Davies N, Austen D E, Wilde M D, Darlington G J, Brownlee G G
Chemical Pathology Unit, Sir William Dunn School of Pathology, University of Oxford.
Br J Haematol. 1997 Dec;99(3):578-9. doi: 10.1046/j.1365-2141.1997.4603263.x.
Previous studies have indicated that C/EBP alpha is involved in the regulation of factor IX and mutations of a C/EBP recognition element in the factor IX promoter result in haemophilia B. We now report that mice homozygous for the deletion of the c/ebp alpha gene are significantly deficient in factor IX transcription.
先前的研究表明,C/EBPα参与因子IX的调控,且因子IX启动子中C/EBP识别元件的突变会导致B型血友病。我们现在报告,c/ebpα基因缺失的纯合小鼠在因子IX转录方面存在显著缺陷。