97 related articles for article (PubMed ID: 17250671)
21. [Mismatch repair (MMR) efficiency and MSH2 gene mutation in human colorectal carcinoma cell line COLO320HSR].
Tronov VA; Kramarenko II; Maĭorova EN; Zakharov SF
Genetika; 2007 Apr; 43(4):537-44. PubMed ID: 17555131
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
Steinke V; Rahner N; Morak M; Keller G; Schackert HK; Görgens H; Schmiegel W; Royer-Pokora B; Dietmaier W; Kloor M; Engel C; Propping P; Aretz S;
Eur J Hum Genet; 2008 May; 16(5):587-92. PubMed ID: 18301448
[TBL] [Abstract][Full Text] [Related]
24. Origins and prevalence of the American Founder Mutation of MSH2.
Clendenning M; Baze ME; Sun S; Walsh K; Liyanarachchi S; Fix D; Schunemann V; Comeras I; Deacon M; Lynch JF; Gong G; Thomas BC; Thibodeau SN; Lynch HT; Hampel H; de la Chapelle A
Cancer Res; 2008 Apr; 68(7):2145-53. PubMed ID: 18381419
[TBL] [Abstract][Full Text] [Related]
25. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):536. PubMed ID: 15991308
[No Abstract] [Full Text] [Related]
26. Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer.
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ
Scand J Gastroenterol; 2007 May; 42(5):628-32. PubMed ID: 17454884
[TBL] [Abstract][Full Text] [Related]
27. The HNPCC associated MSH2*1906G-->C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population.
Sun S; Greenwood CM; Thiffault I; Hamel N; Chong G; Foulkes WD
J Med Genet; 2005 Oct; 42(10):766-8. PubMed ID: 16199548
[TBL] [Abstract][Full Text] [Related]
28. Difference in the role of loss of heterozygosity at 10p15 (KLF6 locus) in colorectal carcinogenesis between sporadic and familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer patients.
Miyaki M; Yamaguchi T; Iijima T; Funata N; Mori T
Oncology; 2006; 71(1-2):131-5. PubMed ID: 17347589
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Germline hMSH2 promoter mutation in a Chinese HNPCC kindred: evidence for dual role of LOH.
Yan H; Jin H; Xue G; Mei Q; Ding F; Hao L; Sun SH
Clin Genet; 2007 Dec; 72(6):556-61. PubMed ID: 17894833
[TBL] [Abstract][Full Text] [Related]
31. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):538. PubMed ID: 15991314
[No Abstract] [Full Text] [Related]
32. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Luo DC; Sun MH; Ni YZ; Cai Q; Li XY; Ni SC; Chen ZJ; Zhou H; Ye YH; Ye ZL; Fang Y; Tao CW; Zhang XM
Hum Genet; 2005 Jul; 117(2-3):298. PubMed ID: 16156026
[No Abstract] [Full Text] [Related]
33. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):410. PubMed ID: 15046099
[No Abstract] [Full Text] [Related]
34. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046096
[No Abstract] [Full Text] [Related]
35. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046093
[No Abstract] [Full Text] [Related]
36. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):408. PubMed ID: 15046091
[No Abstract] [Full Text] [Related]
37. Single nucleotide polymorphism detection in the hMSH2 gene using conformation-sensitive CE.
Chen YL; Jong YJ; Ferrance J; Hsien JS; Shih CJ; Feng CH; Wu MT; Wu SM
Electrophoresis; 2008 Feb; 29(3):634-40. PubMed ID: 18186537
[TBL] [Abstract][Full Text] [Related]
38. Mechanisms of pathogenicity in human MSH2 missense mutants.
Ollila S; Dermadi Bebek D; Jiricny J; Nyström M
Hum Mutat; 2008 Nov; 29(11):1355-63. PubMed ID: 18951462
[TBL] [Abstract][Full Text] [Related]
39. Colorectal cancer in a 9-year-old due to combined EPCAM and MSH2 germline mutations: case report of a unique genotype and immunophenotype.
Li-Chang HH; Driman DK; Levin H; Siu VM; Scanlan NL; Buckley K; Cairney AE; Ainsworth PJ
J Clin Pathol; 2013 Jul; 66(7):631-3. PubMed ID: 23454724
[No Abstract] [Full Text] [Related]
40. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):538. PubMed ID: 15991315
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
