Actl9-KO 基因敲除小鼠

1. Sinaei, Roya, Eslami, Maryam, Dadfar, Mohammadreza, Saberi, Alihossein. . Identification of a new mutation in the ACTL9 gene in men with unexplained infertility. In Molecular genetics & genomic medicine, 12, e2448. doi:10.1002/mgg3.2448. https://pubmed.ncbi.nlm.nih.gov/38769899/

2. 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/

3. Cardona Barberán, Arantxa, Reddy Guggilla, Ramesh, Colenbier, Cora, Vanden Meerschaut, Frauke, Heindryckx, Björn. 2024. High rate of detected variants in male PLCZ1 and ACTL7A genes causing failed fertilization after ICSI. In Human reproduction open, 2024, hoae057. doi:10.1093/hropen/hoae057. https://pubmed.ncbi.nlm.nih.gov/39411542/