Cellular and molecular characterisation of the hyper immunoglobulin m syndrome associated with congenital rubella infection

Journal of Clinical Immunology

Volumn 29, Issue 1, 2009, Pages 99-106

  Ameratunga, Rohan ^a   Woon, See Tarn ^a   Koopmans, Wikke ^a   French, John ^b  

^a AUCKLAND CITY HOSPITAL   (New Zealand)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

Hyper IgM; Isotype switching; Non X linked; Rubella

Indexed keywords

ANTIGEN; CD40 LIGAND; CELL SURFACE IMMUNOGLOBULIN; CYTIDINE DEAMINASE; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M ANTIBODY; INTERLEUKIN 4; LECTIN; URACIL DNA GLYCOSIDASE;

ADULT; ANTIBODY PRODUCTION; APOPTOSIS; ARTICLE; B LYMPHOCYTE; CASE REPORT; CONTROLLED STUDY; DISEASE ASSOCIATION; DRUG MEGADOSE; ENZYME ACTIVATION; FLOW CYTOMETRY; GENE MUTATION; HUMAN; HYPER IGM SYNDROME; IMMUNOGLOBULIN DEFICIENCY; LYMPHOCYTE PROLIFERATION; MALE; MEMORY CELL; PERIPHERAL BLOOD MONONUCLEAR CELL; PRIORITY JOURNAL; RUBELLA; T LYMPHOCYTE ACTIVATION;

B-LYMPHOCYTES; CD40 LIGAND; HUMANS; HYPER-IGM IMMUNODEFICIENCY SYNDROME; IMMUNOGLOBULIN M; IMMUNOLOGIC MEMORY; MALE; MIDDLE AGED; RUBELLA; T-LYMPHOCYTES;

EID: 59449104188     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-008-9219-y     Document Type: Article

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