scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Anastasia N Vlasova | |
Joshua Oluoch Amimo | |||
Juliet Chepngeno | |||
Linda Saif | |||
Yusheng Guo | |||
Alfred Omwando Mainga | |||
Sergei Alekseevich Raev | |||
P2860 | cites work | Rotavirus NSP1 inhibits NFkappaB activation by inducing proteasome-dependent degradation of beta-TrCP: a novel mechanism of IFN antagonism | Q21090517 |
Rotavirus nonstructural protein 1 antagonizes innate immune response by interacting with retinoic acid inducible gene I | Q24299094 | ||
Rotavirus NSP1 inhibits interferon induced non-canonical NFκB activation by interacting with TNF receptor associated factor 2 | Q24311932 | ||
RIG-I/MDA5/MAVS are required to signal a protective IFN response in rotavirus-infected intestinal epithelium | Q24321688 | ||
Rotavirus-encoded nonstructural protein 1 modulates cellular apoptotic machinery by targeting tumor suppressor protein p53 | Q24338301 | ||
MAVS protein is attenuated by rotavirus nonstructural protein 1 | Q24339399 | ||
Mucosal glycan foraging enhances fitness and transmission of a saccharolytic human gut bacterial symbiont | Q24569815 | ||
Rotavirus vaccine protection in low-income and middle-income countries | Q92615051 | ||
Unraveling the role of the secretor antigen in human rotavirus attachment to histo-blood group antigens | Q92937009 | ||
Rotavirus infection induces glycan availability to promote ileum-specific changes in the microbiome aiding rotavirus virulence | Q94667937 | ||
Mechanism and Complex Roles of HSC70 in Viral Infections | Q98735093 | ||
Rotavirus induces intercellular calcium waves through ADP signaling | Q102210267 | ||
Functional refolding of the penetration protein on a non-enveloped virus | Q112581438 | ||
A Continuous Battle for Host-Derived Glycans Between a Mucus Specialist and a Glycan Generalist in vitro and in vivo | Q112581960 | ||
Rotavirus NSP1 Inhibits Type I and Type III Interferon Induction | Q114371217 | ||
Infection of porcine small intestinal enteroids with human and pig rotavirus A strains reveals contrasting roles for histo-blood group antigens and terminal sialic acids | Q114457725 | ||
A novel mechanism of rotavirus infection involving purinergic signaling | Q114457726 | ||
Human group A rotavirus P[25] VP8* specifically binds to A-type histo-blood group antigen | Q114457727 | ||
Decreased rotavirus infection of MA104 cells via probiotic extract binding to Hsc70 and ß3 integrin receptors | Q114457728 | ||
Intestinal Microbiota-A Promising Target for Antiviral Therapy? | Q114457729 | ||
Group C rotavirus requires sialic acid for erythrocyte and cell receptor binding | Q24630296 | ||
Hsp70 chaperones: cellular functions and molecular mechanism | Q24644472 | ||
Comparative genomic analysis of Lactobacillus rhamnosus GG reveals pili containing a human- mucus binding protein | Q24652294 | ||
Rotavirus NSP1 inhibits expression of type I interferon by antagonizing the function of interferon regulatory factors IRF3, IRF5, and IRF7 | Q24683021 | ||
Interferon-λ: Immune Functions at Barrier Surfaces and Beyond | Q26801049 | ||
Rotavirus entry: a deep journey into the cell with several exits | Q26995498 | ||
The battle between rotavirus and its host for control of the interferon signaling pathway | Q27006920 | ||
Interferon-λ in the context of viral infections: production, response and therapeutic implications | Q27013848 | ||
Rotavirus non-structural proteins: structure and function | Q27027535 | ||
Structural basis of glycan interaction in gastroenteric viral pathogens | Q27030776 | ||
Leukocyte-derived IFN-α/β and epithelial IFN-λ constitute a compartmentalized mucosal defense system that restricts enteric virus infections | Q27320523 | ||
Human Intestinal Enteroids: a New Model To Study Human Rotavirus Infection, Host Restriction, and Pathophysiology | Q27321169 | ||
Infectious rotavirus enters cells by direct cell membrane penetration, not by endocytosis | Q27486809 | ||
