UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 142

Sortiert nach

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

Volltextzugriff (PDF)

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

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

2012

Volltextzugriff (PDF)

Viral Nucleases from Herpesviruses and Coronavirus in Recombination and Proofreading: Potential Targets for Antiviral Drug Discovery

Viruses, 2022-07, Vol.14 (7), p.1557

2022

Volltextzugriff (PDF)

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

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

2010

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2022

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Efficient Herpes Simplex Virus 1 Replication Requires Cellular ATR Pathway Proteins

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

2013

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2018

Volltextzugriff (PDF)

HSV Cheats the Executioner

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

2015

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

ATR and ATRIP Are Recruited to Herpes Simplex Virus Type 1 Replication Compartments Even though ATR Signaling Is Disabled

Journal of Virology, 2010-12, Vol.84 (23), p.12152-12164

2010

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Herpes simplex virus eliminates host mitochondrial DNA

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

2007

Volltextzugriff (PDF)

Herpes simplex viruses: mechanisms of DNA replication

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

2012

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

1 – 25 von 142

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(140)
Mit Volltextzugriff
(138)

Publikationsform

Artikel
(142)

Sprache

Englisch
(142)
Japanisch
(34)

Erscheinungsjahr

n.n

Thema

Science & Technology
(113)
Life Sciences & Biomedicine
(107)
Virology
(80)
Animals
(75)
Vero Cells
(55)
Humans
(50)
Herpes Simplex Virus 1
(49)
Microbiology
(49)
Viral Proteins - Metabolism
(44)
Biological And Medical Sciences
(40)
Fundamental And Applied Biological Sciences. Psychology
(38)
Viral Proteins - Genetics
(38)
Cercopithecus Aethiops
(37)
Herpesvirus 1, Human - Genetics
(37)
Herpesvirus 1, Human - Physiology
(31)
Virus Replication
(30)
Cell Line
(26)
Mutation
(26)
Dna-Binding Proteins - Metabolism
(25)
Herpesvirus 1, Human - Metabolism
(23)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

Viral Nucleases from Herpesviruses and Coronavirus in Recombination and Proofreading: Potential Targets for Antiviral Drug Discovery

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

ATR and ATRIP Are Recruited to Herpes Simplex Virus Type 1 Replication Compartments Even though ATR Signaling Is Disabled

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

Suchergebnisse filtern