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Journal of Molecular Medicine, ISSN 0946-2716, 5/2007, Volume 85, Issue 5, pp. 531 - 537
Journal Article
Journal Article
Nature Reviews Rheumatology, ISSN 1759-4790, 12/2016, Volume 12, Issue 12, pp. 716 - 730
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2014, Volume 371, Issue 6, pp. 507 - 518
The stimulator of interferon genes (STING) protein bridges sensors of cytosolic DNA and the inflammatory pathway mediated by interferon-β. Activating mutations... 
MEDICINE, GENERAL & INTERNAL | FAMILIAL CHILBLAIN LUPUS | CYCLIC GMP-AMP | DNA | PROTEASOME SUBUNIT | LIPODYSTROPHY | SENSOR | MONOGENIC AUTOINFLAMMATORY DISEASES | EXPRESSION | I INTERFERON | INBORN-ERRORS | Up-Regulation | Phosphorylation | Humans | Infant | Male | Interferon-gamma - metabolism | Inflammation - metabolism | STAT1 Transcription Factor - metabolism | Skin Diseases, Vascular - genetics | Genes, Dominant | Female | Transcription, Genetic | Interferon-gamma - genetics | Cytokines - genetics | Infant, Newborn | Fibroblasts - metabolism | Skin Diseases, Vascular - metabolism | Cytokines - metabolism | Membrane Proteins - genetics | Sequence Analysis, DNA | Syndrome | Janus Kinases - antagonists & inhibitors | Lung Diseases - genetics | Pedigree | Age of Onset | Inflammation - genetics | Mutation | Pulmonary manifestations of general diseases | Blood circulation disorders | Genetic aspects | Research | Gene mutations | Risk factors | Transcription | Genes | Guanosine | Leukocytes (mononuclear) | Arthritis | Interleukin 6 | Cell activation | Vascular diseases | Lymphocytes | Cyclic GMP | Interleukin 1 | Peripheral blood | Fingers & toes | Fibroblasts | Janus kinase | Skin diseases | Children | Stat1 protein | Age | Deoxyribonucleic acid--DNA | Phenotypes | AMP | Patients | Endothelial cells | Studies | Biopsy | Ligands | Interferon | Autoimmune diseases | Apoptosis
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 11/2011, Volume 1238, Issue 1, pp. 91 - 98
The concept of grouping Mendelian disorders associated with an upregulation of type I interferon is not currently recognized in the medical literature. Here,... 
type I interferon | spondyloenchondrodysplasia | systemic lupus erythematosus | interferonopathy | Aicardi–Goutières syndrome | Systemic lupus erythematosus | Interferonopathy | Type I interferon | Aicardi-Goutières syndrome | Spondyloenchondrodysplasia | SYSTEMIC-LUPUS-ERYTHEMATOSUS | VIRUS INTERFERENCE | MULTIDISCIPLINARY SCIENCES | CONGENITAL INFECTION | EXONUCLEASE TREX1 | PLASMACYTOID DENDRITIC CELLS | GENETIC SUSCEPTIBILITY | AICARDI-GOUTIERES-SYNDROME | FAMILIAL CHILBLAIN LUPUS | Aicardi-Goutieres syndrome | EXPRESSION SIGNATURE | IFN-ALPHA | Immunologic Deficiency Syndromes - therapy | Up-Regulation | Osteochondrodysplasias - immunology | Nervous System Malformations - immunology | Humans | Autoimmune Diseases - immunology | Interferon Type I - immunology | Immunity | Autoimmune Diseases - genetics | Autoimmune Diseases of the Nervous System - immunology | Osteochondrodysplasias - genetics | Complement System Proteins - deficiency | Lupus Erythematosus, Systemic - genetics | Autoimmune Diseases of the Nervous System - genetics | Lupus Erythematosus, Systemic - immunology | Immunologic Deficiency Syndromes - genetics | Interferon Type I - genetics | Interferon Type I - metabolism | Immunologic Deficiency Syndromes - immunology | Nervous System Malformations - genetics | Lupus | Biological response modifiers
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 01/2015, Volume 125, Issue 1, pp. 413 - 424
Journal Article