubMed ID: 15012790)

  • 1. DNA mismatch repair genes and hereditary non-polyposis colorectal cancer.
    J Gastroenterol Hepatol; 2004 Apr; 19(4):465-6. PubMed ID: 15012790
    [No Abstract]   [Full Text] [Related]  

  • 2. 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; 44(2):123-38. PubMed ID: 15942939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Combining clinical investigation with molecular genetics research: to push forward the study of hereditary colorectal carcinoma into a higher level in China].
    Li S
    Zhonghua Yi Xue Za Zhi; 2002 Oct; 82(20):1369-70. PubMed ID: 12613476
    [No Abstract]   [Full Text] [Related]  

  • 4. Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.
    Peltomäki P; Vasen H
    Dis Markers; 2004; 20(4-5):269-76. PubMed ID: 15528792
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Defects of DNA mismatch repair in human prostate cancer.
    Chen Y; Wang J; Fraig MM; Metcalf J; Turner WR; Bissada NK; Watson DK; Schweinfest CW
    Cancer Res; 2001 May; 61(10):4112-21. PubMed ID: 11358834
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.
    de Vos M; Hayward B; Bonthron DT; Sheridan E
    Biochem Soc Trans; 2005 Aug; 33(Pt 4):718-20. PubMed ID: 16042583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer.
    Peltomäki P; Vasen HF
    Gastroenterology; 1997 Oct; 113(4):1146-58. PubMed ID: 9322509
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcription-coupled repair deficiency and mutations in human mismatch repair genes.
    Mellon I; Rajpal DK; Koi M; Boland CR; Champe GN
    Science; 1996 Apr; 272(5261):557-60. PubMed ID: 8614807
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening families with endometrial and colorectal cancers for germline mutations.
    Liu T; Chen J; Salahshor S; Kuismanen S; Holmberg E; Grönberg H; Peltomäki P; Lindblom A
    J Med Genet; 2001 Sep; 38(9):E29. PubMed ID: 11546830
    [No Abstract]   [Full Text] [Related]  

  • 11. Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?
    Jansen M; Menko FH; Brosens LA; Giardiello FM; Offerhaus GJ
    Gastrointest Endosc; 2014 Dec; 80(6):1145-55. PubMed ID: 25434663
    [No Abstract]   [Full Text] [Related]  

  • 12. Lack of PMS2 gene-truncating mutations in patients with hereditary colorectal cancer.
    Viel A; Novella E; Genuardi M; Capozzi E; Fornasarig M; Pedroni M; Santarosa M; De Leon MP; Della Puppa L; Anti M; Boiocchi M
    Int J Oncol; 1998 Sep; 13(3):565-9. PubMed ID: 9683794
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mismatch repair gene deficiency and genetic anticipation in Lynch syndrome: myth or reality?
    Ponti G; Ruini C; Tomasi A
    Dis Colon Rectum; 2015 Jan; 58(1):141-2. PubMed ID: 25489705
    [No Abstract]   [Full Text] [Related]  

  • 14. Anticipating phenotypic differences from genetic mutations.
    You YN
    Dis Colon Rectum; 2015 Jan; 58(1):143-4. PubMed ID: 25489706
    [No Abstract]   [Full Text] [Related]  

  • 15. Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein.
    Raevaara TE; Vaccaro C; Abdel-Rahman WM; Mocetti E; Bala S; Lönnqvist KE; Kariola R; Lynch HT; Peltomäki P; Nyström-Lahti M
    Gastroenterology; 2003 Aug; 125(2):501-9. PubMed ID: 12891553
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening to detect Lynch syndrome and prevent hereditary cancers in relatives.
    Haddow JE; Palomaki GE
    J Med Screen; 2011; 18(4):167-8. PubMed ID: 22184732
    [No Abstract]   [Full Text] [Related]  

  • 17. [Gastric cancer and microsatellite instability].
    Itoh F; Yamamoto H; Horiuchi S; Imai K
    Nihon Shokakibyo Gakkai Zasshi; 2002 Sep; 99(9):1043-9. PubMed ID: 12355890
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. PMS2 mutations in HNPCC.
    Hayward BE; De Vos M; Sheridan E; Bonthron DT
    Clin Genet; 2004 Dec; 66(6):566-7; author reply 568. PubMed ID: 15521988
    [No Abstract]   [Full Text] [Related]  

  • 20. Evaluation and management of Lynch syndrome.
    Boland CR
    Clin Adv Hematol Oncol; 2007 Nov; 5(11):851,873. PubMed ID: 18185481
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.