Ccin-flox 基因敲除小鼠

1. Fan, Yong, Huang, Chenhui, Chen, Juan, Kuang, Yanping, Lei, Ming. 2022. Mutations in CCIN cause teratozoospermia and male infertility. In Science bulletin, 67, 2112-2123. doi:10.1016/j.scib.2022.09.026. https://pubmed.ncbi.nlm.nih.gov/36546111/

2. He, Jiaxin, Liu, Qiang, Wang, Weili, Tu, Chaofeng, Tan, Yue-Qiu. 2023. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. In Clinical genetics, 103, 495-497. doi:10.1111/cge.14281. https://pubmed.ncbi.nlm.nih.gov/36527329/

3. Arora, Manvi, Mehta, Poonam, Sethi, Shruti, Samara, Mary, Singh, Rajender. 2024. Genetic etiological spectrum of sperm morphological abnormalities. In Journal of assisted reproduction and genetics, 41, 2877-2929. doi:10.1007/s10815-024-03274-8. https://pubmed.ncbi.nlm.nih.gov/39417902/

4. Hodžić, Alenka, Maver, Aleš, Zorn, Branko, Kunej, Tanja, Peterlin, Borut. 2023. Transcriptomic signatures for human male infertility. In Frontiers in molecular biosciences, 10, 1226829. doi:10.3389/fmolb.2023.1226829. https://pubmed.ncbi.nlm.nih.gov/37670815/

5. Greither, Thomas, Dejung, Mario, Behre, Hermann M, Butter, Falk, Herlyn, Holger. 2023. The human sperm proteome-Toward a panel for male fertility testing. In Andrology, 11, 1418-1436. doi:10.1111/andr.13431. https://pubmed.ncbi.nlm.nih.gov/36896575/