Expression of the gag-pol fusion protein of Moloney murine leukemia virus without gag protein does not induce virion formation or proteolytic processing.
about
Pseudoknot-dependent read-through of retroviral gag termination codons: importance of sequences in the spacer and loop 2Identification of a cellular factor that modulates HIV-1 programmed ribosomal frameshiftingFunctional Translational Readthrough: A Systems Biology PerspectiveMechanisms and implications of programmed translational frameshiftingAn equilibrium-dependent retroviral mRNA switch regulates translational recodingMutational analysis of the gag-pol junction of Moloney murine leukemia virus: requirements for expression of the gag-pol fusion protein.Threshold number of provirus copies required per cell for efficient virus production and interference in moloney murine leukemia virus-infected NIH 3T3 cells.Achieving a golden mean: mechanisms by which coronaviruses ensure synthesis of the correct stoichiometric ratios of viral proteins.Maintenance of the Gag/Gag-Pol ratio is important for human immunodeficiency virus type 1 RNA dimerization and viral infectivity.Translational control of viral gene expression in eukaryotesA loop 2 cytidine-stem 1 minor groove interaction as a positive determinant for pseudoknot-stimulated -1 ribosomal frameshiftingA rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiaeNovel gene expression mechanism in a fission yeast retroelement: Tf1 proteins are derived from a single primary translation productA genetic screen identifies cellular factors involved in retroviral -1 frameshifting.Profile of Stephen P. Goff. Interview by Greg WilliamsGammaretroviral vectors: biology, technology and applicationAnalysis of natural variants of the human immunodeficiency virus type 1 gag-pol frameshift stem-loop structureA large extension to HIV-1 Gag, like Pol, has negative impacts on virion assemblyInserting a nuclear targeting signal into a replication-competent Moloney murine leukemia virus affects viral export and is not sufficient for cell cycle-independent infection.Identification of putative programmed -1 ribosomal frameshift signals in large DNA databasesA rapid, inexpensive yeast-based dual-fluorescence assay of programmed--1 ribosomal frameshifting for high-throughput screening.The effect of specific mutations at and around the gag-pol gene junction of Moloney murine leukaemia virusMechanisms of mRNA frame maintenance and its subversion during translation of the genetic code.Murine leukemia viruses: objects and organisms.Possible role of splice acceptor site in expression of unspliced gag-containing message of Moloney murine leukemia virus.Large ribosomal protein 4 increases efficiency of viral recoding sequences.Ribosomal protein and biogenesis factors affect multiple steps during movement of the Saccharomyces cerevisiae Ty1 retrotransposon.The retrotransposon Tf1 assembles virus-like particles that contain excess Gag relative to integrase because of a regulated degradation processGenetic analysis of the human immunodeficiency virus type 1 integrase protein.The nonmyristylated Pr160gag-pol polyprotein of human immunodeficiency virus type 1 interacts with Pr55gag and is incorporated into viruslike particles.Amino acids encoded downstream of gag are not required by Rous sarcoma virus protease during gag-mediated assembly.Ribosomal frameshifting efficiency and gag/gag-pol ratio are critical for yeast M1 double-stranded RNA virus propagation.Human immunodeficiency virus type 1 gag-pol frameshifting is dependent on downstream mRNA secondary structure: demonstration by expression in vivo.Incorporation of chimeric gag protein into retroviral particles.Characterization of Moloney murine leukemia virus mutants with single-amino-acid substitutions in the Cys-His box of the nucleocapsid proteinRous sarcoma virus expression in Saccharomyces cerevisiae: processing and membrane targeting of the gag gene product.An RNA pseudoknot and an optimal heptameric shift site are required for highly efficient ribosomal frameshifting on a retroviral messenger RNA.Overexpression of the gag-pol precursor from human immunodeficiency virus type 1 proviral genomes results in efficient proteolytic processing in the absence of virion productionAssembly of gag-beta-galactosidase proteins into retrovirus particles.Spleen necrosis virus gag polyprotein is necessary for particle assembly and release but not for proteolytic processing
P2860
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P2860
Expression of the gag-pol fusion protein of Moloney murine leukemia virus without gag protein does not induce virion formation or proteolytic processing.
description
1988 nî lūn-bûn
@nan
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
1988年论文
@zh
1988年论文
@zh-cn
name
Expression of the gag-pol fusi ...... ion or proteolytic processing.
@en
type
label
Expression of the gag-pol fusi ...... ion or proteolytic processing.
@en
prefLabel
Expression of the gag-pol fusi ...... ion or proteolytic processing.
@en
P2860
P921
P1433
P1476
Expression of the gag-pol fusi ...... ion or proteolytic processing.
@en
P2093
K M Felsenstein
P2860
P304
P407
P577
1988-06-01T00:00:00Z