PubMed (GeneRIF) for id: 8898

Year	Number of Results
2002	3
2003	3
2005	1
2006	1
2007	2
2008	2
2010	1
2011	2
2013	2
2016	1
2017	2
2019	1
2020	2
2023	1
2024	0

1

An integrative analysis reveals the prognostic value and potential functions of MTMR2 in hepatocellular carcinoma.

Yao Y, Lai J, Yang Y, Wang G, Lv J. Yao Y, et al. Sci Rep. 2023 Oct 31;13(1):18701. doi: 10.1038/s41598-023-46089-w. Sci Rep. 2023. PMID: 37907649 Free PMC article.

2

MTMR2 promotes the progression of NK/T cell lymphoma by targeting JAK1.

Wang J, He AL, Zhang WG, Cao XM, Chen YX, Liu J, Zhao WH, Yang Y, Wang JL, Liu HL, Ma XR. Wang J, et al. Eur Rev Med Pharmacol Sci. 2020 Aug;24(15):8057-8066. doi: 10.26355/eurrev_202008_22489. Eur Rev Med Pharmacol Sci. 2020. PMID: 32767332 Free article.

3

Novel MTMR2 mutation causing severe Charcot-Marie-Tooth type 4B1 disease: a case report.

Halperin D, Sapir A, Wormser O, Drabkin M, Yogev Y, Dolgin V, Flusser H, Birk OS. Halperin D, et al. Neurogenetics. 2020 Oct;21(4):301-304. doi: 10.1007/s10048-020-00617-2. Epub 2020 Jun 3. Neurogenetics. 2020. PMID: 32488727

4

MTMR2 promotes invasion and metastasis of gastric cancer via inactivating IFNγ/STAT1 signaling.

Jiang L, Liu JY, Shi Y, Tang B, He T, Liu JJ, Fan JY, Wu B, Xu XH, Zhao YL, Qian F, Cui YH, Yu PW. Jiang L, et al. J Exp Clin Cancer Res. 2019 May 21;38(1):206. doi: 10.1186/s13046-019-1186-z. J Exp Clin Cancer Res. 2019. PMID: 31113461 Free PMC article.

5

Expression of the neuropathy-associated MTMR2 gene rescues MTM1-associated myopathy.

Raess MA, Cowling BS, Bertazzi DL, Kretz C, Rinaldi B, Xuereb JM, Kessler P, Romero NB, Payrastre B, Friant S, Laporte J. Raess MA, et al. Hum Mol Genet. 2017 Oct 1;26(19):3736-3748. doi: 10.1093/hmg/ddx258. Hum Mol Genet. 2017. PMID: 28934386

6

Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature.

Zambon AA, Natali Sora MG, Cantarella G, Cerri F, Quattrini A, Comi G, Previtali SC, Bolino A. Zambon AA, et al. Neuromuscul Disord. 2017 May;27(5):487-491. doi: 10.1016/j.nmd.2017.01.006. Epub 2017 Jan 16. Neuromuscul Disord. 2017. PMID: 28190646 Free PMC article. Review.

7

SOX10 regulates an alternative promoter at the Charcot-Marie-Tooth disease locus MTMR2.

Fogarty EA, Brewer MH, Rodriguez-Molina JF, Law WD, Ma KH, Steinberg NM, Svaren J, Antonellis A. Fogarty EA, et al. Hum Mol Genet. 2016 Sep 15;25(18):3925-3936. doi: 10.1093/hmg/ddw233. Epub 2016 Jul 27. Hum Mol Genet. 2016. PMID: 27466180 Free PMC article.

8

A novel homozygous mutation in the MTMR2 gene in two siblings with 'hypermyelinating neuropathy'.

Luigetti M, Bolino A, Scarlino S, Sabatelli M. Luigetti M, et al. J Peripher Nerv Syst. 2013 Jun;18(2):192-4. doi: 10.1111/jns5.12019. J Peripher Nerv Syst. 2013. PMID: 23781969 No abstract available.

9

Differential phosphorylation of the phosphoinositide 3-phosphatase MTMR2 regulates its association with early endosomal subtypes.

Franklin NE, Bonham CA, Xhabija B, Vacratsis PO. Franklin NE, et al. J Cell Sci. 2013 Mar 15;126(Pt 6):1333-44. doi: 10.1242/jcs.113928. Epub 2013 Feb 1. J Cell Sci. 2013. PMID: 23378027

10

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.

Nouioua S, Hamadouche T, Funalot B, Bernard R, Bellatache N, Bouderba R, Grid D, Assami S, Benhassine T, Levy N, Vallat JM, Tazir M. Nouioua S, et al. Neuromuscul Disord. 2011 Aug;21(8):543-50. doi: 10.1016/j.nmd.2011.04.013. Epub 2011 Jul 7. Neuromuscul Disord. 2011. PMID: 21741241

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