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Does Toll-like receptor 3 play a biological role in virus infections?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/eji.1830251209openalex-snapshot
The roles of perforin‐ and Fas‐dependent cytotoxicity in protection against cytopathic and noncytopathic viruses
inferredcites →https://doi.org/10.1006/viro.1997.8627openalex-snapshot
The Signal Sequence of Lymphocytic Choriomeningitis Virus Contains an Immunodominant Cytotoxic T Cell Epitope That Is Restricted by both H-2Dband H-2KbMolecules
inferredcites →https://doi.org/10.1007/978-1-4684-7032-1_8openalex-snapshot
Defective Interfering Rhabdoviruses
inferredcites →https://doi.org/10.1007/978-3-642-74980-3_8openalex-snapshot
Cellular and Molecular Basis of the Protective Immune Response to Cytomegalovirus Infection
inferredcites →https://doi.org/10.1016/s0006-291x(02)00380-7openalex-snapshot
Establishment of a monoclonal antibody against human Toll-like receptor 3 that blocks double-stranded RNA-mediated signaling
inferredcites →https://doi.org/10.1016/s0165-2478(02)00228-6openalex-snapshot
Recognition of pathogen-associated molecular patterns by TLR family
inferredcites →https://doi.org/10.1016/s0952-7915(99)00045-xopenalex-snapshot
Toll signaling pathways in the innate immune response
inferredcites →https://doi.org/10.1016/s0952-7915(99)80003-xopenalex-snapshot
The Toll-receptor family and control of innate immunity
inferredcites →https://doi.org/10.1016/s1074-7613(00)80470-7openalex-snapshot
Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection
inferredcites →https://doi.org/10.1016/s1074-7613(02)00390-4openalex-snapshot
IRF3 Mediates a TLR3/TLR4-Specific Antiviral Gene Program
inferredcites →https://doi.org/10.1038/35021228openalex-snapshot
Toll-like receptors in the induction of the innate immune response
inferredcites →https://doi.org/10.1038/35047123openalex-snapshot
A Toll-like receptor recognizes bacterial DNA
inferredcites →https://doi.org/10.1038/35099560openalex-snapshot
Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3
inferredcites →https://doi.org/10.1038/80833openalex-snapshot
Pattern recognition receptors TLR4 and CD14 mediate response to respiratory syncytial virus
inferredcites →https://doi.org/10.1038/nature01889openalex-snapshot
Identification of Lps2 as a key transducer of MyD88-independent TIR signalling
inferredcites →https://doi.org/10.1038/ni0901-835openalex-snapshot
TIRAP: an adapter molecule in the Toll signaling pathway
inferredcites →https://doi.org/10.1038/ni886openalex-snapshot
TICAM-1, an adaptor molecule that participates in Toll-like receptor 3–mediated interferon-β induction
inferredcites →https://doi.org/10.1080/13550280260422677openalex-snapshot
Reovirus-induced neuronal apoptosis is mediated by caspase 3 and is associated with the activation of death receptors
inferredcites →https://doi.org/10.1084/jem.160.2.521openalex-snapshot
Selection of genetic variants of lymphocytic choriomeningitis virus in spleens of persistently infected mice. Role in suppression of cytotoxic T lymphocyte response and viral persistence.
inferredcites →https://doi.org/10.1084/jem.170.3.887openalex-snapshot
Antibody inhibits defined stages in the pathogenesis of reovirus serotype 3 infection of the central nervous system.
inferredcites →https://doi.org/10.1084/jem.20011481openalex-snapshot
c-Jun NH2-Terminal Kinase (JNK)1 and JNK2 Signaling Pathways Have Divergent Roles in CD8+ T Cell–mediated Antiviral Immunity
inferredcites →https://doi.org/10.1084/jem.20021652openalex-snapshot
The Poxvirus Protein A52R Targets Toll-like Receptor Signaling Complexes to Suppress Host Defense
inferredcites →https://doi.org/10.1097/00005072-197301000-00002openalex-snapshot
REOVIRUS TYPE III ENCEPHALITIS—A VIROLOGIC AND ULTRASTRUCTURAL STUDY
inferredcites →https://doi.org/10.1099/0022-1317-64-8-1689openalex-snapshot
Genomic and Biological Variation among Commonly Used Lymphocytic Choriomeningitis Virus Strains
inferredcites →https://doi.org/10.1128/jvi.51.1.208-214.1984openalex-snapshot
Protection against lethal viral infection by neutralizing and nonneutralizing monoclonal antibodies: distinct mechanisms of action in vivo
