160 related articles for article (PubMed ID: 11015456)
1. Two common forms of the human MLH1 gene may be associated with functional differences.
Hutter P; Couturier A; Rey-Berthod C
J Med Genet; 2000 Oct; 37(10):776-81. PubMed ID: 11015456
[No Abstract] [Full Text] [Related]
2. 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]
3. Two novel germline mutations (Y548X and K732X) of the MLH1 gene in Czech patients with hereditary nonpolyposis colorectal cancer.
Hajer J; Kepelová A; Zádorová Z; Kment M
Hum Mutat; 2000 Aug; 16(2):181. PubMed ID: 10923051
[No Abstract] [Full Text] [Related]
4. Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.
Chadwick RB; Pyatt RE; Niemann TH; Richards SK; Johnson CK; Stevens MW; Meek JE; Hampel H; Prior TW; de la Chapelle A
J Med Genet; 2001 Jul; 38(7):461-6. PubMed ID: 11474654
[No Abstract] [Full Text] [Related]
5. Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability.
Kuismanen SA; Moisio AL; Schweizer P; Truninger K; Salovaara R; Arola J; Butzow R; Jiricny J; Nyström-Lahti M; Peltomäki P
Am J Pathol; 2002 Jun; 160(6):1953-8. PubMed ID: 12057899
[TBL] [Abstract][Full Text] [Related]
6. Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis.
Andermann A; Thiffault I; Wong N; Gordon P; MacNamara E; Chong G; Foulkes W
J Clin Oncol; 2002 Mar; 20(6):1705-7. PubMed ID: 11896123
[No Abstract] [Full Text] [Related]
7. [Selection criteria for search for germ mutations in colorectal cancer hereditary nonpolyposis].
Ríos A; Rodríguez JM; Carbonel P; Parrilla P
Med Clin (Barc); 2015 Feb; 144(4):185-6. PubMed ID: 25458510
[No Abstract] [Full Text] [Related]
8. Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families.
Wahlberg SS; Schmeits J; Thomas G; Loda M; Garber J; Syngal S; Kolodner RD; Fox E
Cancer Res; 2002 Jun; 62(12):3485-92. PubMed ID: 12067992
[TBL] [Abstract][Full Text] [Related]
9. Microsatellite instability and expression of MLH1 and MSH2 in carcinomas of the small intestine.
Schulmann K; Hahn SA; Brasch F; Schmiegel W
Cancer; 2003 Oct; 98(8):1774-5; author reply 1775-6. PubMed ID: 14534898
[No Abstract] [Full Text] [Related]
10. Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?
Müller-Koch Y; Kopp R; Lohse P; Baretton G; Stoetzer A; Aust D; Daum J; Kerker B; Gross M; Dietmeier W; Holinski-Feder E
Eur J Med Res; 2001 Nov; 6(11):473-82. PubMed ID: 11726306
[TBL] [Abstract][Full Text] [Related]
11. Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
Nakahara M; Yokozaki H; Yasui W; Dohi K; Tahara E
Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):1057-64. PubMed ID: 9419403
[TBL] [Abstract][Full Text] [Related]
12. Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
Mangold E; Pagenstecher C; Friedl W; Mathiak M; Buettner R; Engel C; Loeffler M; Holinski-Feder E; Müller-Koch Y; Keller G; Schackert HK; Krüger S; Goecke T; Moeslein G; Kloor M; Gebert J; Kunstmann E; Schulmann K; Rüschoff J; Propping P
Int J Cancer; 2005 Sep; 116(5):692-702. PubMed ID: 15849733
[TBL] [Abstract][Full Text] [Related]
13. Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States.
Kurzawski G; Suchy J; Kładny J; Safranow K; Jakubowska A; Elsakov P; Kucinskas V; Gardovski J; Irmejs A; Sibul H; Huzarski T; Byrski T; Debniak T; Cybulski C; Gronwald J; Oszurek O; Clark J; Góźdź S; Niepsuj S; Słomski R; Pławski A; Łacka-Wojciechowska A; Rozmiarek A; Fiszer-Maliszewska Ł; Bebenek M; Sorokin D; Stawicka M; Godlewski D; Richter P; Brozek I; Wysocka B; Jawień A; Banaszkiewicz Z; Kowalczyk J; Czudowska D; Goretzki PE; Moeslein G; Lubiński J
J Med Genet; 2002 Oct; 39(10):E65. PubMed ID: 12362047
[No Abstract] [Full Text] [Related]
14. Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families.
Thiffault I; Foulkes WD; Marcus VA; Farber D; Kasprzak L; MacNamara E; Wong N; Hutter P; Radice P; Bertario L; Chong G
Clin Genet; 2004 Aug; 66(2):137-43. PubMed ID: 15253764
[TBL] [Abstract][Full Text] [Related]
15. A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor.
Gazzoli I; Loda M; Garber J; Syngal S; Kolodner RD
Cancer Res; 2002 Jul; 62(14):3925-8. PubMed ID: 12124320
[TBL] [Abstract][Full Text] [Related]
16. Gene symbol: MLH1. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):535. PubMed ID: 15991306
[No Abstract] [Full Text] [Related]
17. Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.
Krüger S; Bier A; Plaschke J; Höhl R; Aust DE; Kreuz FR; Pistorius SR; Saeger HD; Rothhammer V; Al-Taie O; Schackert HK
Hum Mutat; 2004 Oct; 24(4):351-2. PubMed ID: 15365996
[TBL] [Abstract][Full Text] [Related]
18. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.
Piñol V; Castells A; Andreu M; Castellví-Bel S; Alenda C; Llor X; Xicola RM; Rodríguez-Moranta F; Payá A; Jover R; Bessa X;
JAMA; 2005 Apr; 293(16):1986-94. PubMed ID: 15855432
[TBL] [Abstract][Full Text] [Related]
19. [The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation].
Czakó L; Tiszlavicz L; Takács R; Baradnay G; Lonovics J; Cserni G; Závodná K; Bartosova Z
Orv Hetil; 2005 May; 146(20):1009-16. PubMed ID: 15945244
[TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene.
Shin KH; Shin JH; Kim JH; Park JG
Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
