Xk-flox 基因敲除小鼠

1. Peikert, Kevin, Hermann, Andreas, Danek, Adrian. 2022. XK-Associated McLeod Syndrome: Nonhematological Manifestations and Relation to VPS13A Disease. In Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie, 49, 4-12. doi:10.1159/000521417. https://pubmed.ncbi.nlm.nih.gov/35221863/

2. Di, Lin, Fu, Yusi, Sun, Yue, Huang, Yanyi, Wang, Jianbin. 2020. RNA sequencing by direct tagmentation of RNA/DNA hybrids. In Proceedings of the National Academy of Sciences of the United States of America, 117, 2886-2893. doi:10.1073/pnas.1919800117. https://pubmed.ncbi.nlm.nih.gov/31988135/

3. Chen, Pei-Yun, Lai, Szu-Chia, Yang, Chih-Chao, Lu, Chin-Song, Yeh, Tu-Hsueh. 2014. A novel XK gene mutation in a Taiwanese family with McLeod syndrome. In Journal of the neurological sciences, 340, 221-4. doi:10.1016/j.jns.2014.02.027. https://pubmed.ncbi.nlm.nih.gov/24635891/

4. Kong, Xiangfeng, Zhang, Hainan, Li, Guoling, Zhou, Yingsi, Yang, Hui. 2023. Engineered CRISPR-OsCas12f1 and RhCas12f1 with robust activities and expanded target range for genome editing. In Nature communications, 14, 2046. doi:10.1038/s41467-023-37829-7. https://pubmed.ncbi.nlm.nih.gov/37041195/

5. Ying, Yanling, Yu, Shifang, Zhang, Jingjing, Hong, Xiaozhen, Zhu, Faming. 2023. A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report. In Frontiers in genetics, 14, 1073139. doi:10.3389/fgene.2023.1073139. https://pubmed.ncbi.nlm.nih.gov/36816020/