97 related articles for article (PubMed ID: 17250671)
1. Novel germline and somatic mutations of the MSH2 gene in hereditary non-polyposis colorectal cancer.
Ding DC; Huang RL; Chen CH; Chao CF; Chu TY
Clin Genet; 2007 Feb; 71(2):190-2. PubMed ID: 17250671
[No Abstract] [Full Text] [Related]
2. Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancer.
Morak M; Laner A; Scholz M; Madorf T; Holinski-Feder E
Eur J Gastroenterol Hepatol; 2008 Nov; 20(11):1101-5. PubMed ID: 19047842
[TBL] [Abstract][Full Text] [Related]
3. A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.
Park SJ; Lee KA; Park TS; Kim NK; Song J; Kim BY; Choi JR
Cancer Genet Cytogenet; 2008 Apr; 182(2):136-9. PubMed ID: 18406877
[TBL] [Abstract][Full Text] [Related]
4. [Detection of MSH2 gene mutation by PCR].
Zheng D; Liu XP; Li TG; Li J; Tang LJ; Hu WX
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Apr; 31(2):200-3. PubMed ID: 16706114
[TBL] [Abstract][Full Text] [Related]
5. Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer.
Chan TL; Yuen ST; Kong CK; Chan YW; Chan AS; Ng WF; Tsui WY; Lo MW; Tam WY; Li VS; Leung SY
Nat Genet; 2006 Oct; 38(10):1178-83. PubMed ID: 16951683
[TBL] [Abstract][Full Text] [Related]
6. Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
Wehner M; Mangold E; Sengteller M; Friedrichs N; Aretz S; Friedl W; Propping P; Pagenstecher C
Eur J Hum Genet; 2005 Aug; 13(8):983-6. PubMed ID: 15870828
[TBL] [Abstract][Full Text] [Related]
7. Breast cancer in an MSH2 gene mutation carrier.
Westenend PJ; Schütte R; Hoogmans MM; Wagner A; Dinjens WN
Hum Pathol; 2005 Dec; 36(12):1322-6. PubMed ID: 16311127
[TBL] [Abstract][Full Text] [Related]
8. Functional analysis of HNPCC-related missense mutations in MSH2.
Lützen A; de Wind N; Georgijevic D; Nielsen FC; Rasmussen LJ
Mutat Res; 2008 Oct; 645(1-2):44-55. PubMed ID: 18822302
[TBL] [Abstract][Full Text] [Related]
9. Medullary carcinoma of the pancreas in a man with hereditary nonpolyposis colorectal cancer due to a mutation of the MSH2 mismatch repair gene.
Banville N; Geraghty R; Fox E; Leahy DT; Green A; Keegan D; Geoghegan J; O'Donoghue D; Hyland J; Sheahan K
Hum Pathol; 2006 Nov; 37(11):1498-502. PubMed ID: 16996571
[TBL] [Abstract][Full Text] [Related]
10. MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.
Belvederesi L; Bianchi F; Galizia E; Loretelli C; Bracci R; Catalani R; Amati M; Cellerino R
Hum Mutat; 2008 Nov; 29(11):E296-309. PubMed ID: 18781619
[TBL] [Abstract][Full Text] [Related]
11. Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC.
Stella A; Surdo NC; Lastella P; Barana D; Oliani C; Tibiletti MG; Viel A; Natale C; Piepoli A; Marra G; Guanti G
Clin Genet; 2007 Feb; 71(2):130-9. PubMed ID: 17250661
[TBL] [Abstract][Full Text] [Related]
12. Gene symbol: msh2. Disease: hereditary nonpolyposis colorectal cancer.
Leonardis D
Hum Genet; 2006 Jul; 119(6):675. PubMed ID: 17128465
[No Abstract] [Full Text] [Related]
13. 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):407. PubMed ID: 15046088
[No Abstract] [Full Text] [Related]
14. The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences.
Charbonnier F; Baert-Desurmont S; Liang P; Di Fiore F; Martin C; Frerot S; Olschwang S; Wang Q; Buisine MP; Gilbert B; Nilbert M; Lindblom A; Frebourg T
Hum Mutat; 2005 Sep; 26(3):255-61. PubMed ID: 16086322
[TBL] [Abstract][Full Text] [Related]
15. Synchronous lung tumours in a patient with metachronous colorectal carcinoma and a germline MSH2 mutation.
Canney A; Sheahan K; Keegan D; Tolan M; Hyland J; Green A
J Clin Pathol; 2009 May; 62(5):471-3. PubMed ID: 19398597
[TBL] [Abstract][Full Text] [Related]
16. No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer.
Tuupanen S; Karhu A; Järvinen H; Mecklin JP; Launonen V; Aaltonen LA
Oncogene; 2007 Apr; 26(17):2513-7. PubMed ID: 17043646
[TBL] [Abstract][Full Text] [Related]
17. The 10-Mb paracentric inversion of chromosome arm 2p in activating MSH2 and causing hereditary nonpolyposis colorectal cancer: re-annotation and mutational mechanisms.
Chen JM
Genes Chromosomes Cancer; 2008 Jun; 47(6):543-5. PubMed ID: 18335504
[No Abstract] [Full Text] [Related]
18. 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: 15991307
[No Abstract] [Full Text] [Related]
19. Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer.
Ponti G; Losi L; Pellacani G; Wannesson L; Cesinaro AM; Venesio T; Petti C; Seidenari S
Br J Dermatol; 2008 Jul; 159(1):162-8. PubMed ID: 18460031
[TBL] [Abstract][Full Text] [Related]
20. Solitary subungual keratoacanthoma arising in an MSH2 germline mutation carrier: confirmation of a relationship by immunohistochemical analysis.
Stoebner PE; Fabre C; Delfour C; Joujoux JM; Roger P; Dandurand M; Meunier L
Dermatology; 2009; 219(2):174-8. PubMed ID: 19602866
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
