Molecular cloning of the gene encoding the putative polymerase of mouse hepatitis coronavirus, strain A59.
about
Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packagingThe putative helicase of the coronavirus mouse hepatitis virus is processed from the replicase gene polyprotein and localizes in complexes that are active in viral RNA synthesis.RNase L-independent specific 28S rRNA cleavage in murine coronavirus-infected cellsDemyelination determinants map to the spike glycoprotein gene of coronavirus mouse hepatitis virusInduction of apoptosis in murine coronavirus-infected cultured cells and demonstration of E protein as an apoptosis inducer.Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptorsMouse hepatitis virus 3C-like protease cleaves a 22-kilodalton protein from the open reading frame 1a polyprotein in virus-infected cells and in vitro.Importance of the positive-strand RNA secondary structure of a murine coronavirus defective interfering RNA internal replication signal in positive-strand RNA synthesis.Subgenomic negative-strand RNA function during mouse hepatitis virus infection.Mouse hepatitis virus replicase proteins associate with two distinct populations of intracellular membranesPolypyrimidine tract-binding protein binds to the complementary strand of the mouse hepatitis virus 3' untranslated region, thereby altering RNA conformation.Mitochondrial aconitase binds to the 3' untranslated region of the mouse hepatitis virus genome.Heterogeneous nuclear ribonucleoprotein a1 binds to the 3'-untranslated region and mediates potential 5'-3'-end cross talks of mouse hepatitis virus RNA.An in vitro system for the leader-primed transcription of coronavirus mRNAsRepair and mutagenesis of the genome of a deletion mutant of the coronavirus mouse hepatitis virus by targeted RNA recombinationReplication of murine hepatitis virus is regulated by papain-like proteinase 1 processing of nonstructural proteins 1, 2, and 3.The effect of two closely inserted transcription consensus sequences on coronavirus transcription.Identification of the murine coronavirus p28 cleavage site.The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism.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.Identification and characterization of a serine-like proteinase of the murine coronavirus MHV-A59.Characterization of a murine coronavirus defective interfering RNA internal cis-acting replication signal.Function of a 5'-end genomic RNA mutation that evolves during persistent mouse hepatitis virus infection in vitroMolecular anatomy of mouse hepatitis virus persistence: coevolution of increased host cell resistance and virus virulence.Replication of murine coronavirus defective interfering RNA from negative-strand transcripts.The 3' untranslated region of coronavirus RNA is required for subgenomic mRNA transcription from a defective interfering RNA.Murine coronavirus packaging signal confers packaging to nonviral RNA.Assembled coronavirus from complementation of two defective interfering RNAs.Genetic analysis of Murine hepatitis virus nsp4 in virus replicationHeterogeneous nuclear ribonucleoprotein A1 binds to the transcription-regulatory region of mouse hepatitis virus RNA.Optimization of targeted RNA recombination and mapping of a novel nucleocapsid gene mutation in the coronavirus mouse hepatitis virusEvidence for coronavirus discontinuous transcription.Subgenomic RNA synthesis directed by a synthetic defective interfering RNA of mouse hepatitis virus: a study of coronavirus transcription initiation.Map locations of mouse hepatitis virus temperature-sensitive mutants: confirmation of variable rates of recombinationIdentification 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 transcriptionGenetics of mouse hepatitis virus transcription: evidence that subgenomic negative strands are functional templates.Effect of intergenic consensus sequence flanking sequences on coronavirus transcriptionIdentification of the catalytic sites of a papain-like cysteine proteinase of murine coronavirus.Deletion mapping of a mouse hepatitis virus defective interfering RNA reveals the requirement of an internal and discontiguous sequence for replication.
P2860
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P2860
Molecular cloning of the gene encoding the putative polymerase of mouse hepatitis coronavirus, strain A59.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@ast
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@en
type
label
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@ast
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@en
prefLabel
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@ast
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@en
P2093
P1433
P1476
Molecular cloning of the gene ...... titis coronavirus, strain A59.
@en
P2093
P304
P356
10.1016/0042-6822(89)90520-5
P407
P577
1989-07-01T00:00:00Z