723 related articles for article (PubMed ID: 12522549)
21. Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.
Pistorius S; Görgens H; Plaschke J; Hoehl R; Krüger S; Engel C; Saeger HD; Schackert HK
Cancer Lett; 2007 Apr; 248(1):89-95. PubMed ID: 16837128
[TBL] [Abstract][Full Text] [Related]
22. MSH6 germline mutations are rare in colorectal cancer families.
Peterlongo P; Nafa K; Lerman GS; Glogowski E; Shia J; Ye TZ; Markowitz AJ; Guillem JG; Kolachana P; Boyd JA; Offit K; Ellis NA
Int J Cancer; 2003 Nov; 107(4):571-9. PubMed ID: 14520694
[TBL] [Abstract][Full Text] [Related]
23. HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.
de Wind N; Dekker M; Claij N; Jansen L; van Klink Y; Radman M; Riggins G; van der Valk M; van't Wout K; te Riele H
Nat Genet; 1999 Nov; 23(3):359-62. PubMed ID: 10545954
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain.
Caldes T; Godino J; de la Hoya M; Garcia Carbonero I; Perez Segura P; Eng C; Benito M; Diaz-Rubio E
Int J Cancer; 2002 Apr; 98(5):774-9. PubMed ID: 11920650
[TBL] [Abstract][Full Text] [Related]
26. [Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis].
Doré MX; Dieumegard B; Grandjouan S; Avril MF; Martinet C; Ducreux M; Lasser P; Bressac-de Paillerets B
Ann Dermatol Venereol; 1999; 126(8-9):582-6. PubMed ID: 10530344
[TBL] [Abstract][Full Text] [Related]
27. E2F-4 mutation in hereditary non-polyposis colorectal cancer.
Moriyama H; Sasamoto H; Kambara T; Matsubara N; Ikeda M; Baba S; Meltzer SJ; Lynch HT; Shimizu K; Tanaka N
J Exp Clin Cancer Res; 2002 Jun; 21(2):185-9. PubMed ID: 12148576
[TBL] [Abstract][Full Text] [Related]
28. Surveillance on mutation carriers of DNA mismatch repair genes.
Järvinen HJ; Aarnio M
Ann Chir Gynaecol; 2000; 89(3):207-10. PubMed ID: 11079789
[TBL] [Abstract][Full Text] [Related]
29. Phenotypic analysis of hMSH2 mutations in mouse cells carrying human chromosomes.
Marra G; D'Atri S; Yan H; Perrera C; Cannavo' E; Vogelstein B; Jiricny J
Cancer Res; 2001 Nov; 61(21):7719-21. PubMed ID: 11691782
[TBL] [Abstract][Full Text] [Related]
30. Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer.
Renkonen E; Zhang Y; Lohi H; Salovaara R; Abdel-Rahman WM; Nilbert M; Aittomaki K; Jarvinen HJ; Mecklin JP; Lindblom A; Peltomaki P
J Clin Oncol; 2003 Oct; 21(19):3629-37. PubMed ID: 14512394
[TBL] [Abstract][Full Text] [Related]
31. [Diagnosis by directed mutagenesis of a mutation at the hMSH2 gene associated with hereditary nonpolyposis colorectal cancer].
Roqué M; Pusiol E; Giribet G; Perinetti H; Mayorga LS
Medicina (B Aires); 2000; 60(2):188-94. PubMed ID: 10962807
[TBL] [Abstract][Full Text] [Related]
32. Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.
Wagner A; Hendriks Y; Meijers-Heijboer EJ; de Leeuw WJ; Morreau H; Hofstra R; Tops C; Bik E; Bröcker-Vriends AH; van Der Meer C; Lindhout D; Vasen HF; Breuning MH; Cornelisse CJ; van Krimpen C; Niermeijer MF; Zwinderman AH; Wijnen J; Fodde R
J Med Genet; 2001 May; 38(5):318-22. PubMed ID: 11333868
[TBL] [Abstract][Full Text] [Related]
33. Colonic cancer in a 34-yr-old woman: should it prompt microsatellite instability studies and mismatch repair gene testing?
Claro I; Cravo M; Glória L; Gaspar C; Albuquerque C; Lage P; Fidalgo P; Ramalho E; Chaves P; Cardoso P; Nobre Leitão C
Am J Gastroenterol; 1998 Oct; 93(10):1991-2. PubMed ID: 9772075
[TBL] [Abstract][Full Text] [Related]
34. Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes.
Cohn DE; Babb S; Whelan AJ; Mutch DG; Herzog TJ; Rader JS; Elbendary A; Goodfellow PJ
Gynecol Oncol; 2000 Apr; 77(1):18-25. PubMed ID: 10739686
[TBL] [Abstract][Full Text] [Related]
35. [Essential to discover hereditary colorectal and endometrial cancer. Mutations in "HNPCC individuals" can cause several different tumors].
Nilbert M; Grönberg H; Lindblom A
Lakartidningen; 2002 Aug; 99(34):3296-300. PubMed ID: 12362848
[TBL] [Abstract][Full Text] [Related]
36. The mismatch repair gene hMSH2 is mutated in the prostate cancer cell line LNCaP.
Leach FS; Velasco A; Hsieh JT; Sagalowsky AI; McConnell JD
J Urol; 2000 Nov; 164(5):1830-3. PubMed ID: 11025778
[TBL] [Abstract][Full Text] [Related]
37. Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer.
Rey JM; Noruzinia M; Brouillet JP; Sarda P; Maudelonde T; Pujol P
Cancer Genet Cytogenet; 2004 Dec; 155(2):149-51. PubMed ID: 15571801
[TBL] [Abstract][Full Text] [Related]
38. [From gene to disease; from DNA 'mismatch' repair genes to hereditary non-polyposis colorectal carcinoma].
Wijnen JT; Morreau H; Vasen HF
Ned Tijdschr Geneeskd; 2001 Apr; 145(16):780-2. PubMed ID: 11346916
[TBL] [Abstract][Full Text] [Related]
39. Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
Hendriks YM; Jagmohan-Changur S; van der Klift HM; Morreau H; van Puijenbroek M; Tops C; van Os T; Wagner A; Ausems MG; Gomez E; Breuning MH; Bröcker-Vriends AH; Vasen HF; Wijnen JT
Gastroenterology; 2006 Feb; 130(2):312-22. PubMed ID: 16472587
[TBL] [Abstract][Full Text] [Related]
40. Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia.
Bartosova Z; Fridrichova I; Bujalkova M; Wolf B; Ilencikova D; Krizan P; Hlavcak P; Palaj J; Lukac L; Lukacova M; Böör A; Haider R; Jiricny J; Nyström-Lahti M; Marra G
Hum Mutat; 2003 Apr; 21(4):449. PubMed ID: 12655568
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
