Herpes Simplex Virus 1 UL34 Mutants That Affect Membrane Budding Regulation and Nuclear Lamina Disruption
Author:
Affiliation:
1. Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA
2. Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA
Abstract
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
National Science Foundation
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/JVI.00873-21
Reference38 articles.
1. Herpesvirus Nuclear Egress
2. Structural basis of membrane budding by the nuclear egress complex of herpesviruses
3. Membrane deformation and scission by the HSV-1 nuclear egress complex
4. Structural Basis of Vesicle Formation at the Inner Nuclear Membrane
5. Roles for herpes simplex virus type 1 UL34 and US3 proteins in disrupting the nuclear lamina during herpes simplex virus type 1 egress
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1. Herpes simplex virus type-1 cVAC formation in neuronal cells is mediated by dynein motor function and glycoprotein retrieval from the plasma membrane;Journal of Virology;2024-07-23
2. Extragenic suppression of an HSV-1 UL34 nuclear egress mutant reveals role for pUS9 as an inhibitor of epithelial cell-to-cell spread;Journal of Virology;2023-10-31
3. The Knowns and Unknowns of Herpesvirus Nuclear Egress;Annual Review of Virology;2023-09-29
4. HSV Tegument Protein pUL51 Interacts with Host Dynactin for Viral Spread;2022-03-21
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