scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1146/ANNUREV-VIROLOGY-110615-042152 |
P698 | PubMed publication ID | 27482897 |
P50 | author | Susana López Charreton | Q4795076 |
P2093 | author name string | Carlos F Arias | |
Joaquin Moreno | |||
Liliana Sánchez-Tacuba | |||
P2860 | cites work | HIV-1 Vpu neutralizes the antiviral factor Tetherin/BST-2 by binding it and directing its beta-TrCP2-dependent degradation | Q21089617 |
Rotavirus NSP1 inhibits NFkappaB activation by inducing proteasome-dependent degradation of beta-TrCP: a novel mechanism of IFN antagonism | Q21090517 | ||
Role of the interleukin (IL)-28 receptor tyrosine residues for antiviral and antiproliferative activity of IL-29/interferon-lambda 1: similarities with type I interferon signaling | Q24294509 | ||
Rotavirus nonstructural protein 1 antagonizes innate immune response by interacting with retinoic acid inducible gene I | Q24299094 | ||
Recognition of eIF4G by rotavirus NSP3 reveals a basis for mRNA circularization | Q24300425 | ||
Rotavirus NSP1 inhibits interferon induced non-canonical NFκB activation by interacting with TNF receptor associated factor 2 | Q24311932 | ||
IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction | Q24318426 | ||
RIG-I/MDA5/MAVS are required to signal a protective IFN response in rotavirus-infected intestinal epithelium | Q24321688 | ||
IL-28, IL-29 and their class II cytokine receptor IL-28R | Q24323830 | ||
IFN-lambdas mediate antiviral protection through a distinct class II cytokine receptor complex | Q24336912 | ||
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 | ||
Efficient translation of rotavirus mRNA requires simultaneous interaction of NSP3 with the eukaryotic translation initiation factor eIF4G and the mRNA 3' end | Q24527184 | ||
Rotavirus RNA-binding protein NSP3 interacts with eIF4GI and evicts the poly(A) binding protein from eIF4F. | Q24533337 | ||
Rotavirus nonstructural protein 1 subverts innate immune response by inducing degradation of IFN regulatory factor 3 | Q24555785 | ||
Rotavirus Controls Activation of the 2'-5'-Oligoadenylate Synthetase/RNase L Pathway Using at Least Two Distinct Mechanisms | Q38832952 | ||
Rotavirus inhibits IFN-induced STAT nuclear translocation by a mechanism that acts after STAT binding to importin-α. | Q38996491 | ||
MyD88-mediated TLR signaling protects against acute rotavirus infection while inflammasome cytokines direct Ab response | Q39130586 | ||
Rotavirus infection is not associated with small intestinal fluid secretion in the adult mouse. | Q39305964 | ||
Viral determinants of rotavirus pathogenicity in pigs: evidence that the fourth gene of a porcine rotavirus confers diarrhea in the homologous host | Q39579948 | ||
Protein kinase R is responsible for the phosphorylation of eIF2alpha in rotavirus infection | Q39680140 | ||
Interferon regulatory factor 3 is a cellular partner of rotavirus NSP1. | Q39684543 | ||
IRF3 inhibition by rotavirus NSP1 is host cell and virus strain dependent but independent of NSP1 proteasomal degradation. | Q39816481 | ||
Rotavirus infection induces the phosphorylation of eIF2alpha but prevents the formation of stress granules | Q40046408 | ||
Effect of S-adenosylmethionine on human rotavirus RNA synthesis | Q40134092 | ||
Protein kinase R mediates intestinal epithelial gene remodeling in response to double-stranded RNA and live rotavirus | Q40425501 | ||
Development of a pentavalent rotavirus vaccine against prevalent serotypes of rotavirus gastroenteritis | Q40501707 | ||
Phosphorylation and specific ubiquitin acceptor sites are required for ubiquitination and degradation of the IFNAR1 subunit of type I interferon receptor | Q40520820 | ||
Interaction of Epstein-Barr virus latent membrane protein 1 with SCFHOS/beta-TrCP E3 ubiquitin ligase regulates extent of NF-kappaB activation. | Q40629419 | ||
Rotavirus induces alpha-interferon release in children with gastroenteritis. | Q40723253 | ||
The human immunodeficiency virus type 1 Vpu protein inhibits NF-kappa B activation by interfering with beta TrCP-mediated degradation of Ikappa B. | Q40816820 | ||
Innate immune responses to rotavirus infection in macrophages depend on MAVS but involve neither the NLRP3 inflammasome nor JNK and p38 signaling pathways. | Q41158454 | ||
Role of interferon in homologous and heterologous rotavirus infection in the intestines and extraintestinal organs of suckling mice | Q41339221 | ||
Genomic analysis of codon, sequence and structural conservation with selective biochemical-structure mapping reveals highly conserved and dynamic structures in rotavirus RNAs with potential cis-acting functions | Q41350844 | ||
The IRF family of transcription factors: Inception, impact and implications in oncogenesis | Q41888239 | ||
Roles of VP4 and NSP1 in determining the distinctive replication capacities of simian rotavirus RRV and bovine rotavirus UK in the mouse biliary tract | Q41998682 | ||
