Fez1-flox 基因敲除小鼠

1. Malikov, Viacheslav, Meade, Nathan, Simons, Lacy M, Hultquist, Judd F, Naghavi, Mojgan H. . FEZ1 phosphorylation regulates HSPA8 localization and interferon-stimulated gene expression. In Cell reports, 38, 110396. doi:10.1016/j.celrep.2022.110396. https://pubmed.ncbi.nlm.nih.gov/35172151/

2. Gunaseelan, Saravanan, Wang, Ziyin, Tong, Venetia Kok Jing, Lim, Kah-Leong, Chua, John Jia En. . Loss of FEZ1, a gene deleted in Jacobsen syndrome, causes locomotion defects and early mortality by impairing motor neuron development. In Human molecular genetics, 30, 5-20. doi:10.1093/hmg/ddaa281. https://pubmed.ncbi.nlm.nih.gov/33395696/

3. Califano, Daniela, Pignata, Sandro, Pisano, Carmela, Fusco, Alfredo, Chiappetta, Gennaro. . FEZ1/LZTS1 protein expression in ovarian cancer. In Journal of cellular physiology, 222, 382-6. doi:10.1002/jcp.21962. https://pubmed.ncbi.nlm.nih.gov/19885841/