猪血浆中人类血小板聚集活性是血管性血友病因子特性的证据。 - Suppr | 超能文献

Evidnece that human platelet aggregating activity in porcine plasma is a property of von Willbrand factor.

作者信息

Gaetano G, Donati M B, Vermylen J

出版信息

Thromb Diath Haemorrh. 1974 Dec 31;32(2-3):549-53.

Abstract

摘要

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1

Evidnece that human platelet aggregating activity in porcine plasma is a property of von Willbrand factor.猪血浆中人类血小板聚集活性是血管性血友病因子特性的证据。

Thromb Diath Haemorrh. 1974 Dec 31;32(2-3):549-53.

2

Von Willebrand factor: gene dosage relationships and transfusion response in bleeder swine--a new bioassay.血管性血友病因子：出血性猪的基因剂量关系与输血反应——一种新的生物测定法

Proc Natl Acad Sci U S A. 1974 May;71(5):2087-90. doi: 10.1073/pnas.71.5.2087.

3

[On the platelet function in von Willebrand-Juergen's syndrome--Discussion].[关于血管性血友病 - 于尔根综合征中的血小板功能 - 讨论]

Hamatol Bluttransfus. 1969;6:196-9.

4

von Willebrand factor contained in factor VIII concentrates of different purities supports platelet adhesion in blood samples from a heterogeneous group of patients with von Willebrand disease.不同纯度的凝血因子 VIII 浓缩物中所含的血管性血友病因子支持来自异质性血管性血友病患者组的血样中的血小板黏附。

Haematologica. 1998 Nov;83(11):1009-14.

5

von Willebrand's Disease.

Clin Haematol. 1983 Feb;12(1):175-200.

6

[Diagnosis of Von Willebrand's syndrome (author's transl)].血管性血友病综合征的诊断（作者译）

Rev Med Brux. 1981 Mar;2(3):245-50.

7

Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease.血管性血友病因子/凝血因子VIII浓缩物在血管性血友病治疗中的应用

Blood Coagul Fibrinolysis. 2009 Mar;20(2):89-100. doi: 10.1097/MBC.0b013e3283254570.

8

[Action of anti-factor VIII antibodies on platelet adherence to glass beads].[抗凝血因子VIII抗体对血小板黏附于玻璃珠的作用]

Pathol Biol (Paris). 1973 Nov;21:Suppl:72-5.

9

Rationale for the treatment of von Willebrand's disease.

Prog Clin Biol Res. 1981;72:149-62.

10

Restoration of plasma von Willebrand factor deficiency is sufficient to correct thrombus formation after gene therapy for severe von Willebrand disease.恢复血浆血管性血友病因子缺乏足以纠正严重血管性血友病基因治疗后的血栓形成。

Arterioscler Thromb Vasc Biol. 2008 Sep;28(9):1621-6. doi: 10.1161/ATVBAHA.108.168369. Epub 2008 Jun 12.

引用本文的文献

1

Defective ristocetin and bovine factor VIII-induced platelet aggregation in normal rats.正常大鼠中瑞斯托菌素和牛因子VIII诱导的血小板聚集缺陷。

Experientia. 1975 Apr 15;31(4):500-2. doi: 10.1007/BF02026403.

2

Antibody nature of circulating inhibitor of plasma von Willebrand factor.血浆血管性血友病因子循环抑制剂的抗体性质

Proc Natl Acad Sci U S A. 1975 Oct;72(10):4167-71. doi: 10.1073/pnas.72.10.4167.

3

[Alteration of platelet function during intensive replacement therapy in haemophilia A (author's transl)].甲型血友病强化替代治疗期间血小板功能的改变（作者译）

Klin Wochenschr. 1977 Dec 1;55(23):1165-71. doi: 10.1007/BF01478054.