1. Yu, Rong, Wang, Kai, Luo, Wugen, Jiang, Hongqun. 2022. Knockdown and mutation of Pou4f3 gene mutation promotes pyroptosis of cochleae in cisplatin-induced deafness mice by NLRP3/caspase-3/GSDME pathway. In Toxicology, 482, 153368. doi:10.1016/j.tox.2022.153368. https://pubmed.ncbi.nlm.nih.gov/36341876/
2. Xu, Feilong, Yan, Wenya, Cheng, Yanjie. 2019. Pou4f3 gene mutation promotes autophagy and apoptosis of cochlear hair cells in cisplatin-induced deafness mice. In Archives of biochemistry and biophysics, 680, 108224. doi:10.1016/j.abb.2019.108224. https://pubmed.ncbi.nlm.nih.gov/31830441/
3. Aldè, Mirko, Cantarella, Giovanna, Zanetti, Diego, Simon, Francois, Maniaci, Antonino. 2023. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review. In Biomedicines, 11, . doi:10.3390/biomedicines11061616. https://pubmed.ncbi.nlm.nih.gov/37371710/
4. Sharma, Nikhil, Flaherty, Kali, Lezgiyeva, Karina, Klein, Allon M, Ginty, David D. 2020. The emergence of transcriptional identity in somatosensory neurons. In Nature, 577, 392-398. doi:10.1038/s41586-019-1900-1. https://pubmed.ncbi.nlm.nih.gov/31915380/
5. Zhang, Liyan, Chen, Xin, Wang, Xinlin, Chai, Renjie, Qi, Jieyu. 2024. AAV-mediated Gene Cocktails Enhance Supporting Cell Reprogramming and Hair Cell Regeneration. In Advanced science (Weinheim, Baden-Wurttemberg, Germany), 11, e2304551. doi:10.1002/advs.202304551. https://pubmed.ncbi.nlm.nih.gov/38810137/
6. Hertzano, Ronna, Montcouquiol, Mireille, Rashi-Elkeles, Sharon, Kelley, Matthew W, Avraham, Karen B. 2004. Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene. In Human molecular genetics, 13, 2143-53. doi:. https://pubmed.ncbi.nlm.nih.gov/15254021/
7. Masuda, M, Dulon, D, Pak, K, Erkman, L, Ryan, A F. 2011. Regulation of POU4F3 gene expression in hair cells by 5' DNA in mice. In Neuroscience, 197, 48-64. doi:10.1016/j.neuroscience.2011.09.033. https://pubmed.ncbi.nlm.nih.gov/21958861/
8. Bai, Xiaohui, Zhang, Fengguo, Xiao, Yun, Wang, Haibo, Xu, Lei. 2020. Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families. In Journal of cellular and molecular medicine, 24, 6978-6987. doi:10.1111/jcmm.15359. https://pubmed.ncbi.nlm.nih.gov/32390314/