Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Colorectal cancer AND PMS1, hPMS1, 5378, ENSG00000064933, PMSL1, HNPCC3, DKFZp781M0253 AND Diagnosis
33 results:

  • 1. Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome.
    Abildgaard AB; Stein A; Nielsen SV; Schultz-Knudsen K; Papaleo E; Shrikhande A; Hoffmann ER; Bernstein I; Gerdes AM; Takahashi M; Ishioka C; Lindorff-Larsen K; Hartmann-Petersen R
    Elife; 2019 Nov; 8():. PubMed ID: 31697235
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. [A single center study of colorectal cancer screening for Lynch syndrome].
    Pan J; Zhu F; Pan D; Zhang H; Ye Q; Xu P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Mar; 36(3):238-241. PubMed ID: 30835354
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer.
    Ricker CN; Hanna DL; Peng C; Nguyen NT; Stern MC; Schmit SL; Idos GE; Patel R; Tsai S; Ramirez V; Lin S; Shamasunadara V; Barzi A; Lenz HJ; Figueiredo JC
    Cancer; 2017 Oct; 123(19):3732-3743. PubMed ID: 28640387
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. [Founder mutation in Lynch syndrome].
    Cajal AR; Piñero TA; Verzura A; Santino JP; Solano AR; Kalfayan PG; Ferro A; Vaccaro C
    Medicina (B Aires); 2016; 76(3):180-2. PubMed ID: 27295708
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing.
    Marafie MJ; Al-Awadi S; Al-Mosawi F; Elshafey A; Al-Ali W; Al-Mulla F
    Fam Cancer; 2009; 8(4):289-98. PubMed ID: 19669601
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer.
    Koessler T; Azzato EM; Perkins B; Macinnis RJ; Greenberg D; Easton DF; Pharoah PD
    Int J Cancer; 2009 Apr; 124(8):1887-91. PubMed ID: 19115210
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.
    Liu SR; Zhao B; Wang ZJ; Wan YL; Huang YT
    World J Gastroenterol; 2004 Sep; 10(18):2647-51. PubMed ID: 15309712
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Analysis of mismatch repair defects in the familial occurrence of lymphoma and colorectal cancer.
    Teruya-Feldstein J; Greene J; Cohen L; Popplewell L; Ellis NA; Offit K
    Leuk Lymphoma; 2002 Aug; 43(8):1619-26. PubMed ID: 12400605
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Mismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC).
    Müller A; Fishel R
    Cancer Invest; 2002; 20(1):102-9. PubMed ID: 11852992
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. [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]  

  • 11. Germline mutation and genome instability.
    Olschwang S
    Eur J Cancer Prev; 1999 Dec; 8 Suppl 1():S33-7. PubMed ID: 10772416
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree.
    Ponz de Leon M; Benatti P; Percesepe A; Rossi G; Viel A; Santarosa M; Pedroni M; Roncucci L
    Ital J Gastroenterol Hepatol; 1999; 31(6):476-80. PubMed ID: 10575566
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Strategies for screening for hereditary non-polyposis colorectal cancer.
    Loukola A; de la Chapelle A; Aaltonen LA
    J Med Genet; 1999 Nov; 36(11):819-22. PubMed ID: 10544224
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Genetic susceptibility to non-polyposis colorectal cancer.
    Lynch HT; de la Chapelle A
    J Med Genet; 1999 Nov; 36(11):801-18. PubMed ID: 10544223
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Evaluation of the replication error phenotype in relation to molecular and clinicopathological features in hereditary and early onset colorectal cancer.
    Capozzi E; Della Puppa L; Fornasarig M; Pedroni M; Boiocchi M; Viel A
    Eur J Cancer; 1999 Feb; 35(2):289-95. PubMed ID: 10448273
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. 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]  

  • 17. cancer genetics in the new era of molecular biology.
    Lynch HT; Fusaro RM; Lynch JF
    Ann N Y Acad Sci; 1997 Dec; 833():1-28. PubMed ID: 9616736
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer.
    Liu T; Wahlberg S; Rubio C; Holmberg E; Grönberg H; Lindblom A
    Clin Genet; 1998 Feb; 53(2):131-5. PubMed ID: 9611074
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Genetic identification and management of hereditary nonpolyposis colorectal cancer.
    Park JG; Yuan Y
    Int J Oncol; 1998 Apr; 12(4):947-55. PubMed ID: 9499460
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Molecular genetics and clinical-pathology features of hereditary nonpolyposis colorectal carcinoma (Lynch syndrome): historical journey from pedigree anecdote to molecular genetic confirmation.
    Lynch HT; Smyrk T; Lynch JF
    Oncology; 1998; 55(2):103-8. PubMed ID: 9499183
    [TBL] [Abstract] [Full Text] [Related]  


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