F7-flox 基因敲除小鼠

1. Ouardani, Cherifa, Elmahmoudi, Hejer, ELborgi, Wejden, Meriem, Achour, Gouider, Emna. 2022. Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency. In Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 33, 280-284. doi:10.1097/MBC.0000000000001139. https://pubmed.ncbi.nlm.nih.gov/35802509/

2. Quintavalle, Gabriele, Riccardi, Federica, Rivolta, Gianna Franca, Percesepe, Antonio, Tagliaferri, Annarita. 2017. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study. In Thrombosis and haemostasis, 117, 1455-1464. doi:10.1160/TH17-02-0085. https://pubmed.ncbi.nlm.nih.gov/28447100/

3. Friso, Simonetta, Lotto, Valentina, Choi, Sang-Woon, Bernardi, Francesco, Olivieri, Oliviero. 2012. Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease. In Journal of medical genetics, 49, 192-9. doi:10.1136/jmedgenet-2011-100195. https://pubmed.ncbi.nlm.nih.gov/22315437/