Fbn2-KO 基因敲除小鼠

1. Chen, Jing, Xiang, Qinqin, Xiao, Xiao, Yang, Mei, Liu, Shanling. 2022. Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family. In BMC medical genomics, 15, 154. doi:10.1186/s12920-022-01296-8. https://pubmed.ncbi.nlm.nih.gov/35804365/

2. Du, Qiu, Zhang, Dingding, Zhuang, Yue, Wen, Taishen, Jia, Haiping. 2021. The Molecular Genetics of Marfan Syndrome. In International journal of medical sciences, 18, 2752-2766. doi:10.7150/ijms.60685. https://pubmed.ncbi.nlm.nih.gov/34220303/

3. Khoury, L El, Posthumus, M, Collins, M, Cook, J, Raleigh, S M. 2014. ELN and FBN2 gene variants as risk factors for two sports-related musculoskeletal injuries. In International journal of sports medicine, 36, 333-7. doi:10.1055/s-0034-1390492. https://pubmed.ncbi.nlm.nih.gov/25429546/

4. Zhang, Cuiping, Qiao, Fengchang, Cheng, Qing, Hu, Ping, Xu, Zhengfeng. 2023. A Novel Splice Site Mutation in the FBN2 Gene in a Chinese Family with Congenital Contractural Arachnodactyly. In Biochemical genetics, 62, 2495-2503. doi:10.1007/s10528-023-10550-2. https://pubmed.ncbi.nlm.nih.gov/37962692/

5. Lu, Zechao, Lu, Zeguang, Lai, Yongchang, He, Zhaohui, Tang, Fucai. 2023. A comprehensive analysis of FBN2 in bladder cancer: A risk factor and the tumour microenvironment influencer. In IET systems biology, 17, 162-173. doi:10.1049/syb2.12067. https://pubmed.ncbi.nlm.nih.gov/37337404/