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Turkish Journal of Immunology, ISSN 1301-109X, 01/2015, Volume 3, Issue 2, pp. 34 - 35
Journal Article
Turkish Journal of Immunology, ISSN 1301-109X, 08/2015, Volume 3, Issue 2, pp. 34 - 35
Journal Article
Nature Immunology, ISSN 1529-2908, 06/2012, Volume 13, Issue 6, pp. 612 - 620
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 03/2018, Volume 141, Issue 3, pp. 1050 - 1059.e10
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2017, Volume 377, Issue 1, pp. 52 - 61
CD55 prevents convertase enzyme formation in the complement cascade, acting as a brake on complement activation. Inactivating mutations in CD55 result in... 
MEDICINE, GENERAL & INTERNAL | ACTIVATION | INFLAMMATORY-BOWEL-DISEASE | HEMOLYTIC-UREMIC SYNDROME | CELL RESPONSES | COMPLEMENT REGULATORY PROTEIN | INAB PHENOTYPE | DECAY-ACCELERATING FACTOR | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | T-CELLS | Intestine, Small - pathology | Humans | CD55 Antigens - genetics | Child, Preschool | Infant | Male | Protein-Losing Enteropathies - genetics | Syndrome | Complement System Proteins - metabolism | CD55 Antigens - blood | Complement Activation - genetics | Homozygote | T-Lymphocytes - metabolism | Complement Inactivating Agents - pharmacology | Pedigree | Protein-Losing Enteropathies - complications | Statistics, Nonparametric | Immunoglobulin A - blood | Female | Thrombosis - genetics | Mutation | Child | Complement Activation - drug effects | Proteins | Molecular targeted therapy | Gene mutations | Gastrointestinal diseases | Analysis | Homeostasis | Research | Thrombosis | Blood clot | Gastrointestinal tract diseases | Complement component C5a | Lymphocytes T | Cell activation | Immunology | Pain | Intestine | Hepatology | Gastroenterology | Malabsorption | Thromboembolism | Digestive tract | Age | Edema | Medical research | Lymphatic system | Hypersensitivity | Diarrhea | Inflammation | Heredity | Protein deficiency | Patients | Hereditary diseases | Complement activation | Infectious diseases | Decay-accelerating factor
Journal Article
Pediatric Allergy and Immunology, ISSN 0905-6157, 03/2012, Volume 23, Issue 2, p. 204
Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 08/2019, Volume 129, Issue 10, pp. 4194 - 4206
Polymerase δ is essential for eukaryotic genome duplication and synthesizes DNA at both the leading and lagging strands. The polymerase δ complex is a... 
Immunodeficiency | T cell receptors | Adaptive immunity | Genomes | Neurodevelopmental disorders | Patients | DNA biosynthesis | Proteins | Genotype & phenotype | Immunology | Antibiotics | Animal breeding | Etiology | Pedigree | Cell lines | Cell cycle | Replication | Mutation | Age | Deoxyribonucleic acid--DNA
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 135, Issue 2, pp. AB230 - AB230
  Conclusions Our findings suggested impaired NK cell functions in AD patients and imply a decrease of IFN-g production by NK1 cells, which may partially be... 
Allergy and Immunology | Killer cells | Children | Atopic dermatitis | Health aspects | Cytotoxicity | Dermatitis | Immune system
Journal Article
by Barzaghi, Federica and Amaya Hernandez, Laura Cristina and Neven, Benedicte and Ricci, Silvia and Kucuk, Zeynep Yesim and Bleesing, Jack J and Nademi, Zohreh and Slatter, Mary Anne and Ulloa, Erlinda Rose and Shcherbina, Anna and Roppelt, Anna and Worth, Austen and Silva, Juliana and Aiuti, Alessandro and Murguia-Favela, Luis and Speckmann, Carsten and Carneiro-Sampaio, Magda and Fernandes, Juliana Folloni and Baris, Safa and Ozen, Ahmet and Karakoc-Aydiner, Elif and Kiykim, Ayca and Schulz, Ansgar and Steinmann, Sandra and Notarangelo, Lucia Dora and Gambineri, Eleonora and Lionetti, Paolo and Shearer, William Thomas and Forbes, Lisa R and Martinez, Caridad and Moshous, Despina and Blanche, Stephane and Fisher, Alain and Ruemmele, Frank M and Tissandier, Come and Ouachee-Chardin, Marie and Rieux-Laucat, Frédéric and Cavazzana, Marina and Qasim, Waseem and Lucarelli, Barbarella and Albert, Michael H and Kobayashi, Ichiro and Alonso, Laura and Diaz De Heredia, Cristina and Kanegane, Hirokazu and Lawitschka, Anita and Seo, Jong Jin and Gonzalez-Vicent, Marta and Diaz, Miguel Angel and