Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 770

1.

Duodenal tumor risk in Lynch syndrome.

Hammoudi N, Dhooge M, Coriat R, Leblanc S, Barret M, Bordacahar B, Beuvon F, Prat F, Maksimovic F, Chaussade S.

Dig Liver Dis. 2019 Feb;51(2):299-303. doi: 10.1016/j.dld.2018.10.005. Epub 2018 Oct 15.

PMID:
30448460
2.

Rs2303428 of MSH2 Is Associated with Hepatocellular Carcinoma Prognosis in a Chinese Population.

Zhu X, Wang Z, Qiu X, Wang W, Bei C, Tan C, Qin L, Ren Y, Tan S.

DNA Cell Biol. 2018 Jul;37(7):634-641. doi: 10.1089/dna.2018.4224. Epub 2018 Jun 6.

PMID:
29874113
3.

Analysis of MSH2 Loss of Heterozygosity, Expression, and IVS10+12G>A Polymorphism in Sporadic Colon Cancer.

Cacev T, Zapletal E, Musani V, Rako I, Loncar B, Aralica G, Kapitanovic S.

Anticancer Res. 2018 May;38(5):2841-2848.

PMID:
29715107
4.

Association of a novel point mutation in MSH2 gene with familial multiple primary cancers.

Hu H, Li H, Jiao F, Han T, Zhuo M, Cui J, Li Y, Wang L.

J Hematol Oncol. 2017 Oct 3;10(1):158. doi: 10.1186/s13045-017-0523-y.

5.

MSH2 Loss in Primary Prostate Cancer.

Guedes LB, Antonarakis ES, Schweizer MT, Mirkheshti N, Almutairi F, Park JC, Glavaris S, Hicks J, Eisenberger MA, De Marzo AM, Epstein JI, Isaacs WB, Eshleman JR, Pritchard CC, Lotan TL.

Clin Cancer Res. 2017 Nov 15;23(22):6863-6874. doi: 10.1158/1078-0432.CCR-17-0955. Epub 2017 Aug 8.

6.

A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay.

Bianchi F, Maccaroni E, Belvederesi L, Brugiati C, Giampieri R, Bini F, Bracci R, Pagliaretta S, Del Prete M, Piva F, Mandolesi A, Scarpelli M, Berardi R.

Fam Cancer. 2018 Apr;17(2):215-224. doi: 10.1007/s10689-017-0030-x.

PMID:
28785832
7.

Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry.

Goldberg M, Bell K, Aronson M, Semotiuk K, Pond G, Gallinger S, Zbuk K.

J Med Genet. 2017 Nov;54(11):742-746. doi: 10.1136/jmedgenet-2017-104542. Epub 2017 Aug 4.

PMID:
28779004
8.

Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations.

Nielsen SV, Stein A, Dinitzen AB, Papaleo E, Tatham MH, Poulsen EG, Kassem MM, Rasmussen LJ, Lindorff-Larsen K, Hartmann-Petersen R.

PLoS Genet. 2017 Apr 19;13(4):e1006739. doi: 10.1371/journal.pgen.1006739. eCollection 2017 Apr.

9.

[Muir-Torre syndrome and Turcot syndrome].

Velter C, Caussade P, Fricker JP, Cribier B.

Ann Dermatol Venereol. 2017 Aug - Sep;144(8-9):525-529. doi: 10.1016/j.annder.2017.01.017. Epub 2017 Feb 27. French.

PMID:
28256262
10.

Identification of MSH2 inversion of exons 1-7 in clinical evaluation of families with suspected Lynch syndrome.

Mork ME, Rodriguez A, Taggart MW, Rodriguez-Bigas MA, Lynch PM, Bannon SA, You YN, Vilar E.

Fam Cancer. 2017 Jul;16(3):357-361. doi: 10.1007/s10689-016-9960-y.

11.

Overexpression of MutSĪ± Complex Proteins Predicts Poor Prognosis in Oral Squamous Cell Carcinoma.

Wagner VP, Webber LP, Salvadori G, Meurer L, Fonseca FP, Castilho RM, Squarize CH, Vargas PA, Martins MD.

