Omg-KO 基因敲除小鼠

1. Zhao, Peng, Meng, Li, Han, Feiyuan, Liu, Xinxin, Tian, Jinwei. 2024. Use of mendelian randomization to assess the causal associations of circulating plasma proteins with 12-lead ECG parameters. In International immunopharmacology, 143, 113520. doi:10.1016/j.intimp.2024.113520. https://pubmed.ncbi.nlm.nih.gov/39486179/

2. Zheng, Chunfang, Sankoff, David. 2012. Gene order in rosid phylogeny, inferred from pairwise syntenies among extant genomes. In BMC bioinformatics, 13 Suppl 10, S9. doi:10.1186/1471-2105-13-S10-S9. https://pubmed.ncbi.nlm.nih.gov/22759433/

3. Fujii, Tatsuya, Morimoto, Masafumi, Yoshioka, Hiroshi, Wang, Dong, De Vivo, Darryl C. 2010. T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake. In Brain & development, 33, 316-20. doi:10.1016/j.braindev.2010.06.012. https://pubmed.ncbi.nlm.nih.gov/20630673/

4. Heckmann, Jeannine M, Europa, Tarin A, Soni, Aayesha J, Nel, Melissa. 2022. The Epidemiology and Phenotypes of Ocular Manifestations in Childhood and Juvenile Myasthenia Gravis: A Review. In Frontiers in neurology, 13, 834212. doi:10.3389/fneur.2022.834212. https://pubmed.ncbi.nlm.nih.gov/35280301/