inferredcites →https://doi.org/10.1128/jvi.51.3.682-686.1984openalex-snapshot
Biology of cloned cytotoxic T lymphocytes specific for lymphocytic choriomeningitis virus: clearance of virus in vivo
inferredcites →https://doi.org/10.1128/jvi.52.1.119-128.1984openalex-snapshot
Pathogenesis of murine cytomegalovirus infection in natural killer cell-depleted mice
inferredcites →https://doi.org/10.1128/jvi.53.2.552-560.1985openalex-snapshot
Biology of cloned cytotoxic T lymphocytes specific for lymphocytic choriomeningitis virus: clearance of virus and in vitro properties
inferredcites →https://doi.org/10.1128/jvi.66.1.349-358.1992openalex-snapshot
Subunit interactions of vesicular stomatitis virus envelope glycoprotein stabilized by binding to viral matrix protein
inferredcites →https://doi.org/10.1128/jvi.69.4.2153-2158.1995openalex-snapshot
Antiviral protection by vesicular stomatitis virus-specific antibodies in alpha/beta interferon receptor-deficient mice
inferredcites →https://doi.org/10.1128/jvi.71.3.2100-2106.1997openalex-snapshot
Reovirus infection and tissue injury in the mouse central nervous system are associated with apoptosis
inferredcites →https://doi.org/10.1128/jvi.72.10.8281-8288.1998openalex-snapshot
Long-Term CD4 Th1 and Th2 Memory following Acute Lymphocytic Choriomeningitis Virus Infection
inferredcites →https://doi.org/10.1128/jvi.72.11.9208-9216.1998openalex-snapshot
Evidence for an Underlying CD4 Helper and CD8 T-Cell Defect in B-Cell-Deficient Mice: Failure To Clear Persistent Virus Infection after Adoptive Immunotherapy with Virus-Specific Memory Cells from μMT/μMT Mice
inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141126openalex-snapshot
Toll-Like Receptors
inferredcites →https://doi.org/10.1203/00006450-200109000-00004openalex-snapshot
Toll-like Receptors as Sensors of Pathogens
inferredcites →https://doi.org/10.1212/wnl.35.1.88openalex-snapshot
Molecular basis of viral neurotropism
inferredcites →https://doi.org/10.4049/jimmunol.165.10.5392openalex-snapshot
Cutting Edge: TLR2-Deficient and MyD88-Deficient Mice Are Highly Susceptible to Staphylococcus aureus Infection
inferredcites →https://doi.org/10.4049/jimmunol.169.9.4697openalex-snapshot
Cutting Edge: Impaired Toll-Like Receptor Expression and Function in Aging
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470664001.ch12openalex-snapshot
Innate Immune Recognition of Nucleic Acids
inferred← citeshttps://doi.org/10.1002/ange.200704735openalex-snapshot
dsRNA‐funktionalisierte γ‐Fe2O3‐Nanokristalle: ein Instrument zur gezielten Adressierung von Rezeptoren an der Zelloberfläche
inferred← citeshttps://doi.org/10.1002/anie.200704735openalex-snapshot
dsRNA‐Functionalized Multifunctional γ‐Fe2O3 Nanocrystals: A Tool for Targeting Cell Surface Receptors
inferred← citeshttps://doi.org/10.1002/eji.200425583openalex-snapshot
Dendritic cells respond to influenza virus through TLR7‐ and PKR‐independent pathways
inferred← citeshttps://doi.org/10.1002/eji.200425730openalex-snapshot
MyD88 is critical for the development of innate and adaptive immunity during acute lymphocytic choriomeningitis virus infection
inferred← citeshttps://doi.org/10.1002/eji.200535304openalex-snapshot
CD45 is required for type I IFN production by dendritic cells
inferred← citeshttps://doi.org/10.1002/hipo.22129openalex-snapshot
Toll‐like receptor 3 activation modulates hippocampal network excitability, via glial production of interferon‐β
inferred← citeshttps://doi.org/10.1002/iub.1625openalex-snapshot
RNA sensors of the innate immune system and their detection of pathogens
inferred← citeshttps://doi.org/10.1002/rmv.628openalex-snapshot
The role of dendritic cells in alphaherpesvirus infections: archetypes and paradigms
inferred← citeshttps://doi.org/10.1002/rmv.633openalex-snapshot
Recognition of viral nucleic acids in innate immunity
inferred← citeshttps://doi.org/10.1002/rmv.680openalex-snapshot
Antiviral responses induced by the TLR3 pathway
inferred← citeshttps://doi.org/10.1002/sita.200600114openalex-snapshot
Influenza viruses and MAP kinase cascades – Novel targets for an antiviral intervention?
