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Results: 1 to 20 of 929

1.

[Immunohistochemical examination of MSH2, PMS2, MLH1, MSH6 compared with the analysis of microsatellite instability in colon adenocarcinoma].

Raskin GA, Ianus GA, Kornilov AV, Orlova RV, Petrov SV, Protasova AÉ, Pozharisskiĭ KM, Imianitov EN.

Vopr Onkol. 2014;60(2):47-50. Russian.

PMID:
24919261
[PubMed - indexed for MEDLINE]
2.

A de novo germline mutation of APC for inheritable colon cancer in a Chinese family using multigene next generation sequencing.

Zhang Y, Lu G, Hu Q, Wang X, Li C, Mao Y, Cui M.

Biochem Biophys Res Commun. 2014 May 9;447(3):503-7. doi: 10.1016/j.bbrc.2014.04.014. Epub 2014 Apr 13.

PMID:
24735542
[PubMed - indexed for MEDLINE]
3.

Immunohistochemistry for annexin A10 can distinguish sporadic from Lynch syndrome-associated microsatellite-unstable colorectal carcinoma.

Pai RK, Shadrach BL, Carver P, Heald B, Moline J, Church J, Kalady MF, Burke CA, Plesec TP, Lai KK, Gonzalo DH, Pai RK.

Am J Surg Pathol. 2014 Apr;38(4):518-25. doi: 10.1097/PAS.0000000000000148.

PMID:
24625416
[PubMed - indexed for MEDLINE]
4.

Pyloric gland adenoma in Lynch syndrome.

Lee SE, Kang SY, Cho J, Lee B, Chang DK, Woo H, Kim JW, Park HY, Do IG, Kim YE, Kushima R, Lauwers GY, Park CK, Kim KM.

Am J Surg Pathol. 2014 Jun;38(6):784-92. doi: 10.1097/PAS.0000000000000185.

PMID:
24518125
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Association of tumor morphology with mismatch-repair protein status in older endometrial cancer patients: implications for universal versus selective screening strategies for Lynch syndrome.

Rabban JT, Calkins SM, Karnezis AN, Grenert JP, Blanco A, Crawford B, Chen LM.

Am J Surg Pathol. 2014 Jun;38(6):793-800. doi: 10.1097/PAS.0000000000000177.

PMID:
24503759
[PubMed - indexed for MEDLINE]
6.

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families.

Steinke V, Holzapfel S, Loeffler M, Holinski-Feder E, Morak M, Schackert HK, Görgens H, Pox C, Royer-Pokora B, von Knebel-Doeberitz M, Büttner R, Propping P, Engel C; German HNPCC Consortium.

Int J Cancer. 2014 Jul 1;135(1):69-77. doi: 10.1002/ijc.28650. Epub 2014 Feb 20.

PMID:
24493211
[PubMed - indexed for MEDLINE]
7.

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.

Mensenkamp AR, Vogelaar IP, van Zelst-Stams WA, Goossens M, Ouchene H, Hendriks-Cornelissen SJ, Kwint MP, Hoogerbrugge N, Nagtegaal ID, Ligtenberg MJ.

Gastroenterology. 2014 Mar;146(3):643-646.e8. doi: 10.1053/j.gastro.2013.12.002. Epub 2013 Dec 10.

PMID:
24333619
[PubMed - indexed for MEDLINE]
8.

Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.

Petersen SM, Dandanell M, Rasmussen LJ, Gerdes AM, Krogh LN, Bernstein I, Okkels H, Wikman F, Nielsen FC, Hansen TV.

BMC Med Genet. 2013 Oct 3;14:103. doi: 10.1186/1471-2350-14-103.

PMID:
24090359
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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.

PMID:
24040339
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Frequency and variability of genomic rearrangements on MSH2 in Spanish Lynch Syndrome families.

Romero A, Garre P, Valentin O, Sanz J, Pérez-Segura P, Llovet P, Díaz-Rubio E, de la Hoya M, Caldés T.

PLoS One. 2013 Sep 11;8(9):e72195. doi: 10.1371/journal.pone.0072195. eCollection 2013.

PMID:
24039744
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.

Pujol P, Lyonnet DS, Frebourg T, Blin J, Picot MC, Lasset C, Dugast C, Berthet P, de Paillerets BB, Sobol H, Grandjouan S, Soubrier F, Buecher B, Guimbaud R, Lidereau R, Jonveaux P, Houdayer C, Giraud S, Olschwang S, Nogue E, Galibert V, Bara C, Nowak F, Khayat D, Nogues C.

Breast Cancer Res Treat. 2013 Aug;141(1):135-44. doi: 10.1007/s10549-013-2669-9. Epub 2013 Aug 24.

PMID:
23974829
[PubMed - indexed for MEDLINE]
12.

Criteria and prediction models for mismatch repair gene mutations: a review.

Win AK, Macinnis RJ, Dowty JG, Jenkins MA.

J Med Genet. 2013 Dec;50(12):785-93. doi: 10.1136/jmedgenet-2013-101803. Epub 2013 Aug 16. Review.

PMID:
23956446
[PubMed - indexed for MEDLINE]
13.

Microsatellite and genetic instability in patients with Muir-Torre syndrome.

Lorente-Lavirgen AI, Morillo-Andújar M, Zulueta-Dorado T, Conejo-Mir J.

Actas Dermosifiliogr. 2013 Sep;104(7):643-4. doi: 10.1016/j.adengl.2013.02.007. Epub 2013 Jul 23. No abstract available.

PMID:
23891449
[PubMed - indexed for MEDLINE]
14.

EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion.

Spaepen M, Neven E, Sagaert X, De Hertogh G, Beert E, Wimmer K, Matthijs G, Legius E, Brems H.

Genes Chromosomes Cancer. 2013 Sep;52(9):845-54. doi: 10.1002/gcc.22080. Epub 2013 Jun 26.

PMID:
23801599
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
23760948
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.

Grandval P, Fabre AJ, Gaildrat P, Baert-Desurmont S, Buisine MP, Ferrari A, Wang Q, Béroud C, Olschwang S.

Database (Oxford). 2013 May 31;2013:bat036. doi: 10.1093/database/bat036. Print 2013.

PMID:
23729658
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Distinct molecular profiles in Lynch syndrome-associated and sporadic ovarian carcinomas.

Niskakoski A, Kaur S, Renkonen-Sinisalo L, Lassus H, Järvinen HJ, Mecklin JP, Bützow R, Peltomäki P.

Int J Cancer. 2013 Dec 1;133(11):2596-608. doi: 10.1002/ijc.28287. Epub 2013 Jun 21.

PMID:
23716351
[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.

Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome.

Drost M, Lützen A, van Hees S, Ferreira D, Calléja F, Zonneveld JB, Nielsen FC, Rasmussen LJ, de Wind N.

Proc Natl Acad Sci U S A. 2013 Jun 4;110(23):9403-8. doi: 10.1073/pnas.1220537110. Epub 2013 May 20.

PMID:
23690608
[PubMed - indexed for MEDLINE]
Free PMC Article

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