about
Virus entry, assembly, budding, and membrane raftsReplacement of the ectodomains of the hemagglutinin-neuraminidase and fusion glycoproteins of recombinant parainfluenza virus type 3 (PIV3) with their counterparts from PIV2 yields attenuated PIV2 vaccine candidatesReplacement of the F and G proteins of respiratory syncytial virus (RSV) subgroup A with those of subgroup B generates chimeric live attenuated RSV subgroup B vaccine candidates.A matrix-less measles virus is infectious and elicits extensive cell fusion: consequences for propagation in the brain.Cell-cell fusion induced by measles virus amplifies the type I interferon response.The cytoplasmic tail of the human respiratory syncytial virus F protein plays critical roles in cellular localization of the F protein and infectious progeny production.Chimeric bovine respiratory syncytial virus with attachment and fusion glycoproteins replaced by bovine parainfluenza virus type 3 hemagglutinin-neuraminidase and fusion proteinsCell surface delivery of the measles virus nucleoprotein: a viral strategy to induce immunosuppression.Refined methods for propagating vesicular stomatitis virus vectors that are defective for G protein expression.Identification of the respiratory syncytial virus proteins required for formation and passage of helper-dependent infectious particles.Chimeric bovine respiratory syncytial virus with glycoprotein gene substitutions from human respiratory syncytial virus (HRSV): effects on host range and evaluation as a live-attenuated HRSV vaccineMeasles virus structural components are enriched into lipid raft microdomains: a potential cellular location for virus assembly.Pseudotyping of glycoprotein D-deficient herpes simplex virus type 1 with vesicular stomatitis virus glycoprotein G enables mutant virus attachment and entry.Observation of measles virus cell-to-cell spread in astrocytoma cells by using a green fluorescent protein-expressing recombinant virus.Comparison of predicted amino acid sequences of measles virus strains in the Edmonston vaccine lineage.DC-SIGN mediated sphingomyelinase-activation and ceramide generation is essential for enhancement of viral uptake in dendritic cellsRecombinant Newcastle disease virus as a vaccine vectorMeasles viruses with altered envelope protein cytoplasmic tails gain cell fusion competence.Paramyxovirus glycoprotein incorporation, assembly and budding: a three way dance for infectious particle production.Infectivity of a human respiratory syncytial virus lacking the SH, G, and F proteins is efficiently mediated by the vesicular stomatitis virus G protein.Measles virus matrix protein specifies apical virus release and glycoprotein sorting in epithelial cells.Recombinant lymphocytic choriomeningitis virus expressing vesicular stomatitis virus glycoprotein.Matrix protein-specific IgA antibody inhibits measles virus replication by intracellular neutralization.Electron cryotomography of measles virus reveals how matrix protein coats the ribonucleocapsid within intact virions.Broadly neutralizing immune responses against hepatitis C virus induced by vectored measles viruses and a recombinant envelope protein boosterA molecularly cloned Schwarz strain of measles virus vaccine induces strong immune responses in macaques and transgenic mice.Attenuated measles virus as a vaccine vector.Contribution of matrix, fusion, hemagglutinin, and large protein genes of the CAM-70 measles virus vaccine strain to efficient growth in chicken embryonic fibroblasts.Sequence and immunogenicity of a clinically approved novel measles virus vaccine vector.Applications and challenges of multivalent recombinant vaccines.Dimerization Efficiency of Canine Distemper Virus Matrix Protein Regulates Membrane-Budding Activity.F-actin modulates measles virus cell-cell fusion and assembly by altering the interaction between the matrix protein and the cytoplasmic tail of hemagglutinin.Measles virus assembly within membrane rafts.Recombinant rinderpest vaccines expressing membrane-anchored proteins as genetic markers: evidence of exclusion of marker protein from the virus envelope.Recovery and characterization of a chimeric rinderpest virus with the glycoproteins of peste-des-petits-ruminants virus: homologous F and H proteins are required for virus viability.Strength of envelope protein interaction modulates cytopathicity of measles virus.Restriction of measles virus RNA synthesis by a mouse host cell line: trans-complementation by polymerase components or a human cellular factor(s)Importance of the cytoplasmic tails of the measles virus glycoproteins for fusogenic activity and the generation of recombinant measles viruses.The matrix protein of measles virus regulates viral RNA synthesis and assembly by interacting with the nucleocapsid protein.Glycoprotein interactions in paramyxovirus fusion.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Chimeric measles viruses with a foreign envelope
@ast
Chimeric measles viruses with a foreign envelope
@en
Chimeric measles viruses with a foreign envelope
@nl
type
label
Chimeric measles viruses with a foreign envelope
@ast
Chimeric measles viruses with a foreign envelope
@en
Chimeric measles viruses with a foreign envelope
@nl
prefLabel
Chimeric measles viruses with a foreign envelope
@ast
Chimeric measles viruses with a foreign envelope
@en
Chimeric measles viruses with a foreign envelope
@nl
P2093
P2860
P1433
P1476
Chimeric measles viruses with a foreign envelope
@en
P2093
G Christiansen
M A Billeter
P Spielhofer
R Cattaneo
P2860
P304
P577
1998-03-01T00:00:00Z