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DNA Damage Kills Bacterial Spores and Cells Exposed to 222-Nanometer UV Radiation

Applied and environmental microbiology, 2020-04, Vol.86 (8), p.1

2020

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The HSV-1 exonuclease, UL12, stimulates recombination by a single strand annealing mechanism

PLoS pathogens, 2012-08, Vol.8 (8), p.e1002862-e1002862

2012

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Herpes simplex virus reorganizes the cellular DNA repair and protein quality control machinery

PLoS pathogens, 2010-11, Vol.6 (11), p.e1001105-e1001105

2010

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Physical Interaction between the Herpes Simplex Virus Type 1 Exonuclease, UL12, and the DNA Double-Strand Break-Sensing MRN Complex

Journal of Virology, 2010-12, Vol.84 (24), p.12504-12514

2010

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Two-Metal Ion-Dependent Enzymes as Potential Antiviral Targets in Human Herpesviruses

mBio, 2022-02, Vol.13 (1), p.e0322621

2022

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Virus-Induced Chaperone-Enriched (VICE) domains function as nuclear protein quality control centers during HSV-1 infection

PLoS pathogens, 2009-10, Vol.5 (10), p.e1000619-e1000619

2009

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Herpes Simplex Virus Type 1 DNA Polymerase Requires the Mammalian Chaperone Hsp90 for Proper Localization to the Nucleus

Journal of Virology, 2005-08, Vol.79 (16), p.10740-10749

2005

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Herpes simplex virus type I disrupts the ATR-dependent DNA-damage response during lytic infection

Journal of cell science, 2006-07, Vol.119 (13), p.2695-2703

2006

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An Intrinsically Disordered Region of the DNA Repair Protein Nbs1 Is a Species-Specific Barrier to Herpes Simplex Virus 1 in Primates

Cell host & microbe, 2016-08, Vol.20 (2), p.178-188

2016

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Efficient Herpes Simplex Virus 1 Replication Requires Cellular ATR Pathway Proteins

Journal of Virology, 2013-01, Vol.87 (1), p.531-542

2013

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Herpes simplex virus type 1 single strand DNA binding protein and helicase/primase complex disable cellular ATR signaling

PLoS pathogens, 2013-10, Vol.9 (10), p.e1003652-e1003652

2013

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The putative herpes simplex virus 1 chaperone protein UL32 modulates disulfide bond formation during infection

Journal of virology, 2015-01, Vol.89 (1), p.443-453

2015

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Recruitment of Cellular Recombination and Repair Proteins to Sites of Herpes Simplex Virus Type 1 DNA Replication Is Dependent on the Composition of Viral Proteins within Prereplicative Sites and Correlates with the Induction of the DNA Damage Response

Journal of Virology, 2004-05, Vol.78 (9), p.4783-4796

2004

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Viral Proteins U41 and U70 of Human Herpesvirus 6A Are Dispensable for Telomere Integration

Viruses, 2018-11, Vol.10 (11), p.656

2018

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HSV Cheats the Executioner

Cell host & microbe, 2015-02, Vol.17 (2), p.148-151

2015

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DNA Mismatch Repair Proteins Are Required for Efficient Herpes Simplex Virus 1 Replication

Journal of Virology, 2011-12, Vol.85 (23), p.12241-12253

2011

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Disulfide Bond Formation in the Herpes Simplex Virus 1 UL6 Protein Is Required for Portal Ring Formation and Genome Encapsidation

Journal of Virology, 2011-09, Vol.85 (17), p.8616-8624

2011

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Herpes simplex virus eliminates host mitochondrial DNA

EMBO reports, 2007-02, Vol.8 (2), p.188-193

2007

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Herpes simplex viruses: mechanisms of DNA replication

Cold Spring Harbor perspectives in biology, 2012-09, Vol.4 (9), p.a013011-a013011

2012

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Herpes Simplex Virus Type 1 Immediate-Early Protein ICP22 Is Required for VICE Domain Formation during Productive Viral Infection

