Herpes simplex virus amplicon: cleavage of concatemeric DNA is linked to packaging and involves amplification of the terminally reiterated a sequence.
about
Genetic analysis of the filamentous bacteriophage packaging signal and of the proteins that interact with itHuman cytomegalovirus plasmid-based amplicon vector system for gene therapyCloning human herpes virus 6A genome into bacterial artificial chromosomes and study of DNA replication intermediatesUse of amplicon-6 vectors derived from human herpesvirus 6 for efficient expression of membrane-associated and -secreted proteins in T cellsThe DR1 and DR6 first exons of human herpesvirus 6A are not required for virus replication in culture and are deleted in virus stocks that replicate well in T-cell lines.The ends on herpesvirus DNA replicative concatemers contain pac2 cis cleavage/packaging elements and their formation is controlled by terminal cis sequences.Effects of mutations within the herpes simplex virus type 1 DNA encapsidation signal on packaging efficiency.Impact of 2-bromo-5,6-dichloro-1-beta-D-ribofuranosyl benzimidazole riboside and inhibitors of DNA, RNA, and protein synthesis on human cytomegalovirus genome maturation.DNA helicase-mediated packaging of adeno-associated virus type 2 genomes into preformed capsidsHSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part I. HSV-1 structure, replication and pathogenesis.Terminally repeated sequences on a herpesvirus genome are deleted following circularization but are reconstituted by duplication during cleavage and packaging of concatemeric DNA.Herpes simplex virus DNA packaging sequences adopt novel structures that are specifically recognized by a component of the cleavage and packaging machineryCloning of the full-length rhesus cytomegalovirus genome as an infectious and self-excisable bacterial artificial chromosome for analysis of viral pathogenesis.Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences.Circularization and cleavage of guinea pig cytomegalovirus genomesThe infectious BAC genomic DNA expression library: a high capacity vector system for functional genomicsHerpes simplex virus type 1 recombination: the Uc-DR1 region is required for high-level a-sequence-mediated recombination.A novel class of transcripts expressed with late kinetics in the absence of ICP4 spans the junction between the long and short segments of the herpes simplex virus type 1 genomeThe herpes simplex virus type 1 (HSV-1) a sequence serves as a cleavage/packaging signal but does not drive recombinational genome isomerization when it is inserted into the HSV-2 genome.Analysis of the UL36 open reading frame encoding the large tegument protein (ICP1/2) of herpes simplex virus type 1Characterization of DNA sequence-common and sequence-specific proteins binding to cis-acting sites for cleavage of the terminal a sequence of the herpes simplex virus 1 genome.Sequence requirements for DNA rearrangements induced by the terminal repeat of herpes simplex virus type 1 KOS DNAA host cell protein binds to a highly conserved sequence element (pac-2) within the cytomegalovirus a sequence.Functional domains within the a sequence involved in the cleavage-packaging of herpes simplex virus DNA.Herpes simplex virus type 1 oriL is not required for virus replication or for the establishment and reactivation of latent infection in mice.Dramatic effects of 2-bromo-5,6-dichloro-1-beta-D-ribofuranosyl benzimidazole riboside on the genome structure, packaging, and egress of guinea pig cytomegalovirus.The impact of genome length on replication and genome stability of the herpesvirus guinea pig cytomegalovirusEpstein-Barr virus BALF3 has nuclease activity and mediates mature virion production during the lytic cycle.The bipartite geminivirus coat protein aids BR1 function in viral movement by affecting the accumulation of viral single-stranded DNASequences within the herpesvirus-conserved pac1 and pac2 motifs are required for cleavage and packaging of the murine cytomegalovirus genome.Herpesvirus Capsid Assembly and DNA Packaging.Isomerization of a uniquely designed amplicon during herpes simplex virus-mediated 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.Identification of cis sequences required for lytic DNA replication and packaging of murine gammaherpesvirus 68.Analysis of herpes simplex virus type 1 DNA packaging signal mutations in the context of the viral genome.Equimolar generation of the four possible arrangements of adjacent L components in herpes simplex virus type 1 replicative intermediates.Pseudorabies virus protein homologous to herpes simplex virus type 1 ICP18.5 is necessary for capsid maturation.Deletion of the VP16 open reading frame of herpes simplex virus type 1.The pseudorabies virus homology of the herpes simplex virus UL21 gene product is a capsid protein which is involved in capsid maturation.Recombination of the internal direct repeat element DR2 responsible for the fluidity of the a sequence of herpes simplex virus type 1.
P2860
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P2860
Herpes simplex virus amplicon: cleavage of concatemeric DNA is linked to packaging and involves amplification of the terminally reiterated a sequence.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Herpes simplex virus amplicon: ...... minally reiterated a sequence.
@en
type
label
Herpes simplex virus amplicon: ...... minally reiterated a sequence.
@en
prefLabel
Herpes simplex virus amplicon: ...... minally reiterated a sequence.
@en
P2860
P1433
P1476
Herpes simplex virus amplicon: ...... rminally reiterated a sequence
@en
P2093
P2860
P304
P407
P577
1986-03-01T00:00:00Z