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.
176 related articles for article (PubMed ID: 11546830)
1. 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]
2. Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma. Chadwick RB; Pyatt RE; Niemann TH; Richards SK; Johnson CK; Stevens MW; Meek JE; Hampel H; Prior TW; de la Chapelle A J Med Genet; 2001 Jul; 38(7):461-6. PubMed ID: 11474654 [No Abstract] [Full Text] [Related]
3. 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]
4. Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability. Kuismanen SA; Moisio AL; Schweizer P; Truninger K; Salovaara R; Arola J; Butzow R; Jiricny J; Nyström-Lahti M; Peltomäki P Am J Pathol; 2002 Jun; 160(6):1953-8. PubMed ID: 12057899 [TBL] [Abstract][Full Text] [Related]
5. Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers. Lipkin SM; Wang V; Stoler DL; Anderson GR; Kirsch I; Hadley D; Lynch HT; Collins FS Hum Mutat; 2001 May; 17(5):389-96. PubMed ID: 11317354 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation. Nakagawa H; Lockman JC; Frankel WL; Hampel H; Steenblock K; Burgart LJ; Thibodeau SN; de la Chapelle A Cancer Res; 2004 Jul; 64(14):4721-7. PubMed ID: 15256438 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis. Berends MJ; Wu Y; Sijmons RH; van der Sluis T; Ek WB; Ligtenberg MJ; Arts NJ; ten Hoor KA; Kleibeuker JH; de Vries EG; Mourits MJ; Hollema H; Buys CH; Hofstra RM; van der Zee AG J Clin Oncol; 2003 Dec; 21(23):4364-70. PubMed ID: 14645426 [TBL] [Abstract][Full Text] [Related]
10. Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer. Southey MC; Jenkins MA; Mead L; Whitty J; Trivett M; Tesoriero AA; Smith LD; Jennings K; Grubb G; Royce SG; Walsh MD; Barker MA; Young JP; Jass JR; St John DJ; Macrae FA; Giles GG; Hopper JL J Clin Oncol; 2005 Sep; 23(27):6524-32. PubMed ID: 16116158 [TBL] [Abstract][Full Text] [Related]
11. Replication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variables. Johannsdottir JT; Bergthorsson JT; Gretarsdottir S; Kristjansson AK; Ragnarsson G; Jonasson JG; Egilsson V; Ingvarsson S Anticancer Res; 1999; 19(3A):1821-6. PubMed ID: 10470121 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular genetics and endometrial cancer. Lalloo F; Evans G Best Pract Res Clin Obstet Gynaecol; 2001 Jun; 15(3):355-63. PubMed ID: 11476558 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Novel splicing associations of hereditary colon cancer related DNA mismatch repair gene mutations. Renkonen E; Lohi H; Järvinen HJ; Mecklin JP; Peltomäki P J Med Genet; 2004 Jul; 41(7):e95. PubMed ID: 15235038 [No Abstract] [Full Text] [Related]
17. [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]
18. Mutations predisposing to hereditary nonpolyposis colorectal cancer. Peltomäki P; de la Chapelle A Adv Cancer Res; 1997; 71():93-119. PubMed ID: 9111864 [TBL] [Abstract][Full Text] [Related]