inferred← citeshttps://doi.org/10.1007/1-4020-3242-0_1openalex-snapshot
Viruses and the Innate Immune System
inferred← citeshttps://doi.org/10.1007/1-4020-3242-0_10openalex-snapshot
Viral Pathogenesis and Toll-Like Receptors
inferred← citeshttps://doi.org/10.1007/3-7643-7441-1_8openalex-snapshot
Toll-like receptors as key sensors of viral infection
inferred← citeshttps://doi.org/10.1007/82_2012_246openalex-snapshot
Systems Approaches to Dissecting Immunity
inferred← citeshttps://doi.org/10.1007/978-1-0716-4108-8_12openalex-snapshot
Identifying RNA Sensors in Antiviral Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-1-4419-0901-5_2openalex-snapshot
Pattern Recognition by Toll-like Receptors
inferred← citeshttps://doi.org/10.1007/978-3-0346-0279-2_8openalex-snapshot
The Immune Response to Influenza A Viruses
inferred← citeshttps://doi.org/10.1007/978-3-540-71329-6_16openalex-snapshot
Type I Interferon During Viral Infections: Multiple Triggers for a Multifunctional Mediator
inferred← citeshttps://doi.org/10.1007/978-3-540-72167-3_8openalex-snapshot
Dendritic Cell Subsets and Toll-Like Receptors
inferred← citeshttps://doi.org/10.1007/978-3-642-00549-7_4openalex-snapshot
Toll-Like Receptors in CNS Viral Infections
inferred← citeshttps://doi.org/10.1007/978-3-7643-8371-8_6openalex-snapshot
The immune response to influenza A viruses
inferred← citeshttps://doi.org/10.1007/978-90-481-2976-8_8openalex-snapshot
Toll-Like Receptors and Infectious Diseases: Role of Heat Shock Proteins
inferred← citeshttps://doi.org/10.1007/s00109-004-0620-6openalex-snapshot
Reading the viral signature by Toll-like receptors and other pattern recognition receptors
inferred← citeshttps://doi.org/10.1007/s00251-005-0013-1openalex-snapshot
Characterization of Toll-like receptor 3 gene in rainbow trout (Oncorhynchus mykiss)
inferred← citeshttps://doi.org/10.1007/s00251-007-0264-0openalex-snapshot
Toll-like receptor 3 regulates Mx expression in rare minnow Gobiocypris rarus after viral infection
inferred← citeshttps://doi.org/10.1007/s00430-012-0264-zopenalex-snapshot
Live or let die: manipulation of cellular suicide programs by murine cytomegalovirus
inferred← citeshttps://doi.org/10.1007/s00705-010-0863-1openalex-snapshot
Adjuvants and delivery systems in veterinary vaccinology: current state and future developments
inferred← citeshttps://doi.org/10.1007/s00726-009-0374-0openalex-snapshot
Induction of type I interferon by RNA viruses: cellular receptors and their substrates
inferred← citeshttps://doi.org/10.1007/s10495-007-0071-yopenalex-snapshot
Control of apoptosis in influenza virus-infected cells by up-regulation of Akt and p53 signaling
inferred← citeshttps://doi.org/10.1007/s10741-012-9357-4openalex-snapshot
Viral myocarditis: from experimental models to molecular diagnosis in patients
inferred← citeshttps://doi.org/10.1007/s10875-005-8065-4openalex-snapshot
Innate Sensors of Microbial Infection
inferred← citeshttps://doi.org/10.1007/s11259-014-9598-xopenalex-snapshot
Marek’s disease virus may interfere with T cell immunity by TLR3 signals
inferred← citeshttps://doi.org/10.1007/s11515-010-0013-xopenalex-snapshot
Regulation of virus-triggered type I interferon signaling by cellular and viral proteins
inferred← citeshttps://doi.org/10.1007/s12026-009-8113-xopenalex-snapshot
The contribution of direct TLR signaling to T cell responses
inferred← citeshttps://doi.org/10.1007/s12026-014-8617-xopenalex-snapshot
Roles of retinoic acid-inducible gene-I-like receptors (RLRs), Toll-like receptor (TLR) 3 and 2′-5′ oligoadenylate synthetase as viral recognition receptors on human mast cells in response to viral infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.14002-0openalex-snapshot
Dendritic Cells in Viral Infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-387040-7.00006-8openalex-snapshot
Interferon in Rabies Virus Infection
inferred← citeshttps://doi.org/10.1016/b978-0-12-818731-9.00050-1openalex-snapshot
Reovirus and Rotaviruses
inferred← citeshttps://doi.org/10.1016/b978-0-323-04579-7.00002-2openalex-snapshot
Host responses to infection
inferred← citeshttps://doi.org/10.1016/b978-0-323-05659-5.00023-1openalex-snapshot
Biology of Epithelial Cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-89774-7.00011-xopenalex-snapshot
Unconventional functions of miRNAs
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6285-8.00003-4openalex-snapshot
Host Responses to Infection
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4710-0.00013-4openalex-snapshot
Innate Immunity in the Lungs
inferred← citeshttps://doi.org/10.1016/b978-141603158-1.10008-3openalex-snapshot
Toll-like Receptor Responses in Neonatal Dendritic Cells
inferred← citeshttps://doi.org/10.1016/j.abb.2007.03.033openalex-snapshot
Subversion of innate host antiviral strategies by the hepatitis C virus
inferred← citeshttps://doi.org/10.1016/j.addr.2007.11.003openalex-snapshot
Toll-like receptors regulation of viral infection and disease☆
inferred← citeshttps://doi.org/10.1016/j.addr.2007.11.005openalex-snapshot
TLR3: Interferon induction by double-stranded RNA including poly(I:C)☆
