253 related articles for article (PubMed ID: 9354786)
1. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer.
Miyaki M; Konishi M; Tanaka K; Kikuchi-Yanoshita R; Muraoka M; Yasuno M; Igari T; Koike M; Chiba M; Mori T
Nat Genet; 1997 Nov; 17(3):271-2. PubMed ID: 9354786
[No Abstract] [Full Text] [Related]
2. Familial endometrial cancer in female carriers of MSH6 germline mutations.
Wijnen J; de Leeuw W; Vasen H; van der Klift H; Møller P; Stormorken A; Meijers-Heijboer H; Lindhout D; Menko F; Vossen S; Möslein G; Tops C; Bröcker-Vriends A; Wu Y; Hofstra R; Sijmons R; Cornelisse C; Morreau H; Fodde R
Nat Genet; 1999 Oct; 23(2):142-4. PubMed ID: 10508506
[No Abstract] [Full Text] [Related]
3. Multiple epithelial and nonepithelial tumors in hereditary nonpolyposis colorectal cancer: characterization of germline and somatic mutations of the MSH2 gene and heterogeneity of replication error phenotypes.
Huang RL; Chao CF; Ding DC; Yu CP; Chang CC; Lai HC; Yu MH; Liu HS; Chu TY
Cancer Genet Cytogenet; 2004 Sep; 153(2):108-14. PubMed ID: 15350299
[TBL] [Abstract][Full Text] [Related]
4. Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers.
Okamura S; Koyama K; Miyoshi Y; Monden M; Takami M
J Hum Genet; 1998; 43(2):143-5. PubMed ID: 9621522
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of endometrial hyperplasia in HNPCC-suspicious patients may predict progression to endometrial carcinoma.
Sutter C; Dallenbach-Hellweg G; Schmidt D; Baehring J; Bielau S; von Knebel Doeberitz M; Gebert J
Int J Gynecol Pathol; 2004 Jan; 23(1):18-25. PubMed ID: 14668545
[TBL] [Abstract][Full Text] [Related]
6. Novel germline hMSH2 genomic deletion and somatic hMSH2 mutations in a hereditary nonpolyposis colorectal cancer family.
Miyaki M; Iijima T; Yamaguchi T; Shirahama S; Ito T; Yasuno M; Mori T
Mutat Res; 2004 Apr; 548(1-2):19-25. PubMed ID: 15063132
[TBL] [Abstract][Full Text] [Related]
7. Women with synchronous primary cancers of the endometrium and ovary: do they have Lynch syndrome?
Soliman PT; Broaddus RR; Schmeler KM; Daniels MS; Gonzalez D; Slomovitz BM; Gershenson DM; Lu KH
J Clin Oncol; 2005 Dec; 23(36):9344-50. PubMed ID: 16361634
[TBL] [Abstract][Full Text] [Related]
8. [Recognition of congenital endometrial carcinoma: the importance of family history and investigation of microsatellite instability in the tumour].
Hoogerbrugge N; Overbeek LI; de Hullu J; Kets CM; Hebeda KM; Ligtenberg MJ
Ned Tijdschr Geneeskd; 2007 Jun; 151(26):1441-4. PubMed ID: 17633970
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Case records of the Massachusetts General Hospital. Case 13-2007. A 46-year-old woman with gynecologic and intestinal cancers.
Seiden MV; Patel D; O'Neill MJ; Oliva E
N Engl J Med; 2007 Apr; 356(17):1760-9. PubMed ID: 17460231
[No Abstract] [Full Text] [Related]
11. Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue.
Plaschke J; Krüger S; Dietmaier W; Gebert J; Sutter C; Mangold E; Pagenstecher C; Holinski-Feder E; Schulmann K; Möslein G; Rüschoff J; Engel C; Evans G; Schackert HK;
Hum Mutat; 2004 Mar; 23(3):285. PubMed ID: 14974087
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer.
Vahteristo P; Ojala S; Tamminen A; Tommiska J; Sammalkorpi H; Kiuru-Kuhlefelt S; Eerola H; Aaltonen LA; Aittomäki K; Nevanlinna H
J Med Genet; 2005 Apr; 42(4):e22. PubMed ID: 15805151
[TBL] [Abstract][Full Text] [Related]
14. Novel dominant mutations in Saccharomyces cerevisiae MSH6.
Das Gupta R; Kolodner RD
Nat Genet; 2000 Jan; 24(1):53-6. PubMed ID: 10615127
[TBL] [Abstract][Full Text] [Related]
15. Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).
Glasl S; Papatheodorou L; Baretton G; Jung C; Gross M
Hum Mutat; 2000 Jul; 16(1):91-2. PubMed ID: 10874318
[TBL] [Abstract][Full Text] [Related]
16. Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients.
de Leeuw WJ; Dierssen J; Vasen HF; Wijnen JT; Kenter GG; Meijers-Heijboer H; Brocker-Vriends A; Stormorken A; Moller P; Menko F; Cornelisse CJ; Morreau H
J Pathol; 2000 Nov; 192(3):328-35. PubMed ID: 11054716
[TBL] [Abstract][Full Text] [Related]
17. Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancers.
Suchy J; Kurzawski G; Jakubowska K; Rać ME; Safranow K; Kładny J; Rzepka-Górska I; Chosia M; Czeszyńska B; Oszurek O; Scott RJ; Lubiński J
Clin Genet; 2006 Jul; 70(1):68-70. PubMed ID: 16813607
[No Abstract] [Full Text] [Related]
18. [Recognising hereditary non-polyposis colorectal cancer without a clear family history].
de Bruin JH; Nagengast FM; Ligtenberg MJ; van Krieken JH; Niermeijer MF; Hoogerbrugge N
Ned Tijdschr Geneeskd; 2004 Oct; 148(42):2053-7. PubMed ID: 15532325
[TBL] [Abstract][Full Text] [Related]
19. Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer.
Shin KH; Ku JL; Park JG
J Hum Genet; 1999; 44(1):18-21. PubMed ID: 9929971
[TBL] [Abstract][Full Text] [Related]
20. [Hereditary gynecological cancers].
Delaloye JF
Praxis (Bern 1994); 1996 Aug; 85(35):1032-4. PubMed ID: 8848673
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
