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Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 131, Issue 2, pp. 477 - 485.e1
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 2014, Volume 211, Issue 13, pp. 2537 - 2547
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 510, Issue 7504, pp. 288 - 292
Journal Article
Cell, ISSN 0092-8674, 09/2000, Volume 102, Issue 5, pp. 565 - 575
The activation-induced cytidine deaminase (AID) gene, specifically expressed in germinal center B cells in mice, is a member of the cytidine deaminase family.... 
DEFECTIVE EXPRESSION | SIGNAL-TRANSDUCTION | CLASS SWITCH RECOMBINATION | SOMATIC HYPERMUTATION | IMMUNOGLOBULIN GENES | BIOCHEMISTRY & MOLECULAR BIOLOGY | X-LINKED IMMUNODEFICIENCY | CD40 LIGAND | FACTOR-KAPPA-B | GERMINAL-CENTERS | ANTIGEN RECEPTOR | CELL BIOLOGY | Immunologic Deficiency Syndromes - pathology | Lymph Nodes - pathology | Genes, Recessive - genetics | Germinal Center - immunology | Humans | Child, Preschool | Molecular Sequence Data | RNA, Messenger - analysis | Infant | Male | Immunoglobulin M - immunology | Lod Score | Palatine Tonsil - immunology | Hyperplasia - genetics | APOBEC-1 Deaminase | DNA Mutational Analysis | Cell Division | Gene Deletion | Cloning, Molecular | Female | B-Lymphocytes - pathology | Immunologic Deficiency Syndromes - immunology | Child | Chromosomes, Human, Pair 12 - genetics | Cytidine Deaminase - chemistry | Immunoglobulin M - genetics | Amino Acid Sequence | Immunologic Deficiency Syndromes - enzymology | B-Lymphocytes - enzymology | Lymphocyte Activation | Cytidine Deaminase - genetics | RNA, Messenger - genetics | Germinal Center - pathology | Lymph Nodes - immunology | Hyperplasia - pathology | Palatine Tonsil - pathology | B-Lymphocytes - immunology | Hyperplasia - physiopathology | Pedigree | Cytidine Deaminase - metabolism | Adolescent | Cytidine Deaminase - deficiency | Immunologic Deficiency Syndromes - genetics | Physiological aspects | Immunoglobulins | B cells | Differentiation | Genetic recombination | Enzyme activation
Journal Article
Blood, ISSN 0006-4971, 12/2017, Volume 130, Issue 24, pp. 2682 - 2688
Journal Article
Journal Article
Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, 11/2015, Volume 37, Issue 8, pp. 616 - 622
Glucose-6-phosphatase catalytic subunit 3 (G6PC3) deficiency was recently defined as a new severe congenital neutropenia subgroup remarkable with congenital... 
Inflammatory bowel disease | Severe congenital neutropenia | Combined immune deficiency | Intravenous γ-globulin | TYPE-4 | DEFECT | PHENOTYPE | combined immune deficiency | G-CSF THERAPY | intravenous gamma-globulin | inflammatory bowel disease | OSTEOPOROSIS | ONCOLOGY | SYNDROMIC NEUTROPENIA | PEDIATRICS | MUTATIONS | LEUKEMIA | SPECTRUM | HEMATOLOGY | severe congenital neutropenia | Glucose-6-Phosphatase - genetics | Frameshift Mutation | Colitis - genetics | Diarrhea - enzymology | Humans | Male | Failure to Thrive - enzymology | Lymphopenia - enzymology | Thrombocytopenia - genetics | Female | Respiratory Tract Infections - complications | Neutropenia - genetics | Child | Lymphocyte Subsets - pathology | Abnormalities, Multiple - genetics | Immunologic Deficiency Syndromes - enzymology | Catalytic Domain | Failure to Thrive - genetics | RNA Splice Sites - genetics | Thrombocytopenia - congenital | Exons - genetics | Codon, Nonsense | Glycogen Storage Disease Type I - immunology | Lymphopenia - congenital | Neutropenia - enzymology | Cell Lineage | Thrombocytopenia - enzymology | Phenotype | Colitis - enzymology | Glycogen Storage Disease Type I - genetics | Turkey | Diarrhea - genetics | Pedigree | Adolescent | Abnormalities, Multiple - enzymology | Immunologic Deficiency Syndromes - genetics | Consanguinity | Mutagenesis, Insertional | Lymphopenia - genetics | Bronchiectasis - etiology
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