inferred← citeshttps://doi.org/10.1016/j.arcmed.2005.04.007openalex-snapshot
Innate Immune Responses to Dengue Virus
inferred← citeshttps://doi.org/10.1016/j.bbi.2006.12.007openalex-snapshot
The sickness behaviour and CNS inflammatory mediator profile induced by systemic challenge of mice with synthetic double-stranded RNA (poly I:C)
inferred← citeshttps://doi.org/10.1016/j.bbi.2007.10.005openalex-snapshot
Sex differences in the recognition of and innate antiviral responses to Seoul virus in Norway rats
inferred← citeshttps://doi.org/10.1016/j.bbi.2009.10.011openalex-snapshot
Attenuation of the influenza virus sickness behavior in mice deficient in Toll-like receptor 3
inferred← citeshttps://doi.org/10.1016/j.bcp.2010.07.001openalex-snapshot
Innate immune response and viral interference strategies developed by Human Herpesviruses
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.10.010openalex-snapshot
TLRs and chronic inflammation
inferred← citeshttps://doi.org/10.1016/j.cell.2006.01.034openalex-snapshot
Anti-Immunology: Evasion of the Host Immune System by Bacterial and Viral Pathogens
inferred← citeshttps://doi.org/10.1016/j.cell.2006.02.015openalex-snapshot
Pathogen Recognition and Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116210openalex-snapshot
Selective TLR ligand stimulation enhances in vivo mosquito-borne flavivirus pathogenicity
inferred← citeshttps://doi.org/10.1016/j.coi.2012.11.001openalex-snapshot
TLR3 immunity to infection in mice and humans
inferred← citeshttps://doi.org/10.1016/j.coph.2006.11.010openalex-snapshot
Viral-associated exacerbations of asthma and COPD
inferred← citeshttps://doi.org/10.1016/j.coph.2008.05.002openalex-snapshot
Neuroimmunology of central nervous system viral infections: the cells, molecules and mechanisms involved
inferred← citeshttps://doi.org/10.1016/j.coviro.2011.10.006openalex-snapshot
Toll-like receptors: key players in antiviral immunity
inferred← citeshttps://doi.org/10.1016/j.cyto.2015.03.007openalex-snapshot
Insights into antiviral innate immunity revealed by studying hepatitis C virus
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2005.01.006openalex-snapshot
Transcriptional signaling by double-stranded RNA: role of TLR3
inferred← citeshttps://doi.org/10.1016/j.dci.2004.12.002openalex-snapshot
Activation of TLR3 and TLR5 in channel catfish exposed to virulent
inferred← citeshttps://doi.org/10.1016/j.dci.2011.03.006openalex-snapshot
Toll-like receptors in bony fish: From genomics to function
inferred← citeshttps://doi.org/10.1016/j.femsre.2004.12.003openalex-snapshot
Role of apoptosis and cytokines in influenza virus morbidity
inferred← citeshttps://doi.org/10.1016/j.fsi.2005.03.005openalex-snapshot
Response of toll-like receptors, lysozyme, and IGF-I in back-cross hybrid (F1 male (blue×channel)×female channel) catfish challenged with virulent Edwardsiella ictaluri
inferred← citeshttps://doi.org/10.1016/j.fsi.2009.06.009openalex-snapshot
Genomic organization and expression analysis of Toll-like receptor 3 in grass carp (Ctenopharyngodon idella)
inferred← citeshttps://doi.org/10.1016/j.fsi.2018.01.022openalex-snapshot
Basal polarization of the immune responses to Streptococcus agalactiae susceptible and resistant tilapia (Oreochromis niloticus)
inferred← citeshttps://doi.org/10.1016/j.gene.2013.06.014openalex-snapshot
Molecular characterization and functional analysis of Toll-like receptor 3 gene in orange-spotted grouper (Epinephelus coioides)
inferred← citeshttps://doi.org/10.1016/j.imbio.2007.03.011openalex-snapshot
Immunobiology of toll-like receptors in allergic disease
inferred← citeshttps://doi.org/10.1016/j.imbio.2007.09.007openalex-snapshot
The role of viral nucleic acid recognition in dendritic cells for innate and adaptive antiviral immunity
inferred← citeshttps://doi.org/10.1016/j.immuni.2005.09.016openalex-snapshot
Human TLR-7-, -8-, and -9-Mediated Induction of IFN-α/β and -λ Is IRAK-4 Dependent and Redundant for Protective Immunity to Viruses
inferred← citeshttps://doi.org/10.1016/j.immuni.2007.08.012openalex-snapshot
Innate Recognition of Viruses
inferred← citeshttps://doi.org/10.1016/j.immuni.2008.05.005openalex-snapshot
Regulation of Mitochondrial Antiviral Signaling Pathways
inferred← citeshttps://doi.org/10.1016/j.immuni.2008.11.012openalex-snapshot
Toll-like Receptor 7 Mitigates Lethal West Nile Encephalitis via Interleukin 23-Dependent Immune Cell Infiltration and Homing
inferred← citeshttps://doi.org/10.1016/j.immuni.2011.05.006openalex-snapshot
Toll-like Receptors and Their Crosstalk with Other Innate Receptors in Infection and Immunity
inferred← citeshttps://doi.org/10.1016/j.immuni.2011.05.011openalex-snapshot
Innate Immune Sensing of Retroviral Infection via Toll-like Receptor 7 Occurs upon Viral Entry
inferred← citeshttps://doi.org/10.1016/j.immuni.2011.10.010openalex-snapshot
Dying to Replicate: The Orchestration of the Viral Life Cycle, Cell Death Pathways, and Immunity
inferred← citeshttps://doi.org/10.1016/j.it.2005.07.002openalex-snapshot
TLR3 in antiviral immunity: key player or bystander?
