164 related articles for article (PubMed ID: 11429708)
1. HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.
Jäger AC; Rasmussen M; Bisgaard HC; Singh KK; Nielsen FC; Rasmussen LJ
Oncogene; 2001 Jun; 20(27):3590-5. PubMed ID: 11429708
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer.
Guerrette S; Acharya S; Fishel R
J Biol Chem; 1999 Mar; 274(10):6336-41. PubMed ID: 10037723
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC.
Korhonen MK; Raevaara TE; Lohi H; Nyström M
Oncol Rep; 2007 Feb; 17(2):351-4. PubMed ID: 17203173
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2.
Kondo E; Horii A; Fukushige S
Nucleic Acids Res; 2001 Apr; 29(8):1695-702. PubMed ID: 11292842
[TBL] [Abstract][Full Text] [Related]
9. The human PMS2L proteins do not interact with hMLH1, a major DNA mismatch repair protein.
Kondo E; Horii A; Fukushige S
J Biochem; 1999 Apr; 125(4):818-25. PubMed ID: 10101297
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha.
Räschle M; Dufner P; Marra G; Jiricny J
J Biol Chem; 2002 Jun; 277(24):21810-20. PubMed ID: 11948175
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function.
Quaresima B; Alifano P; Tassone P; Avvedimento EV; Costanzo FS; Venuta S
Biochem J; 2003 Apr; 371(Pt 1):183-9. PubMed ID: 12513688
[TBL] [Abstract][Full Text] [Related]
14. Somatic mutation of hPMS2 as a possible cause of sporadic human colon cancer with microsatellite instability.
Ma AH; Xia L; Littman SJ; Swinler S; Lader G; Polinkovsky A; Olechnowicz J; Kasturi L; Lutterbaugh J; Modrich P; Veigl ML; Markowitz SD; Sedwick WD
Oncogene; 2000 Apr; 19(18):2249-56. PubMed ID: 10822375
[TBL] [Abstract][Full Text] [Related]
15. Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.
Räschle M; Marra G; Nyström-Lahti M; Schär P; Jiricny J
J Biol Chem; 1999 Nov; 274(45):32368-75. PubMed ID: 10542278
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer.
Nyström-Lahti M; Perrera C; Räschle M; Panyushkina-Seiler E; Marra G; Curci A; Quaresima B; Costanzo F; D'Urso M; Venuta S; Jiricny J
Genes Chromosomes Cancer; 2002 Feb; 33(2):160-7. PubMed ID: 11793442
[TBL] [Abstract][Full Text] [Related]
18. Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein.
Raevaara TE; Vaccaro C; Abdel-Rahman WM; Mocetti E; Bala S; Lönnqvist KE; Kariola R; Lynch HT; Peltomäki P; Nyström-Lahti M
Gastroenterology; 2003 Aug; 125(2):501-9. PubMed ID: 12891553
[TBL] [Abstract][Full Text] [Related]
19. Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications.
Lynch HT; Lemon SJ; Karr B; Franklin B; Lynch JF; Watson P; Tinley S; Lerman C; Carter C
Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):987-91. PubMed ID: 9419392
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
