193 related articles for article (PubMed ID: 12124176)
1. HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions.
Heinen CD; Wilson T; Mazurek A; Berardini M; Butz C; Fishel R
Cancer Cell; 2002 Jun; 1(5):469-78. PubMed ID: 12124176
[TBL] [Abstract][Full Text] [Related]
2. Hereditary cancer-associated missense mutations in hMSH6 uncouple ATP hydrolysis from DNA mismatch binding.
Cyr JL; Heinen CD
J Biol Chem; 2008 Nov; 283(46):31641-8. PubMed ID: 18790734
[TBL] [Abstract][Full Text] [Related]
3. Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer.
Guerrette S; Wilson T; Gradia S; Fishel R
Mol Cell Biol; 1998 Nov; 18(11):6616-23. PubMed ID: 9774676
[TBL] [Abstract][Full Text] [Related]
4. Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.
Wang Q; Lasset C; Desseigne F; Saurin JC; Maugard C; Navarro C; Ruano E; Descos L; Trillet-Lenoir V; Bosset JF; Puisieux A
Hum Genet; 1999; 105(1-2):79-85. PubMed ID: 10480359
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Human MSH2 (hMSH2) protein controls ATP processing by hMSH2-hMSH6.
Heinen CD; Cyr JL; Cook C; Punja N; Sakato M; Forties RA; Lopez JM; Hingorani MM; Fishel R
J Biol Chem; 2011 Nov; 286(46):40287-95. PubMed ID: 21937421
[TBL] [Abstract][Full Text] [Related]
7. hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden.
Planck M; Koul A; Fernebro E; Borg A; Kristoffersson U; Olsson H; Wenngren E; Mangell P; Nilbert M
Int J Cancer; 1999 Oct; 83(2):197-202. PubMed ID: 10471527
[TBL] [Abstract][Full Text] [Related]
8. Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system.
Trojan J; Zeuzem S; Randolph A; Hemmerle C; Brieger A; Raedle J; Plotz G; Jiricny J; Marra G
Gastroenterology; 2002 Jan; 122(1):211-9. PubMed ID: 11781295
[TBL] [Abstract][Full Text] [Related]
9. Loss or somatic mutations of hMSH2 occur in hereditary nonpolyposis colorectal cancers with hMSH2 germline mutations.
Lu SL; Akiyama Y; Nagasaki H; Nomizu T; Ikeda E; Baba S; Ushio K; Iwama T; Maruyama K; Yuasa Y
Jpn J Cancer Res; 1996 Mar; 87(3):279-87. PubMed ID: 8613431
[TBL] [Abstract][Full Text] [Related]
10. Functional alterations of human exonuclease 1 mutants identified in atypical hereditary nonpolyposis colorectal cancer syndrome.
Sun X; Zheng L; Shen B
Cancer Res; 2002 Nov; 62(21):6026-30. PubMed ID: 12414623
[TBL] [Abstract][Full Text] [Related]
11. The role of mismatched nucleotides in activating the hMSH2-hMSH6 molecular switch.
Gradia S; Acharya S; Fishel R
J Biol Chem; 2000 Feb; 275(6):3922-30. PubMed ID: 10660545
[TBL] [Abstract][Full Text] [Related]
12. Transient mismatch repair gene transfection for functional analysis of genetic hMLH1 and hMSH2 variants.
Brieger A; Trojan J; Raedle J; Plotz G; Zeuzem S
Gut; 2002 Nov; 51(5):677-84. PubMed ID: 12377806
[TBL] [Abstract][Full Text] [Related]
13. Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?
Marcelis CL; van der Putten HW; Tops C; Lutgens LC; Moog U
Fam Cancer; 2001; 1(2):107-9. PubMed ID: 14574006
[TBL] [Abstract][Full Text] [Related]
14. Mutator phenotypes of common polymorphisms and missense mutations in MSH2.
Drotschmann K; Clark AB; Kunkel TA
Curr Biol; 1999 Aug; 9(16):907-10. PubMed ID: 10469597
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch.
Gradia S; Acharya S; Fishel R
Cell; 1997 Dec; 91(7):995-1005. PubMed ID: 9428522
[TBL] [Abstract][Full Text] [Related]
19. Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients.
Spaepen M; Vankeirsbilck B; Van Opstal S; Tejpar S; Van Cutsem E; Geboes K; Legius E; Matthijs G
Fam Cancer; 2006; 5(2):179-89. PubMed ID: 16736289
[TBL] [Abstract][Full Text] [Related]
20. Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.
Plaschke J; Kruppa C; Tischler R; Bocker T; Pistorius S; Dralle H; Rüschoff J; Saeger HD; Fishel R; Schackert HK
Int J Cancer; 2000 Mar; 85(5):606-13. PubMed ID: 10699937
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
