Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

N-terminal VP1 Truncations Favor T = 1 Norovirus-Like Particles

24 Dec 2020

Abstract excerpt

Noroviruses cause immense sporadic gastroenteritis outbreaks worldwide. Emerging genotypes, which are divided based on the sequence of the major capsid protein VP1, further enhance this public threat. Self-assembling properties of the human norovirus major capsid protein VP1 are crucial for using virus-like particles (VLPs) for vaccine development. However, there is no vaccine available yet. Here, VLPs from...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Animal Virus Infections Studies
Share to Viral gastroenteritis research and epidemiology
Share to Virus-based gene therapy research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33374273
DOI: 10.3390/vaccines9010008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

N-terminal VP1 Truncations Favor T = 1 Norovirus-Like ParticlesPMID 33374273Read ↗

N-terminal VP1 truncations favor <i>T</i> =1 norovirus-like particlesSemantic proximity Read ↗

Structural heterogeneity of a human norovirus vaccine candidateSemantic proximity Read ↗

Norovirus assembly and stability.Semantic proximity Read ↗

Novel Structural Features of Human Norovirus CapsidSemantic proximity Read ↗

Noroviruses—The State of the Art, Nearly Fifty Years after Their Initial DiscoverySemantic proximity Read ↗

Virus‐like particles as powerful vaccination strategy against human virusesSemantic proximity Read ↗

Virus-like particles: flexible platforms for vaccine developmentSemantic proximity Read ↗

Advances and challenges in enveloped virus-like particle (VLP)-based vaccinesSemantic proximity Read ↗

Human Norovirus Detection and Production, Quantification, and Storage of Virus‐Like ParticlesSemantic proximity Read ↗

Platforms, advances, and technical challenges in virus-like particles-based vaccinesSemantic proximity Read ↗

Nanobody Binding to a Conserved Epitope Promotes Norovirus Particle DisassemblySemantic proximity Read ↗

Heterologous Expression of Human Norovirus GII.4 VP1 Leads to Assembly of T=4 Virus-Like ParticlesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.