Rescue of vector-expressed fowl plague virus hemagglutinin in biologically active form by acidotropic agents and coexpressed M2 protein.
about
The genomic and epidemiological dynamics of human influenza A virusIdentification of a novel splice variant form of the influenza A virus M2 ion channel with an antigenically distinct ectodomainProteolytic activation of tick-borne encephalitis virus by furinThe influenza A virus M2 cytoplasmic tail is required for infectious virus production and efficient genome packagingThe ion channel activity of the influenza virus M2 protein affects transport through the Golgi apparatusInfluenza A virus M2 ion channel protein: a structure-function analysisHost envelope glycoprotein processing proteases are indispensable for entry into human cells by seasonal and highly pathogenic avian influenza viruses.Novel approach to the development of effective H5N1 influenza A virus vaccines: use of M2 cytoplasmic tail mutants.Influenza virus M2 protein ion channel activity helps to maintain pandemic 2009 H1N1 virus hemagglutinin fusion competence during transport to the cell surface.Inhibition of influenza A virus replication by compounds interfering with the fusogenic function of the viral hemagglutininGenetic analysis of influenza virus NS1 gene: a temperature-sensitive mutant shows defective formation of virus particles.Influenza C virus NS1 protein upregulates the splicing of viral mRNAs.Identification of a membrane targeting and degradation signal in the p42 protein of influenza C virus.Vesicular stomatitis virus G protein acquires pH-independent fusion activity during transport in a polarized endometrial cell line.Influenza A virus can undergo multiple cycles of replication without M2 ion channel activity.Incorporation of fowl plague virus hemagglutinin into murine leukemia virus particles and analysis of the infectivity of the pseudotyped retroviruses.Activation of the M2 ion channel of influenza virus: a role for the transmembrane domain histidine residueInfluenza a virus M2 ion channel activity is essential for efficient replication in tissue culture.Characterization of infectious retroviral pseudotype particles bearing hepatitis C virus glycoproteinsInduction of neutralising antibodies by virus-like particles harbouring surface proteins from highly pathogenic H5N1 and H7N1 influenza virusesReverse genetics system for generation of an influenza A virus mutant containing a deletion of the carboxyl-terminal residue of M2 protein.Characterization of inhibition of M2 ion channel activity by BL-1743, an inhibitor of influenza A virusInfluenza M2 proton channel activity selectively inhibits trans-Golgi network release of apical membrane and secreted proteins in polarized Madin-Darby canine kidney cells.Influenza B virus BM2 protein is transported through the trans-Golgi network as an integral membrane protein.Exploitation of nucleic acid packaging signals to generate a novel influenza virus-based vector stably expressing two foreign genes.Influenza virus M2 protein ion channel activity stabilizes the native form of fowl plague virus hemagglutinin during intracellular transportInfluenza A virus lacking M2 protein as a live attenuated vaccine.Regulation of receptor binding affinity of influenza virus hemagglutinin by its carbohydrate moietyElongation of the cytoplasmic tail interferes with the fusion activity of influenza virus hemagglutinin.Modification of the cytoplasmic domain of influenza virus hemagglutinin affects enlargement of the fusion pore.Novel type II transmembrane serine proteases, MSPL and TMPRSS13, Proteolytically activate membrane fusion activity of the hemagglutinin of highly pathogenic avian influenza viruses and induce their multicycle replication.Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8) infection of human fibroblast cells occurs through endocytosis.Rescue of a synthetic chloramphenicol acetyltransferase RNA into influenza virus-like particles obtained from recombinant plasmidsOligosaccharides in the stem region maintain the influenza virus hemagglutinin in the metastable form required for fusion activity.Restrictions to the adaptation of influenza a virus h5 hemagglutinin to the human host.Acylation-mediated membrane anchoring of avian influenza virus hemagglutinin is essential for fusion pore formation and virus infectivity.Maturation of the trans-Golgi network protease furin: compartmentalization of propeptide removal, substrate cleavage, and COOH-terminal truncation.Influenza Hemifusion Phenotype Depends on Membrane Context: Differences in Cell-Cell and Virus-Cell Fusion.
P2860
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P2860
Rescue of vector-expressed fowl plague virus hemagglutinin in biologically active form by acidotropic agents and coexpressed M2 protein.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Rescue of vector-expressed fow ...... ts and coexpressed M2 protein.
@en
type
label
Rescue of vector-expressed fow ...... ts and coexpressed M2 protein.
@en
prefLabel
Rescue of vector-expressed fow ...... ts and coexpressed M2 protein.
@en
P2093
P2860
P1433
P1476
Rescue of vector-expressed fow ...... ts and coexpressed M2 protein.
@en
P2093
P2860
P304
P407
P577
1994-02-01T00:00:00Z