PubMed (GeneRIF) for id: 7169

Year	Number of Results
2004	1
2007	4
2008	3
2009	4
2010	4
2012	8
2013	9
2014	4
2015	4
2016	6
2017	1
2018	4
2019	3
2020	3
2021	1
2023	1
2024	1

1

Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia.

Wallgren-Pettersson C, Jokela M, Lehtokari VL, Tyynismaa H, Sainio MT, Ylikallio E, Tynninen O, Pelin K, Auranen M. Wallgren-Pettersson C, et al. Neuromuscul Disord. 2024 Feb;35:29-32. doi: 10.1016/j.nmd.2023.12.006. Epub 2023 Dec 15. Neuromuscul Disord. 2024. PMID: 38219297 Free article.

2

Mutations Q93H and E97K in TPM2 Disrupt Ca-Dependent Regulation of Actin Filaments.

Śliwinska M, Robaszkiewicz K, Wasąg P, Moraczewska J. Śliwinska M, et al. Int J Mol Sci. 2021 Apr 14;22(8):4036. doi: 10.3390/ijms22084036. Int J Mol Sci. 2021. PMID: 33919826 Free PMC article.

3

Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln¹⁴⁷Pro Tropomyosin.

Karpicheva OE, Simonyan AO, Rysev NA, Redwood CS, Borovikov YS. Karpicheva OE, et al. Int J Mol Sci. 2020 Oct 14;21(20):7590. doi: 10.3390/ijms21207590. Int J Mol Sci. 2020. PMID: 33066566 Free PMC article.

4

[Expression of tropomyosin 2 in aortic dissection tissue].

Zhong XX, Wei X, Jiang DS, Zhu XH, Liu LG. Zhong XX, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2020 Sep 24;48(9):777-781. doi: 10.3760/cma.j.cn112148-20200707-00540. Zhonghua Xin Xue Guan Bing Za Zhi. 2020. PMID: 32957762 Chinese.

5

A recurrent pathogenic variant in TPM2 reveals further phenotypic and genetic heterogeneity in multiple pterygium syndrome-related disorders.

Vogt J, Al-Saedi A, Willis T, Male A, McKie A, Kiely N, Maher ER. Vogt J, et al. Clin Genet. 2020 Jun;97(6):908-914. doi: 10.1111/cge.13728. Epub 2020 Mar 4. Clin Genet. 2020. PMID: 32092148

6

TPM2 as a potential predictive biomarker for atherosclerosis.

Meng LB, Shan MJ, Qiu Y, Qi R, Yu ZM, Guo P, Di CY, Gong T. Meng LB, et al. Aging (Albany NY). 2019 Sep 5;11(17):6960-6982. doi: 10.18632/aging.102231. Epub 2019 Sep 5. Aging (Albany NY). 2019. PMID: 31487691 Free PMC article.

7

Structural and functional properties of αβ-heterodimers of tropomyosin with myopathic mutations Q147P and K49del in the β-chain.

Matyushenko AM, Shchepkin DV, Susorov DS, Nefedova VV, Kopylova GV, Berg VY, Kleymenov SY, Levitsky DI. Matyushenko AM, et al. Biochem Biophys Res Commun. 2019 Jan 15;508(3):934-939. doi: 10.1016/j.bbrc.2018.12.019. Epub 2018 Dec 10. Biochem Biophys Res Commun. 2019. PMID: 30545627

8

Tropomyosin Tpm 2.1 loss induces glioblastoma spreading in soft brain-like environments.

Mitchell CB, Black B, Sun F, Chrzanowski W, Cooper-White J, Maisonneuve B, Stringer B, Day B, Biro M, O'Neill GM. Mitchell CB, et al. J Neurooncol. 2019 Jan;141(2):303-313. doi: 10.1007/s11060-018-03049-z. Epub 2018 Dec 9. J Neurooncol. 2019. PMID: 30535593

9

Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families.

Li S, You Y, Gao J, Mao B, Cao Y, Zhao X, Zhang X. Li S, et al. BMC Med Genet. 2018 Oct 3;19(1):179. doi: 10.1186/s12881-018-0692-8. BMC Med Genet. 2018. PMID: 30285720 Free PMC article.

10

Hypoxia-Induced TPM2 Methylation is Associated with Chemoresistance and Poor Prognosis in Breast Cancer.

Zhang J, Zhang J, Xu S, Zhang X, Wang P, Wu H, Xia B, Zhang G, Lei B, Wan L, Zhang D, Pang D. Zhang J, et al. Cell Physiol Biochem. 2018;45(2):692-705. doi: 10.1159/000487162. Epub 2018 Jan 31. Cell Physiol Biochem. 2018. PMID: 29414807 Free article.

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