The rhesus rotavirus VP4 sialic acid binding domain has a galectin fold with a novel carbohydrate binding site | Q27638080 | ||
Structure of Rotavirus Outer-Layer Protein VP7 Bound with a Neutralizing Fab | Q27655896 | ||
Cell attachment protein VP8* of a human rotavirus specifically interacts with A-type histo-blood group antigen | Q27678512 | ||
Inhibition of IRF3-dependent antiviral responses by cellular and viral proteins | Q27865225 | ||
The Rotavirus Interferon Antagonist NSP1: Many Targets, Many Questions | Q28067379 | ||
The human HSP70 family of chaperones: where do we stand? | Q28071416 | ||
IFN-λ: A New Inducer of Local Immunity against Cancer and Infections | Q28072995 | ||
Immunoregulatory Effects Triggered by Lactic Acid Bacteria Exopolysaccharides: New Insights into Molecular Interactions with Host Cells | Q28078715 | ||
Toll-like receptor signaling and IRF transcription factors | Q28244355 | ||
IFN-lambda determines the intestinal epithelial antiviral host defense | Q28508039 | ||
Comparative Proteomics Reveals Strain-Specific β-TrCP Degradation via Rotavirus NSP1 Hijacking a Host Cullin-3-Rbx1 Complex | Q28554481 | ||
Glycan Specificity of P[19] Rotavirus and Comparison with Those of Related P Genotypes | Q28821791 | ||
Interferons and viruses: an interplay between induction, signalling, antiviral responses and virus countermeasures | Q29615028 | ||
Histo-blood group antigens as receptors for rotavirus, new understanding on rotavirus epidemiology and vaccine strategy | Q30234848 | ||
Interferon induction and function at the mucosal surface | Q30661545 | ||
Mucin-type O-glycosylation--putting the pieces together. | Q30887465 | ||
Rotavirus infection of MA104 cells is inhibited by Ricinus lectin and separately expressed single binding domains. | Q30936657 | ||
Nlrp9b inflammasome restricts rotavirus infection in intestinal epithelial cells | Q33289420 | ||
Glycosphingolipid binding specificities of rotavirus: identification of a sialic acid-binding epitope | Q39605646 | ||
Epidemiology and genetic diversity of group A rotavirus in acute diarrhea patients in pre-vaccination era in southwest China | Q39626814 | ||
IRF3 inhibition by rotavirus NSP1 is host cell and virus strain dependent but independent of NSP1 proteasomal degradation. | Q39816481 | ||
Binding to sialic acids is not an essential step for the entry of animal rotaviruses to epithelial cells in culture. | Q40046877 | ||
Rotavirus Vaccine Response Correlates with the Infant Gut Microbiota Composition in Pakistan | Q40048009 | ||
Amino acid domains 280-297 of VP6 and 531-554 of VP4 are implicated in heat shock cognate protein hsc70-mediated rotavirus infection | Q40079198 | ||
Exopolysaccharides from Lactobacillus delbrueckii OLL1073R-1 modulate innate antiviral immune response in porcine intestinal epithelial cells | Q40085754 | ||
Systematic Investigation of Multi-TLR Sensing Identifies Regulators of Sustained Gene Activation in Macrophages | Q40116872 | ||
Bifidobacterium adolescentis (DSM 20083) and Lactobacillus casei (Lafti L26-DSL): Probiotics Able to Block the In Vitro Adherence of Rotavirus in MA104 Cells. | Q40232116 | ||
Virus Entry and Release in Polarized Epithelial Cells | Q40431595 | ||
Rotavirus RRV associates with lipid membrane microdomains during cell entry | Q40562535 | ||
Integrin alpha2beta1 mediates the cell attachment of the rotavirus neuraminidase-resistant variant nar3. | Q40838251 | ||
Purified recombinant rotavirus VP7 forms soluble, calcium-dependent trimers | Q40842168 | ||
Entry of rotaviruses is a multistep process | Q40920498 | ||
Ganglioside GM(1a) on the cell surface is involved in the infection by human rotavirus KUN and MO strains | Q40926140 | ||
Productive penetration of rotavirus in cultured cells induces coentry of the translation inhibitor alpha-sarcin | Q41081503 | ||
Phosphatidylserine vesicles enable efficient en bloc transmission of enteroviruses. | Q41484820 | ||
