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.
125 related articles for article (PubMed ID: 11857362)
1. Associations between family history of colorectal cancer and genetic alterations in tumors. Slattery ML; Curtin K; Schaffer D; Anderson K; Samowitz W Int J Cancer; 2002 Feb; 97(6):823-7. PubMed ID: 11857362 [TBL] [Abstract][Full Text] [Related]
2. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene. Shin KH; Shin JH; Kim JH; Park JG Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355 [TBL] [Abstract][Full Text] [Related]
3. Microsatellite instability and p53 mutations in sporadic right and left colon carcinoma: different clinical and molecular implications. Lleonart ME; García-Foncillas J; Sánchez-Prieto R; Martín P; Moreno A; Salas C; Ramón y Cajal S Cancer; 1998 Sep; 83(5):889-95. PubMed ID: 9731891 [TBL] [Abstract][Full Text] [Related]
4. Colorectal cancer without high microsatellite instability and chromosomal instability--an alternative genetic pathway to human colorectal cancer. Tang R; Changchien CR; Wu MC; Fan CW; Liu KW; Chen JS; Chien HT; Hsieh LL Carcinogenesis; 2004 May; 25(5):841-6. PubMed ID: 14729584 [TBL] [Abstract][Full Text] [Related]
5. Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma. Matsumoto N; Yoshida T; Yamashita K; Numata Y; Okayasu I Br J Cancer; 2003 Aug; 89(4):707-12. PubMed ID: 12915883 [TBL] [Abstract][Full Text] [Related]
6. Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. Yamada K; Zhong X; Kanazawa S; Koike J; Tsujita K; Hemmi H Oncol Rep; 2003; 10(4):859-66. PubMed ID: 12792735 [TBL] [Abstract][Full Text] [Related]
7. Association between family history and mismatch repair in colorectal cancer. Coggins RP; Cawkwell L; Bell SM; Crockford GP; Quirke P; Finan PJ; Bishop DT Gut; 2005 May; 54(5):636-42. PubMed ID: 15831908 [TBL] [Abstract][Full Text] [Related]
8. Clinicopathologic and genetic features of nonfamilial colorectal carcinomas with DNA replication errors. Senba S; Konishi F; Okamoto T; Kashiwagi H; Kanazawa K; Miyaki M; Konishi M; Tsukamoto T Cancer; 1998 Jan; 82(2):279-85. PubMed ID: 9445183 [TBL] [Abstract][Full Text] [Related]
9. Sporadic colorectal cancer in elderly people. Koketsu S; Watanabe T; Tada T; Kanazawa T; Ueda E; Nagawa H Hepatogastroenterology; 2003; 50(54):1749-52. PubMed ID: 14696396 [TBL] [Abstract][Full Text] [Related]
10. Two types of sporadic multiple colorectal cancers with and without HNPCC-like genetic instability. Komura K; Masuda H; Esumi M Hepatogastroenterology; 1999; 46(30):3115-20. PubMed ID: 10626171 [TBL] [Abstract][Full Text] [Related]
11. Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer. Curia MC; Palmirotta R; Aceto G; Messerini L; Verì MC; Crognale S; Valanzano R; Ficari F; Fracasso P; Stigliano V; Tonelli F; Casale V; Guadagni F; Battista P; Mariani-Costantini R; Cama A Cancer Res; 1999 Aug; 59(15):3570-5. PubMed ID: 10446963 [TBL] [Abstract][Full Text] [Related]
12. Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes. Thibodeau SN; French AJ; Roche PC; Cunningham JM; Tester DJ; Lindor NM; Moslein G; Baker SM; Liskay RM; Burgart LJ; Honchel R; Halling KC Cancer Res; 1996 Nov; 56(21):4836-40. PubMed ID: 8895729 [TBL] [Abstract][Full Text] [Related]
13. [The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation]. Czakó L; Tiszlavicz L; Takács R; Baradnay G; Lonovics J; Cserni G; Závodná K; Bartosova Z Orv Hetil; 2005 May; 146(20):1009-16. PubMed ID: 15945244 [TBL] [Abstract][Full Text] [Related]
14. Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas. Koinuma K; Shitoh K; Miyakura Y; Furukawa T; Yamashita Y; Ota J; Ohki R; Choi YL; Wada T; Konishi F; Nagai H; Mano H Int J Cancer; 2004 Jan; 108(2):237-42. PubMed ID: 14639609 [TBL] [Abstract][Full Text] [Related]
15. Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis. Young J; Simms LA; Biden KG; Wynter C; Whitehall V; Karamatic R; George J; Goldblatt J; Walpole I; Robin SA; Borten MM; Stitz R; Searle J; McKeone D; Fraser L; Purdie DR; Podger K; Price R; Buttenshaw R; Walsh MD; Barker M; Leggett BA; Jass JR Am J Pathol; 2001 Dec; 159(6):2107-16. PubMed ID: 11733361 [TBL] [Abstract][Full Text] [Related]
17. Prevalence of microsatellite instability, inactivation of mismatch repair genes, p53 mutation, and human papillomavirus infection in Korean oral cancer patients. Shin KH; Park KH; Hong HJ; Kim JM; Oh JE; Choung PH; Min BM Int J Oncol; 2002 Aug; 21(2):297-302. PubMed ID: 12118324 [TBL] [Abstract][Full Text] [Related]
18. Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium. Millar AL; Pal T; Madlensky L; Sherman C; Temple L; Mitri A; Cheng H; Marcus V; Gallinger S; Redston M; Bapat B; Narod S Hum Mol Genet; 1999 May; 8(5):823-9. PubMed ID: 10196371 [TBL] [Abstract][Full Text] [Related]
19. Immunohistochemical detection of the hMLH1 and hMSH2 proteins in hereditary non-polyposis colon cancer and sporadic colon cancer. Plevová P; Krepelová A; Papezová M; Sedláková E; Curík R; Foretová L; Navrátilová M; Novotný J; Zapletalová J; Palas J; Nieslanik J; Horácek J; Dvorácková J; Kolár Z Neoplasma; 2004; 51(4):275-84. PubMed ID: 15254659 [TBL] [Abstract][Full Text] [Related]
20. Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression. Scartozzi M; Bianchi F; Rosati S; Galizia E; Antolini A; Loretelli C; Piga A; Bearzi I; Cellerino R; Porfiri E J Clin Oncol; 2002 Mar; 20(5):1203-8. PubMed ID: 11870161 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]