Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
about
Functional analysis of the CAAT box in the major late promoter of the subgroup C human adenovirusesDissection of the adenoviral VA RNAI central domain structure reveals minimum requirements for RNA-mediated inhibition of PKR.RNA binding and intramolecular interactions modulate the regulation of gene expression by nuclear factor 110.Coexpressed RIG-I agonist enhances humoral immune response to influenza virus DNA vaccine.Novel rapidly evolving hominid RNAs bind nuclear factor 90 and display tissue-restricted distributionStructural features of adenovirus 2 virus-associated RNA required for binding to the protein kinase DAI.Identification of RISC-associated adenoviral microRNAs, a subset of their direct targets, and global changes in the targetome upon lytic adenovirus 5 infection.Effect of single-base substitutions in the central domain of virus-associated RNA I on its function.A phylogenetically conserved RNA structure in the poliovirus open reading frame inhibits the antiviral endoribonuclease RNase L.Structure, function, and evolution of adenovirus-associated RNA: a phylogenetic approach.High level of transgene expression in cell cultures and in the mouse by replication-incompetent adenoviruses harboring modified VAI genesActivities of adenovirus virus-associated RNAs: purification and characterization of RNA binding proteins.In vitro analysis of virus-associated RNA I (VAI RNA): inhibition of the double-stranded RNA-activated protein kinase PKR by VAI RNA mutants correlates with the in vivo phenotype and the structural integrity of the central domain.Dicer functions as an antiviral system against human adenoviruses via cleavage of adenovirus-encoded noncoding RNAPersistently adenovirus-infected lymphoid cells express microRNAs derived from the viral VAI and especially VAII RNA.Adenovirus Vector-Derived VA-RNA-Mediated Innate Immune Responses.Domain interactions in adenovirus VAI RNA mediate high-affinity PKR binding.Systematic deletion of the adenovirus-associated RNAI terminal stem reveals a surprisingly active RNA inhibitor of double-stranded RNA-activated protein kinase.Rapid subgenus identification of human adenovirus isolates by a general PCR.Adenovirus virus-associated RNA is processed to functional interfering RNAs involved in virus production.Analysis of adenovirus VA RNAI structure and stability using compensatory base pair modifications.The PKR-binding domain of adenovirus VA RNAI exists as a mixture of two functionally non-equivalent structures
P2860
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P2860
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@ast
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@en
type
label
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@ast
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@en
prefLabel
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@ast
Comparative analysis of the structure and function of adenovirus virus-associated RNAs.
@en
P2860
P1433
P1476
Comparative analysis of the structure and function of adenovirus virus-associated RNAs
@en
P2093
P2860
P304
P407
P577
1993-11-01T00:00:00Z