• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Infusion of human and canine factor VIII in dogs with von Willebrand's disease: studies of the von Willebrand and factor VIII synthesis stimulating factors.

作者信息

Bouma B N, Dodds W J, van Mourik J A, Sixma J J, Webster W P

出版信息

Scand J Haematol. 1976 Oct;17(4):263-75. doi: 10.1111/j.1600-0609.1976.tb01184.x.

DOI:10.1111/j.1600-0609.1976.tb01184.x
PMID:825957
Abstract

Dogs with von Willebrand's disease (VWD) were infused with a highly purified human and canine factor VIII preparation. Control infusions were performed using isotonic saline solution. Following all of the concentrate infusions, the bleeding times were shortened to within the normal range for up to 4 h. Factor VIII activity rose immediately after infusion, rapidly returned to preinfusion levels, and then increased again at 18 h. The levels of factor VIII-related antigen (F VIII-RA) as measured with anticanine factor VIII also increased after infusion and then gradually declined. There was no further increase in F VIII-RA at 18 h, when the factor VIII activity showed the secondary increase characteristic of VWD. With antihuman factor VIII, two identifiable antigens were present in the plasma of the dogs given human factor VIII. The reduced platelet retention of these animals was not significantly altered following infusion, whereas ristocetin-induced platelet aggregation was corrected in one of the dogs given human factor VIII. These studies indicate that factor VIII procoagulalant and von Willebrand factor activities reside on a single molecule or form part of a molecular complex. In addition, the factor VIII preparations appeared to contain the factor VIII synthesis-stimulating factor and/or a precursor of factor VIII procoagulant activity.

摘要

相似文献

1
Infusion of human and canine factor VIII in dogs with von Willebrand's disease: studies of the von Willebrand and factor VIII synthesis stimulating factors.
Scand J Haematol. 1976 Oct;17(4):263-75. doi: 10.1111/j.1600-0609.1976.tb01184.x.
2
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.
3
Factor VIII/von Willebrand factor binding to von Willebrand's disease platelets.因子VIII/血管性血友病因子与血管性血友病血小板的结合。
Blood. 1982 Aug;60(2):328-32.
4
Dissociation between factor VIII (activity and antigen) and ristocetin-induced platelet aggregation in von Willebrand's disease.血管性血友病中因子VIII(活性与抗原)及瑞斯托霉素诱导的血小板聚集之间的解离
Acta Haematol. 1975;53(1):44-8. doi: 10.1159/000208154.
5
Factor VIII (Willebrand) antigen and ristocetin-Willebrand factor in pigs with von Willebrand's disease.患血管性血友病猪的凝血因子VIII(血管性血友病因子)抗原及瑞斯托霉素-血管性血友病因子
Thromb Res. 1976 Mar;8(3):319-27. doi: 10.1016/0049-3848(76)90025-6.
6
Diagnosis of von Willebrand's disease. A comparative study of diagnostic tests on nine families with von Willebrand's disease and its differential diagnosis from hemophilia and thrombocytopathy.血管性血友病的诊断。对九个血管性血友病家族的诊断试验及其与血友病和血小板病的鉴别诊断的比较研究。
Am J Med. 1976 Mar;60(3):344-56. doi: 10.1016/0002-9343(76)90750-6.
7
Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's disease.正常因子VIII/血管性血友病因子蛋白的电泳异质性,以及血管性血友病患者的异常电泳迁移率。
J Lab Clin Med. 1976 Feb;87(2):185-94.
8
Ristocetin in the diagnosis of von willebrand's disease: a comparison of rate and percent of aggregation with levels of the plasma factor(s) necessary for ristocetin aggregation.瑞斯托霉素在血管性血友病诊断中的应用:瑞斯托霉素诱导聚集率和聚集百分比与瑞斯托霉素诱导聚集所需血浆因子水平的比较。
Thromb Diath Haemorrh. 1975 Nov 15;34(2):465-74.
9
The effects of epinephrine infusion in patients with von Willebrand's disease.肾上腺素输注对血管性血友病患者的影响。
J Clin Invest. 1976 Jun;57(6):1618-25. doi: 10.1172/JCI108432.
10
An atypical von Willebrand's disease with hyperreactivity of platelet aggregation.一种伴有血小板聚集反应性增强的非典型血管性血友病。
Acta Haematol. 1984;71(3):158-64. doi: 10.1159/000206579.

引用本文的文献

1
One Health: Animal Models of Heritable Human Bleeding Diseases.同一健康:遗传性人类出血性疾病的动物模型
Animals (Basel). 2022 Dec 26;13(1):87. doi: 10.3390/ani13010087.
2
Survival of 125iodine-labeled Factor VIII in normals and patients with classic hemophilia. Observations on the heterogeneity of human Factor VIII.125碘标记的凝血因子VIII在正常人和典型血友病患者体内的存活情况。关于人凝血因子VIII异质性的观察。
J Clin Invest. 1978 Aug;62(2):223-34. doi: 10.1172/JCI109120.