Association of rs35006907 Polymorphism with Risk of Dilated Cardiomyopathy in Han Chinese Population

1. Deacon DC, Happe CL, Chen C, Tedeschi N, Manso AM, Li T, et al. Combinatorial interactions of genetic variants in human cardiomyopathy. Nat Biomed Eng. 2019;3:147–57. DeaconDC HappeCL ChenC TedeschiN MansoAM LiT Combinatorial interactions of genetic variants in human cardiomyopathy Nat Biomed Eng 2019 3 147 57 Search in Google Scholar

2. Li K, Zhong Y, Peng Y, Zhou B, Wang Y, Li Q, et al. Association Between AXIN1 Gene Polymorphisms and Dilated Cardiomyopathy in a Chinese Han Population. DNA Cell Biol. 2019;38:436–42. LiK ZhongY PengY ZhouB WangY LiQ Association Between AXIN1 Gene Polymorphisms and Dilated Cardiomyopathy in a Chinese Han Population DNA Cell Biol 2019 38 436 42 Search in Google Scholar

3. Shen C, Zhong Y, Huang X, Wang Y, Peng Y, Li K, et al. Associations between TAB2 gene polymorphisms and dilated cardiomyopathy in a Chinese population. Biomark Med. 2020;14:441–50. ShenC ZhongY HuangX WangY PengY LiK Associations between TAB2 gene polymorphisms and dilated cardiomyopathy in a Chinese population Biomark Med 2020 14 441 50 Search in Google Scholar

4. Levitas A, Muhammad E, Zhang Y, Perea Gil I, Serrano R, Diaz N, et al. A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy. PLoS Genet. 2020;16:e1009000. LevitasA MuhammadE ZhangY Perea GilI SerranoR DiazN A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy PLoS Genet 2020 16 e1009000 Search in Google Scholar

5. Jordan E, Peterson L, Ai T, Asatryan B, Bronicki L, Brown E, et al. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation. 2021;144:7–19. JordanE PetersonL AiT AsatryanB BronickiL BrownE Evidence-Based Assessment of Genes in Dilated Cardiomyopathy Circulation 2021 144 7 19 Search in Google Scholar

6. Pirruccello JP, Bick A, Wang M, Chaffin M, Friedman S, Yao J, et al. Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Nat Commun. 2020;11:2254. PirruccelloJP BickA WangM ChaffinM FriedmanS YaoJ Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy Nat Commun 2020 11 2254 Search in Google Scholar

7. Chen FF, Xia YL, Xu CQ, Li SS, Zhao YY, Wang XJ, et al. Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population. Int J Clin Exp Med. 2015;8:1188–96. ChenFF XiaYL XuCQ LiSS ZhaoYY WangXJ Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population Int J Clin Exp Med 2015 8 1188 96 Search in Google Scholar

8. Li C, Wang L, Li Y, Feng Z, Wang Q, Luo W. Common Variants in the ARG1 Gene Contribute to the Risk of Dilated Cardiomyopathy in the Han Chinese Population. Genet Test Mol Biomarkers. 2020;24:584–91. LiC WangL LiY FengZ WangQ LuoW Common Variants in the ARG1 Gene Contribute to the Risk of Dilated Cardiomyopathy in the Han Chinese Population Genet Test Mol Biomarkers 2020 24 584 91 Search in Google Scholar

9. Xie F, Ye L, Ta M, Zhang L, Jiang WG. MTSS1: A multifunctional protein and its role in cancer invasion and metastasis. Front Biosci (Schol Ed). 2011;3:621–31. XieF YeL TaM ZhangL JiangWG MTSS1: A multifunctional protein and its role in cancer invasion and metastasis Front Biosci (Schol Ed) 2011 3 621 31 Search in Google Scholar

10. Du P, Wang S, Tang X, An C, Yang Y, Jiang WG. Reduced Expression of Metastasis Suppressor-1 (MTSS1) Accelerates Progression of Human Bladder Uroepithelium Cell Carcinoma. Anticancer Res. 2017;37:4499–505. DuP WangS TangX AnC YangY JiangWG Reduced Expression of Metastasis Suppressor-1 (MTSS1) Accelerates Progression of Human Bladder Uroepithelium Cell Carcinoma Anticancer Res 2017 37 4499 505 Search in Google Scholar

11. Grandits AM, Nguyen CH, Schlerka A, Hackl H, Sill H, Etzler J, et al. Downregulation of MTSS1 in acute myeloid leukemia is associated with a poor prognosis, chemotherapy resistance, and disease aggressiveness. Leukemia. 2021;35:2827–39. GranditsAM NguyenCH SchlerkaA HacklH SillH EtzlerJ Downregulation of MTSS1 in acute myeloid leukemia is associated with a poor prognosis, chemotherapy resistance, and disease aggressiveness Leukemia 2021 35 2827 39 Search in Google Scholar

12. Li T, Zuo X, Meng X. Circ_002059 suppresses cell proliferation and migration of gastric cancer via miR-182/MTSS1 axis. Acta Biochim Biophys Sin (Shanghai). 2021;53:454–62. LiT ZuoX MengX Circ_002059 suppresses cell proliferation and migration of gastric cancer via miR-182/MTSS1 axis Acta Biochim Biophys Sin (Shanghai) 2021 53 454 62 Search in Google Scholar

