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Purification and partial characterization of a hereditary abnormal antithrombin III fraction of a patient with recurrent thrombophlebitis.

作者信息

Tran T H, Bounameaux H, Bondeli C, Honkanen H, Marbet G A, Duckert F

出版信息

Thromb Haemost. 1980 Oct 31;44(2):87-91.

PMID:7455996
Abstract
摘要

相似文献

1
Purification and partial characterization of a hereditary abnormal antithrombin III fraction of a patient with recurrent thrombophlebitis.复发性血栓性静脉炎患者遗传性异常抗凝血酶III组分的纯化及部分特性分析
Thromb Haemost. 1980 Oct 31;44(2):87-91.
2
Purification and characterization of hereditary abnormal antithrombin III with impaired thrombin binding.凝血酶结合受损的遗传性异常抗凝血酶III的纯化与特性分析
J Lab Clin Med. 1984 Aug;104(2):245-56.
3
Isolation and characterization of a hereditary abnormal antithrombin III 'Antithrombin III Toyama'.
Thromb Res. 1983 Jul 15;31(2):319-28. doi: 10.1016/0049-3848(83)90334-1.
4
A functional abnormal antithrombin III (AT III) deficiency: AT III Charleville.一种功能性异常抗凝血酶III（AT III）缺乏症：夏勒维尔AT III。
Thromb Res. 1985 Sep 1;39(5):559-70. doi: 10.1016/0049-3848(85)90236-1.
5
[Hereditary abnormalities of antithrombin III in patients with recurrent thrombophlebitis].[复发性血栓性静脉炎患者抗凝血酶III的遗传性异常]
Med Arh. 1986;40(1-2):51-3.
6
Antithrombin III Toyama: a congenital antithrombin III abnormality with recurrent thrombophlebitis.富山抗凝血酶III：一种伴有复发性血栓性静脉炎的先天性抗凝血酶III异常。
Nihon Ketsueki Gakkai Zasshi. 1985 Dec;48(8):1895-905.
7
Antithrombin III Toyama: a hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitis.富山抗凝血酶III：一名复发性血栓性静脉炎患者的遗传性异常抗凝血酶III 。
Thromb Res. 1983 Jul 15;31(2):305-17. doi: 10.1016/0049-3848(83)90333-x.
8
Abnormal reactivity with thrombin of a new variant of dysfunctional antithrombin (AT 'Vicenza').功能异常抗凝血酶新变体（抗凝血酶“维琴察”）与凝血酶的异常反应性
Ric Clin Lab. 1984 Jul-Sep;14(3):515-9. doi: 10.1007/BF02904879.
9
[Comparative studies of the antithrombin III level and plasminogen activator activity in patients with thrombophlebitis].[血栓性静脉炎患者抗凝血酶III水平与纤溶酶原激活物活性的比较研究]
Pol Tyg Lek. 1985 Oct 28;40(43):1202-4.
10
Simultaneous isolation and partial characterization of antithrombin III and alpha 1-proteinase inhibitor from horse plasma.从马血浆中同时分离抗凝血酶III和α1-蛋白酶抑制剂并进行部分特性鉴定。
Acta Biochim Pol. 1982;29(1-2):95-103.

引用本文的文献

1
Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease.
Blut. 1983 Aug;47(2):93-103. doi: 10.1007/BF02482643.
2
Antithrombin III Toyama: replacement of arginine-47 by cysteine in hereditary abnormal antithrombin III that lacks heparin-binding ability.富山抗凝血酶III：遗传性异常抗凝血酶III中精氨酸-47被半胱氨酸取代，该抗凝血酶III缺乏肝素结合能力。
Proc Natl Acad Sci U S A. 1984 Jan;81(2):289-93. doi: 10.1073/pnas.81.2.289.
3
Isolation and sequence characterization of a cDNA clone of human antithrombin III.人抗凝血酶III cDNA克隆的分离与序列特征分析
Proc Natl Acad Sci U S A. 1983 Apr;80(7):1845-8. doi: 10.1073/pnas.80.7.1845.
4
Familial venous thrombosis.家族性静脉血栓形成
Postgrad Med J. 1983 Nov;59(697):677-89. doi: 10.1136/pgmj.59.697.677.
5
Genetic mapping of the structural gene for antithrombin III to human chromosome 1.抗凝血酶III结构基因在人类1号染色体上的基因定位。
Hum Genet. 1984;67(1):34-6. doi: 10.1007/BF00270555.
6
Interaction of antithrombin III with bovine aortic segments. Role of heparin in binding and enhanced anticoagulant activity.抗凝血酶III与牛主动脉段的相互作用。肝素在结合及增强抗凝活性中的作用。
J Clin Invest. 1985 Jan;75(1):272-9. doi: 10.1172/JCI111685.