Circularization and cleavage of guinea pig cytomegalovirus genomes
about
Cloning the complete guinea pig cytomegalovirus genome as an infectious bacterial artificial chromosome with excisable origin of replication.The ends on herpesvirus DNA replicative concatemers contain pac2 cis cleavage/packaging elements and their formation is controlled by terminal cis sequences.Reactivation of the human cytomegalovirus major immediate-early regulatory region and viral replication in embryonal NTera2 cells: role of trichostatin A, retinoic acid, and deletion of the 21-base-pair repeats and modulator.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.Terminally repeated sequences on a herpesvirus genome are deleted following circularization but are reconstituted by duplication during cleavage and packaging of concatemeric DNA.Anti-cytomegalovirus activity of the anthraquinone atanyl blue PRL.Cloning of the full-length rhesus cytomegalovirus genome as an infectious and self-excisable bacterial artificial chromosome for analysis of viral pathogenesis.Bacterial artificial chromosome clones of viruses comprising the towne cytomegalovirus vaccine.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 cytomegalovirusDNA virus replication compartments.Sequences within the herpesvirus-conserved pac1 and pac2 motifs are required for cleavage and packaging of the murine cytomegalovirus genome.Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.A human cytomegalovirus deleted of internal repeats replicates with near wild type efficiency but fails to undergo genome isomerizationMolecular, biological, and in vivo characterization of the guinea pig cytomegalovirus (CMV) homologs of the human CMV matrix proteins pp71 (UL82) and pp65 (UL83).Circularization of the herpes simplex virus type 1 genome upon lytic infectionAnalysis of the nucleotide sequence of the guinea pig cytomegalovirus (GPCMV) genomeA 128-base-pair sequence containing the pac1 and a presumed cryptic pac2 sequence includes cis elements sufficient to mediate efficient genome maturation of human cytomegalovirus.Definition of the minimal cis-acting sequences necessary for genome maturation of the herpesvirus murine cytomegalovirus.A Guinea pig cytomegalovirus resistant to the DNA maturation inhibitor BDCRB.
P2860
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P2860
Circularization and cleavage of guinea pig cytomegalovirus genomes
description
1997 nî lūn-bûn
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1997年の論文
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1997年論文
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1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
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1997年論文
@zh-tw
1997年论文
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1997年论文
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1997年论文
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name
Circularization and cleavage of guinea pig cytomegalovirus genomes
@ast
Circularization and cleavage of guinea pig cytomegalovirus genomes
@en
type
label
Circularization and cleavage of guinea pig cytomegalovirus genomes
@ast
Circularization and cleavage of guinea pig cytomegalovirus genomes
@en
prefLabel
Circularization and cleavage of guinea pig cytomegalovirus genomes
@ast
Circularization and cleavage of guinea pig cytomegalovirus genomes
@en
P2093
P2860
P1433
P1476
Circularization and cleavage of guinea pig cytomegalovirus genomes
@en
P2093
P2860
P304
P407
P577
1997-06-01T00:00:00Z