Nyx-flox 基因敲除小鼠

1. Dai, Shuzhen, Ying, Ming, Wang, Kai, Hao, Peng, Li, Ningdong. 2015. Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness. In Scientific reports, 5, 12679. doi:10.1038/srep12679. https://pubmed.ncbi.nlm.nih.gov/26234941/

2. Pesch, Katrin, Zeitz, Christina, Fries, Julia E, Berger, Wolfgang, Wissinger, Bernd. . Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina. In Investigative ophthalmology & visual science, 44, 2260-6. doi:. https://pubmed.ncbi.nlm.nih.gov/12714669/

3. 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/