Requirement for double-strand breaks but not for specific DNA sequences in herpes simplex virus type 1 genome isomerization events.
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The HSV-1 exonuclease, UL12, stimulates recombination by a single strand annealing mechanismRecruitment 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 respoContributions of nucleotide excision repair, DNA polymerase eta, and homologous recombination to replication of UV-irradiated herpes simplex virus type 1Herpes simplex virus genome isomerization: origins of adjacent long segments in concatemeric viral DNA.Recombination promoted by DNA viruses: phage λ to herpes simplex virus.Rad51 and Rad52 are involved in homologous recombination of replicating herpes simplex virus DNA.Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences.Herpes simplex virus type 1 alkaline nuclease is required for efficient processing of viral DNA replication intermediates.The a sequence is dispensable for isomerization of the herpes simplex virus type 1 genome.Characterization of ICP6::lacZ insertion mutants of the UL15 gene of herpes simplex virus type 1 reveals the translation of two proteins.Structural variability of the herpes simplex virus 1 genome in vitro and in vivo.Replication-Coupled Recruitment of Viral and Cellular Factors to Herpes Simplex Virus Type 1 Replication Forks for the Maintenance and Expression of Viral Genomes.Epstein-Barr virus intrastrain recombination in oral hairy leukoplakia.Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.Cleavage in and around the DR1 element of the A sequence of herpes simplex virus type 1 relevant to the excision of DNA fragments with length corresponding to one and two units of the A sequenceRequirement for uracil-DNA glycosylase during the transition to late-phase cytomegalovirus DNA replication.Intracellular Cre-mediated deletion of the unique packaging signal carried by a herpes simplex virus type 1 recombinant and its relationship to the cleavage-packaging process.A human cytomegalovirus deleted of internal repeats replicates with near wild type efficiency but fails to undergo genome isomerizationBranched structures in the intracellular DNA of herpes simplex virus type 1.Inhibition of generation of authentic genomic termini of herpes simplex virus type 1 DNA in temperature-sensitive mutant BHK-21 cells with a mutated CCG1/TAF(II)250 gene.Direct repeats of the herpes simplex virus a sequence promote nonconservative homologous recombination that is not dependent on XPF/ERCC4Equimolar generation of the four possible arrangements of adjacent L components in herpes simplex virus type 1 replicative intermediates.Co-opting the Fanconi anemia genomic stability pathway enables herpesvirus DNA synthesis and productive growth
P2860
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P2860
Requirement for double-strand breaks but not for specific DNA sequences in herpes simplex virus type 1 genome isomerization events.
description
1994 nî lūn-bûn
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1994年の論文
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1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Requirement for double-strand ...... 1 genome isomerization events.
@ast
Requirement for double-strand ...... 1 genome isomerization events.
@en
type
label
Requirement for double-strand ...... 1 genome isomerization events.
@ast
Requirement for double-strand ...... 1 genome isomerization events.
@en
prefLabel
Requirement for double-strand ...... 1 genome isomerization events.
@ast
Requirement for double-strand ...... 1 genome isomerization events.
@en
P2860
P1433
P1476
Requirement for double-strand ...... 1 genome isomerization events
@en
P2093
R T Sarisky
P2860
P407
P577
1994-01-01T00:00:00Z