Multiple beta 1 chain integrins are receptors for invasin, a protein that promotes bacterial penetration into mammalian cells | Q41511934 | ||
Revisiting the role of histo-blood group antigens in rotavirus host-cell invasion. | Q41564793 | ||
Sialic acid dependence in rotavirus host cell invasion | Q45112469 | ||
Characterization of homotypic and heterotypic VP7 neutralization sites of rhesus rotavirus | Q46141039 | ||
Influence of the intestinal microbiota on the immunogenicity of oral rotavirus vaccine given to infants in south India | Q46164556 | ||
Differences of Rotavirus Vaccine Effectiveness by Country: Likely Causes and Contributing Factors | Q46243057 | ||
Structural basis of glycan specificity of P[19] VP8*: Implications for rotavirus zoonosis and evolution. | Q47100074 | ||
Bacteria and bacterial envelope components enhance mammalian reovirus thermostability | Q47142697 | ||
The biology of mucus: Composition, synthesis and organization | Q47609256 | ||
Histoblood Group Antigen Phenotype Determines Susceptibility to Genotype-specific Rotavirus Infections and Impacts Measures of Rotavirus Vaccine Efficacy | Q47699205 | ||
TRAF molecules in cell signaling and in human diseases | Q36972287 | ||
The VP8* domain of neonatal rotavirus strain G10P[11] binds to type II precursor glycans | Q36978982 | ||
Rotavirus NSP1 Associates with Components of the Cullin RING Ligase Family of E3 Ubiquitin Ligases | Q37002502 | ||
Mechanisms of action of probiotics | Q37053062 | ||
Silencing the alarms: Innate immune antagonism by rotavirus NSP1 and VP3 | Q37083338 | ||
Homologous 2',5'-phosphodiesterases from disparate RNA viruses antagonize antiviral innate immunity | Q37088604 | ||
Toll-like receptor and innate cytokine responses induced by lactobacilli colonization and human rotavirus infection in gnotobiotic pigs. | Q37121858 | ||
Histo-blood group antigen-like substances of human enteric bacteria as specific adsorbents for human noroviruses. | Q37123423 | ||
Rotavirus NSP1 mediates degradation of interferon regulatory factors through targeting of the dimerization domain | Q37123575 | ||
Rotavirus antagonizes cellular antiviral responses by inhibiting the nuclear accumulation of STAT1, STAT2, and NF-kappaB. | Q37192229 | ||
Innate immune response to viral infection | Q37241258 | ||
Variation in antagonism of the interferon response to rotavirus NSP1 results in differential infectivity in mouse embryonic fibroblasts | Q37248029 | ||
Structure-based antigen design: a strategy for next generation vaccines | Q37314536 | ||
P[8] and P[4] Rotavirus Infection Associated with Secretor Phenotypes Among Children in South China | Q37314849 | ||
Viral evasion and subversion of pattern-recognition receptor signalling | Q37319381 | ||
VP7 mediates the interaction of rotaviruses with integrin alphavbeta3 through a novel integrin-binding site | Q37567855 | ||
Bacterial lipopolysaccharide binding enhances virion stability and promotes environmental fitness of an enteric virus | Q37576028 | ||
Cell-line-induced mutation of the rotavirus genome alters expression of an IRF3-interacting protein | Q37592530 | ||
Association between norovirus and rotavirus infection and histo-blood group antigen types in Vietnamese children | Q37713694 | ||
Relevance of secretor status genotype and microbiota composition in susceptibility to rotavirus and norovirus infections in humans | Q37728352 | ||
Mucus enhances gut homeostasis and oral tolerance by delivering immunoregulatory signals | Q37734574 | ||
Characterization of a porcine intestinal epithelial cell line for in vitro studies of microbial pathogenesis in swine | Q37863771 | ||
Innate cellular responses to rotavirus infection. | Q38088957 | ||
ABH and related histo-blood group antigens; immunochemical differences in carrier isotypes and their distribution | Q38197599 | ||
