Ganglioside-linked terminal sialic acid moieties on murine macrophages function as attachment receptors for murine noroviruses. - Wikidata - awgldk - TriplyDB

Ganglioside-linked terminal sialic acid moieties on murine macrophages function as attachment receptors for murine noroviruses.

Ganglioside-linked terminal sialic acid moieties on murine macrophages function as attachment receptors for murine noroviruses.

http://www.wikidata.org/entity/Q39879555

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The G428A nonsense mutation in FUT2 provides strong but not absolute protection against symptomatic GII.4 Norovirus infection Viruses and sialic acids: rules of engagement Critical review of norovirus surrogates in food safety research: rationale for considering volunteer studies Experimental inoculation of juvenile rhesus macaques with primate enteric caliciviruses High-Resolution X-Ray Structure and Functional Analysis of the Murine Norovirus 1 Capsid Protein Protruding Domain Glycosphingolipid-Protein Interaction in Signal Transduction Norovirus immunology: Of mice and mechanisms Pathogenesis of noroviruses, emerging RNA viruses Antiviral activity of a small molecule deubiquitinase inhibitor occurs via induction of the unfolded protein response Both α2,3- and α2,6-linked sialic acids on O-linked glycoproteins act as functional receptors for porcine Sapovirus Functional receptor molecules CD300lf and CD300ld within the CD300 family enable murine noroviruses to infect cells Rabbit haemorrhagic disease (RHD) and rabbit haemorrhagic disease virus (RHDV): a review Norovirus Regulation by Host and Microbe.Norovirus drug candidates that inhibit viral capsid attachment to human histo-blood group antigens.Antibodies against Lewis antigens inhibit the binding of human norovirus GII.4 virus-like particles to saliva but not to intestinal Caco-2 cells Norovirus gastroenteritis, carbohydrate receptors, and animal models.Efficient norovirus and reovirus replication in the mouse intestine requires microfold (M) cells.Inactivation of the Tulane virus, a novel surrogate for the human norovirus Murine norovirus: propagation, quantification, and genetic manipulation Viral plaque analysis on a wide field-of-view, time-lapse, on-chip imaging platform Norwalk virus does not replicate in human macrophages or dendritic cells derived from the peripheral blood of susceptible humans.Gangliosides are ligands for human noroviruses.Susceptibility to winter vomiting disease: a sweet matter.Genogroup IV and VI canine noroviruses interact with histo-blood group antigens.LT-IIc, a new member of the type II heat-labile enterotoxin family encoded by an Escherichia coli strain obtained from a nonmammalian host.High-resolution functional profiling of the norovirus genome Evaluation of the porcine gastric mucin binding assay for high-pressure-inactivation studies using murine norovirus and tulane virus Qualitative and quantitative analysis of the binding of GII.4 norovirus variants onto human blood group antigens.Norovirus-host interaction: multi-selections by human histo-blood group antigens.Transient or persistent norovirus infection does not alter the pathology of Salmonella typhimurium induced intestinal inflammation and fibrosis in mice A working model of how noroviruses infect the intestine Tulane virus recognizes sialic acids as cellular receptors.Protruding domain of capsid protein is necessary and sufficient to determine murine norovirus replication and pathogenesis in vivo Isolation and Analysis of Rare Norovirus Recombinants from Coinfected Mice Using Drop-Based Microfluidics Interactions between Human Norovirus Surrogates and Acanthamoeba spp.Murine noroviruses bind glycolipid and glycoprotein attachment receptors in a strain-dependent manner.Spike protein VP8* of human rotavirus recognizes histo-blood group antigens in a type-specific manner.Internalization and dissemination of human norovirus and animal caliciviruses in hydroponically grown romaine lettuce.Rotavirus VP8*: phylogeny, host range, and interaction with histo-blood group antigens Norovirus vaccines and potential antinorovirus drugs: recent advances and future perspectives

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Ganglioside-linked terminal sialic acid moieties on murine macrophages function as attachment receptors for murine noroviruses.

http://www.wikidata.org/entity/Q39879555

description

2009 nî lūn-bûn

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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2009年學術文章

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name

Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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type

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Ganglioside-linked terminal si ...... eptors for murine noroviruses.

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Chang Hoon Lee

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Heather Auble

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Hesham F Nawar

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James A Shayman

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Kristen Yetming

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Liming Shu

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Sagar P Patel

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Terry D Connell

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P2860

How Viruses Enter Animal Cells

Replication of Norovirus in cell culture reveals a tropism for dendritic cells and macrophages

Human caliciviruses and pediatric gastroenteritis

Molecular and epidemiologic trends of caliciviruses associated with outbreaks of acute gastroenteritis in the United States, 2000-2004

Food-related illness and death in the United States

Avian flu: influenza virus receptors in the human airway

Sialic acid is a cellular receptor for coxsackievirus A24 variant, an emerging virus with pandemic potential.

Junctional adhesion molecule 1 is a functional receptor for feline calicivirus.

Norovirus and its histo-blood group antigen receptors: an answer to a historical puzzle.

Mucosal adjuvant properties of mutant LT-IIa and LT-IIb enterotoxins that exhibit altered ganglioside-binding activities.

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4092-4101

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10.1128/JVI.02245-08

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9

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83

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Christiane Wobus

Jeffrey W Perry

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24041602

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2668497

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