Donald Coen, PhD
Professor of Biological Chemistry and Molecular Pharmacology, Harvard Medical School
A small molecule exerts selective antiviral activity by targeting the human cytomegalovirus nuclear egress complex
Authors: Authors: Han Chen, Ming F Lye, Christoph Gorgulla, Scott B Ficarro, Gregory D Cuny, David A Scott, Fan Wu, Paul W Rothlauf, Xiaoou Wang, Rosio Fernandez, Jean M Pesola, Sorin Draga, Jarrod A Marto, James M Hogle, Haribabu Arthanari, Donald M Coen
PLoS
View full abstract on Pubmed
PLoS
View full abstract on Pubmed
High-Throughput Small Interfering RNA Screening Identifies Phosphatidylinositol 3-Kinase Class II Alpha as Important for Production of Human Cytomegalovirus Virions.
Authors: Authors: Polachek WS, Moshrif HF, Franti M, Coen DM, Sreenu VB, Strang BL.
J Virol
View full abstract on Pubmed
J Virol
View full abstract on Pubmed
Expression of herpes simplex virus 1 microRNAs in cell culture models of quiescent and latent infection.
Authors: Authors: Jurak I, Hackenberg M, Kim JY, Pesola JM, Everett RD, Preston CM, Wilson AC, Coen DM.
J Virol
View full abstract on Pubmed
J Virol
View full abstract on Pubmed
Mammalian alphaherpesvirus miRNAs.
Role of homodimerization of human cytomegalovirus DNA polymerase accessory protein UL44 in origin-dependent DNA replication in cells.
Authors: Authors: Sinigalia E, Alvisi G, Mercorelli B, Coen DM, Pari GS, Jans DA, Ripalti A, Palù G, Loregian A.
J Virol
View full abstract on Pubmed
J Virol
View full abstract on Pubmed
Low-level expression and reversion both contribute to reactivation of herpes simplex virus drug-resistant mutants with mutations on homopolymeric sequences in thymidine kinase.
The herpes simplex virus processivity factor, UL42, binds DNA as a monomer.
Quantitation of rare DNAs by PCR.
Herpes simplex virus processivity factor UL42 imparts increased DNA-binding specificity to the viral DNA polymerase and decreased dissociation from primer-template without reducing the elongation rate.
Temporal regulation of herpes simplex virus type 1 UL24 mRNA expression via differential polyadenylation.