inferred← citeshttps://doi.org/10.1016/j.it.2007.01.005openalex-snapshot
Astrocytes are active players in cerebral innate immunity
inferred← citeshttps://doi.org/10.1016/j.jcpa.2005.06.011openalex-snapshot
Cytokine and Toll-like Receptor mRNAs in the Nasal-associated Lymphoid Tissues of Cattle During Foot-and-mouth Disease Virus Infection
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2014.12.011openalex-snapshot
Central mediators involved in the febrile response induced by polyinosinic–polycytidylic acid: Lack of involvement of endothelins and substance P
inferred← citeshttps://doi.org/10.1016/j.jns.2016.11.034openalex-snapshot
Toll like receptor 3 and viral infections of nervous system
inferred← citeshttps://doi.org/10.1016/j.jviromet.2007.05.002openalex-snapshot
Analysis of foot-and-mouth disease virus replication using strand-specific quantitative RT-PCR
inferred← citeshttps://doi.org/10.1016/j.mce.2016.07.033openalex-snapshot
Mumps virus induces innate immune responses in mouse ovarian granulosa cells through the activation of Toll-like receptor 2 and retinoic acid-inducible gene I
inferred← citeshttps://doi.org/10.1016/j.micinf.2004.08.013openalex-snapshot
Viruses and Toll-like receptors
inferred← citeshttps://doi.org/10.1016/j.micinf.2005.02.001openalex-snapshot
Interferons (IFNs) are key cytokines in both innate and adaptive antiviral immune responses—and viruses counteract IFN action
inferred← citeshttps://doi.org/10.1016/j.micinf.2005.06.014openalex-snapshot
Flavivirus induces interferon-beta gene expression through a pathway involving RIG-I-dependent IRF-3 and PI3K-dependent NF-κB activation
inferred← citeshttps://doi.org/10.1016/j.micinf.2007.06.008openalex-snapshot
Signalling pathways mediating type I interferon gene expression
inferred← citeshttps://doi.org/10.1016/j.micinf.2012.06.006openalex-snapshot
Realities of virus sensing
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.05.012openalex-snapshot
Toll-Like Receptors and RNA Helicases: Two Parallel Ways to Trigger Antiviral Responses
inferred← citeshttps://doi.org/10.1016/j.molimm.2004.11.005openalex-snapshot
Functional characterization of full-length TLR3, IRAK-4, and TRAF6 in zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.molimm.2004.11.007openalex-snapshot
The role of Toll-like receptors in the host response to viruses
inferred← citeshttps://doi.org/10.1016/j.molmed.2005.07.006openalex-snapshot
Interferon gene regulation: not all roads lead to Tolls
inferred← citeshttps://doi.org/10.1016/j.nbd.2009.07.025openalex-snapshot
Viral-like brain inflammation during development causes increased seizure susceptibility in adult rats
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.12.005openalex-snapshot
Virus-induced modulation of lower airway diseases: Pathogenesis and pharmacologic approaches to treatment
inferred← citeshttps://doi.org/10.1016/j.rvsc.2022.08.023openalex-snapshot
Expression of Toll-like receptor and cytokine mRNAs in feline odontoclastic resorptive lesion (FORL) and feline oral health
inferred← citeshttps://doi.org/10.1016/j.semreu.2010.04.005openalex-snapshot
ABC de los «Toll-like receptors»: relación con el desarrollo y progresión de enfermedades autoinmunes
inferred← citeshttps://doi.org/10.1016/j.smim.2005.05.008openalex-snapshot
Plasmacytoid dendritic cells—virus experts of innate immunity
inferred← citeshttps://doi.org/10.1016/j.smim.2007.01.003openalex-snapshot
Viral recognition by Toll-like receptors
inferred← citeshttps://doi.org/10.1016/j.vaccine.2006.05.015openalex-snapshot
Zebrafish (Danio rerio) as a model for the study of vaccination against viral haemorrhagic septicemia virus (VHSV)
inferred← citeshttps://doi.org/10.1016/j.vaccine.2021.01.047openalex-snapshot
Recombinant lymphocytic choriomeningitis virus-based vaccine vector protects type I interferon receptor deficient mice from viral challenge
inferred← citeshttps://doi.org/10.1016/j.vetimm.2012.11.016openalex-snapshot
The influence of oral bacteria on tissue levels of Toll-like receptor and cytokine mRNAs in feline chronic gingivostomatitis and oral health
inferred← citeshttps://doi.org/10.1016/j.virol.2005.07.021openalex-snapshot
West Nile virus replication interferes with both poly(I:C)-induced interferon gene transcription and response to interferon treatment
inferred← citeshttps://doi.org/10.1016/j.virol.2013.02.015openalex-snapshot
Interferon regulatory factor 7 (IRF7) is required for the optimal initial control but not subsequent clearance of lymphocytic choriomeningitis virus infection in mice
inferred← citeshttps://doi.org/10.1016/j.virusres.2013.06.003openalex-snapshot