Goyal, Rakesh Kumar and Sauer, Martin G and Yesilipek, Akif and Kim, Minsoo and Yilmaz-Demirdag, Yesim and Bhatia, Monica and Khlevner, Julie and Richmond Padilla, Erick J and Martino, Silvana and Montin, Davide and Neth, Olaf and Molinos-Quintana, Agueda and Valverde-Fernandez, Justo and Broides, Arnon and Pinsk, Vered and Ballauf, Antje and Haerynck, Filomeen and Bordon, Victoria and Dhooge, Catharina and Garcia-Lloret, Maria Laura and Bredius, Robbert G and Kałwak, Krzysztof and Haddad, Elie and Seidel, Markus Gerhard and Duckers, Gregor and Pai, Sung-Yun and Dvorak, Christopher C and Ehl, Stephan and Locatelli, Franco and Goldman, Frederick and Gennery, Andrew Richard and Cowan, Mort J and Roncarolo, Maria-Grazia and Bacchetta, Rosa and PIDTC and IEWP and European Soc Blood Marrow and Primary Immune Deficiency Treatment Consortium (PIDTC) and the Inborn Errors Working Party (IEWP) of the European Society for Blood and Marrow Transplantation (EBMT)
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 03/2018, Volume 141, Issue 3, pp. 1036 - 1049.e5
Journal Article
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 1/2019, Volume 39, Issue 1, pp. 37 - 44
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2016, Volume 36, Issue 7, pp. 641 - 648
Loss and gain-of-function (GOF) mutations in human signal transducer and activator of transcription 1 (STAT1) lead to distinct phenotypes. Although recurrent... 
gain-of-function mutation | ruxolitinib | autoimmunity | STAT1 | mucocutaneous candidiasis | combined immunodeficiency | IMMUNITY | IMMUNOLOGY | CHRONIC MUCOCUTANEOUS CANDIDIASIS | DEFICIENCY | INBORN-ERRORS | ACTIVATOR | SIGNAL TRANSDUCER | T-Lymphocyte Subsets - immunology | Phosphorylation | Humans | Autoimmunity - genetics | Infant | Male | Tomography, X-Ray Computed | Janus Kinases - metabolism | Infection - etiology | STAT1 Transcription Factor - metabolism | Genes, Dominant | DNA Mutational Analysis | Infection - diagnosis | Female | Gain of Function Mutation | Cytokines - genetics | Pyrazoles - pharmacology | Gene Expression | Cytokines - metabolism | Severe Combined Immunodeficiency - diagnosis | Immunophenotyping | Severe Combined Immunodeficiency - immunology | STAT1 Transcription Factor - genetics | Janus Kinases - antagonists & inhibitors | Severe Combined Immunodeficiency - complications | Severe Combined Immunodeficiency - genetics | Immunoglobulin Isotypes - blood | Turkey | Interferon-beta - metabolism | Interferon-beta - pharmacology | Pedigree | T-Lymphocyte Subsets - metabolism | Age of Onset | Biomarkers | Heterozygote | Immunoglobulin Isotypes - immunology | Autoimmunity | Pneumonia | Bacterial pneumonia | Immunodeficiency | Mycoses | Biological response modifiers | T cells | Genetic research | Cytomegalovirus infections | Genetic aspects | Interferon | Nucleotide sequencing | DNA sequencing | Ruxolitinib | gain-of function mutation
Journal Article
Balkan Medical Journal, ISSN 2146-3123, 09/2016, Volume 33, Issue 5, pp. 539 - 542
Background: Allergic diseases with a potential for anaphylaxis pose a critical public health issue in schools. Aims: This study was carried out to identify the... 
Epinephrine | Food allergy | School board policy | Anaphylaxis | MEDICINE, GENERAL & INTERNAL | COMMUNITY | school board policy | ALLERGIC REACTIONS | PRESCHOOLS | epinephrine | food allergy | CARE | T?p | Original
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 2/2019, Volume 39, Issue 2, pp. 144 - 147
(4) 0000 0001 0671 7131, grid.24956.3c, Department of Genetics and Bioengineering, Istanbul Bilgi University, Istanbul, Turkey 
Medical Microbiology | Infectious Diseases | Internal Medicine | Biomedicine | Immunology | IMMUNOLOGY | GENE | DEFICIENCY | MUTATION | Bone marrow | Allergy | Transplantation | Molecular biology | Allergic reaction | Severe combined immunodeficiency
Journal Article
Turk pediatri arsivi, ISSN 1306-0015, 03/2016, Volume 51, Issue 1, pp. 8 - 14
Immunoglobulin replacement therapy is required to reduce the frequency and severity of infections in patients with primary antibody deficiencies.... 
Treatment outcome | Care and treatment | Immunoglobulins | Usage | Analysis | Immunodeficiency | Children | Research | Health aspects
Journal Article