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NEMO is a key component of NF-κB– and IRF-3–dependent TLR3-mediated immunity to herpes simplex virus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archderm.144.3.342openalex-snapshot
X-Linked Ectodermal Dysplasia With Immunodeficiency Caused by NEMO Mutation
inferredcites →https://doi.org/10.1002/1096-8628(2001)9999:9999<::aid-ajmg1155>3.0.co;2-yopenalex-snapshot
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
inferredcites →https://doi.org/10.1002/eji.200425221openalex-snapshot
Bacillus Calmette Guérin triggers the IL‐12/IFN‐γ axis by an IRAK‐4‐ and NEMO‐dependent, non‐cognate interaction between monocytes, NK, and T lymphocytes
inferredcites →https://doi.org/10.1006/clim.1999.4688openalex-snapshot
IL-12-Independent Costimulation Pathways for Interferon-γ Production in Familial DisseminatedMycobacterium aviumComplex Infection
inferredcites →https://doi.org/10.1007/bf01805582openalex-snapshot
Transient B cell immaturity with intractable diarrhoea: A possible new immunodeficiency syndrome
inferredcites →https://doi.org/10.1007/bf02075774openalex-snapshot
Anhidrotic ectodermal dysplasia associated with specific antibody deficiency
inferredcites →https://doi.org/10.1007/s00439-005-0068-yopenalex-snapshot
A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency
inferredcites →https://doi.org/10.1016/j.antiviral.2006.04.002openalex-snapshot
Herpes simplex encephalitis: Adolescents and adults
inferredcites →https://doi.org/10.1016/j.coi.2003.11.013openalex-snapshot
Inherited disorders of NF-κB-mediated immunity in man
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.immuni.2010.08.014openalex-snapshot
Human TRAF3 Adaptor Molecule Deficiency Leads to Impaired Toll-like Receptor 3 Response and Susceptibility to Herpes Simplex Encephalitis
inferredcites →https://doi.org/10.1016/j.jaad.2004.05.032openalex-snapshot
Characteristics of mycobacterial infection in patients with immunodeficiency and nuclear factor–κB essential modulator mutation, with or without ectodermal dysplasia
inferredcites →https://doi.org/10.1016/j.jaad.2007.02.024openalex-snapshot
A male infant with anhidrotic ectodermal dysplasia/immunodeficiency accompanied by incontinentia pigmenti and a mutation in the NEMO pathway
inferredcites →https://doi.org/10.1016/j.jaci.2004.01.762openalex-snapshot
The presentation and natural history of immunodeficiency caused by nuclear factor κB essential modulator mutation
inferredcites →https://doi.org/10.1016/j.jaci.2004.06.052openalex-snapshot
Human nuclear factor κB essential modulator mutation can result in immunodeficiency without ectodermal dysplasia
inferredcites →https://doi.org/10.1016/j.jaci.2004.08.047openalex-snapshot
Nuclear factor κB essential modulator–deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia
inferredcites →https://doi.org/10.1016/j.jaci.2006.08.006openalex-snapshot
Interleukin receptor-associated kinase-4 deficiency impairs Toll-like receptor–dependent innate antiviral immune responses
inferredcites →https://doi.org/10.1016/j.jaci.2007.11.014openalex-snapshot
IKBKG (nuclear factor-κB essential modulator) mutation can be associated with opportunistic infection without impairing Toll-like receptor function
inferredcites →https://doi.org/10.1016/j.jaci.2008.08.018openalex-snapshot
Hypomorphic nuclear factor-κB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity
inferredcites →https://doi.org/10.1016/j.jaci.2010.04.026openalex-snapshot
Immune deficiency caused by impaired expression of nuclear factor-κB essential modifier (NEMO) because of a mutation in the 5′ untranslated region of the NEMO gene
inferredcites →https://doi.org/10.1016/j.jpeds.2010.04.020openalex-snapshot
Age-Dependent Mendelian Predisposition to Herpes Simplex Virus Type 1 Encephalitis in Childhood
inferredcites →https://doi.org/10.1016/j.smim.2006.07.010openalex-snapshot
Inborn errors of IL-12/23- and IFN-γ-mediated immunity: molecular, cellular, and clinical features
inferredcites →https://doi.org/10.1038/35013114openalex-snapshot
Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti
inferredcites →https://doi.org/10.1038/85277openalex-snapshot
Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia
inferredcites →https://doi.org/10.1038/85837openalex-snapshot
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
inferredcites →https://doi.org/10.1038/nature03464openalex-snapshot
IRF-7 is the master regulator of type-I interferon-dependent immune responses
inferredcites →https://doi.org/10.1038/ng1097openalex-snapshot
Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency
inferredcites →https://doi.org/10.1038/ni1465openalex-snapshot
The NEMO adaptor bridges the nuclear factor-κB and interferon regulatory factor signaling pathways
inferredcites →https://doi.org/10.1038/ni921openalex-snapshot
IKKε and TBK1 are essential components of the IRF3 signaling pathway
inferredcites →https://doi.org/10.1056/nejm199405123301904openalex-snapshot
Treatment of Refractory Disseminated Nontuberculous Mycobacterial Infection With Interferon Gamma: A Preliminary Report
inferredcites →https://doi.org/10.1074/jbc.m205069200openalex-snapshot
Association of the Adaptor TANK with the IκB Kinase (IKK) Regulator NEMO Connects IKK Complexes with IKKε and TBK1 Kinases
inferredcites →https://doi.org/10.1084/jem.20030701openalex-snapshot
Distinct Mutations in IRAK-4 Confer Hyporesponsiveness to Lipopolysaccharide and Interleukin-1 in a Patient with Recurrent Bacterial Infections
inferredcites →https://doi.org/10.1084/jem.20060085openalex-snapshot
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
inferredcites →https://doi.org/10.1084/jem.20070628openalex-snapshot
Selective predisposition to bacterial infections in IRAK-4–deficient children: IRAK-4–dependent TLRs are otherwise redundant in protective immunity
inferredcites →https://doi.org/10.1086/316914openalex-snapshot
A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO)
inferredcites →https://doi.org/10.1086/318806openalex-snapshot
Atypical Forms of Incontinentia Pigmenti in Male Individuals Result from Mutations of a Cytosine Tract in Exon 10 of NEMO (IKK-γ)
inferredcites →https://doi.org/10.1086/323003openalex-snapshot
Female Patient Showing Hypohidrotic Ectodermal Dysplasia and Immunodeficiency (HED-ID)
inferredcites →https://doi.org/10.1086/422319openalex-snapshot
Nontuberculous Mycobacterial Infection in Children: A 2-Year Prospective Surveillance Study in The Netherlands
inferredcites →https://doi.org/10.1086/501532openalex-snapshot
The NEMO Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation
inferredcites →https://doi.org/10.1093/hmg/11.20.2371openalex-snapshot
The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
inferredcites →https://doi.org/10.1093/hmg/ddh192openalex-snapshot
Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF- B activation
inferredcites →https://doi.org/10.1097/aci.0b013e3282f151d2openalex-snapshot
Genetic susceptibility to herpes simplex virus 1 encephalitis in mice and humans
inferredcites →https://doi.org/10.1097/md.0b013e3181fd8ec3openalex-snapshot
Clinical Features and Outcome of Patients With IRAK-4 and MyD88 Deficiency
inferredcites →https://doi.org/10.1111/j.0105-2896.2005.00221.xopenalex-snapshot
Human disease resulting from gene mutations that interfere with appropriate nuclear factor‐κB activation
inferredcites →https://doi.org/10.1111/j.0105-2896.2005.00235.xopenalex-snapshot
Inherited disorders of human Toll‐like receptor signaling: immunological implications
inferredcites →https://doi.org/10.1111/j.1600-065x.2007.00564.xopenalex-snapshot
Human Toll‐like receptor‐dependent induction of interferons in protective immunity to viruses
inferredcites →https://doi.org/10.1111/j.1600-065x.2008.00698.xopenalex-snapshot
Inborn errors of interferon (IFN)‐mediated immunity in humans: insights into the respective roles of IFN‐α/β, IFN‐γ, and IFN‐λ in host defense
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05834.xopenalex-snapshot
Life‐threatening infectious diseases of childhood: single‐gene inborn errors of immunity?
