Rhag-KO 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. Kawano, M, Iwamoto, S, Okuda, H, Hasegawa, N, Kajii, E. . A splicing mutation of the RHAG gene associated with the Rhnull phenotype. In Annals of human genetics, 62, 107-13. doi:. https://pubmed.ncbi.nlm.nih.gov/9759472/

3. Miyazaki, Toru, Isa, Kazumi, Kurita, Ryo, Miyata, Shigeki, Satake, Masahiro. 2023. DSLK and Kg: Antithetical antigens in the RHAG blood group system, and characterization of anti-DSLK antibody. In Vox sanguinis, 118, 392-397. doi:10.1111/vox.13425. https://pubmed.ncbi.nlm.nih.gov/36908196/

4. 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/