Structural diversity and specific distribution of O-glycans in normal human mucins along the intestinal tract | Q38336832 | ||
Guarding the frontiers: the biology of type III interferons | Q38550956 | ||
Rotavirus Controls Activation of the 2'-5'-Oligoadenylate Synthetase/RNase L Pathway Using at Least Two Distinct Mechanisms | Q38832952 | ||
Rotavirus Strategies Against the Innate Antiviral System | Q38916023 | ||
Mammalian Lipopolysaccharide Receptors Incorporated into the Retroviral Envelope Augment Virus Transmission. | Q39097992 | ||
Intestinal microbiota promote enteric virus replication and systemic pathogenesis | Q39306213 | ||
Roles of intestinal epithelial cells in the maintenance of gut homeostasis | Q39331432 | ||
Rotavirus capsid protein VP5* permeabilizes membranes. | Q39549991 | ||
Cellular entry of hantaviruses which cause hemorrhagic fever with renal syndrome is mediated by beta3 integrins. | Q39550459 | ||
Trypsin cleavage stabilizes the rotavirus VP4 spike | Q39603255 | ||
Differential Effects of Escherichia coli Nissle and Lactobacillus rhamnosus Strain GG on Human Rotavirus Binding, Infection, and B Cell Immunity | Q35901914 | ||
Spike protein VP8* of human rotavirus recognizes histo-blood group antigens in a type-specific manner | Q35943850 | ||
Immunobiotic Bifidobacteria Strains Modulate Rotavirus Immune Response in Porcine Intestinal Epitheliocytes via Pattern Recognition Receptor Signaling | Q35972991 | ||
Distinct Roles of Type I and Type III Interferons in Intestinal Immunity to Homologous and Heterologous Rotavirus Infections | Q36003428 | ||
Detailed O-glycomics of the Muc2 mucin from colon of wild-type, core 1- and core 3-transferase-deficient mice highlights differences compared with human MUC2. | Q36056064 | ||
Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus | Q36110059 | ||
Rotavirus immune responses and correlates of protection | Q36173819 | ||
Rotavirus VP8*: phylogeny, host range, and interaction with histo-blood group antigens | Q36246385 | ||
Both Lewis and secretor status mediate susceptibility to rotavirus infections in a rotavirus genotype-dependent manner | Q36293984 | ||
Host Genetic Susceptibility to Enteric Viruses: A Systematic Review and Metaanalysis | Q36373327 | ||
Role of sialic acids in rotavirus infection | Q36436772 | ||
Integrin-using rotaviruses bind alpha2beta1 integrin alpha2 I domain via VP4 DGE sequence and recognize alphaXbeta2 and alphaVbeta3 by using VP7 during cell entry | Q36464766 | ||
Innate immune response to homologous rotavirus infection in the small intestinal villous epithelium at single-cell resolution. | Q36483624 | ||
Murine rotavirus genes encoding outer capsid proteins VP4 and VP7 are not major determinants of host range restriction and virulence | Q36644973 | ||
Viral infection. Prevention and cure of rotavirus infection via TLR5/NLRC4-mediated production of IL-22 and IL-18 | Q36677605 | ||
The sweet spot: defining virus-sialic acid interactions | Q36685206 | ||
Rotavirus contains integrin ligand sequences and a disintegrin-like domain that are implicated in virus entry into cells. | Q36773071 | ||
A pathogenic picornavirus acquires an envelope by hijacking cellular membranes | Q36781367 | ||
Rotaviruses specifically bind to the neutral glycosphingolipid asialo-GM1. | Q36783978 | ||
Enterobacter cloacae inhibits human norovirus infectivity in gnotobiotic pigs. | Q36835594 | ||
Epidemiologic Association Between FUT2 Secretor Status and Severe Rotavirus Gastroenteritis in Children in the United States | Q36867575 | ||
IFN-lambda (IFN-lambda) is expressed in a tissue-dependent fashion and primarily acts on epithelial cells in vivo | Q33325913 | ||
The VP8 fragment of VP4 is the rhesus rotavirus hemagglutinin | Q33337017 | ||
Site directed processing: role of amino acid sequences and glycosylation of acceptor glycopeptides in the assembly of extended mucin type O-glycan core 2. | Q33467206 | ||
