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Journal of the Pediatric Infectious Diseases Society, ISSN 2048-7193, 12/2018, Volume 7, Issue 2, pp. S79 - S82
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 133, Issue 5, pp. 1400 - 1409.e5
Background Identifying genetic syndromes that lead to significant atopic disease can open new pathways for investigation and intervention in allergy. Objective... 
Allergy and Immunology | immune deficiency | autoimmunity | phosphoglucomutase 3 | glycosylation | allergy | hyper-IgE | neurocognitive impairment | Atopy | STAT3 MUTATIONS | DOCK8 | NUCLEOTIDE SUGARS | HEALTHY | IMMUNOLOGY | O-GLCNACYLATION | CONGENITAL DISORDERS | Common Variable Immunodeficiency - immunology | CD8-Positive T-Lymphocytes - pathology | Hypersensitivity - enzymology | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Hypersensitivity - immunology | Male | Th2 Cells - immunology | Genetic Diseases, Inborn - pathology | Common Variable Immunodeficiency - enzymology | Autoimmune Diseases - genetics | Young Adult | Immunoglobulin E - immunology | Immunoglobulin E - genetics | Female | Hypersensitivity - genetics | B-Lymphocytes - pathology | Cognition Disorders - immunology | Autoimmune Diseases - pathology | Child | Th2 Cells - pathology | Phosphoglucomutase - metabolism | Th17 Cells - pathology | Cognition Disorders - enzymology | B-Lymphocytes - enzymology | Th17 Cells - enzymology | Autoimmune Diseases - enzymology | Autoimmune Diseases - immunology | Cognition Disorders - pathology | Common Variable Immunodeficiency - pathology | Genetic Diseases, Inborn - immunology | Common Variable Immunodeficiency - genetics | Cognition Disorders - genetics | CD8-Positive T-Lymphocytes - enzymology | B-Lymphocytes - immunology | Hypersensitivity - pathology | Pedigree | Genetic Diseases, Inborn - enzymology | Th17 Cells - immunology | Family | Phosphoglucomutase - immunology | Mutation | CD8-Positive T-Lymphocytes - immunology | Th2 Cells - enzymology | Phosphoglucomutase - genetics | Autoimmunity | Nervous system diseases | Genomics | Immunodeficiency | Genetic research | Disease susceptibility | Genetic aspects | Food allergies | Enzymes | Nuclear magnetic resonance--NMR | Disease | Infections | Dermatitis | Patients | Allergies | Asthma | Defects | Proteins | Lasers | Spectrum analysis | Viral infections
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2015, Volume 112, Issue 10, pp. 3056 - 3061
Journal Article
Journal Article
Immunology and Cell Biology, ISSN 0818-9641, 04/2019, Volume 97, Issue 4, pp. 389 - 402
Inherited defects in genes encoding for proteins that are involved in the assembly and dynamics of the actin skeleton have increasingly been identified in... 
primary immunodeficiency | RAC2 | Coronin 1A | DOCK2–DOCK8 | cytoskeleton | T-CELL SURVIVAL | SUPEROXIDE-PRODUCTION | THYMIC EGRESS | ARP2/3 COMPLEX | RAC ACTIVATOR | IMMUNOLOGY | AUTOINFLAMMATORY DISEASE | CELL BIOLOGY | COMBINED IMMUNODEFICIENCY | DOCK2-DOCK8 | RHO GTPASES | DOCK2 DEFICIENCY
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 131, Issue 3, pp. 840 - 848
Journal Article
International Reviews of Immunology, ISSN 0883-0185, 01/2016, Volume 35, Issue 1, pp. 39 - 56
In recent years a number of primary immunodeficiencies (PIDs) characterized by elevated Immunoglobulin E (IgE) levels have been uncovered and termed as... 
DOCK8 | herpes virus infections | STAT3 | primary immunodeficiency | JAK-STAT signaling | TYK2 | atypical mycobacteriosis | chronic mucocutaneous candidiasis | hyper-IgE syndrome | staphylococcus aureus | STAT3 MUTATIONS | JOBS-SYNDROME | HUMAN IL-17 | T-CELL MEMORY | IL-21 RECEPTOR | IMMUNOLOGY | INBORN-ERRORS | B-CELLS | HYPERIMMUNOGLOBULIN-E SYNDROME | DOCK8 DEFICIENCY | COLD STAPHYLOCOCCAL ABSCESSES | Job Syndrome - genetics | Job Syndrome - therapy | Humans | TYK2 Kinase - metabolism | Immunoglobulin E - blood | Antifungal Agents - therapeutic use | TYK2 Kinase - immunology | Anti-Bacterial Agents - therapeutic use | T-Lymphocytes - metabolism | Guanine Nucleotide Exchange Factors - metabolism | Bone Marrow Transplantation | Severe Combined Immunodeficiency - metabolism | Job Syndrome - metabolism | B-Lymphocytes - metabolism | STAT3 Transcription Factor - genetics | STAT3 Transcription Factor - metabolism | Cytokines - immunology | Phosphoglucomutase - metabolism | Diagnosis, Differential | Guanine Nucleotide Exchange Factors - genetics | Cytokines - metabolism | Job Syndrome - diagnosis | Signal Transduction | Antiviral Agents - therapeutic use | Severe Combined Immunodeficiency - diagnosis | Immunoglobulin E - metabolism | Severe Combined Immunodeficiency - therapy | Severe Combined Immunodeficiency - genetics | Phenotype | B-Lymphocytes - immunology | Guanine Nucleotide Exchange Factors - immunology | T-Lymphocytes - immunology | Phosphoglucomutase - immunology | Mutation | STAT3 Transcription Factor - immunology | TYK2 Kinase - genetics | Phosphoglucomutase - genetics
Journal Article
INDIAN JOURNAL OF PEDIATRICS, ISSN 0019-5456, 10/2016, Volume 83, Issue 10, pp. 1104 - 1108
Objectives To assess the utility of T helper17 (T(H)17) cell enumeration vis-a-vis National Institutes of Health (NIH) scoring in Hyper IgE syndrome (HIES).... 
ATOPIC-DERMATITIS | Hyper-IgE syndrome | DOCK8 | STAT3 | PEDIATRICS | MUTATIONS | T(H)17 cells | NIH scoring
Journal Article
Journal Article