Rhag-flox 基因敲除小鼠

1. Tian, Li, Song, Ning, Yao, Zhi-Qiang, Huang, Mei, Hou, Li. 2011. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene. In Transfusion, 51, 2686-9. doi:10.1111/j.1537-2995.2011.03218.x. https://pubmed.ncbi.nlm.nih.gov/21682734/

2. Mu, S, Cui, Y, Wang, W, Zhu, O, Zhu, D. 2018. A RHAG point mutation selectively disrupts Rh antigen expression. In Transfusion medicine (Oxford, England), 29, 121-127. doi:10.1111/tme.12519. https://pubmed.ncbi.nlm.nih.gov/29508504/

3. Wen, Jizhi, Verhagen, Onno J H M, Jia, Shuangshuang, Ji, Yanli, van der Schoot, C Ellen. 2018. A variant RhAG protein encoded by the RHAG*572A allele causes serological weak D expression while maintaining normal RhCE phenotypes. In Transfusion, 59, 405-411. doi:10.1111/trf.14969. https://pubmed.ncbi.nlm.nih.gov/30284303/

4. Goossens, Dominique, da Silva, Nelly, Metral, Sylvain, Mouro-Chanteloup, Isabelle, Cartron, Jean-Pierre. 2013. Mice expressing RHAG and RHD human blood group genes. In PloS one, 8, e80460. doi:10.1371/journal.pone.0080460. https://pubmed.ncbi.nlm.nih.gov/24260394/