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Components of the REST/CoREST/histone deacetylase repressor complex are disrupted, modified, and translocated in HSV-1-infected cells.
The CoREST/REST repressor is both necessary and inimical for expression of herpes simplex virus genes.
Herpes simplex virus-infected cell protein 0 blocks the silencing of viral DNA by dissociating histone deacetylases from the CoREST-REST complex.
The checkpoints of viral gene expression in productive and latent infection: the role of the HDAC/CoREST/LSD1/REST repressor complex.
The two functions of herpes simplex virus 1 ICP0, inhibition of silencing by the CoREST/REST/HDAC complex and degradation of PML, are executed in tandem.
Engagement of the lysine-specific demethylase/HDAC1/CoREST/REST complex by herpes simplex virus 1.
Disruption of HDAC/CoREST/REST repressor by dnREST reduces genome silencing and increases virulence of herpes simplex virus.
HSV carrying WT REST establishes latency but reactivates only if the synthesis of REST is suppressed.
The role of the CoREST/REST repressor complex in herpes simplex virus 1 productive infection and in latency.
Dissection of the Functions of Herpes Simplex Virus ICPO
MECHANISMS OF VIRAL INFECTION IN RELATION TO CANCER