HIV Env reduction postreceptor binding: a new target for AIDS treatment?

被引：4

作者：

Fenouillet, E ^{[1
]}

Barbouche, R ^{[1
]}

Jones, IM ^{[1
]}

机构：

[1] CNRS, Sch Med, Dept Biochem, F-13015 Marseille, France

来源：

BLOOD | 2004年 / 104卷 / 01期

基金：

英国医学研究理事会;

关键词：

D O I：

10.1182/blood-2004-03-1176

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：296 / 296

页数：1

共 8 条

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[2] The catalytic activity of protein disulfide isomerase is involved in human immunodeficiency virus envelope- mediated membrane fusion after CD4 cell binding
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[3] Inhibitors of protein-disulfide isomerase prevent cleavage of disulfide bonds in receptor-bound glycoprotein 120 and prevent HIV-1 entry
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[4] KOMBLUTH RS, 2004, BLOOD, V103, P1567
[5] Thiol/disulfide exchange is a prerequisite for CXCR4-tropic HIV-1 envelope-mediated T-cell fusion during viral entry
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[8] INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION BY AGENTS THAT INTERFERE WITH THIOL-DISULFIDE INTERCHANGE UPON VIRUS-RECEPTOR INTERACTION
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