Col18a1-KO 基因敲除小鼠

1. Suri, Fatemeh, Yazdani, Shahin, Chapi, Marjan, Turk, Casey, Elahi, Elahe. . COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. In Human molecular genetics, 27, 3772-3786. doi:10.1093/hmg/ddy256. https://pubmed.ncbi.nlm.nih.gov/30007336/

2. Jiang, Zixuan, Sun, Wenmin, Zhang, Qingjiong, Wang, Panfeng. 2023. Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1. In Stem cell research, 70, 103131. doi:10.1016/j.scr.2023.103131. https://pubmed.ncbi.nlm.nih.gov/37269665/

3. Irene Díez García-Prieto, I, Lopez-Martín, Sara, Albert, Jacobo, Izzi, Valerio, Fernández-Jaén, Alberto. 2022. Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings. In Neurocase, 28, 11-18. doi:10.1080/13554794.2021.1928228. https://pubmed.ncbi.nlm.nih.gov/35253627/

4. Lourenço, Gustavo J, Cardoso-Filho, Cassio, Gonçales, Neiva S L, Gurgel, Maria S C, Lima, Carmen S P. 2006. A high risk of occurrence of sporadic breast cancer in individuals with the 104NN polymorphism of the COL18A1 gene. In Breast cancer research and treatment, 100, 335-8. doi:. https://pubmed.ncbi.nlm.nih.gov/16807676/