The Cellular Thioredoxin-1/Thioredoxin Reductase-1 Driven Oxidoreduction Represents a Chemotherapeutic Target for HIV-1 Entry Inhibition

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The Cellular Thioredoxin-1/Thioredoxin Reductase-1 Driven Oxidoreduction Represents a Chemotherapeutic Target for HIV-1 Entry Inhibition

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2016 nî lūn-bûn

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2016 թուականին հրատարակուած գիտական յօդուած

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2016 թվականին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

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The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

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The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

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Item

label

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

@ast

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

@en

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

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The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

@ast

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

@en

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

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P1476

The Cellular Thioredoxin-1/Thi ...... get for HIV-1 Entry Inhibition

@en

P2093

Kathrin Reiser

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Lars Engman

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Leen Mathys

http://www.w3.org/2001/XMLSchema#string

Mathias Lundberg

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Sandra Liekens

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Sophie Curbo

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P2860

Identification of gammaretroviruses constitutively released from cell lines used for human immunodeficiency virus research

Structure and mechanism of mammalian thioredoxin reductase: the active site is a redox-active selenolthiol/selenenylsulfide formed from the conserved cysteine-selenocysteine sequence

HIV Drug Resistance: Problems and Perspectives

Thioltransferase (glutaredoxin) is detected within HIV-1 and can regulate the activity of glutathionylated HIV-1 protease in vitro

Clinical pharmacology of gold

The thioredoxin antioxidant system

Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1-specific nucleoside analogue [2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]-3'-spiro-5 "- (4"-amino-1",2"-oxathiole-2",2"-di

Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives

Inhibition of human immunodeficiency virus infection by agents that interfere with thiol-disulfide interchange upon virus-receptor interaction

Standardized peripheral blood mononuclear cell culture assay for determination of drug susceptibilities of clinical human immunodeficiency virus type 1 isolates. The RV-43 Study Group, the AIDS Clinical Trials Group Virology Committee Resistance Wor

P304

e0147773

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scholarly article

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10.1371/JOURNAL.PONE.0147773

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English

P433

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P478

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P50

Jan Balzarini

Anna Karlsson

Christophe Pannecouque

Sam Noppen

P577

2016-01-01T00:00:00Z

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P5875

292142523

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P698

26816344

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P921

chemotherapy

P932

4729491

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