13. Chen L, Chen Q, Wu Y, Zhu M, Hu J, Zhuang Z. MTSS1 inhibits colorectal cancer metastasis by regulating the CXCR4/CXCL12 signaling axis. Int J Mol Med 2021. ChenL ChenQ WuY ZhuM HuJ ZhuangZ MTSS1 inhibits colorectal cancer metastasis by regulating the CXCR4/CXCL12 signaling axis Int J Mol Med 2021 Search in Google Scholar

14. Zhang L, Wang X, Liu X, Lv M, Shen E, Zhu G, Sun Z. miR-28-5p targets MTSS1 to regulate cell proliferation and apoptosis in esophageal cancer. Acta Biochim Biophys Sin (Shanghai). 2020;52:842–52. ZhangL WangX LiuX LvM ShenE ZhuG SunZ miR-28-5p targets MTSS1 to regulate cell proliferation and apoptosis in esophageal cancer Acta Biochim Biophys Sin (Shanghai) 2020 52 842 52 Search in Google Scholar

15. Mattila PK, Salminen M, Yamashiro T, Lappalainen P. Mouse MIM, a tissue-specific regulator of cytoskeletal dynamics, interacts with ATP-actin monomers through its C-terminal WH2 domain. J Biol Chem. 2003;278:8452–9. MattilaPK SalminenM YamashiroT LappalainenP Mouse MIM, a tissue-specific regulator of cytoskeletal dynamics, interacts with ATP-actin monomers through its C-terminal WH2 domain J Biol Chem 2003 278 8452 9 Search in Google Scholar

16. Aung N, Vargas JD, Yang C, Cabrera CP, Warren HR, Fung K, et al. Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development. Circulation. 2019;140:1318–30. AungN VargasJD YangC CabreraCP WarrenHR FungK Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development Circulation 2019 140 1318 30 Search in Google Scholar

17. Andersson C, Lin H, Liu C, Levy D, Mitchell GF, Larson MG, Vasan RS. Integrated Multiomics Approach to Identify Genetic Underpinnings of Heart Failure and Its Echocardiographic Precursors: Framingham Heart Study. Circ Genom Precis Med. 2019;12:e002489. AnderssonC LinH LiuC LevyD MitchellGF LarsonMG VasanRS Integrated Multiomics Approach to Identify Genetic Underpinnings of Heart Failure and Its Echocardiographic Precursors: Framingham Heart Study Circ Genom Precis Med 2019 12 e002489 Search in Google Scholar

18. Morley MP, Wang X, Hu R, Brandimarto J, Tucker NR, Felix JF, et al. Cardioprotective Effects of MTSS1 Enhancer Variants. Circulation. 2019;139:2073–6. MorleyMP WangX HuR BrandimartoJ TuckerNR FelixJF Cardioprotective Effects of MTSS1 Enhancer Variants Circulation 2019 139 2073 6 Search in Google Scholar

19. Kaski JP, Elliott P. The classification concept of the ESC Working Group on myocardial and pericardial diseases for dilated cardiomyopathy. Herz. 2007;32:446–51. KaskiJP ElliottP The classification concept of the ESC Working Group on myocardial and pericardial diseases for dilated cardiomyopathy Herz 2007 32 446 51 Search in Google Scholar

20. Hu D, Huang J, Hu S, Zhang Y, Li S, Sun Y, et al. A common variant of RIP3 promoter region is associated with poor prognosis in heart failure patients by influencing SOX17 binding. J Cell Mol Med. 2019;23:5317–28. HuD HuangJ HuS ZhangY LiS SunY A common variant of RIP3 promoter region is associated with poor prognosis in heart failure patients by influencing SOX17 binding J Cell Mol Med 2019 23 5317 28 Search in Google Scholar

21. Giri P, Mukhopadhyay A, Gupta M, Mohapatra B. Dilated cardiomyopathy: A new insight into the rare but common cause of heart failure. Heart Fail Rev. 2022;27:431–54. GiriP MukhopadhyayA GuptaM MohapatraB Dilated cardiomyopathy: A new insight into the rare but common cause of heart failure Heart Fail Rev 2022 27 431 54 Search in Google Scholar

22. Lin J, Liu J, Wang Y, Zhu J, Zhou K, Smith N, Zhan X. Differential regulation of cortactin and N-WASP-mediated actin polymerization by missing in metastasis (MIM) protein. Oncogene. 2005;24:2059–66. LinJ LiuJ WangY ZhuJ ZhouK SmithN ZhanX Differential regulation of cortactin and N-WASP-mediated actin polymerization by missing in metastasis (MIM) protein Oncogene 2005 24 2059 66 Search in Google Scholar

23. Wild PS, Felix JF, Schillert A, Teumer A, Chen M-H, Leening MJG, et al. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J Clin Invest. 2017;127:1798–812. WildPS FelixJF SchillertA TeumerA ChenM-H LeeningMJG Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function J Clin Invest 2017 127 1798 812 Search in Google Scholar

24. Chang AN, Potter JD. Sarcomeric protein mutations in dilated cardiomyopathy. Heart Fail Rev. 2005;10:225–35. ChangAN PotterJD Sarcomeric protein mutations in dilated cardiomyopathy Heart Fail Rev 2005 10 225 35 Search in Google Scholar