• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

AT III Barcelona: a familial quantitative-qualitative AT III deficiency.

作者信息

Grau E, Fontcuberta J, Félez J, de Diego I, Soto R, Rutllant M L

机构信息

Servei d'Hematologia, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Thromb Haemost. 1988 Feb 25;59(1):13-7.

PMID:3363529
Abstract

A quantitative and qualitative deficiency of antithrombin III (ATIII) was found in four members of a Spanish family with thrombotic tendency. In all affected members, levels of ATIII antigen and activity (heparin cofactor activity) were reduced to 50% of the normal range. When crossed immunoelectrophoresis (CIE) was performed in the presence of heparin, an abnormal slow-moving peak was found. Crossed immunoelectrofocusing (CIEF) from normal and affected individuals showed that normal ATIII migrated between pH 4.9-5.3 while the ATIII under study was asymmetrically distributed between two pH ranges: 4.9-5.3 and 4.6-4.8. Affinity adsorption of affected members' plasma to heparin-sepharose beads revealed one population of ATIII in the supernatant corresponding to the abnormal ATIII, devoid of heparin cofactor activity and showing a peak between pH range: 4.6-4.8 in CIEF. Our data supports the view that a quantitative-qualitative deficiency was present in the heterozygous state in all the affected family members. Both normal and abnormal ATIII were present in plasma of the affected individuals. This abnormal ATIII was characterized by a lack of affinity for heparin. This familial ATIII deficiency was named ATIII Barcelona.

摘要

相似文献

1
AT III Barcelona: a familial quantitative-qualitative AT III deficiency.
Thromb Haemost. 1988 Feb 25;59(1):13-7.
2
Quantitative and qualitative congenital deficiency of antithrombin III: a new molecular variant called ATIII-Barcelona 2.
Thromb Res. 1988 Jul 1;51(1):75-81. doi: 10.1016/0049-3848(88)90284-8.
3
Homozygous variant of antithrombin III that lacks affinity for heparin, AT III Kumamoto.抗凝血酶III的纯合变体,对肝素缺乏亲和力,即熊本抗凝血酶III。
Thromb Haemost. 1989 Feb 28;61(1):20-4.
4
Antithrombin III "Northwick Park": a variant antithrombin with normal affinity for heparin but reduced heparin cofactor activity.
Thromb Haemost. 1985 Jun 24;53(3):314-9.
5
Antithrombin III deficiency.
Rom J Intern Med. 1994 Apr-Jun;32(2):119-27.
6
Antithrombin III molecular variants with defective binding to heparin or to serine proteases: evidence of two different abnormal patterns identified by crossed immunoelectrofocusing.
Thromb Haemost. 1988 Aug 30;60(1):8-12.
7
Homozygous variant of antithrombin III: AT III Fontainebleau.
Thromb Haemost. 1986 Aug 20;56(1):18-22.
8
Antithrombin III Alger: a new homozygous AT III variant.
Thromb Haemost. 1986 Apr 30;55(2):218-21.
9
Antithrombin III Geneva: a hereditary abnormal AT III with defective heparin cofactor activity.抗凝血酶III日内瓦型:一种遗传性异常抗凝血酶III,其肝素辅助因子活性存在缺陷。
Thromb Haemost. 1987 Apr 7;57(2):154-7.
10
A tentative classification of AT III congenital abnormalities.
Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(5):661-9.