inferredcites →https://doi.org/10.1126/science.1081315openalex-snapshot
Triggering the Interferon Antiviral Response Through an IKK-Related Pathway
inferredcites →https://doi.org/10.1126/science.1081902openalex-snapshot
Pyogenic Bacterial Infections in Humans with IRAK-4 Deficiency
inferredcites →https://doi.org/10.1126/science.1128346openalex-snapshot
Herpes Simplex Virus Encephalitis in Human UNC-93B Deficiency
inferredcites →https://doi.org/10.1126/science.1139522openalex-snapshot
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
inferredcites →https://doi.org/10.1126/science.1142963openalex-snapshot
Primary Immunodeficiencies: A Field in Its Infancy
inferredcites →https://doi.org/10.1126/science.1158298openalex-snapshot
Pyogenic Bacterial Infections in Humans with MyD88 Deficiency
inferredcites →https://doi.org/10.1136/adc.88.4.340openalex-snapshot
Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO
inferredcites →https://doi.org/10.1136/jmg.2006.044446openalex-snapshot
IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal disease
inferredcites →https://doi.org/10.1172/jci0214858openalex-snapshot
Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations
inferredcites →https://doi.org/10.1172/jci14858openalex-snapshot
Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations
inferredcites →https://doi.org/10.1172/jci200421345openalex-snapshot
Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation
inferredcites →https://doi.org/10.1172/jci37083openalex-snapshot
A partial form of recessive STAT1 deficiency in humans
inferredcites →https://doi.org/10.1172/jci38111openalex-snapshot
Human genetics of infectious diseases: between proof of principle and paradigm
inferredcites →https://doi.org/10.1182/blood-2003-10-3655openalex-snapshot
X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival
inferredcites →https://doi.org/10.1182/blood-2003-12-4420openalex-snapshot
Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome
inferredcites →https://doi.org/10.1542/peds.109.6.e97openalex-snapshot
Osteopetrosis, Lymphedema, Anhidrotic Ectodermal Dysplasia, and Immunodeficiency in a Boy and Incontinentia Pigmenti in His Mother
inferredcites →https://doi.org/10.1542/peds.2004-1754openalex-snapshot
NEMO Mutations in 2 Unrelated Boys With Severe Infections and Conical Teeth
inferredcites →https://doi.org/10.1542/peds.2005-2062openalex-snapshot
Transient Hemophagocytosis With Deficient Cellular Cytotoxicity, Monoclonal Immunoglobulin M Gammopathy, Increased T-Cell Numbers, and HypomorphicNEMOMutation
inferredcites →https://doi.org/10.4049/jimmunol.0903944openalex-snapshot
Synoviocyte Innate Immune Responses: II. Pivotal Role of IFN Regulatory Factor 3
inferredcites →https://doi.org/10.4049/jimmunol.157.1.411openalex-snapshot
Defective monocyte costimulation for IFN-γ production in familial disseminated Mycobacterium avium complex infection: abnormal IL-12 regulation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Inborn Errors of Nucleic Acid Sensing and Type I Interferon Signaling Determine Viral Susceptibility in Humans
inferred← citeshttps://doi.org/10.1002/rmv.1848openalex-snapshot
Innate immune response during herpes simplex virus encephalitis and development of immunomodulatory strategies
inferred← citeshttps://doi.org/10.1002/rmv.2048openalex-snapshot
Toll‐like receptors as novel therapeutic targets for herpes simplex virus infection
inferred← citeshttps://doi.org/10.1007/978-3-031-74853-0_71openalex-snapshot
Herpes Simplex Viruses in Children
inferred← citeshttps://doi.org/10.1007/978-981-10-7230-7_5openalex-snapshot
Neurological Disorders Associated with Human Alphaherpesviruses
inferred← citeshttps://doi.org/10.1007/s00011-023-01768-2openalex-snapshot
USP10 regulates macrophage inflammation responses via stabilizing NEMO in LPS-induced sepsis
inferred← citeshttps://doi.org/10.1007/s00335-018-9772-5openalex-snapshot
Insights into the pathogenesis of herpes simplex encephalitis from mouse models
inferred← citeshttps://doi.org/10.1007/s00439-020-02127-5openalex-snapshot
