A mechanistic basis for potent, glycoprotein B-directed gammaherpesvirus neutralization
Author:
Affiliation:
1. Division of Virology, Department of Pathology, University of Cambridge, Cambridge, UK
2. Immunology-Vaccinology, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium
Abstract
Publisher
Microbiology Society
Subject
Virology
Reference52 articles.
1. Cloning and Mutagenesis of the Murine Gammaherpesvirus 68 Genome as an Infectious Bacterial Artificial Chromosome
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3. Hydrophobic Residues That Form Putative Fusion Loops of Epstein-Barr Virus Glycoprotein B Are Critical for Fusion Activity
4. Structure of a trimeric variant of the Epstein–Barr virus glycoprotein B
5. Vaccinal control of Marek's disease: Current challenges, and future strategies to maximize protection
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1. Antibody arrests γ-herpesvirus olfactory super-infection independently of neutralization;Journal of General Virology;2019-02-01
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3. Deletion of Murid Herpesvirus 4 ORF63 Affects the Trafficking of Incoming Capsids toward the Nucleus;Journal of Virology;2016-03
4. Cells transformed by murine herpesvirus 68 (MHV-68) release compounds with transforming and transformed phenotype suppressing activity resembling growth factors;ACTA VIROL;2015
5. Forces and Structures of the Herpes Simplex Virus (HSV) Entry Mechanism;ACS Infectious Diseases;2015-08-27
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