Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
about
Jumping species-a mechanism for coronavirus persistence and survival.MERS-CoV spike protein: a key target for antivirals.Pre-fusion structure of a human coronavirus spike protein.Characterization of Chinese Porcine Epidemic Diarrhea Virus with Novel Insertions and Deletions in Genome.Receptor-binding domain of MERS-CoV with optimal immunogen dosage and immunization interval protects human transgenic mice from MERS-CoV infection.Structure, Function, and Evolution of Coronavirus Spike Proteins.Receptor usage and cell entry of porcine epidemic diarrhea coronavirusIdentification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1.Two Mutations Were Critical for Bat-to-Human Transmission of Middle East Respiratory Syndrome CoronavirusIdentification and Comparison of Receptor Binding Characteristics of the Spike Protein of Two Porcine Epidemic Diarrhea Virus Strains.Introduction of neutralizing immunogenicity index to the rational design of MERS coronavirus subunit vaccines.Detection and phylogenetic analysis of porcine epidemic diarrhea virus in central China based on the ORF3 gene and the S1 gene.Recombinant Receptor-Binding Domains of Multiple Middle East Respiratory Syndrome Coronaviruses (MERS-CoVs) Induce Cross-Neutralizing Antibodies against Divergent Human and Camel MERS-CoVs and Antibody Escape Mutants.Cell Entry of Porcine Epidemic Diarrhea Coronavirus Is Activated by Lysosomal Proteases.Carcinoembryonic Antigen-Related Cell Adhesion Molecule 5 Is an Important Surface Attachment Factor That Facilitates Entry of Middle East Respiratory Syndrome CoronavirusVaccines for the prevention against the threat of MERS-CoV.Comparison of lentiviruses pseudotyped with S proteins from coronaviruses and cell tropisms of porcine coronaviruses.Middle East respiratory syndrome: current status and future prospects for vaccine development.Coexistence of multiple genotypes of porcine epidemic diarrhea virus with novel mutant S genes in the Hubei Province of China in 2016.Crystal structure of the receptor binding domain of the spike glycoprotein of human betacoronavirus HKU1.Interpatient mutational spectrum of human coronavirus-OC43 revealed by illumina sequencing.Structural and Molecular Evidence Suggesting Coronavirus-driven Evolution of Mouse Receptor.Cryo-electron microscopy structures of the SARS-CoV spike glycoprotein reveal a prerequisite conformational state for receptor binding.A recombinant receptor-binding domain of MERS-CoV in trimeric form protects human dipeptidyl peptidase 4 (hDPP4) transgenic mice from MERS-CoV infection.The evidence of porcine hemagglutinating encephalomyelitis virus induced nonsuppurative encephalitis as the cause of death in pigletsThe bulky and the sweet: How neutralizing antibodies and glycan receptors compete for virus binding.Porcine hemagglutinating encephalomyelitis virus enters Neuro-2a cells via clathrin-mediated endocytosis in a Rab5-, cholesterol-, and pH-dependent manner.Cryo-EM structure of porcine delta coronavirus spike protein in the pre-fusion state.Molecular characterization of the spike gene of the porcine epidemic diarrhea virus in Mexico, 2013-2016.Oral recombinant Lactobacillus vaccine targeting the intestinal microfold cells and dendritic cells for delivering the core neutralizing epitope of porcine epidemic diarrhea virus.Engineering a stable CHO cell line for the expression of a MERS-coronavirus vaccine antigen.Cryo-EM structure of infectious bronchitis coronavirus spike protein reveals structural and functional evolution of coronavirus spike proteins.Tetraspanin Assemblies in Virus Infection.Characterization of peritoneal cells from cats with experimentally-induced feline infectious peritonitis (FIP) using RNA-seqA planarian nidovirus expands the limits of RNA genome sizeA Novel Nanobody Targeting Middle East Respiratory Syndrome Coronavirus (MERS-CoV) Receptor-Binding Domain Has Potent Cross-Neutralizing Activity and Protective Efficacy against MERS-CoV
P2860
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P2860
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
description
2014 nî lūn-bûn
@nan
2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@ast
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@en
type
label
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@ast
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@en
prefLabel
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@ast
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@en
P2860
P356
P1433
P1476
Receptor recognition mechanisms of coronaviruses: a decade of structural studies.
@en
P2093
P2860
P304
P356
10.1128/JVI.02615-14
P407
P577
2014-11-26T00:00:00Z