Herpes simplex virus encephalitis of childhood: inborn errors of central nervous system cell-intrinsic immunity
inferred← citeshttps://doi.org/10.1007/s10875-017-0400-zopenalex-snapshot
Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency
inferred← citeshttps://doi.org/10.1016/b978-0-12-405546-9.00034-0openalex-snapshot
Other TLR Pathway Defects
inferred← citeshttps://doi.org/10.1016/b978-0-12-407179-7.00003-5openalex-snapshot
Evolution of the Definition of Primary Immunodeficiencies
inferred← citeshttps://doi.org/10.1016/b978-0-12-407675-4.00002-xopenalex-snapshot
Genetics of Immune Recognition and Response in Drosophila host defense
inferred← citeshttps://doi.org/10.1016/b978-0-12-816768-7.00039-9openalex-snapshot
Inherited disorders of TLR, IL-1R, and NFκB immunity
inferred← citeshttps://doi.org/10.1016/b978-0-323-82763-8.00158-8openalex-snapshot
Herpes Simplex Viruses 1 and 2
inferred← citeshttps://doi.org/10.1016/b978-0-444-52910-7.00027-1openalex-snapshot
Mendelian predisposition to herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1016/j.cell.2016.12.012openalex-snapshot
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
inferred← citeshttps://doi.org/10.1016/j.cell.2022.07.004openalex-snapshot
From rare disorders of immunity to common determinants of infection: Following the mechanistic thread
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.coi.2019.03.008openalex-snapshot
Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism
inferred← citeshttps://doi.org/10.1016/j.coi.2020.01.004openalex-snapshot
Human inborn errors of immunity to herpes viruses
inferred← citeshttps://doi.org/10.1016/j.coi.2021.07.004openalex-snapshot
Neuron-intrinsic immunity to viruses in mice and humans
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.coviro.2011.10.016openalex-snapshot
Inborn errors of anti-viral interferon immunity in humans
inferred← citeshttps://doi.org/10.1016/j.ejphar.2025.177435openalex-snapshot
Nonadditive transcriptional change analysis identifies regulators for ginsenoside Rg3 to alleviate synergistic cytokine production in TLR2/3 dual-stimulated macrophages
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Interferons at the crossroad of cell death pathways during gastrointestinal inflammation and infection
inferred← citeshttps://doi.org/10.1016/j.ijpam.2018.05.004openalex-snapshot
Approach to recurrent Herpes Simplex Encephalitis in children
inferred← citeshttps://doi.org/10.1016/j.immbio.2013.04.001openalex-snapshot
Prédisposition génétique aux maladies infectieuses chez l’homme
inferred← citeshttps://doi.org/10.1016/j.immuni.2024.03.004openalex-snapshot
Decoding Toll-like receptors: Recent insights and perspectives in innate immunity
inferred← citeshttps://doi.org/10.1016/j.intimp.2016.10.012openalex-snapshot
The important roles of type I interferon and interferon-inducible genes in systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1016/j.jaci.2011.11.047openalex-snapshot
Advances in basic and clinical immunology in 2011
inferred← citeshttps://doi.org/10.1016/j.jaci.2013.02.039openalex-snapshot
Herpesviruses and the microbiome
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The monogenic landscape of human infectious diseases
inferred← citeshttps://doi.org/10.1016/j.jmb.2013.11.024openalex-snapshot
Toll-Like Receptors in Antiviral Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2017.03.006openalex-snapshot
Molecular mechanisms of neuroinflammation and injury during acute viral encephalitis
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2017.12.011openalex-snapshot
Functional failure of TLR3 and its signaling components contribute to herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1016/j.micinf.2020.07.009openalex-snapshot
SNW1 interacts with IKKγ to positively regulate antiviral innate immune responses against influenza A virus infection
inferred← citeshttps://doi.org/10.1016/j.tig.2020.08.017openalex-snapshot
Genetic Lesions of Type I Interferon Signalling in Human Antiviral Immunity
inferred← citeshttps://doi.org/10.1016/j.yexcr.2012.03.032openalex-snapshot
Controlling systems of nucleic acid sensing-TLRs restrict homeostatic inflammation
inferred← citeshttps://doi.org/10.1038/gene.2015.46openalex-snapshot
Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1038/nrm3644openalex-snapshot
Molecular control of the NEMO family of ubiquitin-binding proteins
inferred← citeshttps://doi.org/10.1038/s41390-025-03830-7openalex-snapshot
The immunogenetic basis of severe herpes simplex infections in neonates and children: a review
inferred← citeshttps://doi.org/10.1038/s41423-024-01181-7openalex-snapshot
Orchestration of antiviral responses within the infected central nervous system
inferred← citeshttps://doi.org/10.1038/s41586-024-07745-xopenalex-snapshot
Human TMEFF1 is a restriction factor for herpes simplex virus in the brain
inferred← citeshttps://doi.org/10.1038/s41586-024-08119-zopenalex-snapshot
Genetic defects of brain immunity in childhood herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1038/s41591-019-0672-3openalex-snapshot
Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1038/srep24530openalex-snapshot
Dengue virus infection induces interferon-lambda1 to facilitate cell migration
inferred← citeshttps://doi.org/10.1080/21505594.2021.1982373openalex-snapshot
Pathogenesis and virulence of herpes simplex virus
inferred← citeshttps://doi.org/10.1084/jem.20111316openalex-snapshot
Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood
inferred← citeshttps://doi.org/10.1084/jem.20142274openalex-snapshot
Functional IRF3 deficiency in a patient with herpes simplex encephalitis
inferred← citeshttps://doi.org/10.1084/jem.20181621openalex-snapshot
Severe influenza pneumonitis in children with inherited TLR3 deficiency
inferred← citeshttps://doi.org/10.1084/jem.20240843openalex-snapshot
Mutations disrupting the kinase domain of IKKα lead to immunodeficiency and immune dysregulation in humans
inferred← citeshttps://doi.org/10.1084/jem.20250064openalex-snapshot
Role for NF-κB in herpes encephalitis pathology in mice genocopying an inborn error of IRF3-IFN immunity
inferred← citeshttps://doi.org/10.1084/jem.20251760openalex-snapshot
Autoantibodies neutralizing type I IFNs in patients with fulminant herpes simplex virus hepatitis
inferred← citeshttps://doi.org/10.1089/dna.2017.3668openalex-snapshot
The Type I Interferon Response and Age-Dependent Susceptibility to Herpes Simplex Virus Infection
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/cei/uxaf074openalex-snapshot
Autoantibodies against type I interferons correlate with low CD169/SIGLEC1 and severe non-viral infections in ER patients
inferred← citeshttps://doi.org/10.1126/science.abd4570openalex-snapshot
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
inferred← citeshttps://doi.org/10.1128/cmr.00105-19openalex-snapshot
Immunomodulatory Strategies in Herpes Simplex Virus Encephalitis
inferred← citeshttps://doi.org/10.1128/mbio.00921-20openalex-snapshot
The Innate Immune Response to Herpes Simplex Virus 1 Infection Is Dampened in the Newborn Brain and Can Be Modulated by Exogenous Interferon Beta To Improve Survival
inferred← citeshttps://doi.org/10.1136/bcr-2015-213999openalex-snapshot
Group B streptococcal meningitis in a previously healthy man
inferred← citeshttps://doi.org/10.1146/annurev-genet-120116-023425openalex-snapshot
Human Genetic Determinants of Viral Diseases
inferred← citeshttps://doi.org/10.1146/annurev-genom-091212-153448openalex-snapshot
The Genetic Theory of Infectious Diseases: A Brief History and Selected Illustrations
inferred← citeshttps://doi.org/10.1172/jci128808openalex-snapshot
Genetically programmed alternative splicing of NEMO mediates an autoinflammatory disease phenotype
inferred← citeshttps://doi.org/10.1172/jci134529openalex-snapshot
TLR3 controls constitutive IFN-β antiviral immunity in human fibroblasts and cortical neurons
inferred← citeshttps://doi.org/10.1172/jci139980openalex-snapshot
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency
inferred← citeshttps://doi.org/10.1172/jci166283openalex-snapshot
Unlocking life-threatening COVID-19 through two types of inborn errors of type I IFNs
inferred← citeshttps://doi.org/10.1172/jci59259openalex-snapshot
Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency
inferred← citeshttps://doi.org/10.1172/jci92280openalex-snapshot
Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections
inferred← citeshttps://doi.org/10.1186/s43042-020-00122-zopenalex-snapshot
Understanding the genetic determinant of severity in viral diseases: a case of SARS-Cov-2 infection
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008168openalex-snapshot
Herpes simplex encephalitis in adult patients with MASP-2 deficiency
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010857openalex-snapshot
RIPK3 and caspase 8 collaborate to limit herpes simplex encephalitis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3846667/v1openalex-snapshot
Oxymatrine Modulation of TLR3 Signaling Pathway: A Dual-Action Mechanism Against H9N2 Avian Influenza Virus and Immune Regulation
inferred← citeshttps://doi.org/10.3389/fimmu.2020.569331openalex-snapshot
Unveiling Interindividual Variability of Human Fibroblast Innate Immune Response Using Robust Cell-Based Protocols
inferred← citeshttps://doi.org/10.3389/fimmu.2021.685768openalex-snapshot
Corrigendum: Unveiling Interindividual Variability of Human Fibroblast Innate Immune Response Using Robust Cell-Based Protocols
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1751672openalex-snapshot
The cell-mediated adaptive immune response to herpes simplex virus type 1 encephalitis: mechanisms and clinical implications
inferred← citeshttps://doi.org/10.3390/biology15181648openalex-snapshot
Host Genetic Susceptibility and Antiviral Immunity Shape the Pathogenesis and Outcomes of Herpes Simplex Encephalitis
inferred← citeshttps://doi.org/10.3390/cells14040304openalex-snapshot
NEMO Family of Proteins as Polyubiquitin Receptors: Illustrating Non-Degradative Polyubiquitination’s Roles in Health and Disease
inferred← citeshttps://doi.org/10.3390/ijms23010242openalex-snapshot
Disrupting Neurons and Glial Cells Oneness in the Brain—The Possible Causal Role of Herpes Simplex Virus Type 1 (HSV-1) in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules29091945openalex-snapshot
Oxymatrine Modulation of TLR3 Signaling: A Dual-Action Mechanism for H9N2 Avian Influenza Virus Defense and Immune Regulation
inferred← citeshttps://doi.org/10.3390/pathogens12020310openalex-snapshot
Inborn Errors of Immunity Predisposing to Herpes Simplex Virus Infections of the Central Nervous System
inferred← citeshttps://doi.org/10.4049/jimmunol.1700699openalex-snapshot
NEMO–IKKβ Are Essential for IRF3 and NF-κB Activation in the cGAS–STING Pathway
inferred← citeshttps://doi.org/10.4049/jimmunol.1800063openalex-snapshot
Rel-Dependent Immune and Central Nervous System Mechanisms Control Viral Replication and Inflammation during Mouse Herpes Simplex Encephalitis
inferred← citeshttps://doi.org/10.70675/2a45c06fz18c3z4c07z88e2ze0e6ce5a17d0openalex-snapshot
Cinétique des effecteurs immunologiques impliqués dans la protection contre le virus Herpès simplex type 1 (HSV1) après primo-infection par une autre souche non neurovirulente : vers un modèle vaccinal
inferred← citeshttps://doi.org/10.70675/65d5a9daz9e88z43a5zb640zffa61798d4f1openalex-snapshot
Impaired TLR3 signaling and childhood herpes simplex encephalitis in autosomal recessive MEX3B deficiency
inferred← citeshttps://doi.org/10.70675/a1c17eadz8e32z4ae6z8f5dzbe60fed472deopenalex-snapshot
Rare bi-allelic MEX3B mutations in childhood herpes simplex encephalitis
inferred← citeshttps://doi.org/10.70675/b19ae5a1z0ff8z4de6zb2bczca89c6e7a7daopenalex-snapshot
Systematic Study of OX40 Ligand Context-Dependent Function on Human T Helper Cell Polarization
inferred← citeshttps://doi.org/10.70675/b75973b8z6f0dz4909z86acz3d7b45348403openalex-snapshot
Fulminant viral hepatitis in human inherited IL-10RB deficiency
inferred← citeshttps://doi.org/10.70675/da7bdf03zf68cz400dzbefbz7410b63d4e40openalex-snapshot
Autoantibodies to type I interferons : key factors in severe viral infections and emerging clinical applications
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