Lmbrd2-flox 基因敲除小鼠

1. Malhotra, Alka, Ziegler, Alban, Shu, Li, Mao, Xiao, Bonneau, Dominique. 2020. De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features. In Journal of medical genetics, 58, 712-716. doi:10.1136/jmedgenet-2020-107137. https://pubmed.ncbi.nlm.nih.gov/32820033/

2. Babii, Anna V, Arkhipova, Anna L, Kovalchuk, Svetlana N. 2022. Identification of novel integration sites for bovine leukemia virus proviral DNA in cancer driver genes in cattle with persistent lymphocytosis. In Virus research, 317, 198813. doi:10.1016/j.virusres.2022.198813. https://pubmed.ncbi.nlm.nih.gov/35584733/

3. Cheng, Qi, Chen, Mo, Chen, Xin, Wu, Huaxiang, Du, Yan. 2021. Novel Long Non-coding RNA Expression Profile of Peripheral Blood Mononuclear Cells Reveals Potential Biomarkers and Regulatory Mechanisms in Systemic Lupus Erythematosus. In Frontiers in cell and developmental biology, 9, 639321. doi:10.3389/fcell.2021.639321. https://pubmed.ncbi.nlm.nih.gov/34150746/