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 *

78 related articles for article (PubMed ID: 21882197)

  • 1. Six primary cancers in one Lynch syndrome patient with chronic arsenic exposure.
    Chen PC; Chen WC; Chao SC; Lin BW; Lin SC; Chen CJ; Lee JC
    J Surg Oncol; 2012 Mar; 105(3):329-30. PubMed ID: 21882197
    [No Abstract]   [Full Text] [Related]  

  • 2. Upper urinary tract carcinoma in Lynch syndrome cases.
    Crockett DG; Wagner DG; Holmäng S; Johansson SL; Lynch HT
    J Urol; 2011 May; 185(5):1627-30. PubMed ID: 21419447
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers.
    Okamura S; Koyama K; Miyoshi Y; Monden M; Takami M
    J Hum Genet; 1998; 43(2):143-5. PubMed ID: 9621522
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Editorial comment on: upper urinary tract urothelial cell carcinomas and other urological malignancies involved in the hereditary nonpolyposis colorectal cancer (Lynch syndrome) tumor spectrum.
    Mongiat-Artus P
    Eur Urol; 2008 Dec; 54(6):1235-6. PubMed ID: 18715693
    [No Abstract]   [Full Text] [Related]  

  • 5. Editorial comment on: upper urinary tract urothelial cell carcinomas and other urological malignancies involved in the hereditary nonpolyposis colorectal cancer (Lynch syndrome) tumor spectrum.
    Burger M
    Eur Urol; 2008 Dec; 54(6):1236. PubMed ID: 18715704
    [No Abstract]   [Full Text] [Related]  

  • 6. Multifocal transitional cell carcinoma in a patient with hereditary nonpolyposis colon cancer.
    Ong E; Joseph JV; Bramwell SP; Haites NE
    BJU Int; 2003 Feb; 91(3):297. PubMed ID: 12581024
    [No Abstract]   [Full Text] [Related]  

  • 7. Mechanisms of arsenic carcinogenicity: genetic or epigenetic mechanisms?
    Simeonova PP; Luster MI
    J Environ Pathol Toxicol Oncol; 2000; 19(3):281-6. PubMed ID: 10983894
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Muir Torre syndrome and MSH2 mutations: the importance of dermatological awareness.
    Tischkowitz M; Gologan A; Srolovitz H; Khanna M; Foulkes WD
    Br J Cancer; 2006 Jul; 95(2):243-4. PubMed ID: 16786041
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Upper urinary tract urothelial cell carcinomas and other urological malignancies involved in the hereditary nonpolyposis colorectal cancer (lynch syndrome) tumor spectrum.
    Rouprêt M; Yates DR; Comperat E; Cussenot O
    Eur Urol; 2008 Dec; 54(6):1226-36. PubMed ID: 18715695
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Muir-Torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hMSH2 mutation.
    Suspiro A; Fidalgo P; Cravo M; Albuquerque C; Ramalho E; Leitão CN; Costa Mira F
    Am J Gastroenterol; 1998 Sep; 93(9):1572-4. PubMed ID: 9732950
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synchronous breast cancers with different morphologic and molecular phenotypes occurring in Lynch syndrome: what does the heterogeneity imply?
    D'Arcy C; Wen YH; Stadler ZK; Brogi E; Shia J
    Am J Surg Pathol; 2011 Nov; 35(11):1743-8. PubMed ID: 21997695
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene symbol: msh2. Disease: hereditary nonpolyposis colorectal cancer.
    Leonardis D
    Hum Genet; 2006 Jul; 119(6):675. PubMed ID: 17128465
    [No Abstract]   [Full Text] [Related]  

  • 14. A novel germline mutation of MSH2 in a hereditary nonpolyposis colorectal cancer patient with liposarcoma.
    Hirata K; Kanemitsu S; Nakayama Y; Nagata N; Itoh H; Ohnishi H; Ishikawa H; Furukawa Y;
    Am J Gastroenterol; 2006 Jan; 101(1):193-6. PubMed ID: 16405554
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene symbol: hMSH2. Disease: hereditary nonpolyposis colorectal cancer.
    Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
    Hum Genet; 2005 Dec; 118(3-4):546. PubMed ID: 16521300
    [No Abstract]   [Full Text] [Related]  

  • 16. Mutational spectrum of p53 gene in arsenic-related skin cancers from the blackfoot disease endemic area of Taiwan.
    Hsu CH; Yang SA; Wang JY; Yu HS; Lin SR
    Br J Cancer; 1999 Jun; 80(7):1080-6. PubMed ID: 10362120
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Small cell carcinoma: arising in Lynch syndrome: a previously undocumented occurrence.
    Oman SA; Ballinger L; Cerilli LA
    Int J Surg Pathol; 2009 Feb; 17(1):46-50. PubMed ID: 18480399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel nonsense mutation of MSH2 gene in a Taiwanese family with hereditary nonpolyposis colorectal cancer.
    Chen WC; Lin SC; Lee JC
    Kaohsiung J Med Sci; 2011 Feb; 27(2):68-71. PubMed ID: 21354521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The frequency of Muir-Torre syndrome among Lynch syndrome families.
    South CD; Hampel H; Comeras I; Westman JA; Frankel WL; de la Chapelle A
    J Natl Cancer Inst; 2008 Feb; 100(4):277-81. PubMed ID: 18270343
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.
    Park SJ; Lee KA; Park TS; Kim NK; Song J; Kim BY; Choi JR
    Cancer Genet Cytogenet; 2008 Apr; 182(2):136-9. PubMed ID: 18406877
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.