Medicine (Baltimore). 2016 May;95(22):e3725. doi: 10.1097/MD.0000000000003725.

12.

Causes of Cancer Death Among First-Degree Relatives in Japanese Families with Lynch Syndrome.

Tanakaya K, Yamaguchi T, Ishikawa H, Hinoi T, Furukawa Y, Hirata K, Saida Y, Shimokawa M, Arai M, Matsubara N, Tomita N, Tamura K, Sugano K, Ishioka C, Yoshida T, Ishida H, Watanabe T, Sugihara K; for HNPCC Registry and Genetic Testing Project of the Japanese Society for Cancer of the Colon and Rectum.

Anticancer Res. 2016 Apr;36(4):1985-9.

PMID:
27069191
13.

MSH2 rs2303425 Polymorphism is Associated with Early-Onset Breast Cancer in Taiwan.

Hsieh YC, Cho EC, Tu SH, Wu CH, Hung CS, Hsieh MC, Su CT, Liu YR, Lee CH, Ho YS, Chiou HY.

Ann Surg Oncol. 2017 Feb;24(2):603-610. doi: 10.1245/s10434-016-5168-5. Epub 2016 Mar 14.

PMID:
26975740
14.

Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.

Houlleberghs H, Dekker M, Lantermans H, Kleinendorst R, Dubbink HJ, Hofstra RM, Verhoef S, Te Riele H.

Proc Natl Acad Sci U S A. 2016 Apr 12;113(15):4128-33. doi: 10.1073/pnas.1520813113. Epub 2016 Mar 7.

15.

A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.

Liu Q, Hesson LB, Nunez AC, Packham D, Williams R, Ward RL, Sloane MA.

Carcinogenesis. 2016 Jan;37(1):10-17. doi: 10.1093/carcin/bgv154. Epub 2015 Oct 24.

PMID:
26498247
16.

MSH2 role in BRCA1-driven tumorigenesis: A preliminary study in yeast and in human tumors from BRCA1-VUS carriers.

Maresca L, Spugnesi L, Lodovichi S, Cozzani C, Naccarato AG, Tancredi M, Collavoli A, Falaschi E, Rossetti E, Aretini P, Cervelli T, Galli A, Caligo MA.

Eur J Med Genet. 2015 Oct;58(10):531-9. doi: 10.1016/j.ejmg.2015.09.005. Epub 2015 Sep 14.

PMID:
26381082
17.

Family with MSH2 mutation presenting with keratoacanthoma and precancerous skin lesions.

Hatta N, Takata A, Ishizawa S, Niida Y.

J Dermatol. 2015 Nov;42(11):1087-90. doi: 10.1111/1346-8138.12949. Epub 2015 Jun 16.

PMID:
26077460
18.

Minor Changes in Expression of the Mismatch Repair Protein MSH2 Exert a Major Impact on Glioblastoma Response to Temozolomide.

McFaline-Figueroa JL, Braun CJ, Stanciu M, Nagel ZD, Mazzucato P, Sangaraju D, Cerniauskas E, Barford K, Vargas A, Chen Y, Tretyakova N, Lees JA, Hemann MT, White FM, Samson LD.

Cancer Res. 2015 Aug 1;75(15):3127-38. doi: 10.1158/0008-5472.CAN-14-3616. Epub 2015 May 29.

19.

[Lynch syndrome and risk of prostate cancer; review of the literature].

Maillard F, Manouvrier S, Biardeau X, Ouzzane A, Villers A.

Prog Urol. 2015 Apr;25(5):225-32. doi: 10.1016/j.purol.2015.01.001. Epub 2015 Jan 29. Review. French.

PMID:
25640028
20.

Down-regulation of MSH2 expression by Hsp90 inhibition enhances cytotoxicity affected by tamoxifen in human lung cancer cells.

Ko JC, Chiu HC, Syu JJ, Chen CY, Jian YT, Huang YJ, Wo TY, Jian YJ, Chang PY, Wang TJ, Lin YW.

Biochem Biophys Res Commun. 2015 Jan 2;456(1):506-12. doi: 10.1016/j.bbrc.2014.11.116. Epub 2014 Dec 6.

PMID:
25490383

Supplemental Content

Support Center