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Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 2176 - 15
Microbial nucleic acid recognition serves as the major stimulus to an antiviral response, implying a requirement to limit the misrepresentation of self nucleic... 
AICARDI-GOUTIERES-SYNDROME | SYSTEMIC-LUPUS-ERYTHEMATOSUS | ACTIVE ENZYME | MAMMALIAN DNA | MULTIDISCIPLINARY SCIENCES | ALPHA | INFLAMMATORY DISEASE | DEOXYRIBONUCLEASE-II | MUTATIONS | EXONUCLEASE TREX1 | NUCLEIC-ACIDS | Endodeoxyribonucleases - immunology | Phosphorylation | Deoxyribonucleases - deficiency | Humans | RNA, Messenger - analysis | Male | Gene Expression Profiling | Erythroblasts - immunology | Signal Transduction - immunology | Deoxyribonucleases - immunology | STAT1 Transcription Factor - metabolism | Female | Endodeoxyribonucleases - deficiency | Child | STAT3 Transcription Factor - metabolism | Interferon-alpha - metabolism | Antiviral Agents - pharmacology | Hereditary Autoinflammatory Diseases - blood | Hereditary Autoinflammatory Diseases - enzymology | Hereditary Autoinflammatory Diseases - immunology | Interferon-alpha - immunology | Up-Regulation - drug effects | Deoxyribonucleases - genetics | Hematopoiesis - immunology | Endodeoxyribonucleases - genetics | Sequence Analysis, RNA | Interferon-alpha - blood | Adolescent | Mutation | Hereditary Autoinflammatory Diseases - genetics | Glomerulonephritis | Neonates | Deformation | Liver | Antibodies | α-Interferon | Microorganisms | Lymphocytes | Hematopoiesis | Peripheral blood | Anti-DNA antibodies | Stat1 protein | Enzyme-linked immunosorbent assay | Deoxyribonucleic acid--DNA | Deoxyribonuclease | Hematology | Anemia | Stat3 protein | Nucleic acids | Ribonucleic acid--RNA | Hemopoiesis | Signaling | Monocytes | Erythroblasts | Fibrosis | Interferon | Endonuclease | Life Sciences | Immunology
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 12/2017, Volume 76, Issue 12, pp. 2085 - 2094
ObjectivePyrin-Associated Autoinflammation with Neutrophilic Dermatosis (PAAND) is a recently described monogenic autoinflammatory disease. The causal p.S242R... 
14-3-3 | PAAND | pyrin | autoinflammatory disease | FMF | ASC | PROTEIN | RECOGNITION | NLRP3 INFLAMMASOME ACTIVATION | INFEVERS | DISORDERS | RHEUMATOLOGY | NF-KAPPA-B | REGISTRY | Leukocytes, Mononuclear - metabolism | Diagnosis, Differential | Hereditary Autoinflammatory Diseases - blood | Humans | Lipopolysaccharides - administration & dosage | Familial Mediterranean Fever - genetics | Caspase 1 - metabolism | Hereditary Autoinflammatory Diseases - diagnosis | Sweet Syndrome - genetics | Pyrin - blood | Case-Control Studies | Familial Mediterranean Fever - blood | Flow Cytometry | 14-3-3 Proteins - blood | Protein Binding | Familial Mediterranean Fever - diagnosis | Mutation | Sweet Syndrome - blood | Sweet Syndrome - diagnosis | Cytokines - blood | Hereditary Autoinflammatory Diseases - genetics | Care and treatment | Research | Cytokines | Gene mutations | Autoimmune diseases | Flow cytometry | Cell culture | Immunoprecipitation | Leukocytes (mononuclear) | Caspase-1 | Lipopolysaccharides | Proteins | Peripheral blood mononuclear cells | Skin diseases | Familial Mediterranean fever | Enzyme-linked immunosorbent assay | Blood & organ donations | Secretion | Caspase | Leukocytes (neutrophilic) | Inflammation | Fever | Interleukin 18 | Monocytes | 14-3-3 protein | Pyrin protein | Mutagenesis | Cell death | Speck | Apoptosis | Autoinflammatory Disease | Pyrin
Journal Article
Journal Article
Pediatric Emergency Care, ISSN 0749-5161, 07/2013, Volume 29, Issue 7, pp. 842 - 851
ABSTRACTPeriodic fevers are acquired or inherited disorders of innate immunity, which were first described in the 1940s. The patients are typically young at... 
hyperimmunoglobulinemia D syndrome | pharyngitis | aphthous stomatitis | tumor necrosis factor receptor 1Yassociated periodic syndrome | and cervical adenitis syndrome | cryopyrin-associated periodic syndromes | autoinflammatory diseases | familial Mediterranean fever | periodic fever | periodic fever syndromes | PFAPA SYNDROME | CONTROLLED-TRIAL | APHTHOUS STOMATITIS | RECURRENT FEVER | aphthous stomatitis, pharyngitis, and cervical adenitis syndrome | ENCODING MEVALONATE KINASE | HYPERIMMUNOGLOBULINEMIA-D SYNDROME | SYNDROME TRAPS | EMERGENCY MEDICINE | FAMILIAL-MEDITERRANEAN-FEVER | PEDIATRICS | tumor necrosis factor receptor 1-associated periodic syndrome | INFLAMMATORY ATTACKS | HYPER-IGD SYNDROME | NLR Family, Pyrin Domain-Containing 3 Protein | Colchicine - therapeutic use | Humans | Mevalonate Kinase Deficiency - genetics | Mevalonate Kinase Deficiency - blood | Receptors, Tumor Necrosis Factor - therapeutic use | Cryopyrin-Associated Periodic Syndromes - blood | Etanercept | Amyloidosis - etiology | Stomatitis, Aphthous - etiology | Lymphadenitis - etiology | Pharyngitis - etiology | Cryopyrin-Associated Periodic Syndromes - genetics | Hereditary Autoinflammatory Diseases - blood | Familial Mediterranean Fever - genetics | Periodicity | Emergencies | Fever - diagnosis | Immunoglobulin G - therapeutic use | Familial Mediterranean Fever - drug therapy | Hereditary Autoinflammatory Diseases - diagnosis | Receptors, Tumor Necrosis Factor, Type I - genetics | Cold Temperature - adverse effects | Hereditary Autoinflammatory Diseases - drug therapy | Mevalonate Kinase Deficiency - diagnosis | Familial Mediterranean Fever - blood | Carrier Proteins - genetics | Cryopyrin-Associated Periodic Syndromes - diagnosis | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Fever - genetics | Familial Mediterranean Fever - diagnosis | Fever - classification | Prednisone - therapeutic use | Hereditary Autoinflammatory Diseases - genetics
Journal Article
Journal Article
Journal Article