1.
The Preparation, Identification and Application of Rabbit Polyclonal Antibody Against Human FⅩⅢ A Subunit;
兔抗人凝血因子ⅩⅢ A亚单位多克隆抗体的制备、鉴定及应用研究
2.
coagulation factor deficiency
凝血因子缺乏性疾病
3.
The precursor of any of various blood factors necessary for coagulation.
前凝血剂血液凝结所必须的凝血因子的凝血酶原
4.
A pharmacogenetic effect of factor XIII valine 34 leucine polymorphism on fibrinolytic therapy for acute myocardial infarction
因子ⅩⅢ氨酸34亮氨酸多态性在急性心肌梗死纤维蛋白溶解疗法中的遗传药理学作用
5.
Study of Extraction of Three Porcine Coagulation Factors from the Blood of Pig and Coagulation Factor X Protein Analysis
猪血液中三种凝血因子的提取及凝血因子X的蛋白分析研究
6.
Full Length cDNA Cloning of Human Coagulation Factor C Homology
人凝血因子C同源物基因全长cDNA克隆
7.
von Willebrand factor
Von Willebrand因子[由血管内皮细胞释放到血中，参与凝血]
8.
Correlation of Val34Leu and Pro564Leu Polymorphism in the a Subunit of Coagulation Factor XⅢ with Cerebral Hemorrhage;
凝血因子XⅢA Val34Leu、Pro564Leu基因多态性与脑出血关系研究
9.
Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI.
在典型的血友病中缺乏的是凝血因子VIII;其它的血友病是因缺乏凝血因子IX或XI。
10.
The Correlation Analysis of Venous Thromboembolism and Acute Myocardial Infarction with the Levels and Polymorphisms of Coagulation and Anticoagulation Factors;
凝血及抗凝血因子与静脉血栓栓塞和心肌梗死关系的初步研究
11.
coagulation factor IX
干燥浓缩人血凝固第IX因子
12.
Study on Expression and Purification of Recombinant Human Coagulation Factor Ⅶ in Mammalian Cell Line;
重组人凝血因子Ⅶ的表达与纯化研究
13.
Expression of Human Coagulation Factor IX in Transgenic Tomato;
利用番茄表达人凝血IX因子的研究
14.
Development of human coagulation factor Ⅷ,Ⅸ,Ⅺ in the healthy fetuses
胎儿期凝血因子Ⅷ、Ⅸ、Ⅺ的生成趋势
15.
Preclinical Research of Inherited Anti-coagulation Factor and Acquired Coagulation Factor Deficiency;
遗传性抗凝因子和获得性凝血因子缺陷症的基础研究
16.
Effect of the Blood Plasma Separation Time on Unstable Clotting Factors
血浆分离时间对不稳定凝血因子活性的影响
17.
The Correlation Analysis of Venous Thromboembolism with the Levels and Polymorphisms of Coagulation Factor Ⅷ
凝血因子Ⅷ与静脉血栓栓塞症相关性研究
18.
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
血友病: 一种遗传性出血性疾病,因先天性缺乏某种凝血因子而引起。