1. Donaudy, F, Zheng, L, Ficarella, R, Bartles, J R, Gasparini, P. 2005. Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. In Journal of medical genetics, 43, 157-61. doi:. https://pubmed.ncbi.nlm.nih.gov/15930085/
2. Nicholson, Kathleen R, Cronin, Rachel M, Menon, Aruna R, Tobin, David M, Champion, Patricia A. 2023. The EspN transcription factor is an infection-dependent regulator of the ESX-1 system in M. marinum. In bioRxiv : the preprint server for biology, , . doi:10.1101/2023.02.15.528779. https://pubmed.ncbi.nlm.nih.gov/36824794/
3. Nicholson, Kathleen R, Cronin, Rachel M, Prest, Rebecca J, Tobin, David M, Champion, Patricia A. 2024. The antagonistic transcription factors, EspM and EspN, regulate the ESX-1 secretion system in M. marinum. In mBio, 15, e0335723. doi:10.1128/mbio.03357-23. https://pubmed.ncbi.nlm.nih.gov/38445877/
4. Ahmed, Zubair M, Jaworek, Thomas J, Sarangdhar, Gowri N, Riazuddin, Sheikh, Riazuddin, Saima. 2018. Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment. In Journal of medical genetics, 55, 479-488. doi:10.1136/jmedgenet-2017-105221. https://pubmed.ncbi.nlm.nih.gov/29572253/
5. Liu, Xinhua, Peng, Yonglin, Wang, Ju. . Integrative analysis of DNA methylation and gene expression profiles identified potential breast cancer-specific diagnostic markers. In Bioscience reports, 40, . doi:10.1042/BSR20201053. https://pubmed.ncbi.nlm.nih.gov/32412047/
6. Li, Zhan, Hu, Yuru, Song, Yuan, Li, Tao, Wang, Hui. 2024. Diversity, Distribution and Structural Prediction of the Pathogenic Bacterial Effectors EspN and EspS. In Genes, 15, . doi:10.3390/genes15101250. https://pubmed.ncbi.nlm.nih.gov/39457374/
7. Jackson, Torrance, Thomas, James, Green, Eric D, Noben-Trauth, Konrad. . Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4. In Biochemical and biophysical research communications, 296, 1143-7. doi:. https://pubmed.ncbi.nlm.nih.gov/12207892/
8. Naz, S, Griffith, A J, Riazuddin, S, Wilcox, E R, Friedman, T B. . Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. In Journal of medical genetics, 41, 591-5. doi:. https://pubmed.ncbi.nlm.nih.gov/15286153/
智鼠故事 
