about
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMCAcquisition of macrophage tropism during the pathogenesis of feline infectious peritonitis is determined by mutations in the feline coronavirus spike proteinCD200 receptor controls sex-specific TLR7 responses to viral infectionCellular entry of the porcine epidemic diarrhea virusCryo-electron microscopy structure of a coronavirus spike glycoprotein trimerThe Coronavirus Spike Protein Is a Class I Virus Fusion Protein: Structural and Functional Characterization of the Fusion Core ComplexRole of Endocytosis and Low pH in Murine Hepatitis Virus Strain A59 Cell EntryMouse Hepatitis Coronavirus RNA Replication Depends on GBF1-Mediated ARF1 ActivationTopology and Membrane Anchoring of the Coronavirus Replication Complex: Not All Hydrophobic Domains of nsp3 and nsp6 Are Membrane SpanningDynamics of coronavirus replication-transcription complexes.Dissection of the influenza A virus endocytic routes reveals macropinocytosis as an alternative entry pathwayA single immunization with soluble recombinant trimeric hemagglutinin protects chickens against highly pathogenic avian influenza virus H5N1Evolution of the hemagglutinin protein of the new pandemic H1N1 influenza virus: maintaining optimal receptor binding by compensatory substitutions.Recombinant soluble, multimeric HA and NA exhibit distinctive types of protection against pandemic swine-origin 2009 A(H1N1) influenza virus infection in ferretsCrucial steps in the structure determination of a coronavirus spike glycoprotein using cryo-electron microscopy.Only two residues are responsible for the dramatic difference in receptor binding between swine and new pandemic H1 hemagglutinin.Protective efficacy of Newcastle disease virus expressing soluble trimeric hemagglutinin against highly pathogenic H5N1 influenza in chickens and mice.Cryo-electron tomography of mouse hepatitis virus: Insights into the structure of the coronavirion.The coronavirus nucleocapsid protein is dynamically associated with the replication-transcription complexes.Mobility and interactions of coronavirus nonstructural protein 4.Improved microarray gene expression profiling of virus-infected cells after removal of viral RNAType I interferon receptor-independent and -dependent host transcriptional responses to mouse hepatitis coronavirus infection in vivoDissecting virus entry: replication-independent analysis of virus binding, internalization, and penetration using minimal complementation of β-galactosidaseInhibition of the ubiquitin-proteasome system affects influenza A virus infection at a postfusion step.Pathogenic characteristics of persistent feline enteric coronavirus infection in cats.Single-cell analysis of population context advances RNAi screening at multiple levels.Anguillid herpesvirus 1 transcriptome.Coronaviruses maintain viability despite dramatic rearrangements of the strictly conserved genome organizationSevere acute respiratory syndrome coronavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides.Competition between influenza A virus genome segmentsGenome-wide gene expression analysis of anguillid herpesvirus 1.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.Switching species tropism: an effective way to manipulate the feline coronavirus genome.Manipulation of the porcine epidemic diarrhea virus genome using targeted RNA recombination.A protective and safe intranasal RSV vaccine based on a recombinant prefusion-like form of the F protein bound to bacterium-like particles.Coronavirus cell entry occurs through the endo-/lysosomal pathway in a proteolysis-dependent manner.Identification and localization of the structural proteins of anguillid herpesvirus 1.Rapid Emergence of Highly Pathogenic Avian Influenza Subtypes from a Subtype H5N1 Hemagglutinin Variant.A field-proven yeast two-hybrid protocol used to identify coronavirus-host protein-protein interactions.Recombinant Soluble Respiratory Syncytial Virus F Protein That Lacks Heptad Repeat B, Contains a GCN4 Trimerization Motif and Is Not Cleaved Displays Prefusion-Like Characteristics.
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description
emeritus hoogleraar virologie
@nl
researcher (ORCID 0000-0001-5373-732X)
@en
name
Peter J M Rottier
@en
Peter Rottier
@nl
type
label
Peter J M Rottier
@en
Peter Rottier
@nl
altLabel
P.J.M. (Peter) Rottier
@nl
P.J.M. Rottier
@nl
Peter J.M. Rottier
@nl
prefLabel
Peter J M Rottier
@en
Peter Rottier
@nl
P106
P21
P213
0000 0000 2965 4607
P31
P496
0000-0001-5373-732X
P569
1947-01-01T00:00:00Z
P7449
PRS1238373