Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in turkish patients with common variable immunodeficiency

Journal of Clinical Immunology

Volumn 32, Issue 6, 2012, Pages 1165-1179

  Kutukculer, Necil ^a   Gulez, Nesrin ^a   Karaca, Neslihan E ^a   Aksu, Guzide ^a   Berdeli, Afig ^a  

^a EGE UNIVERSITY   (Turkey)

Author keywords

B lymphocyte subpopulations; childhood; Common variable immunodeficiency

Indexed keywords

APRIL PROTEIN; B CELL ACTIVATING FACTOR RECEPTOR; CD19 ANTIGEN; CD27 ANTIGEN; COMPLEMENT COMPONENT C3D RECEPTOR; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; IMMUNOGLOBULIN A; IMMUNOGLOBULIN D; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; INDUCIBLE T CELL COSTIMULATOR; TRANSMEMBRANE ACTIVATOR AND CAML INTERACTOR; ICOS PROTEIN, HUMAN; TNFRSF13B PROTEIN, HUMAN; TNFRSF13C PROTEIN, HUMAN; TNFSF13 PROTEIN, HUMAN;

3' UNTRANSLATED REGION; ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOIMMUNE DISEASE; B LYMPHOCYTE; BRONCHIECTASIS; CHILD; CLINICAL ARTICLE; COMMON VARIABLE IMMUNODEFICIENCY; CONSANGUINITY; CONTROLLED STUDY; CTLA 4 GENE; CYTOPENIA; DISEASE CLASSIFICATION; DISEASE SEVERITY; ETHNIC GROUP; EXON; FEMALE; FLOW CYTOMETRY; GENE MUTATION; GENETIC RISK; GRANULOMATOSIS; HETEROZYGOSITY; HUMAN; HUMAN CELL; ICOS GENE; IMMUNOGLOBULIN BLOOD LEVEL; INFECTION; LYMPHADENOPATHY; LYMPHOCYTE SUBPOPULATION; MALE; MEMORY CELL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPLENOMEGALY; TNFRSF13B GENE; TNFRSF13C GENE; TNFSF13 GENE; TURKISH; ADULT; CASE CONTROL STUDY; CLASSIFICATION; GENETIC POLYMORPHISM; GENETICS; IMMUNOLOGICAL MEMORY; IMMUNOLOGY; LYMPHATIC SYSTEM DISEASE; METABOLISM; MUTATION; PATHOLOGY; SEVERITY OF ILLNESS INDEX; TURKEY (REPUBLIC);

ADOLESCENT; B-CELL ACTIVATION FACTOR RECEPTOR; B-LYMPHOCYTES; CASE-CONTROL STUDIES; CHILD; COMMON VARIABLE IMMUNODEFICIENCY; CONSANGUINITY; CTLA-4 ANTIGEN; FEMALE; HUMANS; IMMUNOLOGIC MEMORY; INDUCIBLE T-CELL CO-STIMULATOR PROTEIN; LYMPHATIC DISEASES; MALE; MUTATION; POLYMORPHISM, GENETIC; SEVERITY OF ILLNESS INDEX; SPLENOMEGALY; TRANSMEMBRANE ACTIVATOR AND CAML INTERACTOR PROTEIN; TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY MEMBER 13; TURKEY; YOUNG ADULT;

EID: 84878244909     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-012-9717-9     Document Type: Article

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