Comparative distribution of human and avian type sialic acid influenza receptors in the pig | Q33526849 | ||
Antigen structure and genetic basis of histo-blood groups A, B and O: their changes associated with human cancer | Q33783766 | ||
Integrins alpha2beta1 and alpha4beta1 can mediate SA11 rotavirus attachment and entry into cells | Q33794692 | ||
The VP5 domain of VP4 can mediate attachment of rotaviruses to cells | Q33795796 | ||
Rotavirus stimulates release of serotonin (5-HT) from human enterochromaffin cells and activates brain structures involved in nausea and vomiting | Q33967946 | ||
Extracellular proteins secreted by probiotic bacteria as mediators of effects that promote mucosa–bacteria interactions | Q34139719 | ||
Targeted mutation of the outer membrane protein P66 disrupts attachment of the Lyme disease agent, Borrelia burgdorferi , to integrin α v β 3 | Q34197056 | ||
Cytokine responses in gnotobiotic pigs after infection with virulent or attenuated human rotavirus. | Q34233101 | ||
VLA-2 (alpha2beta1) integrin promotes rotavirus entry into cells but is not necessary for rotavirus attachment | Q34329341 | ||
Interactions between rotavirus and gastrointestinal cells | Q34331554 | ||
Initial interaction of rotavirus strains with N-acetylneuraminic (sialic) acid residues on the cell surface correlates with VP4 genotype, not species of origin | Q34335469 | ||
Heat shock cognate protein 70 is involved in rotavirus cell entry | Q34335581 | ||
ABH and Lewis histo-blood group antigens, a model for the meaning of oligosaccharide diversity in the face of a changing world | Q34346443 | ||
Proteolytic enhancement of human rotavirus infectivity | Q34355532 | ||
Pathogenesis of rotavirus diarrhea | Q34439852 | ||
Helicobacter pylori adhesin binding fucosylated histo-blood group antigens revealed by retagging | Q34452414 | ||
Sialic acid glycoproteins inhibit in vitro and in vivo replication of rotaviruses | Q34555040 | ||
The interferons: 50 years after their discovery, there is much more to learn | Q34628245 | ||
To sialylate, or not to sialylate: that is the question | Q34712591 | ||
Diversity of interferon antagonist activities mediated by NSP1 proteins of different rotavirus strains | Q34742076 | ||
Entry of viruses through the epithelial barrier: pathogenic trickery | Q35038289 | ||
The early interferon response to rotavirus is regulated by PKR and depends on MAVS/IPS-1, RIG-I, MDA-5, and IRF3. | Q35076535 | ||
Cryoelectron microscopy structures of rotavirus NSP2-NSP5 and NSP2-RNA complexes: implications for genome replication. | Q35139285 | ||
Interaction of rotaviruses with Hsc70 during cell entry is mediated by VP5 | Q35149035 | ||
Convergence of the NF-kappaB and interferon signaling pathways in the regulation of antiviral defense and apoptosis | Q35700309 | ||
Virus entry: molecular mechanisms and biomedical applications | Q35712985 | ||
Binding Patterns of Rotavirus Genotypes P[4], P[6], and P[8] in China with Histo-Blood Group Antigens | Q35746089 | ||
Multistep entry of rotavirus into cells: a Versaillesque dance | Q35785633 | ||
Integrin alpha(v)beta(3) mediates rotavirus cell entry | Q35852198 | ||
Genetic mapping indicates that VP4 is the rotavirus cell attachment protein in vitro and in vivo | Q35853803 | ||
Trypsin activation pathway of rotavirus infectivity. | Q35867736 | ||
Human group C rotavirus VP8*s recognize type A histo-blood group antigens as ligands. | Q51782798 | ||
STAG2 deficiency induces interferon responses via cGAS-STING pathway and restricts virus infection. | Q52319679 | ||
Core 3-derived O-glycans are essential for intestinal mucus barrier function. | Q52603396 | ||
Glycan Binding Specificity and Mechanism of Human and Porcine P[6]/P[19] Rotavirus VP8*s. | Q54222566 | ||
Comparison of human, simian, and bovine rotaviruses for requirement of sialic acid in hemagglutination and cell adsorption. | Q54346185 | ||
Glycan recognition in globally dominant human rotaviruses. | Q55510040 | ||
