about
The parasitophorous vacuole membrane of Toxoplasma gondii is targeted for disruption by ubiquitin-like conjugation systems of autophagy.Unraveling a three-step spatiotemporal mechanism of triggering of receptor-induced Nipah virus fusion and cell entry.N-Glycans on the Nipah virus attachment glycoprotein modulate fusion and viral entry as they protect against antibody neutralizationIndividual N-glycans added at intervals along the stalk of the Nipah virus G protein prevent fusion but do not block the interaction with the homologous F protein.Viral Replication Complexes Are Targeted by LC3-Guided Interferon-Inducible GTPases.Quo vadis? Interferon-inducible GTPases go to their target membranes via the LC3-conjugation system of autophagy.Targeting by AutophaGy proteins (TAG): Targeting of IFNG-inducible GTPases to membranes by the LC3 conjugation system of autophagy.LC3s hire membrane breakers to attack viral shelters.Demarcation of Viral Shelters Results in Destruction by Membranolytic GTPases: Antiviral Function of Autophagy Proteins and Interferon-Inducible GTPases.Murine Norovirus Infection Induces T1 Inflammatory Responses to Dietary AntigensFlavivirus NS1 Triggers Tissue-Specific Vascular Endothelial Dysfunction Reflecting Disease TropismInsight Into the Interaction Between RNA Polymerase and VPg for Murine Norovirus Replication.Endocytosis of flavivirus NS1 is required for NS1-mediated endothelial hyperpermeability and is abolished by a single N-glycosylation site mutation
P50
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P50
description
researcher ORCID id 0000-0003-1991-629X
@en
wetenschapper
@nl
name
Scott B Biering
@ast
Scott B Biering
@en
Scott B Biering
@es
Scott B Biering
@nl
type
label
Scott B Biering
@ast
Scott B Biering
@en
Scott B Biering
@es
Scott B Biering
@nl
prefLabel
Scott B Biering
@ast
Scott B Biering
@en
Scott B Biering
@es
Scott B Biering
@nl
P106
P1153
57190299860
P31
P496
0000-0003-1991-629X