Understanding and altering cell tropism of vesicular stomatitis virus
inferred← citeshttps://doi.org/10.1016/s0065-3527(06)69001-5openalex-snapshot
The Innate Antiviral Response: New Insights Into A Continuing Story
inferred← citeshttps://doi.org/10.1016/s0076-6879(08)02405-1openalex-snapshot
In Vivo Analysis of the Decay of Transcripts Generated by Cytoplasmic RNA Viruses
inferred← citeshttps://doi.org/10.1016/s2222-1808(16)61089-7openalex-snapshot
Bridging the importance of Toll like receptors in human viral infections
inferred← citeshttps://doi.org/10.1038/cmi.2013.40openalex-snapshot
The interaction between the helicase DHX33 and IPS-1 as a novel pathway to sense double-stranded RNA and RNA viruses in myeloid dendritic cells
inferred← citeshttps://doi.org/10.1038/cmi.2014.73openalex-snapshot
Mast cells as rapid innate sensors of cytomegalovirus by TLR3/TRIF signaling-dependent and -independent mechanisms
inferred← citeshttps://doi.org/10.1038/nature03326openalex-snapshot
Toll-like receptor 3 promotes cross-priming to virus-infected cells
inferred← citeshttps://doi.org/10.1038/nature04193openalex-snapshot
Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus
inferred← citeshttps://doi.org/10.1038/nature04946openalex-snapshot
Intracellular pattern recognition receptors in the host response
inferred← citeshttps://doi.org/10.1038/ni1303openalex-snapshot
Innate immune recognition of viral infection
inferred← citeshttps://doi.org/10.1038/nm1140openalex-snapshot
Toll-like receptor 3 mediates West Nile virus entry into the brain causing lethal encephalitis
inferred← citeshttps://doi.org/10.1038/nm1204-1294openalex-snapshot
West Nile virus: crossing the blood-brain barrier
inferred← citeshttps://doi.org/10.1038/nri2436openalex-snapshot
Viral evasion and subversion of pattern-recognition receptor signalling
inferred← citeshttps://doi.org/10.1038/sj.cr.7290309openalex-snapshot
The host type I interferon response to viral and bacterial infections
inferred← citeshttps://doi.org/10.1038/sj.gt.3302625openalex-snapshot
Cellular factors influencing Semliki Forest Virus vector biology
inferred← citeshttps://doi.org/10.1038/sj.icb.7100100openalex-snapshot
Toll‐like receptors, RIG‐I‐like RNA helicases and the antiviral innate immune response
inferred← citeshttps://doi.org/10.1042/bj20090272openalex-snapshot
Pathogen recognition in the innate immune response
inferred← citeshttps://doi.org/10.1051/medsci/20062211961openalex-snapshot
Immunité innée antivirale : Rôle des mécanismesToll-dépendants etToll-indépendants
inferred← citeshttps://doi.org/10.1073/pnas.0603082103openalex-snapshot
Essential role of mda-5 in type I IFN responses to polyriboinosinic:polyribocytidylic acid and encephalomyocarditis picornavirus
inferred← citeshttps://doi.org/10.1073/pnas.0800168105openalex-snapshot
Inhibition of proinflammatory and innate immune signaling pathways by a cytomegalovirus RIP1-interacting protein
inferred← citeshttps://doi.org/10.1073/pnas.0810372105openalex-snapshot
A critical link between Toll-like receptor 3 and type II interferon signaling pathways in antiviral innate immunity
inferred← citeshttps://doi.org/10.1074/jbc.m113.538009openalex-snapshot
Interleukin-1 Receptor-associated Kinase-2 Genetic Variant rs708035 Increases NF-κB Activity through Promoting TRAF6 Ubiquitination
inferred← citeshttps://doi.org/10.1074/jbc.m410592200openalex-snapshot
Involvement of Toll-like Receptor 3 in the Immune Response of Lung Epithelial Cells to Double-stranded RNA and Influenza A Virus
inferred← citeshttps://doi.org/10.1074/jbc.m414139200openalex-snapshot
Distinct Poly(I-C) and Virus-activated Signaling Pathways Leading to Interferon-β Production in Hepatocytes
inferred← citeshttps://doi.org/10.1074/jbc.m507163200openalex-snapshot
Recognition of Double-stranded RNA by Human Toll-like Receptor 3 and Downstream Receptor Signaling Requires Multimerization and an Acidic pH
inferred← citeshttps://doi.org/10.1074/jbc.m510442200openalex-snapshot
Structural and Functional Analyses of the Human Toll-like Receptor 3
inferred← citeshttps://doi.org/10.1074/jbc.m707264200openalex-snapshot
MyD88 Functions as a Negative Regulator of TLR3/TRIF-induced Corneal Inflammation by Inhibiting Activation of c-Jun N-terminal Kinase
inferred← citeshttps://doi.org/10.1080/08830185.2017.1298749openalex-snapshot
Cytosolic nucleic acid sensors and innate immune regulation
inferred← citeshttps://doi.org/10.1080/08830185.2017.1380200openalex-snapshot
Toll-like receptors: Significance, ligands, signaling pathways, and functions in mammals
inferred← citeshttps://doi.org/10.1080/10495398.2023.2214189openalex-snapshot
