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Molecular Biology

D-Index
85
Citations
21312
World Ranking
858
National Ranking
65

Overview

Roger D. Everett is affiliated with the University of Glasgow in the United Kingdom. Their research primarily focuses on viral infections and the molecular mechanisms involved in virus-host interactions. The work contributes to multiple fields, including agricultural and biological sciences, biochemistry, genetics and molecular biology, and immunology and microbiology.

Their research includes significant studies related to animal virus infections, virus-based gene therapy, and the roles of interferon and immune responses. These topics align with subfields such as animal science and zoology, genetics, and immunology, illustrating a multidisciplinary approach to understanding viral pathogenesis and immune system modulation.

Recent publications authored or co-authored by Roger D. Everett include the following:

  • Suppression of TRIM19 by arterivirus nonstructural protein 1 promotes viral replication, 2023, Virus Research
  • Nonstructural protein 1 of swine arterivirus PRRSV downregulates promyelocytic leukemia nuclear bodies and promotes viral replication, 2023, bioRxiv (Cold Spring Harbor Laboratory)

These publications investigate how specific viral proteins affect host cellular structures and immune responses to enhance viral replication. The study of arterivirus nonstructural proteins and their interaction with cellular components provides insight into viral strategies for immune evasion.

Roger D. Everett collaborates frequently with other researchers in the field. Notable co-authors include:

  • Chia-Ming Su
  • Mingyuan Han
  • Dongwan Yoo
  • Yu Fan Hung
  • Junyu Tang

Publication venues for their work include Virus Research and bioRxiv, representing both peer-reviewed journals and preprint servers recognized in virology and molecular biology research communities.

Best Publications

  • The SV40 72 base repair repeat has a striking effect on gene expression both in SV40 and other chimeric recombinants

    P. Moreau;R. Hen;B. Wasylyk;R. Everett

  • A novel ubiquitin-specific protease is dynamically associated with the PML nuclear domain and binds to a herpesvirus regulatory protein

    Roger D. Everett;Michayla Meredith;Anne Orr;Anne Cross

  • PML and PML nuclear bodies: Implications in antiviral defence

    Roger D. Everett;Mounira K. Chelbi-Alix

  • Trans activation of transcription by herpes virus products: requirement for two HSV-1 immediate-early polypeptides for maximum activity

    Everett Rd

  • HSV-1 IE protein Vmw110 causes redistribution of PML.

    R.D. Everett;G.G. Maul

  • The Disruption of ND10 during Herpes Simplex Virus Infection Correlates with the Vmw110- and Proteasome-Dependent Loss of Several PML Isoforms

    Roger D. Everett;Paul Freemont;Hisato Saitoh;Mary Dasso

  • Herpes Simplex Virus Type 1 Immediate-Early Protein ICP0 and Its Isolated RING Finger Domain Act as Ubiquitin E3 Ligases In Vitro

    Chris Boutell;Seth Sadis;Roger D. Everett

  • PML Contributes to a Cellular Mechanism of Repression of Herpes Simplex Virus Type 1 Infection That Is Inactivated by ICP0

    Roger D. Everett;Sabine Rechter;Peer Papior;Nina Tavalai

  • ICP0, a regulator of herpes simplex virus during lytic and latent infection

    Roger D. Everett

  • The nuclear location of PML, a cellular member of the C3HC4 zinc-binding domain protein family, is rearranged during herpes simplex virus infection by the C3HC4 viral protein ICP0

    Gerd G. Maul;Roger D. Everett

  • Structure of the C3HC4 Domain by 1H-nuclear Magnetic Resonance Spectroscopy.: A New Structural Class of Zinc-finger

    Paul Barlow;B Luisi;A Milner;M Elliott

  • Nuclear Domain 10 as Preexisting Potential Replication Start Sites of Herpes Simplex Virus Type-1

    Gerd G. Maul;Alexander M. Ishov;Roger D. Everett

  • The Herpes Simplex Virus ICP0 RING Finger Domain Inhibits IRF3- and IRF7-Mediated Activation of Interferon-Stimulated Genes

    Rongtuan Lin;Ryan S. Noyce;Susan E. Collins;Roger D. Everett

  • DNA viruses and viral proteins that interact with PML nuclear bodies.

    Roger D Everett

  • Specific destruction of kinetochore protein CENP-C and disruption of cell division by herpes simplex virus immediate-early protein Vmw110.

    Roger D. Everett;William C. Earnshaw;John Findlay;Patrick Lomonte

  • Herpes Simplex Virus Type 1 Immediate-Early Protein Vmw110 Induces the Proteasome-Dependent Degradation of the Catalytic Subunit of DNA-Dependent Protein Kinase

    Jane Parkinson;Susan P. Lees-Miller;Roger D. Everett

  • ND10 Components Relocate to Sites Associated with Herpes Simplex Virus Type 1 Nucleoprotein Complexes during Virus Infection

    Roger D. Everett;Jill Murray

  • Replication of ICP0-Null Mutant Herpes Simplex Virus Type 1 Is Restricted by both PML and Sp100

    Roger D. Everett;Carlos Parada;Philippe Gripon;Hüseyin Sirma

  • Characterization of the IE110 gene of herpes simplex virus type 1.

    Lise J. Perry;Frazer J. Rixon;Roger D. Everett;Margaret C. Frame

  • Cell cycle regulation of PML modification and ND10 composition

    R.D. Everett;P. Lomonte;T. Sternsdorf;R. van Driel

Frequent Co-Authors

Chris M. Preston
Chris M. Preston University of Glasgow
Pierre Chambon
Pierre Chambon Institute of Genetics and Molecular and Cellular Biology
Ronald T. Hay
Ronald T. Hay University of Dundee
Jessica K. Tyler
Jessica K. Tyler Cornell University
Thomas Dobner
Thomas Dobner Heinrich-Pette-Institute
Gerd G. Maul
Gerd G. Maul The Wistar Institute
Peter O'Hare
Peter O'Hare Imperial College London
Frazer J. Rixon
Frazer J. Rixon University of Glasgow
Nigel W. Fraser
Nigel W. Fraser University of Pennsylvania
Duncan J. McGeoch
Duncan J. McGeoch University of Glasgow

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