Permissive replication of homologous murine rotavirus in the mouse intestine is primarily regulated by VP4 and NSP1. | Q43079549 | ||
Determinants of rotavirus host range restriction--a heterologous bovine NSP1 gene does not affect replication kinetics in the pig. | Q43406052 | ||
Interferon gamma and interleukin 1, but not interferon alfa, inhibit rotavirus entry into human intestinal cell lines | Q46474616 | ||
Rotavirus open cores catalyze 5'-capping and methylation of exogenous RNA: evidence that VP3 is a methyltransferase. | Q53920399 | ||
The role of interferons in rotavirus infections and protection. | Q54526298 | ||
Lack of a Role for Type I and Type II Interferons in the Resolution of Rotavirus-Induced Diarrhea and Infection in Mice | Q60321338 | ||
Identification of group A rotavirus genes associated with virulence of a porcine rotavirus and host range restriction of a human rotavirus in the gnotobiotic piglet model | Q72230220 | ||
New insights into the role of RNase L in innate immunity | Q24597466 | ||
Length-dependent recognition of double-stranded ribonucleic acids by retinoic acid-inducible gene-I and melanoma differentiation-associated gene 5 | Q24648192 | ||
Rotavirus protein NSP3 (NS34) is bound to the 3' end consensus sequence of viral mRNAs in infected cells | Q24657379 | ||
Viral encounters with 2',5'-oligoadenylate synthetase and RNase L during the interferon antiviral response | Q24681387 | ||
Rotavirus NSP1 inhibits expression of type I interferon by antagonizing the function of interferon regulatory factors IRF3, IRF5, and IRF7 | Q24683021 | ||
NF-κB, the first quarter-century: remarkable progress and outstanding questions | Q26822516 | ||
Rotavirus entry: a deep journey into the cell with several exits | Q26995498 | ||
Rotaviruses | Q26996393 | ||
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 | ||
Leukocyte-derived IFN-α/β and epithelial IFN-λ constitute a compartmentalized mucosal defense system that restricts enteric virus infections | Q27320523 | ||
Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses | Q27860455 | ||
RIG-I-mediated antiviral responses to single-stranded RNA bearing 5'-phosphates | Q27861007 | ||
Pattern recognition receptors and inflammation | Q27861115 | ||
Identification and characterization of MAVS, a mitochondrial antiviral signaling protein that activates NF-kappaB and IRF 3 | Q27861127 | ||
5'-Triphosphate RNA is the ligand for RIG-I | Q28131726 | ||
VISA is an adapter protein required for virus-triggered IFN-beta signaling | Q28131814 | ||
Comparison of the rotavirus nonstructural protein NSP1 (NS53) from different species by sequence analysis and northern blot hybridization | Q28244835 | ||
Activation of innate immune defense mechanisms by signaling through RIG-I/IPS-1 in intestinal epithelial cells | Q28251813 | ||
A novel human WD protein, h-beta TrCp, that interacts with HIV-1 Vpu connects CD4 to the ER degradation pathway through an F-box motif | Q28276184 | ||
Zinc-binding domain of rotavirus NSP1 is required for proteasome-dependent degradation of IRF3 and autoregulatory NSP1 stability | Q28284962 | ||
Global burden of childhood pneumonia and diarrhoea | Q28288886 | ||
IFN-lambda determines the intestinal epithelial antiviral host defense | Q28508039 | ||
STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity | Q28509328 | ||
Gene-specific regulation by general translation factors | Q28611181 | ||
Interferons and viruses: an interplay between induction, signalling, antiviral responses and virus countermeasures | Q29615028 | ||
The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling | Q29615457 | ||
Interferon induction and function at the mucosal surface | Q30661545 | ||
IFN-lambda (IFN-lambda) is expressed in a tissue-dependent fashion and primarily acts on epithelial cells in vivo | Q33325913 | ||
Rotavirus structural proteins and dsRNA are required for the human primary plasmacytoid dendritic cell IFNalpha response | Q33598425 | ||
Viral phosphodiesterases that antagonize double-stranded RNA signaling to RNase L by degrading 2-5A | Q33714369 | ||
Analysis of host range restriction determinants in the rabbit model: comparison of homologous and heterologous rotavirus infections. | Q33782483 | ||
Predicted structure and domain organization of rotavirus capping enzyme and innate immune antagonist VP3 | Q34059087 | ||
Interferon-lambda: a new addition to an old family | Q34077324 | ||
It takes two to tango: IκBs, the multifunctional partners of NF-κB. | Q37995679 | ||
Regulation of NF-κB by ubiquitination and degradation of the IκBs | Q37995680 | ||
The JAK-STAT pathway at twenty | Q38004201 | ||
Rotavirus vaccination in developing countries | Q38018763 | ||
Innate cellular responses to rotavirus infection. | Q38088957 | ||
The estimated mortality impact of vaccinations forecast to be administered during 2011-2020 in 73 countries supported by the GAVI Alliance. | Q38100050 | ||
Interferon-stimulated genes: roles in viral pathogenesis | Q38203069 | ||
