Biased small‐molecule ligands for selective inhibition of HIV‐1 cell entry via CCR5
Author:
Affiliation:
1. Department of Neuroscience and Pharmacology Faculty of Health and Medical Sciences The Panum Institute University of Copenhagen Copenhagen Denmark
2. Department of Medicine Infectious Disease Unit Herlev Hospital Copenhagen Denmark
Funder
AIDS Fondet
Københavns Universitet
Publisher
Wiley
Subject
General Pharmacology, Toxicology and Pharmaceutics,Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prp2.262
Reference59 articles.
1. CC CKR5: A RANTES, MIP-1α, MIP-1β Receptor as a Fusion Cofactor for Macrophage-Tropic HIV-1
2. G Protein-Dependent CCR5 Signaling Is Not Required for Efficient Infection of Primary T Lymphocytes and Macrophages by R5 Human Immunodeficiency Virus Type 1 Isolates
3. Resistance to CCR5 inhibitors caused by sequence changes in the fusion peptide of HIV-1 gp41
4. Considerations in the rationale, design and methods of the Strategic Timing of AntiRetroviral Treatment (START) study
5. International Union of Basic and Clinical Pharmacology. LXXXIX. Update on the Extended Family of Chemokine Receptors and Introducing a New Nomenclature for Atypical Chemokine Receptors
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