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Results: 1 to 20 of 68

Related Articles by Review for PubMed (Select 17453358)

1.

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

Loughrey MB, Waring PM, Tan A, Trivett M, Kovalenko S, Beshay V, Young MA, McArthur G, Boussioutas A, Dobrovic A.

Fam Cancer. 2007;6(3):301-10. Epub 2007 Apr 24.

PMID:
17453358
2.

Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification.

Parsons MT, Buchanan DD, Thompson B, Young JP, Spurdle AB.

J Med Genet. 2012 Mar;49(3):151-7. doi: 10.1136/jmedgenet-2011-100714. Review.

PMID:
22368298
3.

Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.

Bonis PA, Trikalinos TA, Chung M, Chew P, Ip S, DeVine DA, Lau J.

Evid Rep Technol Assess (Full Rep). 2007 May;(150):1-180. Review.

4.

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors.

Vasen HF, Hendriks Y, de Jong AE, van Puijenbroek M, Tops C, Bröcker-Vriends AH, Wijnen JT, Morreau H.

Dis Markers. 2004;20(4-5):207-13. Review.

5.

Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review.

Metcalf AM, Spurdle AB.

Fam Cancer. 2014 Mar;13(1):1-12. doi: 10.1007/s10689-013-9671-6. Review.

PMID:
23880961
6.
7.

Microsatellite instability and colorectal cancer.

Geiersbach KB, Samowitz WS.

Arch Pathol Lab Med. 2011 Oct;135(10):1269-77. doi: 10.5858/arpa.2011-0035-RA. Review.

PMID:
21970482
8.

Soft tissue sarcoma and the hereditary non-polyposis colorectal cancer (HNPCC) syndrome: formulation of an hypothesis.

Urso E, Agostini M, Pucciarelli S, Bedin C, D'angelo E, Mescoli C, Viel A, Maretto I, Mammi I, Nitti D.

Mol Biol Rep. 2012 Oct;39(10):9307-10. doi: 10.1007/s11033-012-1729-2. Epub 2012 Jul 11. Review.

PMID:
22782591
9.

Lynch or not Lynch? Is that always a question?

Colas C, Coulet F, Svrcek M, Collura A, Fléjou JF, Duval A, Hamelin R.

Adv Cancer Res. 2012;113:121-66. doi: 10.1016/B978-0-12-394280-7.00004-X. Review.

PMID:
22429854
10.

Prognosis in DNA mismatch repair deficient colorectal cancer: are all MSI tumours equivalent?

Clark AJ, Barnetson R, Farrington SM, Dunlop MG.

Fam Cancer. 2004;3(2):85-91. Review.

PMID:
15340258
11.
12.

A meta-analysis of the prevalence of somatic mutations in the hMLH1 and hMSH2 genes in colorectal cancer.

Zhang R, Qin W, Xu GL, Zeng FF, Li CX.

Colorectal Dis. 2012 Mar;14(3):e80-9. doi: 10.1111/j.1463-1318.2011.02858.x. Review.

PMID:
21988782
13.

MSI-testing in hereditary non-polyposis colorectal carcinoma (HNPCC).

Müller A, Edmonston TB, Dietmaier W, Büttner R, Fishel R, Rüschoff J.

Dis Markers. 2004;20(4-5):225-36. Review.

14.

Lynch Syndrome.

Kohlmann W, Gruber SB.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2004 Feb 5 [updated 2014 May 22].

15.

[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].

Olschwang S, Bonaïti C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F.

Bull Cancer. 2004 Apr;91(4):303-15. Review. French.

PMID:
15242312
16.

[EPICOLON project: contribution to the knowledge of Lynch syndrome and other familial or hereditary colorectal cancer].

Castells A, Andreu M; Grupo de Oncología Gastrointestinal de la Asociación Española de Gastroenterología.

Med Clin (Barc). 2007 Jan 20;128(2):55-60. Review. Spanish. No abstract available.

PMID:
17266903
17.

Interrelationship between microsatellite instability and microRNA in gastrointestinal cancer.

Yamamoto H, Adachi Y, Taniguchi H, Kunimoto H, Nosho K, Suzuki H, Shinomura Y.

World J Gastroenterol. 2012 Jun 14;18(22):2745-55. doi: 10.3748/wjg.v18.i22.2745. Review.

18.
19.

MLH1 promoter methylation frequency in colorectal cancer patients and related clinicopathological and molecular features.

Li X, Yao X, Wang Y, Hu F, Wang F, Jiang L, Liu Y, Wang D, Sun G, Zhao Y.

PLoS One. 2013;8(3):e59064. doi: 10.1371/journal.pone.0059064. Epub 2013 Mar 29. Review.

20.

[Hereditary nonpolyposis colorectal carcinoma (HNPCC). Current review of etiology, clinical aspects, diagnosis and therapy].

al-Taie O, Mörk H, Seufert J, Treis H, Jakob F, Scheurlen M.

Med Klin (Munich). 2001 Sep 15;96(9):529-38. Review. German.

PMID:
11603116
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