The impact of the interferon-lambda family on the innate and adaptive immune response to viral infections | Q38514365 | ||
Guarding the frontiers: the biology of type III interferons | Q38550956 | ||
IFN-lambda therapy: current status and future perspectives. | Q38629043 | ||
Intestinal epithelia activate anti-viral signaling via intracellular sensing of rotavirus structural components | Q34213447 | ||
2008 estimate of worldwide rotavirus-associated mortality in children younger than 5 years before the introduction of universal rotavirus vaccination programmes: a systematic review and meta-analysis | Q34227701 | ||
Age-dependent TLR3 expression of the intestinal epithelium contributes to rotavirus susceptibility | Q34263052 | ||
Rotavirus-host cell interactions: an arms race | Q34278554 | ||
Poxvirus targeting of E3 ligase β-TrCP by molecular mimicry: a mechanism to inhibit NF-κB activation and promote immune evasion and virulence | Q34611139 | ||
The interferons: 50 years after their discovery, there is much more to learn | Q34628245 | ||
Nuclear localization of cytoplasmic poly(A)-binding protein upon rotavirus infection involves the interaction of NSP3 with eIF4G and RoXaN. | Q34830104 | ||
Characterization of rotavirus RNAs that activate innate immune signaling through the RIG-I-like receptors | Q34874614 | ||
Rotavirus Nonstructural Protein NSP3 is not required for viral protein synthesis | Q35024231 | ||
Putative E3 ubiquitin ligase of human rotavirus inhibits NF-κB activation by using molecular mimicry to target β-TrCP. | Q35072342 | ||
The early interferon response to rotavirus is regulated by PKR and depends on MAVS/IPS-1, RIG-I, MDA-5, and IRF3. | Q35076535 | ||
Rotavirus replication: plus-sense templates for double-stranded RNA synthesis are made in viroplasms | Q35122641 | ||
The rhesus rotavirus gene encoding VP4 is a major determinant in the pathogenesis of biliary atresia in newborn mice | Q35192854 | ||
Structural basis for 2'-5'-oligoadenylate binding and enzyme activity of a viral RNase L antagonist. | Q35745380 | ||
Multistep entry of rotavirus into cells: a Versaillesque dance | Q35785633 | ||
Interferon-λ and interleukin 22 act synergistically for the induction of interferon-stimulated genes and control of rotavirus infection | Q36108222 | ||
β-TrCP-mediated IRAK1 degradation releases TAK1-TRAF6 from the membrane to the cytosol for TAK1-dependent NF-κB activation | Q36277255 | ||
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 | ||
Rotavirus prevents the expression of host responses by blocking the nucleocytoplasmic transport of polyadenylated mRNAs | Q36827188 | ||
Molecular basis of rotavirus virulence: role of gene segment 4. | Q36855328 | ||
Capped and conserved terminal structures in human rotavirus genome double-stranded RNA segments | Q36906867 | ||
TRAF molecules in cell signaling and in human diseases | Q36972287 | ||
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 | ||
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 | ||
Variation in antagonism of the interferon response to rotavirus NSP1 results in differential infectivity in mouse embryonic fibroblasts | Q37248029 | ||
Innate immunity to virus infection. | Q37361448 | ||
Rotavirus NSP1 protein inhibits interferon-mediated STAT1 activation | Q37547591 | ||
Sensing and signaling in antiviral innate immunity | Q37731032 | ||
IFN-λs | Q37917252 | ||
Recognition of nucleic acids by pattern-recognition receptors and its relevance in autoimmunity | Q37925064 | ||
Viral subversion of the host protein synthesis machinery | Q37946208 | ||
P433 | issue | 1 | |
P921 | main subject | Rotavirus | Q164778 |
modulation by virus of host process | Q14818042 | ||
P304 | page(s) | 591-609 | |
P577 | publication date | 2016-07-29 | |
P1433 | published in | Annual Review of Virology | Q19962702 |
P1476 | title | Rotavirus Strategies Against the Innate Antiviral System | |
P478 | volume | 3 |
Q37612580 | A paradox of transcriptional and functional innate interferon responses of human intestinal enteroids to enteric virus infection |
Q90715237 | A single mutation in the mammalian orthoreovirus S1 gene is responsible for increased interferon sensitivity in a virus mutant selected in Vero cells |
Q92989195 | How Many Mammalian Reovirus Proteins are involved in the Control of the Interferon Response? |
Q47547819 | Multiple proteins differing between laboratory stocks of mammalian orthoreoviruses affect both virus sensitivity to interferon and induction of interferon production during infection |
Q40088701 | Reverse Genetics System Demonstrates that Rotavirus Nonstructural Protein NSP6 Is Not Essential for Viral Replication in Cell Culture |
Q114370871 | Rotavirus Interactions With Host Intestinal Epithelial Cells |
Q46152582 | Rotavirus infection |
Q60934864 | Rotavirus infection beyond the gut |
Q36407402 | Rotavirus replication is correlated with S/G2 interphase arrest of the host cell cycle |
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