Myl1-flox 基因敲除小鼠

1. Ravenscroft, Gianina, Zaharieva, Irina T, Bortolotti, Carlo A, Laing, Nigel G, Muntoni, Francesco. . Bi-allelic mutations in MYL1 cause a severe congenital myopathy. In Human molecular genetics, 27, 4263-4272. doi:10.1093/hmg/ddy320. https://pubmed.ncbi.nlm.nih.gov/30215711/

2. Lin, Xiang, Wang, Dianpeng, Wen, Li, Hu, Yang, Zhang, Yong. 2015. Intron polymorphism in MYL1 gene is associated with individual cardiac trainability to endurance training in human myocardium. In The Journal of sports medicine and physical fitness, 57, 144-153. doi:10.23736/S0022-4707.16.05780-7. https://pubmed.ncbi.nlm.nih.gov/26473445/

3. Li, Ce, Guan, Rui, Li, Wenming, Wu, Kainan, Lei, Dapeng. 2023. Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC. In BMC cancer, 23, 840. doi:10.1186/s12885-023-11349-5. https://pubmed.ncbi.nlm.nih.gov/37679666/