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2. Zhou, Yuan, Bian, Shuhui, Zhou, Xin, Fu, Wei, Tang, Fuchou. 2020. Single-Cell Multiomics Sequencing Reveals Prevalent Genomic Alterations in Tumor Stromal Cells of Human Colorectal Cancer. In Cancer cell, 38, 818-828.e5. doi:10.1016/j.ccell.2020.09.015. https://pubmed.ncbi.nlm.nih.gov/33096021/
3. Megarbane, Andre, Bizzari, Sami, Deepthi, Asha, Delague, Valérie, Urtizberea, J Andoni. . A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort. In Journal of neuromuscular diseases, 9, 193-210. doi:10.3233/JND-210652. https://pubmed.ncbi.nlm.nih.gov/34602496/
4. Mroczek, Magdalena, Kabzińska, Dagmara, Chrzanowska, Krystyna H, Pronicki, Maciej, Kochański, Andrzej. 2016. A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features. In Journal of applied genetics, 58, 199-203. doi:10.1007/s13353-016-0368-z. https://pubmed.ncbi.nlm.nih.gov/27726070/
5. Hsu, Wei L, Ma, Yun L, Liu, Yen C, Lee, Eminy H Y. 2017. Smad4 SUMOylation is essential for memory formation through upregulation of the skeletal myopathy gene TPM2. In BMC biology, 15, 112. doi:10.1186/s12915-017-0452-9. https://pubmed.ncbi.nlm.nih.gov/29183317/
6. Zhou, Xingchen, Li, Zhishuang, Chen, Huan, Zhou, Chengjun, Li, Hui. 2024. Relevance Analysis of TPM2 and Clinicopathological Characteristics in Breast Cancer. In International journal of general medicine, 17, 59-74. doi:10.2147/IJGM.S442004. https://pubmed.ncbi.nlm.nih.gov/38221941/
7. Mokbel, Nancy, Ilkovski, Biljana, Kreissl, Michaela, North, Kathryn N, Clarke, Nigel F. 2013. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. In Brain : a journal of neurology, 136, 494-507. doi:10.1093/brain/aws348. https://pubmed.ncbi.nlm.nih.gov/23378224/