Identification of spike protein residues of murine coronavirus responsible for receptor-binding activity by use of soluble receptor-resistant mutants.
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The soluble form of the EIAV receptor encoded by an alternative splicing variant inhibits EIAV infection of target cellsConformational Changes in the Capsid of a Calicivirus upon Interaction with Its Functional ReceptorA single amino acid change within antigenic domain II of the spike protein of bovine coronavirus confers resistance to virus neutralizationCharacterization of murine coronavirus neutralization epitopes with phage-displayed peptidesProduction and characterization of a soluble, active form of Tva, the subgroup A avian sarcoma and leukosis virus receptorReceptor-independent spread of a highly neurotropic murine coronavirus JHMV strain from initially infected microglial cells in mixed neural culturesPurified, soluble recombinant mouse hepatitis virus receptor, Bgp1(b), and Bgp2 murine coronavirus receptors differ in mouse hepatitis virus binding and neutralizing activitiesIdentification of key residues in subgroup A avian leukosis virus envelope determining receptor binding affinity and infectivity of cells expressing chicken or quail Tva receptor.Pathogenesis of murine coronavirus in the central nervous system.Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus.Monoclonal antibodies targeting the HR2 domain and the region immediately upstream of the HR2 of the S protein neutralize in vitro infection of severe acute respiratory syndrome coronavirus.Soluble receptor potentiates receptor-independent infection by murine coronavirus.Receptor-induced conformational changes of murine coronavirus spike protein.Molecular epidemiology of bovine coronavirus on the basis of comparative analyses of the S geneN-terminal domain of the murine coronavirus receptor CEACAM1 is responsible for fusogenic activation and conformational changes of the spike proteinReceptor-independent infection of murine coronavirus: analysis by spinoculationAmino acid substitutions in the S2 subunit of mouse hepatitis virus variant V51 encode determinants of host range expansionProtease-mediated entry via the endosome of human coronavirus 229E.Proteolytic processing of Middle East respiratory syndrome coronavirus spikes expands virus tropismThe N-terminal domain of the murine coronavirus spike glycoprotein determines the CEACAM1 receptor specificity of the virus strain.Cooperative involvement of the S1 and S2 subunits of the murine coronavirus spike protein in receptor binding and extended host range.Mutations conferring resistance to neutralization by a soluble form of the neurotrophin receptor (p75NTR) map outside of the known antigenic sites of the rabies virus glycoprotein.Pathogenesis of neurotropic murine coronavirus is multifactorial.
P2860
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P2860
Identification of spike protein residues of murine coronavirus responsible for receptor-binding activity by use of soluble receptor-resistant mutants.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Identification of spike protei ...... le receptor-resistant mutants.
@ast
Identification of spike protei ...... le receptor-resistant mutants.
@en
type
label
Identification of spike protei ...... le receptor-resistant mutants.
@ast
Identification of spike protei ...... le receptor-resistant mutants.
@en
prefLabel
Identification of spike protei ...... le receptor-resistant mutants.
@ast
Identification of spike protei ...... le receptor-resistant mutants.
@en
P2093
P2860
P1433
P1476
Identification of spike protei ...... ble receptor-resistant mutants
@en
P2093
P2860
P304
P407
P577
1997-12-01T00:00:00Z