PubMed for id: 4439

Year	Number of Results
1989	1
1996	1
1998	2
1999	2
2002	1
2003	4
2004	5
2005	2
2006	3
2007	5
2008	6
2009	5
2010	6
2011	1
2012	2
2013	1
2014	1
2015	4
2017	5
2019	1
2020	4
2021	3
2022	2
2024	0

1

A Homozygous Loss-of-Function Mutation in MSH5 Abolishes MutSγ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals.

Gong C, Abbas T, Muhammad Z, Zhou J, Khan R, Ma H, Zhang H, Shi Q, Shi B. Gong C, et al. Int J Mol Sci. 2022 Jun 10;23(12):6522. doi: 10.3390/ijms23126522. Int J Mol Sci. 2022. PMID: 35742973 Free PMC article.

2

Association of hMSH5 C85T polymorphism with radiation sensitivity of testicular cell lines GC-1, GC-2, TM3, and TM4.

Lin M, Guo L, Cheng Z, Huan X, Huang Y, Xu K. Lin M, et al. Andrology. 2020 Sep;8(5):1174-1183. doi: 10.1111/andr.12803. Epub 2020 May 8. Andrology. 2020. PMID: 32306546 Free article.

3

MutS homologue hMSH5: recombinational DSB repair and non-synonymous polymorphic variants.

Wu X, Xu Y, Feng K, Tompkins JD, Her C. Wu X, et al. PLoS One. 2013 Sep 4;8(9):e73284. doi: 10.1371/journal.pone.0073284. eCollection 2013. PLoS One. 2013. PMID: 24023853 Free PMC article.

4

The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage.

Bannwarth S, Figueroa A, Fragaki K, Destroismaisons L, Lacas-Gervais S, Lespinasse F, Vandenbos F, Pradelli LA, Ricci JE, Rötig A, Michiels JF, Vande Velde C, Paquis-Flucklinger V. Bannwarth S, et al. Mitochondrion. 2012 Nov;12(6):654-65. doi: 10.1016/j.mito.2012.07.111. Epub 2012 Aug 11. Mitochondrion. 2012. PMID: 22917773

5

hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization.

Lahaye F, Lespinasse F, Staccini P, Palin L, Paquis-Flucklinger V, Santucci-Darmanin S. Lahaye F, et al. Nucleic Acids Res. 2010 Jun;38(11):3655-71. doi: 10.1093/nar/gkq098. Epub 2010 Feb 25. Nucleic Acids Res. 2010. PMID: 20185565 Free PMC article.

6

Mutations of MSH5 in nonobstructive azoospermia (NOA) and rescued via in vivo gene editing.

Chen M, Yao C, Qin Y, Cui X, Li P, Ji Z, Lin L, Wu H, Zhou Z, Gui Y, Li Z, Gao F. Chen M, et al. Signal Transduct Target Ther. 2022 Jan 3;7(1):1. doi: 10.1038/s41392-021-00710-4. Signal Transduct Target Ther. 2022. PMID: 34980881 Free PMC article. No abstract available.

7

Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.

Wyrwoll MJ, van Walree ES, Hamer G, Rotte N, Motazacker MM, Meijers-Heijboer H, Alders M, Meißner A, Kaminsky E, Wöste M, Krallmann C, Kliesch S, Hunt TJ, Clark AT, Silber S, Stallmeyer B, Friedrich C, van Pelt AMM, Mathijssen IB, Tüttelmann F. Wyrwoll MJ, et al. Hum Reprod. 2021 Dec 27;37(1):178-189. doi: 10.1093/humrep/deab230. Hum Reprod. 2021. PMID: 34755185

8

Mutations in MSH5 in primary ovarian insufficiency.

Guo T, Zhao S, Zhao S, Chen M, Li G, Jiao X, Wang Z, Zhao Y, Qin Y, Gao F, Chen ZJ. Guo T, et al. Hum Mol Genet. 2017 Apr 15;26(8):1452-1457. doi: 10.1093/hmg/ddx044. Hum Mol Genet. 2017. PMID: 28175301 Free PMC article.

9

hMSH5 Facilitates the Repair of Camptothecin-induced Double-strand Breaks through an Interaction with FANCJ.

Xu Y, Wu X, Her C. Xu Y, et al. J Biol Chem. 2015 Jul 24;290(30):18545-58. doi: 10.1074/jbc.M115.642884. Epub 2015 Jun 8. J Biol Chem. 2015. PMID: 26055704 Free PMC article.

10

MSH5 is not a genetic predisposing factor for immunoglobulin A deficiency but marks the HLA-DRB1*0102 subgroup carrying susceptibility.

Pozo ND, Medrano LM, Cénit MC, Fernández-Arquero M, Ferreira A, García-Rodríguez MC, de la Concha EG, Urcelay E, Núñez C. Pozo ND, et al. Hum Immunol. 2010 Sep;71(9):861-4. doi: 10.1016/j.humimm.2010.06.007. Epub 2010 Jun 11. Hum Immunol. 2010. PMID: 20542071

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