Diverse pathogen-associated molecular patterns affect transcription of genes in the toll-like receptor signaling pathway in goat blood
inferred← citeshttps://doi.org/10.1080/13550280500384982openalex-snapshot
Differential responses of human brain cells to West Nile virus infection
inferred← citeshttps://doi.org/10.1080/13550280802298120openalex-snapshot
Association of toll-like receptor 3 gene polymorphism with subacute sclerosing panencephalitis
inferred← citeshttps://doi.org/10.1080/17471060701286559openalex-snapshot
Study of hepatocytes using RNA interference
inferred← citeshttps://doi.org/10.1084/jem.20041442openalex-snapshot
Vaccinia virus protein A46R targets multiple Toll-like–interleukin-1 receptor adaptors and contributes to virulence
inferred← citeshttps://doi.org/10.1084/jem.20041930openalex-snapshot
Type I interferon dependence of plasmacytoid dendritic cell activation and migration
inferred← citeshttps://doi.org/10.1084/jem.20061587openalex-snapshot
Type I interferons produced by hematopoietic cells protect mice against lethal infection by mammalian reovirus
inferred← citeshttps://doi.org/10.1084/jem.20101568openalex-snapshot
Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity
inferred← citeshttps://doi.org/10.1089/dna.2005.24.614openalex-snapshot
Interferon-β Induction Through Toll-Like Receptor 3 Depends on Double-Stranded RNA Structure
inferred← citeshttps://doi.org/10.1089/jir.2006.0050openalex-snapshot
Enlarged Spleens Without Enlarged Lymph Nodes in tlr3 −/− pkr −/− Mice
inferred← citeshttps://doi.org/10.1089/jir.2009.0064openalex-snapshot
Multifaceted Evasion of the Interferon Response by Cytomegalovirus
inferred← citeshttps://doi.org/10.1089/jir.2009.0068openalex-snapshot
Rhabdovirus Evasion of the Interferon System
inferred← citeshttps://doi.org/10.1089/jir.2009.0073openalex-snapshot
The Interferon System and Vaccinia Virus Evasion Mechanisms
inferred← citeshttps://doi.org/10.1089/jir.2010.0117openalex-snapshot
Type I Interferon Production Induced by RIG-I-Like Receptors
inferred← citeshttps://doi.org/10.1089/vim.2005.18.584openalex-snapshot
Dendritic Cells, Toll-Like Receptors, and T-Cell Responses: Lessons from Viral Infections in Vivo
inferred← citeshttps://doi.org/10.1089/vim.2005.18.89openalex-snapshot
Mechanisms of Reovirus-Induced Cell Death and Tissue Injury: Role of Apoptosis and Virus-Induced Perturbation of Host-Cell Signaling and Transcription Factor Activation
inferred← citeshttps://doi.org/10.1093/abbs/gms122openalex-snapshot
Recognition of pathogen-associated nucleic acids by endosomal nucleic acid-sensing toll-like receptors
inferred← citeshttps://doi.org/10.1093/femsec/fiw188openalex-snapshot
Differences in CD8αα and cecal microbiome community during proliferation and late cytolytic phases of Marek's disease virus infection are associated with genetic resistance to Marek's disease
inferred← citeshttps://doi.org/10.1093/intimm/dxp017openalex-snapshot
The roles of TLRs, RLRs and NLRs in pathogen recognition
inferred← citeshttps://doi.org/10.1093/intimm/dxr019openalex-snapshot
Bacterial LPS up-regulated TLR3 expression is critical for antiviral response in human monocytes: evidence for negative regulation by CYLD
inferred← citeshttps://doi.org/10.1093/jb/mvm032openalex-snapshot
Antiviral Signaling Through Pattern Recognition Receptors
inferred← citeshttps://doi.org/10.1093/nar/gkaf1302openalex-snapshot
The lysosomal catabolism of nucleic acids—critical regulators of the innate immune system
inferred← citeshttps://doi.org/10.1099/jgv.0.000867openalex-snapshot
uS10, a novel Npro-interacting protein, inhibits classical swine fever virus replication
inferred← citeshttps://doi.org/10.1099/vir.0.83391-0openalex-snapshot
Interferons and viruses: an interplay between induction, signalling, antiviral responses and virus countermeasures
inferred← citeshttps://doi.org/10.1101/2023.12.31.573785openalex-snapshot
An ATP-Binding Cassette Transporter Gene Links Innate and Adaptive Immune Responses
inferred← citeshttps://doi.org/10.1111/are.15044openalex-snapshot
Transcriptome analysis of Giant grouper ( Epinephelus lanceolatus ) kidney and spleen in response to spotted knifejaw iridovirus (SKIV) infection
inferred← citeshttps://doi.org/10.1111/cei.13514openalex-snapshot
Association of the polymorphism of the Toll-like receptor (TLR)-3 and TLR-9 genes with hepatitis C virus-specific cell-mediated immunity outcomes among Egyptian health-care workers
inferred← citeshttps://doi.org/10.1111/imm.12143openalex-snapshot
Toll‐like receptor 3 in viral pathogenesis: friend or foe?
