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Results by year

Year	Number of Results
1985	1
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818 results

Results by year

Page 1

Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.

Jia X, Burugula BB, Chen V, Lemons RM, Jayakody S, Maksutova M, Kitzman JO. Jia X, et al. Am J Hum Genet. 2021 Jan 7;108(1):163-175. doi: 10.1016/j.ajhg.2020.12.003. Epub 2020 Dec 23. Am J Hum Genet. 2021. PMID: 33357406 Free PMC article.

Correlation of MSH2 exonic deletions and protein downregulation with breast cancer biomarkers and outcome in Pakistani women/patients.

Malik SS, Mubarik S, Aftab A, Khan R, Masood N, Asif M, Bano R. Malik SS, et al. Environ Sci Pollut Res Int. 2021 Jan;28(3):3066-3077. doi: 10.1007/s11356-020-10717-z. Epub 2020 Sep 9. Environ Sci Pollut Res Int. 2021. PMID: 32902747

Molecular characteristics of synchronous multiple gastric cancer.

Wang A, Li Z, Wang M, Jia S, Chen J, Ji K, Ji X, Zong X, Wu X, Zhang J, Li Z, Zhang L, Hu Y, Bu Z, Zheng Q, Ji J. Wang A, et al. Theranostics. 2020 Apr 7;10(12):5489-5500. doi: 10.7150/thno.42814. eCollection 2020. Theranostics. 2020. PMID: 32373223 Free PMC article.

Hypermethylation of mismatch repair gene hMSH2 associates with platinum-resistant disease in epithelial ovarian cancer.

Tian H, Yan L, Xiao-Fei L, Hai-Yan S, Juan C, Shan K. Tian H, et al. Clin Epigenetics. 2019 Oct 30;11(1):153. doi: 10.1186/s13148-019-0748-4. Clin Epigenetics. 2019. PMID: 31666131 Free PMC article.

MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.

Vermaut C, Leclerc J, Vasseur F, Wacrenier A, Lovecchio T, Boidin D, Rebergue MH, Cattan S, Manouvrier S, Lejeune S, Buisine MP. Vermaut C, et al. Genes Chromosomes Cancer. 2020 Feb;59(2):111-118. doi: 10.1002/gcc.22804. Epub 2019 Sep 3. Genes Chromosomes Cancer. 2020. PMID: 31433521

Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins.

Jaballah-Gabteni A, Tounsi H, Kabbage M, Hamdi Y, Elouej S, Ben Ayed I, Medhioub M, Mahmoudi M, Dallali H, Yaiche H, Ben Jemii N, Maaloul A, Mezghani N, Abdelhak S, Hamzaoui L, Azzouz M, Boubaker S. Jaballah-Gabteni A, et al. J Transl Med. 2019 Jun 27;17(1):212. doi: 10.1186/s12967-019-1961-9. J Transl Med. 2019. PMID: 31248416 Free PMC article.

Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestine.

Herberg M, Siebert S, Quaas M, Thalheim T, Rother K, Hussong M, Altmüller J, Kerner C, Galle J, Schweiger MR, Aust G. Herberg M, et al. Clin Epigenetics. 2019 Apr 27;11(1):65. doi: 10.1186/s13148-019-0639-8. Clin Epigenetics. 2019. PMID: 31029155 Free PMC article.

Structural debilitation of mutation G322D associated with MSH2 and their role in triple negative breast cancer.

Sriroopreddy R, Raghuraman P, Sudandiradoss C. Sriroopreddy R, et al. J Biomol Struct Dyn. 2020 Feb;38(3):771-780. doi: 10.1080/07391102.2019.1587512. Epub 2019 Mar 19. J Biomol Struct Dyn. 2020. PMID: 30806579

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. Hammoudi N, et al. Dig Liver Dis. 2019 Feb;51(2):299-303. doi: 10.1016/j.dld.2018.10.005. Epub 2018 Oct 15. Dig Liver Dis. 2019. PMID: 30448460

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. Zhu X, et al. DNA Cell Biol. 2018 Jul;37(7):634-641. doi: 10.1089/dna.2018.4224. Epub 2018 Jun 6. DNA Cell Biol. 2018. PMID: 29874113