Donald Coen, PhD
Professor of Biological Chemistry and Molecular Pharmacology, Harvard Medical School
A mutation deleting sequences encoding the amino terminus of human cytomegalovirus UL84 impairs interaction with UL44 and capsid localization.
Authors: Authors: Strang BL, Bender BJ, Sharma M, Pesola JM, Sanders RL, Spector DH, Coen DM.
J Virol
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J Virol
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Numerous conserved and divergent microRNAs expressed by herpes simplex viruses 1 and 2.
Authors: Authors: Jurak I, Kramer MF, Mellor JC, van Lint AL, Roth FP, Knipe DM, Coen DM.
J Virol
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J Virol
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Herpes simplex virus mutants with multiple substitutions affecting DNA binding of UL42 are impaired for viral replication and DNA synthesis.
Authors: Authors: Jiang C, Hwang YT, Wang G, Randell JC, Coen DM, Hwang CB.
J Virol
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J Virol
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Effects of substitutions of arginine residues on the basic surface of herpes simplex virus UL42 support a role for DNA binding in processive DNA synthesis.
Authors: Authors: Randell JC, Komazin G, Jiang C, Hwang CB, Coen DM.
J Virol
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J Virol
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Effect of immunization on herpes simplex virus type 1 latent infection in the trigeminal ganglion.
Authors: Authors: Kramer M, Riley J, Spoering A, Coen D, Knipe D.
Curr Eye Res
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Curr Eye Res
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Enzymatic amplification of DNA by PCR: standard procedures and optimization.
Importance of the herpes simplex virus UL24 gene for productive ganglionic infection in mice.
Authors: Authors: Jacobson JG, Chen SH, Cook WJ, Kramer MF, Coen DM.
Virology
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Virology
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Quantification of transcripts from the ICP4 and thymidine kinase genes in mouse ganglia latently infected with herpes simplex virus.
Functional analysis of the herpes simplex virus UL42 protein.
Engineered herpes simplex virus DNA polymerase point mutants: the most highly conserved region shared among alpha-like DNA polymerases is involved in substrate recognition.