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Nature Genetics, ISSN 1061-4036, 12/2015, Volume 48, Issue 1, pp. 67 - 73
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 03/2012, Volume 167, Issue 3, pp. 391 - 404
OTHER THEMES PUBLISHED IN THIS IMMUNOLOGY IN THE CLINIC REVIEW SERIES Allergy, Host Responses, Cancer, Type 1 diabetes and viruses, Metabolic diseases. Summary... 
CANDLE | DIRA | CAPS | neonatal disorder | NOMID | Neonatal disorder | GENERALIZED PUSTULAR PSORIASIS | HYPER-GAMMA-GLOBULINEMIA | JUVENILE IDIOPATHIC ARTHRITIS | IMMUNOLOGY | ATYPICAL NEUTROPHILIC DERMATOSIS | ENCODING MEVALONATE KINASE | AICARDI-GOUTIERES-SYNDROME | FAMILIAL MEDITERRANEAN FEVER | RECEPTOR ANTAGONIST ANAKINRA | ONSET STILLS-DISEASE | MULTISYSTEM INFLAMMATORY DISEASE | Cryopyrin-Associated Periodic Syndromes - immunology | Interleukin 1 Receptor Antagonist Protein - immunology | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Inflammatory Bowel Diseases - immunology | Hereditary Autoinflammatory Diseases - immunology | Cryopyrin-Associated Periodic Syndromes - therapy | Interleukins - genetics | Models, Immunological | Animals | Interleukins - immunology | Inflammatory Bowel Diseases - genetics | Interleukin-1 - immunology | Cytokines - antagonists & inhibitors | Interleukin-1 - antagonists & inhibitors | Hereditary Autoinflammatory Diseases - therapy | Receptors, Interleukin-1 - antagonists & inhibitors | Carrier Proteins - immunology | Cytokines - immunology | Hereditary Autoinflammatory Diseases - genetics | Type 2 diabetes | Rheumatoid factor | Genetic disorders | Interleukins | Type 1 diabetes | Rheumatoid arthritis | Skin diseases | Coronary heart disease | Drug approval | Cardiovascular disease | Metabolic disorders | Diabetes | Review
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 07/2017, Volume 76, Issue 7, pp. 1191 - 1198
ObjectivesInflammasomes are multiprotein complexes that sense pathogens and trigger biological mechanisms to control infection. Nucleotide-binding... 
Arthritis | Inflammation | Fever Syndromes | Juvenile Idiopathic Arthritis | CELLS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | DISEASES | SUBPOPULATIONS | FAMILIAL MEDITERRANEAN FEVER | JUVENILE IDIOPATHIC ARTHRITIS | MECHANISMS | INFLAMMASOMES | RHEUMATOLOGY | PYRIN | BLOOD | Interleukin-18 - immunology | Skin Diseases - genetics | Humans | Male | Precursor Cells, B-Lymphoid - immunology | Caspase 1 - immunology | Autoimmune Diseases - genetics | Netherlands | Apoptosis Regulatory Proteins - genetics | Female | Algeria | Child | Autoimmune Diseases - complications | Autoimmune Diseases - immunology | Hereditary Autoinflammatory Diseases - immunology | European Continental Ancestry Group | Skin Diseases - immunology | Arthritis, Juvenile - genetics | Syndrome | Hereditary Autoinflammatory Diseases - complications | Homozygote | Skin Diseases - complications | B-Lymphocytes - immunology | Arthritis, Juvenile - immunology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Arthritis, Juvenile - complications | Consanguinity | Mutation | African Continental Ancestry Group | Hereditary Autoinflammatory Diseases - genetics | Research | Gene mutations | Autoimmune diseases | NLRP proteins | Dyskeratosis | Pathogens | Cytokines | Transcription | Caspase | Patients | Inflammatory diseases | Caspase-1 | Interleukin 18 | Proteins | Vitiligo | Pyrin protein | Lymphocytes B | Rheumatoid arthritis | Gene mapping | Age | Immune system | Life Sciences | Human health and pathology | Rhumatology and musculoskeletal system
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2016, Volume 113, Issue 36, pp. 10127 - 10132
Systemic autoinflammatory diseases are caused by mutations in genes that function in innate immunity. Here, we report an autoinflammatory disease caused by... 
Autoinflammatory disease | Cytokines | Nf-κb pathway | Linear deubiquitinase | OTULIN | ACTIVATION | AMYLOPECTINOSIS | NF-kappa B pathway | UBIQUITIN | MULTIDISCIPLINARY SCIENCES | linear deubiquitinase | ASSEMBLY COMPLEX | CELL-DEATH | HOIP | SHARPIN | autoinflammatory disease | INFLAMMATION | LUBAC DEFICIENCY | cytokines | IMMUNODEFICIENCY | Fibroblasts - enzymology | Humans | NF-kappa B - immunology | Child, Preschool | Male | Fever - physiopathology | Leukocytes, Mononuclear - immunology | HEK293 Cells | Female | Child | Cytokines - genetics | Failure to Thrive - physiopathology | Hereditary Autoinflammatory Diseases - pathology | Cytokines - immunology | Dermatitis - physiopathology | Signal Transduction | Hereditary Autoinflammatory Diseases - enzymology | Gene Expression Regulation | Ubiquitin - genetics | Endopeptidases - deficiency | Hereditary Autoinflammatory Diseases - diagnosis | Fibroblasts - pathology | Endopeptidases - immunology | Leukocytes, Mononuclear - pathology | Endopeptidases - genetics | NF-kappa B - genetics | Pedigree | Age of Onset | Alleles | Fibroblasts - immunology | Leukocytes, Mononuclear - enzymology | Panniculitis - physiopathology | Consanguinity | Mutation | Ubiquitin - immunology | Hereditary Autoinflammatory Diseases - genetics | Allelomorphism | Genetic aspects | Gene mutations | Autoimmune diseases | Health aspects | Biological Sciences | NF-κB pathway
Journal Article
Nature Immunology, ISSN 1529-2908, 07/2017, Volume 18, Issue 8, pp. 832 - 842
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 12/2014, Volume 73, Issue 12, pp. 2160 - 2167
Journal Article
Clinical Immunology, ISSN 1521-6616, 2012, Volume 147, Issue 3, pp. 185 - 196
Journal Article