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HIV-1 Protease Inhibitors Are Substrates for theMDR1 Multidrug Transporter

Data up to Jan 2025

Published1998
Citations480
References15

Total Citations Per Year

Abstract

References (15)

BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTER

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Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues.

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In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors

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1989 • 606 citations

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HIV‐1, macrophages, glial cells, and cytokines in AIDS nervous system disease

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1990 • 277 citations

P-glycoprotein is strongly expressed in the luminal membranes of the endothelium of blood vessels in the brain

1997 • 249 citations

Brain Microvascular and Astrocyte Localization of P‐Glycoprotein

1997 • 146 citations

Identification of residues in the first cytoplasmic loop of P-glycoprotein involved in the function of chimeric human MDR1-MDR2 transporters.

1992 • 114 citations

Molecular Biology of Membrane Transport Disorders

1996 • 110 citations

Photoaffinity probes for the alpha 1-adrenergic receptor and the calcium channel bind to a common domain in P-glycoprotein.

1990 • 108 citations

Decreased biotolerability for ivermectin and cyclosporin a in mice exposed to potent P‐glycoprotein inhibitors

1995 • 73 citations

Heterogeneity in P‐glycoprotein (multidrug resistance) activity among murine peripheral T cells: Correlation with surface phenotype and effector function

1994 • 34 citations

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HIV-1 Protease Inhibitors Are Substrates for theMDR1 Multidrug Transporter (1998) – Biochemistry | Metascience Observatory Explorer