Primary structure and translation of a defective interfering RNA of murine coronavirus.
about
cis-acting sequences required for coronavirus infectious bronchitis virus defective-RNA replication and packaging.SYNCRIP, a member of the heterogeneous nuclear ribonucleoprotein family, is involved in mouse hepatitis virus RNA synthesisImportance of the positive-strand RNA secondary structure of a murine coronavirus defective interfering RNA internal replication signal in positive-strand RNA synthesis.Host protein interactions with the 3' end of bovine coronavirus RNA and the requirement of the poly(A) tail for coronavirus defective genome replication.Liver-specific alpha 2 interferon gene expression results in protection from induced hepatitis.Heterogeneous nuclear ribonucleoprotein a1 binds to the 3'-untranslated region and mediates potential 5'-3'-end cross talks of mouse hepatitis virus RNA.Secondary structural elements within the 3' untranslated region of mouse hepatitis virus strain JHM genomic RNAAn in vitro system for the leader-primed transcription of coronavirus mRNAsDependence of coronavirus RNA replication on an NH2-terminal partial nonstructural protein 1 in cis.Effect of mutations in the mouse hepatitis virus 3'(+)42 protein binding element on RNA replication.RNA recombination in brome mosaic virus: effects of strand-specific stem-loop inserts.Switching species tropism: an effective way to manipulate the feline coronavirus genome.The structure and functions of coronavirus genomic 3' and 5' ends.The effect of two closely inserted transcription consensus sequences on coronavirus transcription.Specific binding of host cellular proteins to multiple sites within the 3' end of mouse hepatitis virus genomic RNA.Two murine coronavirus genes suffice for viral RNA synthesis.Characterization of a murine coronavirus defective interfering RNA internal cis-acting replication signal.cis Requirement for N-specific protein sequence in bovine coronavirus defective interfering RNA replication.Replication of murine coronavirus defective interfering RNA from negative-strand transcripts.Assembled coronavirus from complementation of two defective interfering RNAs.Requirement of the 5'-end genomic sequence as an upstream cis-acting element for coronavirus subgenomic mRNA transcription.Identification of the cis-acting signal for minus-strand RNA synthesis of a murine coronavirus: implications for the role of minus-strand RNA in RNA replication and transcriptionDeletion mapping of a mouse hepatitis virus defective interfering RNA reveals the requirement of an internal and discontiguous sequence for replication.Mechanism of coronavirus transcription: duration of primary transcription initiation activity and effects of subgenomic RNA transcription on RNA replication.Identification and characterization of a coronavirus packaging signalCoronavirus mRNA transcription: UV light transcriptional mapping studies suggest an early requirement for a genomic-length templateAnalysis of efficiently packaged defective interfering RNAs of murine coronavirus: localization of a possible RNA-packaging signalA system for study of coronavirus mRNA synthesis: a regulated, expressed subgenomic defective interfering RNA results from intergenic site insertion.High-frequency leader sequence switching during coronavirus defective interfering RNA replication.Efficient homologous RNA recombination and requirement for an open reading frame during replication of equine arteritis virus defective interfering RNAsIsolation and characterization of an arterivirus defective interfering RNA genomeTranscription regulatory sequences and mRNA expression levels in the coronavirus transmissible gastroenteritis virus.Translation but not the encoded sequence is essential for the efficient propagation of the defective interfering RNAs of the coronavirus mouse hepatitis virusReplication and packaging of coronavirus infectious bronchitis virus defective RNAs lacking a long open reading frame.Nonhomologous RNA recombination in tombusviruses: generation and evolution of defective interfering RNAs by stepwise deletions.Enhanced competitiveness of tomato bushy stunt virus defective interfering RNAs by segment duplication or nucleotide insertion.Three different cellular proteins bind to complementary sites on the 5'-end-positive and 3'-end-negative strands of mouse hepatitis virus RNA.Coding capacity determines in vivo accumulation of a defective RNA of clover yellow mosaic virus.Recombination between satellite RNAs of turnip crinkle virus.
P2860
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P2860
Primary structure and translation of a defective interfering RNA of murine coronavirus.
description
1988 nî lūn-bûn
@nan
1988 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@ast
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@en
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@nl
type
label
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@ast
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@en
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@nl
prefLabel
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@ast
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@en
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@nl
P2093
P1433
P1476
Primary structure and translation of a defective interfering RNA of murine coronavirus.
@en
P2093
P304
P356
10.1016/0042-6822(88)90526-0
P407
P577
1988-10-01T00:00:00Z