1. Gu, Xue, Yuan, Fang-Fen, Huang, Xin, Lin, Jun, Wu, Jing. 2017. Association of PIK3CG gene polymorphisms with attention-deficit/hyperactivity disorder: A case-control study. In Progress in neuro-psychopharmacology & biological psychiatry, 81, 169-177. doi:10.1016/j.pnpbp.2017.10.020. https://pubmed.ncbi.nlm.nih.gov/29097255/
2. Hu, Dong, Xiao, Lei, Li, Shiyang. . A common variant in PIK3CG gene associated with the prognosis of heart failure. In Journal of cellular and molecular medicine, 28, e70069. doi:10.1111/jcmm.70069. https://pubmed.ncbi.nlm.nih.gov/39245801/
3. Kaneda, Megan M, Messer, Karen S, Ralainirina, Natacha, Cohen, Ezra E W, Varner, Judith A. 2016. PI3Kγ is a molecular switch that controls immune suppression. In Nature, 539, 437-442. doi:10.1038/nature19834. https://pubmed.ncbi.nlm.nih.gov/27642729/
4. Kelly, Lois M, Rutter, Justine C, Lin, Kevin H, Wood, Kris C, Puissant, Alexandre. 2024. Targeting a lineage-specific PI3Kɣ-Akt signaling module in acute myeloid leukemia using a heterobifunctional degrader molecule. In Nature cancer, 5, 1082-1101. doi:10.1038/s43018-024-00782-5. https://pubmed.ncbi.nlm.nih.gov/38816660/
5. Serajee, F J, Nabi, R, Zhong, H, Mahbubul Huq, A H M. . Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism. In Journal of medical genetics, 40, e119. doi:. https://pubmed.ncbi.nlm.nih.gov/14627686/
6. Ramirez, Neftali J, Posadas-Cantera, Sara, Caballero-Oteyza, Andrés, Camacho-Ordonez, Nadezhda, Grimbacher, Bodo. 2021. There is no gene for CVID - novel monogenetic causes for primary antibody deficiency. In Current opinion in immunology, 72, 176-185. doi:10.1016/j.coi.2021.05.010. https://pubmed.ncbi.nlm.nih.gov/34153571/
智鼠故事 
