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- Factor VIII antigen assay 因子Ⅷ抗原测定
- Factor VIII related antigen assay 因子Ⅷ有关的抗原测定
- Factor VIII antigen 因子Ⅷ抗原
- The endothelial cells are immunoreactive for CD34 and Factor VIII related antigen. 内皮细胞呈CD34+和VIII因子相关抗原+。
- With anti-CDV antigen assay, the ependymal cells with inclusion bodies showed an intensive positive reaction. 部分锥体细胞，神经核细胞和浦氏细胞变性、溶解或胞浆深染，胞核浓缩。
- Hemophilia caused by a congenital deficiency of factor VIII,occurs almost exclusively in men. 由于先天缺乏凝血银子VIII而引起的血友病,通常出现在男性。
- The drug is a recombinant protein, called Factor VIII, which is necessary to help blood clot. 该药是一种重组蛋白质，叫第8因子，能有效地帮助血液凝固。
- 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。
- 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。
- People with hemophilia A, the most common form of the disease, are deficient in Factor VIII and suffer episodes of uncontrolled bleeding. A型血友病是血友病中最常见的类型。 病人第8因子缺失，罹患无法控制的出血。
- Now, the domestic production of blood products, including the coagulation factor VIII, have been strictly dealt with inactivated virus. 现在，国内生产的血液制品，包括第八凝血因子，均经严格病毒灭活处理。
- A unit of factor VIII currently costs more than 1 yuan in China.In case of a hemorrhage, 1,000 units are required to stop a potentially fatal bout of bleeding. 中国目前1单位VIII因子花费超过1元.;对于血友病患者要阻断1次潜在的致命流血需要1000单位
- Plasminogen activator inhibitor antigen assay 纤维蛋白溶酶原激活剂抑制剂抗原测定
- alpha-2 Antiplasmin antigen assay α-2抗纤维蛋白溶酶抗原测定
- Before Baxter's biotech treatment, hemophilia patients relied solely on Factor VIII proteins derived from plasma, and the supply of plasma is dependent on blood donations, which can carry the risk of contamination. 在有贝克斯特生物治剂治疗之前，血友病人完全依赖摄取自血浆的第8因子蛋白质。 不过血浆的供应又必须依赖献血，这会遇到血源污染的危险。
- Antigenicity assay showed the AWTE CTB protein expressed in the transgenic soybean tissue can combine with CTB antibody. 抗原性分析实验结果表明 ,特异表达的融合蛋白可与 CTB和 AWTE抗体结合 ,具有 CTB抗原性。
- Subsequent pathological examination indicated a histiocytic proliferation positive for CD68 and factor VIII, and negative for CD1a and S100, with Touton giant cells characteristic of ECD. 其后的病理检查表现出ECD特征性的组织细胞增生：CD68和VIII因子阳性，CD1a和S100阴性，伴Touton巨细胞。
- Congenital factor VIII deficiency disease 先天性因子Ⅷ缺乏性疾病
- Acquired factor VIII deficiency disease 获得性因子Ⅷ缺乏性疾病
- Less than 1% of normal factor VIII 因子Ⅷ少于正常的1%25
