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Volumn 7, Issue 1, 2005, Pages
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Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome.
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Author keywords
[No Author keywords available]
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Indexed keywords
CD56 ANTIGEN;
GRANZYME;
GZMB PROTEIN, HUMAN;
MEMBRANE PROTEIN;
PERFORIN;
PORE FORMING CYTOTOXIC PROTEIN;
SERINE PROTEINASE;
ADOLESCENT;
ADULT;
ARTICLE;
AUTOIMMUNE DISEASE;
BLOOD;
CD8+ T LYMPHOCYTE;
CELL STRAIN K 562;
CHEMISTRY;
CHILD;
CLASSIFICATION;
COCULTURE;
COMPARATIVE STUDY;
CYTOTOXICITY;
CYTOTOXICITY TEST;
FEMALE;
FLOW CYTOMETRY;
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS;
HUMAN;
IMMUNE DEFICIENCY;
IMMUNOLOGY;
JUVENILE RHEUMATOID ARTHRITIS;
MACROPHAGE ACTIVATION;
MALE;
MONONUCLEAR CELL;
NATURAL KILLER CELL;
PRESCHOOL CHILD;
SYNDROME;
ADOLESCENT;
ADULT;
ANTIGENS, CD56;
ARTHRITIS, JUVENILE RHEUMATOID;
AUTOIMMUNE DISEASES;
CD8-POSITIVE T-LYMPHOCYTES;
CHILD;
CHILD, PRESCHOOL;
COCULTURE TECHNIQUES;
CYTOTOXICITY TESTS, IMMUNOLOGIC;
CYTOTOXICITY, IMMUNOLOGIC;
FEMALE;
FLOW CYTOMETRY;
GRANZYMES;
HUMANS;
IMMUNOLOGIC DEFICIENCY SYNDROMES;
K562 CELLS;
KILLER CELLS, NATURAL;
LEUKOCYTES, MONONUCLEAR;
LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC;
MACROPHAGE ACTIVATION;
MALE;
MEMBRANE GLYCOPROTEINS;
PORE FORMING CYTOTOXIC PROTEINS;
SERINE ENDOPEPTIDASES;
SYNDROME;
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EID: 21744452702
PISSN: None
EISSN: 14786362
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (213)
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References (0)
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