inferred← citeshttps://doi.org/10.1111/imr.12195openalex-snapshot
The role of type I interferons in intestinal infection, homeostasis, and inflammation
inferred← citeshttps://doi.org/10.1111/j.0959-9673.2005.00440.xopenalex-snapshot
Dendritic cells in viral pathogenesis: protective or defective?
inferred← citeshttps://doi.org/10.1111/j.1365-2249.2006.03079.xopenalex-snapshot
Expression of Toll-like receptors and their association with cytokine responses in peripheral blood mononuclear cells of children with acute rotavirus diarrhoea
inferred← citeshttps://doi.org/10.1111/j.1365-2249.2006.03301.xopenalex-snapshot
Translational Mini-Review Series on Toll-like Receptors: Recent advances in understanding the role of Toll-like receptors in anti-viral immunity
inferred← citeshttps://doi.org/10.1111/j.1365-2249.2010.04196.xopenalex-snapshot
Recent insights into the role of Toll-like receptors in viral infection
inferred← citeshttps://doi.org/10.1111/j.1365-2567.2006.02363.xopenalex-snapshot
CD45 negatively regulates tumour necrosis factor and interleukin‐6 production in dendritic cells
inferred← citeshttps://doi.org/10.1111/j.1365-3083.2012.02754.xopenalex-snapshot
Administration of Interferon (IFN)‐α Exacerbates Reovirus Type‐2‐Triggered Autoimmune Insulitis in DBA/1J Mice
inferred← citeshttps://doi.org/10.1111/j.1399-0039.2006.00583.xopenalex-snapshot
Toll‐like receptors and innate antiviral immunity
inferred← citeshttps://doi.org/10.1111/j.1440-1746.2005.03977.xopenalex-snapshot
Rotavirus double‐stranded RNA induces apoptosis and diminishes wound repair in rat intestinal epithelial cells
inferred← citeshttps://doi.org/10.1111/j.1462-5822.2005.00678.xopenalex-snapshot
Ringing the alarm bells: signalling and apoptosis in influenza virus infected cells
inferred← citeshttps://doi.org/10.1111/j.1462-5822.2006.00841.xopenalex-snapshot
IFN? induction by influenza A virus is mediated by RIG-I which is regulated by the viral NS1 protein
inferred← citeshttps://doi.org/10.1111/j.1462-5822.2007.00965.xopenalex-snapshot
How important are Toll-like receptors for antimicrobial responses?
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2007.00564.xopenalex-snapshot
Human Toll‐like receptor‐dependent induction of interferons in protective immunity to viruses
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2008.00721.xopenalex-snapshot
Systems biology of innate immunity
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2008.00726.xopenalex-snapshot
Viral sensors: diversity in pathogen recognition
inferred← citeshttps://doi.org/10.1111/j.1600-065x.2011.01033.xopenalex-snapshot
Epithelial cells and airway diseases
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2009.04932.xopenalex-snapshot
Brain Tumor Immunotherapy with Type‐1 Polarizing Strategies
inferred← citeshttps://doi.org/10.1111/jnc.15716openalex-snapshot
Poly(I:C) promotes neurotoxic amyloid β accumulation through reduced degradation by decreasing neprilysin protein levels in astrocytes
inferred← citeshttps://doi.org/10.1126/science.1139522openalex-snapshot
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
inferred← citeshttps://doi.org/10.1128/9781555815493.ch19openalex-snapshot
Toll-Like Receptors: Novel Molecular Targets for Antiviral Immunotherapy
inferred← citeshttps://doi.org/10.1128/9781555815561.ch13openalex-snapshot
RNA Virus Families: Distinguishing Characteristics, Differences, and Similarities
inferred← citeshttps://doi.org/10.1128/9781555815561.ch14openalex-snapshot
Rhabdoviruses and Mechanisms of Type I Interferon Antagonism
inferred← citeshttps://doi.org/10.1128/9781555815561.ch2openalex-snapshot
Role of Toll-Like Receptors in the Innate Immune Response to RNA Viruses
inferred← citeshttps://doi.org/10.1128/9781555815561.ch25openalex-snapshot
Innate Immune Responses Elicited by Reovirus and Rotavirus
inferred← citeshttps://doi.org/10.1128/9781555816834.ch54openalex-snapshot
Innate Immunity and Host Defense against Microbial Infection
inferred← citeshttps://doi.org/10.1128/cmr.00022-07openalex-snapshot
Sensing of Viral Infection and Activation of Innate Immunity by Toll-Like Receptor 3
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