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• W2125018159 abstract "ABSTRACT Recent studies have explored the chromatin structures associated with the herpes simplex virus type 1 (HSV-1) genome during latency, particularly with regard to specific histone tail modifications such as acetylation and dimethylation. The objective of our present study was to develop a rapid systemic method of in vivo HSV-1 reactivation to further explore the changes that occur in the chromatin structures associated with HSV-1 at early time points after the initiation of HSV reactivation. We present a uniform, rapid, and reliable method of in vivo HSV-1 reactivation in mice that yields high reactivation frequencies (75 to 100%) by using sodium butyrate, a histone deacetylase inhibitor, and demonstrate that the reactivating virus can be detected at the original site of infection." @default.
• W2125018159 created "2016-06-24" @default.
• W2125018159 creator A5030022089 @default.
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• W2125018159 date "2007-06-01" @default.
• W2125018159 modified "2023-10-10" @default.
• W2125018159 title "Sodium Butyrate: a Chemical Inducer of In Vivo Reactivation of Herpes Simplex Virus Type 1 in the Ocular Mouse Model" @default.
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• W2125018159 doi "https://doi.org/10.1128/jvi.00070-07" @default.
• W2125018159 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1900314" @default.
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