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Properties of the platelet retention (von Willebrand) factor and its similarity to the antihemophilic factor (AHF).

作者信息

Weiss H J, Rogers J, Brand H

出版信息

Blood. 1973 Jun;41(6):809-15.

PMID:4541271
Abstract
摘要

相似文献

1
Properties of the platelet retention (von Willebrand) factor and its similarity to the antihemophilic factor (AHF).
Blood. 1973 Jun;41(6):809-15.
2
Von Willebrand factor and platelet adhesiveness.血管性血友病因子与血小板黏附性。
J Clin Pathol. 1970 Apr;23(3):228-31. doi: 10.1136/jcp.23.3.228.
3
Letter: Nature of the von Willebrand factor.信件:血管性血友病因子的性质。
N Engl J Med. 1974 Feb 21;290(8):464. doi: 10.1056/NEJM197402212900820.
4
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.
5
Willebrand factor: immunological and biological study.血管性血友病因子:免疫学与生物学研究
Pathol Biol (Paris). 1973 Nov;21:Suppl:66-71.
6
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.
7
[Biological diagnosis of von Willebrand's disease (author's transl)].血管性血友病的生物学诊断(作者译)
Sangre (Barc). 1978;23(5B):728-45.
8
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.
9
Willebrand factor and ristocetin. II. Relationship between Willebrand factor, Willebrand antigen and factor VIII activity.血管性血友病因子与瑞斯托霉素。II. 血管性血友病因子、血管性血友病抗原与凝血因子VIII活性之间的关系。
Br J Haematol. 1974 Dec;28(4):579-99. doi: 10.1111/j.1365-2141.1974.tb06676.x.
10
[Sugar-chain of factor VIII/von Willebrand factor in von Willebrand's disease. Analysis by immuno-affinoelectrophoresis using lectin].[血管性血友病中凝血因子VIII/血管性血友病因子的糖链。使用凝集素的免疫亲和电泳分析]
Nihon Ketsueki Gakkai Zasshi. 1983 Sep;46(5):1117-23.

引用本文的文献

1
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.
2
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.
3
Acquired von Willebrand's disease and hypothyroidism: report of a case presenting with menorrhagia.
获得性血管性血友病综合征与甲状腺功能减退症:一例以月经过多为表现的病例报告。
Postgrad Med J. 1990 Jun;66(776):474-6. doi: 10.1136/pgmj.66.776.474.
4
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.
5
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.