1. Liang, Guozheng, Wang, ShengPeng, Shao, Jingchen, Wang, Lei, Offermanns, Stefan. 2022. Tenascin-X Mediates Flow-Induced Suppression of EndMT and Atherosclerosis. In Circulation research, 130, 1647-1659. doi:10.1161/CIRCRESAHA.121.320694. https://pubmed.ncbi.nlm.nih.gov/35443807/
2. Kaufman, Carolyn S, Butler, Merlin G. . Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome. In World journal of medical genetics, 6, 17-21. doi:10.5496/wjmg.v6.i2.17. https://pubmed.ncbi.nlm.nih.gov/28344932/
3. Shi, Xiao, Sun, Yaoting, Shen, Cenkai, Ji, Qinghai, Wei, Wenjun. 2022. Integrated proteogenomic characterization of medullary thyroid carcinoma. In Cell discovery, 8, 120. doi:10.1038/s41421-022-00479-y. https://pubmed.ncbi.nlm.nih.gov/36344509/
4. Gao, Yinjie, Lu, Lin, Yu, Bingqing, Nie, Min, Wu, Xueyan. . The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. In The Journal of clinical endocrinology and metabolism, 105, . doi:10.1210/clinem/dgaa199. https://pubmed.ncbi.nlm.nih.gov/32291442/
5. Lee, Hsien-Hsiung. 2004. Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module. In Molecular genetics and metabolism, 84, 4-8. doi:. https://pubmed.ncbi.nlm.nih.gov/15639189/