1. Geng, Sha, Liu, Song-Bai, He, Wei, Li, Yangxin, Song, Yao-Hua. 2024. Deletion of TECRL promotes skeletal muscle repair by up-regulating EGR2. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2317495121. doi:10.1073/pnas.2317495121. https://pubmed.ncbi.nlm.nih.gov/38753506/
2. Hou, Cuilan, Jiang, Xunwei, Zhang, Han, Xie, Lijian, Xiao, Tingting. 2022. TECRL deficiency results in aberrant mitochondrial function in cardiomyocytes. In Communications biology, 5, 470. doi:10.1038/s42003-022-03414-9. https://pubmed.ncbi.nlm.nih.gov/35577932/
3. Porretta, Alessandra Pia, Le Bloa, Mathieu, Bhuiyan, Zahurul Alam, Extramiana, Fabrice, Pruvot, Etienne. 2025. Arrhythmogenic Potential of Heterozygous TECRL Variants in Type 3 Catecholaminergic Polymorphic Ventricular Tachycardia. In JACC. Clinical electrophysiology, , . doi:10.1016/j.jacep.2024.12.015. https://pubmed.ncbi.nlm.nih.gov/39945714/
4. Webster, Gregory, Aburawi, Elhadi H, Chaix, Marie A, Wilde, Arthur A M, Bhuiyan, Zahurul A. . Life-threatening arrhythmias with autosomal recessive TECRL variants. In Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 23, 781-788. doi:10.1093/europace/euaa376. https://pubmed.ncbi.nlm.nih.gov/33367594/
5. Jones, Douglas, Hartung, Jacob, Lasalle, Elizabeth, Kingsmore, Stephen F, Coufal, Nicole G. 2024. Novel variants in TECRL leading to catecholaminergic polymorphic ventricular tachycardia. In Life science alliance, 7, . doi:10.26508/lsa.202402572. https://pubmed.ncbi.nlm.nih.gov/38777371/
6. Devalla, Harsha D, Gélinas, Roselle, Aburawi, Elhadi H, Bhuiyan, Zahurul A, Passier, Robert. 2016. TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT. In EMBO molecular medicine, 8, 1390-1408. doi:10.15252/emmm.201505719. https://pubmed.ncbi.nlm.nih.gov/27861123/
智鼠故事 
