Actrt1-KO 基因敲除小鼠

1. Zhang, Qi, Jin, Huijuan, Long, Shunhua, Chen, Suren, Lin, Tingting. . Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human. In Human reproduction (Oxford, England), 39, 880-891. doi:10.1093/humrep/deae031. https://pubmed.ncbi.nlm.nih.gov/38414365/

2. Sha, Yanwei, Liu, Wensheng, Li, Lin, Wang, Yifeng, Wei, Xiaoli. 2021. Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. In Frontiers in cell and developmental biology, 9, 676246. doi:10.3389/fcell.2021.676246. https://pubmed.ncbi.nlm.nih.gov/34422805/

3. Schafer, D A, Schroer, T A. . Actin-related proteins. In Annual review of cell and developmental biology, 15, 341-63. doi:. https://pubmed.ncbi.nlm.nih.gov/10611965/

4. Bal, Elodie, Park, Hyun-Sook, Belaid-Choucair, Zakia, Munnich, Arnold, Smahi, Asma. 2017. Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas. In Nature medicine, 23, 1226-1233. doi:10.1038/nm.4368. https://pubmed.ncbi.nlm.nih.gov/28869610/