Journal of Virology, 2010-03, Vol.84 (5), p.2384-2394

2010

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The Herpes Simplex Virus 1 Immediate Early Protein ICP22 Is a Functional Mimic of a Cellular J Protein

Journal of virology, 2020-01, Vol.94 (4)

2020

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Nuclear Sequestration of Cellular Chaperone and Proteasomal Machinery during Herpes Simplex Virus Type 1 Infection

Journal of Virology, 2004-07, Vol.78 (13), p.7175-7185

2004

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Oligomerization of ICP4 and Rearrangement of Heat Shock Proteins May Be Important for Herpes Simplex Virus Type 1 Prereplicative Site Formation

Journal of Virology, 2008-07, Vol.82 (13), p.6324-6336

2008

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New model integrates innate responses, PML‐NB formation, epigenetic control and reactivation from latency

EMBO reports, 2021-09, Vol.22 (9), p.e53496-n/a

2021

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Disulfide Bond Formation Contributes to Herpes Simplex Virus Capsid Stability and Retention of Pentons

Journal of Virology, 2011-09, Vol.85 (17), p.8625-8634

2011

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DNA Damage Kills Bacterial Spores and Cells Exposed to 222-Nanometer UV Radiation

The HSV-1 exonuclease, UL12, stimulates recombination by a single strand annealing mechanism

Herpes simplex virus reorganizes the cellular DNA repair and protein quality control machinery

Physical Interaction between the Herpes Simplex Virus Type 1 Exonuclease, UL12, and the DNA Double-Strand Break-Sensing MRN Complex

Two-Metal Ion-Dependent Enzymes as Potential Antiviral Targets in Human Herpesviruses

Virus-Induced Chaperone-Enriched (VICE) domains function as nuclear protein quality control centers during HSV-1 infection

Herpes Simplex Virus Type 1 DNA Polymerase Requires the Mammalian Chaperone Hsp90 for Proper Localization to the Nucleus

Herpes simplex virus type I disrupts the ATR-dependent DNA-damage response during lytic infection

An Intrinsically Disordered Region of the DNA Repair Protein Nbs1 Is a Species-Specific Barrier to Herpes Simplex Virus 1 in Primates

Efficient Herpes Simplex Virus 1 Replication Requires Cellular ATR Pathway Proteins

Herpes simplex virus type 1 single strand DNA binding protein and helicase/primase complex disable cellular ATR signaling

The putative herpes simplex virus 1 chaperone protein UL32 modulates disulfide bond formation during infection

Recruitment of Cellular Recombination and Repair Proteins to Sites of Herpes Simplex Virus Type 1 DNA Replication Is Dependent on the Composition of Viral Proteins within Prereplicative Sites and Correlates with the Induction of the DNA Damage Response

Viral Proteins U41 and U70 of Human Herpesvirus 6A Are Dispensable for Telomere Integration

HSV Cheats the Executioner

DNA Mismatch Repair Proteins Are Required for Efficient Herpes Simplex Virus 1 Replication

Disulfide Bond Formation in the Herpes Simplex Virus 1 UL6 Protein Is Required for Portal Ring Formation and Genome Encapsidation

Herpes simplex virus eliminates host mitochondrial DNA

Herpes simplex viruses: mechanisms of DNA replication

Herpes Simplex Virus Type 1 Immediate-Early Protein ICP22 Is Required for VICE Domain Formation during Productive Viral Infection

The Herpes Simplex Virus 1 Immediate Early Protein ICP22 Is a Functional Mimic of a Cellular J Protein

Nuclear Sequestration of Cellular Chaperone and Proteasomal Machinery during Herpes Simplex Virus Type 1 Infection

Oligomerization of ICP4 and Rearrangement of Heat Shock Proteins May Be Important for Herpes Simplex Virus Type 1 Prereplicative Site Formation

New model integrates innate responses, PML‐NB formation, epigenetic control and reactivation from latency

Disulfide Bond Formation Contributes to Herpes Simplex Virus Capsid Stability and Retention of Pentons

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