人凝血因子VIII的异质性。II. 存在瑞斯托菌素时凝血因子VIII与血小板结合形式的特征 - Suppr

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超能文献

Heterogeneity of human factor VIII. II. Characterization of forms of factor VIII binding to platelets in the presence of ristocetin.

作者信息

Doucet-de Bruïne M H, Sixma J J, Over J, Beeser-Visser N H

出版信息

J Lab Clin Med. 1978 Jul;92(1):96-107.

PMID:659967

Abstract

摘要

相似文献

Heterogeneity of human factor VIII. II. Characterization of forms of factor VIII binding to platelets in the presence of ristocetin.人凝血因子VIII的异质性。II. 存在瑞斯托菌素时凝血因子VIII与血小板结合形式的特征

J Lab Clin Med. 1978 Jul;92(1):96-107.

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.

Studies on the mechanism of ristocetin-induced platelet aggregation: binding of factor VIII to platelets.瑞斯托菌素诱导血小板聚集机制的研究：因子VIII与血小板的结合

Br J Haematol. 1979 Sep;43(1):99-112. doi: 10.1111/j.1365-2141.1979.tb03725.x.

Survival of iodine-125-labeled factor VIII in patients with von Willebrand's disease.125碘标记的因子VIII在血管性血友病患者中的存活情况。

J Lab Clin Med. 1981 Mar;97(3):332-44.

Interactions of purified rat factor VIII/von Willebrand factor with rat and human platelets--effect of albumin and ristocetin.纯化的大鼠因子VIII/血管性血友病因子与大鼠和人血小板的相互作用——白蛋白和瑞斯托菌素的影响

Thromb Haemost. 1984 Aug 31;52(1):57-9.

[Pathophysiology of platelet anomalies and its analysis. (4). Abnormality of the platelet function in von Willebrand's disease].血小板异常的病理生理学及其分析。（4）血管性血友病中血小板功能异常

Rinsho Byori. 1983 Nov;31(11):1176-85.

[Binding of factor VIII/Willebrand to Bernard-Soulier and thrombasthenic platelets (author's transl)].因子VIII/血管性血友病因子与Bernard-Soulier综合征及血小板无力症血小板的结合（作者译）

Nouv Rev Fr Hematol (1978). 1981;23(2):89-93.

Heterogeneity of human factor VIII. I. Characterization of factor VIII present in the supernatant of cryoprecipitate.人凝血因子VIII的异质性。I. 冷沉淀上清液中存在的凝血因子VIII的特性

J Lab Clin Med. 1978 Jan;91(1):32-46.

Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.血管性血友病中瑞斯托霉素诱导的血小板聚集缺陷及其通过因子VIII的纠正。

J Clin Invest. 1973 Nov;52(11):2697-707. doi: 10.1172/JCI107464.

Proceedings: Interaction of ristocetin (R), von Willebrand factor (vWF), factor VIII clotting activity (VIIIc) and platelets.论文：瑞斯托霉素（R）、血管性血友病因子（vWF）、凝血因子 VIII 活性（VIIIc）与血小板的相互作用

Thromb Diath Haemorrh. 1975 Nov 15;34(2):582.

引用本文的文献

von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease.血管性血友病因子与血小板结合，并在血小板型而非IIB型血管性血友病中诱导血小板聚集。

J Clin Invest. 1983 Nov;72(5):1532-42. doi: 10.1172/JCI111112.

Botrocetin (venom coagglutinin): reaction with a broad spectrum of multimeric forms of factor VIII macromolecular complex.蛇毒凝固素（毒液凝集素）：与多种多聚体形式的凝血因子VIII大分子复合物发生反应。

Proc Natl Acad Sci U S A. 1983 Mar;80(5):1463-6. doi: 10.1073/pnas.80.5.1463.

Functional domains on von Willebrand factor. Recognition of discrete tryptic fragments by monoclonal antibodies that inhibit interaction of von Willebrand factor with platelets and with collagen.血管性血友病因子的功能结构域。通过抑制血管性血友病因子与血小板及胶原蛋白相互作用的单克隆抗体识别离散的胰蛋白酶片段。

J Clin Invest. 1984 Sep;74(3):736-44. doi: 10.1172/JCI111489.

Expression of variant von Willebrand factor (vWF) cDNA in heterologous cells: requirement of the pro-polypeptide in vWF multimer formation.血管性血友病因子（vWF）变异体cDNA在异源细胞中的表达：前体多肽在vWF多聚体形成中的需求

EMBO J. 1987 Oct;6(10):2885-90. doi: 10.1002/j.1460-2075.1987.tb02591.x.

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