ICP8 Filament Formation Is Essential for Replication Compartment Formation during Herpes Simplex Virus Infection

Item

http://www.wikidata.org/entity/Q39605405

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

ICP8 Filament Formation Is Ess ...... Herpes Simplex Virus Infection

@en

ICP8 Filament Formation Is Ess ...... erpes Simplex Virus Infection.

@nl

type

Item

label

ICP8 Filament Formation Is Ess ...... Herpes Simplex Virus Infection

@en

ICP8 Filament Formation Is Ess ...... erpes Simplex Virus Infection.

@nl

prefLabel

ICP8 Filament Formation Is Ess ...... Herpes Simplex Virus Infection

@en

ICP8 Filament Formation Is Ess ...... erpes Simplex Virus Infection.

@nl

P1476

ICP8 Filament Formation Is Ess ...... Herpes Simplex Virus Infection

@en

P2093

Anthar S Darwish

http://www.w3.org/2001/XMLSchema#string

Lorry M Grady

http://www.w3.org/2001/XMLSchema#string

Ping Bai

http://www.w3.org/2001/XMLSchema#string

Sandra K Weller

http://www.w3.org/2001/XMLSchema#string

P2860

Formation of nuclear foci of the herpes simplex virus type 1 regulatory protein ICP4 at early times of infection: localization, dynamics, recruitment of ICP27, and evidence for the de novo induction of ND10-like complexes

The herpes simplex virus type 1 alkaline nuclease and single-stranded DNA binding protein mediate strand exchange in vitro

Phase transitions and size scaling of membrane-less organelles

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

The bipolar filaments formed by herpes simplex virus type 1 SSB/recombination protein (ICP8) suggest a mechanism for DNA annealing.

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 respo

Proteomics of herpes simplex virus replication compartments: association of cellular DNA replication, repair, recombination, and chromatin remodeling proteins with ICP8.

A dominant-negative herpesvirus protein inhibits intranuclear targeting of viral proteins: effects on DNA replication and late gene expression.

ATR and ATRIP are recruited to herpes simplex virus type 1 replication compartments even though ATR signaling is disabled.

Mutations in the putative zinc-binding motif of UL52 demonstrate a complex interdependence between the UL5 and UL52 subunits of the human herpes simplex virus type 1 helicase/primase complex.

P304

2561-2570

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1128/JVI.02854-15

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-12-16T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26676794

http://www.w3.org/2001/XMLSchema#string

P932

4810729

http://www.w3.org/2001/XMLSchema#string