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Results: 1 to 20 of 43

Cited In for PubMed (Select 20028993)

1.

Advances in the study of Lynch syndrome in China.

Lu JY, Sheng JQ.

World J Gastroenterol. 2015 Jun 14;21(22):6861-6871. Review.

2.

Replicative DNA polymerase δ but not ε proofreads errors in Cis and in Trans.

Flood CL, Rodriguez GP, Bao G, Shockley AH, Kow YW, Crouse GF.

PLoS Genet. 2015 Mar 5;11(3):e1005049. doi: 10.1371/journal.pgen.1005049. eCollection 2015 Mar.

3.

The genetic basis of Lynch syndrome and its implications for clinical practice and risk management.

Cohen SA, Leininger A.

Appl Clin Genet. 2014 Jul 22;7:147-58. doi: 10.2147/TACG.S51483. eCollection 2014. Review.

4.

Familial cancer among consecutive uterine cancer patients in Sweden.

Tzortzatos G, Wersäll O, Danielsson KG, Lindblom A, Tham E, Mints M.

Hered Cancer Clin Pract. 2014 May 7;12(1):14. doi: 10.1186/1897-4287-12-14. eCollection 2014.

5.

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Thompson BA, Spurdle AB, Plazzer JP, Greenblatt MS, Akagi K, Al-Mulla F, Bapat B, Bernstein I, Capellá G, den Dunnen JT, du Sart D, Fabre A, Farrell MP, Farrington SM, Frayling IM, Frebourg T, Goldgar DE, Heinen CD, Holinski-Feder E, Kohonen-Corish M, Robinson KL, Leung SY, Martins A, Moller P, Morak M, Nystrom M, Peltomaki P, Pineda M, Qi M, Ramesar R, Rasmussen LJ, Royer-Pokora B, Scott RJ, Sijmons R, Tavtigian SV, Tops CM, Weber T, Wijnen J, Woods MO, Macrae F, Genuardi M; InSiGHT.

Nat Genet. 2014 Feb;46(2):107-15. doi: 10.1038/ng.2854. Epub 2013 Dec 22.

7.

Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients.

Wielders EA, Houlleberghs H, Isik G, te Riele H.

PLoS One. 2013 Sep 10;8(9):e74766. doi: 10.1371/journal.pone.0074766. eCollection 2013.

8.

History, genetics, and strategies for cancer prevention in Lynch syndrome.

Kastrinos F, Stoffel EM.

Clin Gastroenterol Hepatol. 2014 May;12(5):715-27; quiz e41-3. doi: 10.1016/j.cgh.2013.06.031. Epub 2013 Jul 23.

9.

Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention.

Lu KH, Daniels M.

Fam Cancer. 2013 Jun;12(2):273-7. doi: 10.1007/s10689-013-9664-5. Review.

10.

Molecular pathogenesis of endometrial cancers in patients with Lynch syndrome.

Huang M, Djordjevic B, Yates MS, Urbauer D, Sun C, Burzawa J, Daniels M, Westin SN, Broaddus R, Lu K.

Cancer. 2013 Aug 15;119(16):3027-33. doi: 10.1002/cncr.28152. Epub 2013 Jun 12.

11.

Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testing.

Flander L, Speirs-Bridge A, Rutstein A, Niven H, Win AK, Ait Ouakrim D, Hopper JL, Macrae F, Keogh L, Gaff C, Jenkins M.

J Genet Couns. 2014 Feb;23(1):79-88. doi: 10.1007/s10897-013-9614-2. Epub 2013 Jun 9.

12.

CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein.

Terui H, Akagi K, Kawame H, Yura K.

J Biomed Sci. 2013 Apr 28;20:25. doi: 10.1186/1423-0127-20-25.

13.

Risk of breast cancer in Lynch syndrome: a systematic review.

Win AK, Lindor NM, Jenkins MA.

Breast Cancer Res. 2013 Mar 19;15(2):R27. doi: 10.1186/bcr3405. Review.

14.

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

Win AK, Hopper JL, Buchanan DD, Young JP, Tenesa A, Dowty JG, Giles GG, Goldblatt J, Winship I, Boussioutas A, Young GP, Parry S, Baron JA, Duggan D, Gallinger S, Newcomb PA, Haile RW, Le Marchand L, Lindor NM, Jenkins MA.

Eur J Cancer. 2013 May;49(7):1578-87. doi: 10.1016/j.ejca.2013.01.029. Epub 2013 Feb 22.

15.

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.

Vasen HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I, Bertario L, Burn J, Capella G, Colas C, Engel C, Frayling IM, Genuardi M, Heinimann K, Hes FJ, Hodgson SV, Karagiannis JA, Lalloo F, Lindblom A, Mecklin JP, Møller P, Myrhoj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Sijmons RH, Tejpar S, Thomas HJ, Rahner N, Wijnen JT, Järvinen HJ, Möslein G; Mallorca group.

Gut. 2013 Jun;62(6):812-23. doi: 10.1136/gutjnl-2012-304356. Epub 2013 Feb 13.

16.

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome.

Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, Marchand LL, Gallinger S, Haile RW, Newcomb PA, Hopper JL, Jenkins MA.

J Natl Cancer Inst. 2013 Feb 20;105(4):274-9. doi: 10.1093/jnci/djs525. Epub 2013 Feb 5.

17.

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers.

Win AK, Parry S, Parry B, Kalady MF, Macrae FA, Ahnen DJ, Young GP, Lipton L, Winship I, Boussioutas A, Young JP, Buchanan DD, Arnold J, Le Marchand L, Newcomb PA, Haile RW, Lindor NM, Gallinger S, Hopper JL, Jenkins MA.

Ann Surg Oncol. 2013 Jun;20(6):1829-36. doi: 10.1245/s10434-012-2858-5. Epub 2013 Jan 29.

18.

Prospective study of family history and colorectal cancer risk by tumor LINE-1 methylation level.

Ogino S, Nishihara R, Lochhead P, Imamura Y, Kuchiba A, Morikawa T, Yamauchi M, Liao X, Qian ZR, Sun R, Sato K, Kirkner GJ, Wang M, Spiegelman D, Meyerhardt JA, Schernhammer ES, Chan AT, Giovannucci E, Fuchs CS.

J Natl Cancer Inst. 2013 Jan 16;105(2):130-40. doi: 10.1093/jnci/djs482. Epub 2012 Nov 21.

19.

Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer.

Kast K, Neuhann TM, Görgens H, Becker K, Keller K, Klink B, Aust D, Distler W, Schröck E, Schackert HK.

BMC Cancer. 2012 Nov 20;12:531. doi: 10.1186/1471-2407-12-531.

20.

A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry.

Thompson BA, Goldgar DE, Paterson C, Clendenning M, Walters R, Arnold S, Parsons MT, Michael D W, Gallinger S, Haile RW, Hopper JL, Jenkins MA, Lemarchand L, Lindor NM, Newcomb PA, Thibodeau SN; Colon Cancer Family Registry, Young JP, Buchanan DD, Tavtigian SV, Spurdle AB.

Hum Mutat. 2013 Jan;34(1):200-9. doi: 10.1002/humu.22213. Epub 2012 Oct 11.

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