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Evidence that factor VIII and the ristocetin aggregating factor (VIIIRist) are separate molecular entities.

作者信息

Hougie C, Sargeant R B, Brown J E, Baugh R F

出版信息

Proc Soc Exp Biol Med. 1974 Oct;147(1):58-61. doi: 10.3181/00379727-147-38280.

DOI:10.3181/00379727-147-38280
PMID:4548194
Abstract
摘要

相似文献

1
Evidence that factor VIII and the ristocetin aggregating factor (VIIIRist) are separate molecular entities.凝血因子VIII与瑞斯托菌素聚集因子（VIIIRist）是不同分子实体的证据。
Proc Soc Exp Biol Med. 1974 Oct;147(1):58-61. doi: 10.3181/00379727-147-38280.
2
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.
3
Relationship between ristocetin-induced platelet aggregation and factor VIII (activity and antigen) in v. Willebrand's disease.血管性血友病中瑞斯托霉素诱导的血小板聚集与因子VIII（活性和抗原）之间的关系。
Blut. 1974 Oct;29(4):260-4. doi: 10.1007/BF01635547.
4
[Studies on the effects of five monoclonal antibodies, polyclonal rabbit antibody and homologous antibody to human F VIII/vWF on ristocetin-induced platelet agglutination and platelet retention by glass bead column].[关于五种单克隆抗体、兔多克隆抗体及人F VIII/vWF同源抗体对瑞斯托菌素诱导的血小板凝集及玻璃珠柱血小板滞留作用的研究]
Rinsho Ketsueki. 1985 Jul;26(7):1042-9.
5
Willebrand factor and ristocetin. I. Mechanism of rustocetin-induced platelet aggregation.血管性血友病因子与瑞斯托霉素。I. 瑞斯托霉素诱导血小板聚集的机制。
Br J Haematol. 1974 Dec;28(4):561-78. doi: 10.1111/j.1365-2141.1974.tb06675.x.
6
Acquired von Willebrand syndrome with inhibitors both to factor VIII clotting activity and ristocetin-induced platelet aggregation.获得性血管性血友病综合征，同时伴有针对凝血因子VIII凝血活性和瑞斯托霉素诱导的血小板聚集的抑制剂。
Br J Haematol. 1976 Aug;33(4):565-73. doi: 10.1111/j.1365-2141.1976.tb03575.x.
7
Separation of human factor VIII activity from the von Willebrand's antigen and ristocetin platelet aggregating activity.从血管性血友病因子抗原和瑞斯托霉素血小板聚集活性中分离人凝血因子VIII活性。
Biochim Biophys Acta. 1974 Dec 18;371(2):360-7. doi: 10.1016/0005-2795(74)90032-4.
8
Recent advances in haemophilia and von Willebrand's disease.血友病和血管性血友病的最新进展
Vox Sang. 1975;28(6):409-21. doi: 10.1111/j.1423-0410.1975.tb02790.x.
9
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.
10
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.

引用本文的文献

1
Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome.血管性血友病因子裂解蛋白酶与舒-尤二氏综合征
Int J Hematol. 2002 Jan;75(1):25-34. doi: 10.1007/BF02981975.
2
Presence of factor VIII-related antigen in blood platelets of patients with Von Willebrand's disease.血管性血友病患者血小板中存在VIII因子相关抗原。
Nature. 1975 Oct 9;257(5526):510-12. doi: 10.1038/257510a0.
3
The properties of immune complexes formed by human antibodies to factor VIII.人抗凝血因子 VIII 抗体形成的免疫复合物的特性
J Clin Invest. 1977 Nov;60(5):1070-9. doi: 10.1172/JCI108858.
4
Stabilization of factor VIII in plasma by the von Willebrand factor. Studies on posttransfusion and dissociated factor VIII and in patients with von Willebrand's disease.血管性血友病因子对血浆中凝血因子VIII的稳定作用。关于输血后及解离的凝血因子VIII的研究以及血管性血友病患者的研究。
J Clin Invest. 1977 Aug;60(2):390-404. doi: 10.1172/JCI108788.