Translational control of the innate immune response through IRF-7 | Q57203299 | ||
Four Modes of Adhesion are Used During Helicobacter pylori Binding to Human Mucins in the Oral and Gastric Niches | Q57282793 | ||
Hsc70 is a component of bacterially generated Actin-Rich Structures; an immunolocalization study | Q57470053 | ||
Lactic Acid Bacteria (LAB) Bind to Human B- or H-Antigens Expressed on Intestinal Mucosa | Q57709944 | ||
Glycan binding patterns of human rotavirus P[10] VP8* protein | Q57811802 | ||
Histo-blood group antigen-binding specificities of human rotaviruses are associated with gastroenteritis but not with in vitro infection | Q58699643 | ||
The Dual Nature of Type I and Type II Interferons | Q58750649 | ||
Rotavirus VP3 targets MAVS for degradation to inhibit type III interferon expression in intestinal epithelial cells | Q59350438 | ||
Type III Interferons in Viral Infection and Antiviral Immunity | Q59350891 | ||
Vesicle-Cloaked Virus Clusters Are Optimal Units for Inter-organismal Viral Transmission | Q59354859 | ||
Collective properties of viral infectivity | Q59356748 | ||
Nucleocapsid protein from porcine epidemic diarrhea virus isolates can antagonize interferon-λ production by blocking the nuclear factor-κB nuclear translocation | Q59357653 | ||
Histo-Blood Group Antigens in Children with Symptomatic Rotavirus Infection | Q63880512 | ||
Genetic Susceptibility to Human Norovirus Infection: An Update | Q64060326 | ||
Why viruses sometimes disperse in groups?†. | Q64956414 | ||
Characterization of binding of simian rotavirus SA-11 to cultured epithelial cells | Q69822321 | ||
Chinese adult rotavirus is a group B rotavirus | Q69872264 | ||
The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo | Q73727591 | ||
Growth of rotaviruses in continuous human and monkey cell lines that vary in their expression of integrins | Q74198319 | ||
Human and most animal rotavirus strains do not require the presence of sialic acid on the cell surface for efficient infectivity | Q77352836 | ||
Indigenous microbes and their soluble factors differentially modulate intestinal glycosylation steps in vivo. Use of a "lectin assay" to survey in vivo glycosylation changes | Q81210660 | ||
Homeostasis and function of goblet cells during rotavirus infection in mice | Q81729712 | ||
'Sialidase sensitivity' of rotaviruses revisited | Q83195414 | ||
Rotavirus receptor proteins Hsc70 and integrin αvβ3 are located in the lipid microdomains of animal intestinal cells | Q83614552 | ||
The Double Face of Mucin-Type O-Glycans in Lectin-Mediated Infection and Immunity | Q88643509 | ||
Reverse genetics reveals a role of the rotavirus VP3 phosphodiesterase activity in inhibiting RNase L signaling and contributing to intestinal viral replication in vivo | Q89685625 | ||
Genetic Manipulation of Human Intestinal Enteroids Demonstrates the Necessity of a Functional Fucosyltransferase 2 Gene for Secretor-Dependent Human Norovirus Infection | Q90406906 | ||
The Impact of Human Genetic Polymorphisms on Rotavirus Susceptibility, Epidemiology, and Vaccine Take | Q90462445 | ||
Segmented Filamentous Bacteria Prevent and Cure Rotavirus Infection | Q90677812 | ||
Mucin degradation niche as a driver of microbiome composition and Akkermansia muciniphila abundance in a dynamic gut model is donor independent | Q91618391 | ||
Investigation of a large waterborne acute gastroenteritis outbreak caused by group B rotavirus in Maharashtra state, India | Q91647824 | ||
Glycans in drug discovery | Q91791746 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Rotavirus | Q164778 |
viral entry into host cell | Q4118894 | ||
modulation by virus of host process | Q14818042 | ||
P304 | page(s) | 793841 | |
P577 | publication date | 2021-01-01 | |
P1433 | published in | Frontiers in Immunology | Q27723748 |
P1476 | title | Rotavirus Interactions With Host Intestinal Epithelial Cells | |
P478 | volume | 12 |