Identification of a receptor-binding domain of the spike glycoprotein of human coronavirus HCoV-229E.
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Genetic characterization of Betacoronavirus lineage C viruses in bats reveals marked sequence divergence in the spike protein of pipistrellus bat coronavirus HKU5 in Japanese pipistrelle: implications for the origin of the novel Middle East respiratCurrent advancements and potential strategies in the development of MERS-CoV vaccinesStructural Bases of Coronavirus Attachment to Host Aminopeptidase N and Its Inhibition by Neutralizing AntibodiesA 193-amino acid fragment of the SARS coronavirus S protein efficiently binds angiotensin-converting enzyme 2Immune responses against severe acute respiratory syndrome coronavirus induced by virus-like particles in mice.Molecular and biological characterization of human monoclonal antibodies binding to the spike and nucleocapsid proteins of severe acute respiratory syndrome coronavirus.Detection of alpha- and betacoronaviruses in rodents from Yunnan, ChinaA conformation-dependent neutralizing monoclonal antibody specifically targeting receptor-binding domain in Middle East respiratory syndrome coronavirus spike protein.Development of a transgenic mouse model susceptible to human coronavirus 229E.The spike protein of SARS-CoV--a target for vaccine and therapeutic development.Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus.Severe acute respiratory syndrome coronavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides.An exposed domain in the severe acute respiratory syndrome coronavirus spike protein induces neutralizing antibodies.The receptor binding domain of the new Middle East respiratory syndrome coronavirus maps to a 231-residue region in the spike protein that efficiently elicits neutralizing antibodies.Human coronavirus 229E: receptor binding domain and neutralization by soluble receptor at 37 degrees C.Reconstitution of the receptor-binding motif of the SARS coronavirus.Identification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1.Animal origins of the severe acute respiratory syndrome coronavirus: insight from ACE2-S-protein interactions.Peptide mimicrying between SARS coronavirus spike protein and human proteins reacts with SARS patient serum.Receptor-binding domains of spike proteins of emerging or re-emerging viruses as targets for development of antiviral vaccines.Entry from the cell surface of severe acute respiratory syndrome coronavirus with cleaved S protein as revealed by pseudotype virus bearing cleaved S protein.Protease-mediated entry via the endosome of human coronavirus 229E.Link of a ubiquitous human coronavirus to dromedary camels.Proteolytic activation of the spike protein at a novel RRRR/S motif is implicated in furin-dependent entry, syncytium formation, and infectivity of coronavirus infectious bronchitis virus in cultured cellsAmino acids 270 to 510 of the severe acute respiratory syndrome coronavirus spike protein are required for interaction with receptor.Recombination, reservoirs, and the modular spike: mechanisms of coronavirus cross-species transmissionVaccines for the prevention against the threat of MERS-CoV.Prediction and In Silico Identification of Novel B-Cells and T-Cells Epitopes in the S1-Spike Glycoprotein of M41 and CR88 (793/B) Infectious Bronchitis Virus Serotypes for Application in Peptide VaccinesTMPRSS2 activates the human coronavirus 229E for cathepsin-independent host cell entry and is expressed in viral target cells in the respiratory epithelium.Cooperative involvement of the S1 and S2 subunits of the murine coronavirus spike protein in receptor binding and extended host range.Murine coronavirus with an extended host range uses heparan sulfate as an entry receptor.Single-dose treatment with a humanized neutralizing antibody affords full protection of a human transgenic mouse model from lethal Middle East respiratory syndrome (MERS)-coronavirus infectionThe S proteins of human coronavirus NL63 and severe acute respiratory syndrome coronavirus bind overlapping regions of ACE2.Crystal structure of the receptor binding domain of the spike glycoprotein of human betacoronavirus HKU1.Highly conserved regions within the spike proteins of human coronaviruses 229E and NL63 determine recognition of their respective cellular receptors.SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells.Mosaic evolution of the severe acute respiratory syndrome coronavirus.Coronavirus spike glycoprotein, extended at the carboxy terminus with green fluorescent protein, is assembly competent.Luxury at a cost? Recombinant mouse hepatitis viruses expressing the accessory hemagglutinin esterase protein display reduced fitness in vitro.Identification and characterization of a Penaeus monodon lymphoid cell-expressed receptor for the yellow head virus.
P2860
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P2860
Identification of a receptor-binding domain of the spike glycoprotein of human coronavirus HCoV-229E.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@en
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@nl
type
label
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@en
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@nl
prefLabel
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@en
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@nl
P2093
P2860
P1433
P1476
Identification of a receptor-b ...... f human coronavirus HCoV-229E.
@en
P2093
Aurelio Bonavia
Bruce D Zelus
Pierre J Talbot
P2860
P304
P356
10.1128/JVI.77.4.2530-2538.2003
P407
P577
2003-02-01T00:00:00Z