Nyx-KO 基因敲除小鼠

1. Zeitz, Christina, Scherthan, Harry, Freier, Susanne, Schweiger, Susann, Berger, Wolfgang. . NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. In Investigative ophthalmology & visual science, 44, 4184-91. doi:. https://pubmed.ncbi.nlm.nih.gov/14507859/

2. Ivanova, Marianna E, Zolnikova, Inna V, Gorgisheli, Ketevan V, Ghosh, Preetam, Barh, Debmalya. 2019. Novel frameshift mutation in NYX gene in a Russian family with complete congenital stationary night blindness. In Ophthalmic genetics, 40, 558-563. doi:10.1080/13816810.2019.1698617. https://pubmed.ncbi.nlm.nih.gov/31826698/

3. Zhou, Lin, Li, Tuo, Song, Xiusheng, Li, Hongyan, Dan, Handong. 2015. NYX mutations in four families with high myopia with or without CSNB1. In Molecular vision, 21, 213-23. doi:. https://pubmed.ncbi.nlm.nih.gov/25802485/

4. Zhang, Qingjiong, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Hejtmancik, J Fielding. 2007. Mutations in NYX of individuals with high myopia, but without night blindness. In Molecular vision, 13, 330-6. doi:. https://pubmed.ncbi.nlm.nih.gov/17392683/