Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination
We are sorry, but NCBI web applications do not support your browser and may not function properly. More information

Results: 1 to 20 of 229

1.

Molecular characteristics of mismatch repair genes in sporadic colorectal tumors in Czech patients.

Vymetalkova VP, Slyskova J, Korenkova V, Bielik L, Langerova L, Prochazka P, Rejhova A, Schwarzova L, Pardini B, Naccarati A, Vodicka P.

BMC Med Genet. 2014 Jan 31;15:17. doi: 10.1186/1471-2350-15-17.

PMID:
24484585
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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.

PMID:
24362816
[PubMed - indexed for MEDLINE]
3.

High-stage urachal adenocarcinoma can be associated with microsatellite instability and KRAS mutations.

Sirintrapun SJ, Ward M, Woo J, Cimic A.

Hum Pathol. 2014 Feb;45(2):327-30. doi: 10.1016/j.humpath.2013.09.008. Epub 2013 Oct 3.

PMID:
24355196
[PubMed - indexed for MEDLINE]
4.

Contributions of molecular analysis to the diagnosis and treatment of gastrointestinal neoplasms.

Bellizzi AM.

Semin Diagn Pathol. 2013 Nov;30(4):329-61. doi: 10.1053/j.semdp.2013.11.001. Epub 2013 Nov 13. Review.

PMID:
24342289
[PubMed - indexed for MEDLINE]
5.

Mismatch repair deficiency in ovarian cancer -- molecular characteristics and clinical implications.

Xiao X, Melton DW, Gourley C.

Gynecol Oncol. 2014 Feb;132(2):506-12. doi: 10.1016/j.ygyno.2013.12.003. Epub 2013 Dec 10. Review.

PMID:
24333356
[PubMed - indexed for MEDLINE]
6.

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

Buchanan DD, Tan YY, Walsh MD, Clendenning M, Metcalf AM, Ferguson K, Arnold ST, Thompson BA, Lose FA, Parsons MT, Walters RJ, Pearson SA, Cummings M, Oehler MK, Blomfield PB, Quinn MA, Kirk JA, Stewart CJ, Obermair A, Young JP, Webb PM, Spurdle AB.

J Clin Oncol. 2014 Jan 10;32(2):90-100. doi: 10.1200/JCO.2013.51.2129. Epub 2013 Dec 9.

PMID:
24323032
[PubMed - indexed for MEDLINE]
7.

Immunochemistry screening for Lynch syndrome in colorectal adenocarcinoma using an initial two antibody panel can replace a four antibody panel.

O'Regan T, Chau K, Tatton M, Smith T, Parry S, Bissett I.

N Z Med J. 2013 Sep 13;126(1382):70-7.

PMID:
24154771
[PubMed - indexed for MEDLINE]
8.

Microsatellite instability analysis for the screening of synchronous endometrial and ovarian cancer in Lynch syndrome.

Bats AS, Roussel H, Narjoz C, Le Frere-Belda MA, Chamming's F, Blons H, Laurent-Puig P, Lecuru F.

Anticancer Res. 2013 Sep;33(9):3977-81.

PMID:
24023337
[PubMed - indexed for MEDLINE]
9.

Immunophenotypic analysis of ovarian endometrioid adenocarcinoma: correlation with KRAS mutation and the presence of endometriosis.

Stewart CJ, Walsh MD, Budgeon CA, Crook ML, Buchanan DB.

Pathology. 2013 Oct;45(6):559-66. doi: 10.1097/PAT.0b013e3283650ad7.

PMID:
24018808
[PubMed - indexed for MEDLINE]
10.

Two co-existing germline mutations P53 V157D and PMS2 R20Q promote tumorigenesis in a familial cancer syndrome.

Wang Z, Sun Y, Gao B, Lu Y, Fang R, Gao Y, Xiao T, Liu XY, Pao W, Zhao Y, Chen H, Ji H.

Cancer Lett. 2014 Jan 1;342(1):36-42. doi: 10.1016/j.canlet.2013.08.032. Epub 2013 Aug 24.

PMID:
23981578
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

MMR deficiency is common in high-grade endometrioid carcinomas and is associated with an unfavorable outcome.

Nelson GS, Pink A, Lee S, Han G, Morris D, Ogilvie T, Duggan MA, Köbel M.

Gynecol Oncol. 2013 Nov;131(2):309-14. doi: 10.1016/j.ygyno.2013.08.003. Epub 2013 Aug 11.

PMID:
23938375
[PubMed - indexed for MEDLINE]
12.

BRAF V600E mutation analysis simplifies the testing algorithm for Lynch syndrome.

Jin M, Hampel H, Zhou X, Schunemann L, Yearsley M, Frankel WL.

Am J Clin Pathol. 2013 Aug;140(2):177-83. doi: 10.1309/AJCPB9FOVH1HGKFR.

PMID:
23897252
[PubMed - indexed for MEDLINE]
13.

Mismatch repair deficiency screening via immunohistochemical staining in young Asians with colorectal cancers.

Chew MH, Koh PK, Tan M, Lim KH, Carol L, Tang CL.

World J Surg. 2013 Oct;37(10):2468-75. doi: 10.1007/s00268-013-2134-2.

PMID:
23887594
[PubMed - indexed for MEDLINE]
14.

Clinicopathologic features of synchronous colorectal carcinoma: A distinct subset arising from multiple sessile serrated adenomas and associated with high levels of microsatellite instability and favorable prognosis.

Hu H, Chang DT, Nikiforova MN, Kuan SF, Pai RK.

Am J Surg Pathol. 2013 Nov;37(11):1660-70. doi: 10.1097/PAS.0b013e31829623b8.

PMID:
23887157
[PubMed - indexed for MEDLINE]
15.

Hereditary genes and SNPs associated with breast cancer.

Mahdi KM, Nassiri MR, Nasiri K.

Asian Pac J Cancer Prev. 2013;14(6):3403-9. Review.

PMID:
23886119
[PubMed - indexed for MEDLINE]
Free Article
16.

Reduced FHIT expression is associated with mismatch repair deficient and high CpG island methylator phenotype colorectal cancer.

Al-Temaimi RA, Jacob S, Al-Ali W, Thomas DA, Al-Mulla F.

J Histochem Cytochem. 2013 Sep;61(9):627-38. doi: 10.1369/0022155413497367. Epub 2013 Jun 24.

PMID:
23797051
[PubMed - indexed for MEDLINE]
18.

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies.

Walter AW, Ennis S, Best H, Vaughn CP, Swensen JJ, Openshaw A, Gripp KW.

Pediatr Blood Cancer. 2013 Nov;60(11):E135-6. doi: 10.1002/pbc.24613. Epub 2013 Jun 1.

PMID:
23729388
[PubMed - indexed for MEDLINE]
19.

Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.

Borràs E, Pineda M, Cadiñanos J, Del Valle J, Brieger A, Hinrichsen I, Cabanillas R, Navarro M, Brunet J, Sanjuan X, Musulen E, van der Klift H, Lázaro C, Plotz G, Blanco I, Capellá G.

J Med Genet. 2013 Aug;50(8):552-63. doi: 10.1136/jmedgenet-2012-101511. Epub 2013 May 24.

PMID:
23709753
[PubMed - indexed for MEDLINE]
20.

Stable expression of MutLγ in human cells reveals no specific response to mismatched DNA, but distinct recruitment to damage sites.

Roesner LM, Mielke C, Fähnrich S, Merkhoffer Y, Dittmar KE, Drexler HG, Dirks WG.

J Cell Biochem. 2013 Oct;114(10):2405-14. doi: 10.1002/jcb.24591.

PMID:
23696135
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk