Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhood |
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Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis |
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Cleaved/associated TLR3 represents the primary form of the signaling receptor |
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Deciphering Human Cell-Autonomous Anti-HSV-1 Immunity in the Central Nervous System |
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Déficit autosomique récessive de MEX3B : défaut de réponse à TLR3 et l’encéphalite herpétique de l’enfant. |
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Déficit héréditaire dans TLR3 chez l'homme : étiologie génétique de l'encéphalite herpétique et de la grippe sévère infantile. |
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EVER2 deficiency is associated with mild T-cell abnormalities |
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Genome-wide Innate Immune Responsiveness Profiles of Patients with Inborn Errors of Toll-like Receptor Signaling |
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Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency |
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Herpes simplex encephalitis in children : deficiences in Toll-Like receptor 3 signalling pathway |
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Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis |
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HGCS: an online tool for prioritizing disease-causing gene variants by biological distance |
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Host genetics of severe influenza: from mouse Mx1 to human IRF7 |
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Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors |
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The human gene connectome as a map of short cuts for morbid allele discovery |
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The human gene damage index as a gene-level approach to prioritizing exome variants |
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Human genetic and immunological determinants of critical COVID-19 pneumonia |
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Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism |
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Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation |
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Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis |
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Human TBK1: A Gatekeeper of Neuroinflammation |
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Human TBK1 is required for early autophagy induction upon HSV1 infection |
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Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses |
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IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients |
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Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells |
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Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense |
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Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection. |
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 |
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Inborn errors underlying herpes simplex encephalitis: From TLR3 to IRF3. |
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Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency |
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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections |
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Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines |
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Inherited MST1 deficiency underlies susceptibility to EV-HPV infections |
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IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans |
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L'encéphalite herpétique de l'enfant : défaut génétique humaine sur la voie de signalisation de Toll-like récepteur 3. |
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Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency |
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De l'étude des défauts génétiques innés de l’immunité de l’interféron de type I à leur phénocopie auto-immune. |
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Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation |
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A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes |
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The mutation significance cutoff: gene-level thresholds for variant predictions |
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Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance |
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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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A novel kindred with inherited STAT2 deficiency and severe viral illness |
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Parsing the Interferon Transcriptional Network and Its Disease Associations |
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A partial form of recessive STAT1 deficiency in humans |
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PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations |
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The proteome of Toll-like receptor 3-stimulated human immortalized fibroblasts: implications for susceptibility to herpes simplex virus encephalitis |
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Revisiting human primary immunodeficiencies |
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The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies |
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Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity |
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Severe COVID-19 in the young and healthy: monogenic inborn errors of immunity? |
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Severe influenza pneumonitis in children with inherited TLR3 deficiency |
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T-cell Responses to HSV-1 in Persons Who Have Survived Childhood Herpes Simplex Encephalitis |
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TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk |
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TLR3 immunity to infection in mice and humans |
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Varicella-zoster virus CNS vasculitis and RNA polymerase III gene mutation in identical twins |
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WITHDRAWN: Genetic infectious susceptibility and TLR defects in human |
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