المؤلفون: Burmeister, Thomas

المساهمون: Charite, Med. Klinik fur Hamatologie, Onkologie und Tumorimmunologie, Hindenburgdamm 30, 12200 Berlin, Germany

مصطلحات موضوعية: CEBPE, Transcription factor, Neutrophil specific granule deficiency, Acute lymphoblastic leukemia, Translocation, Genes Section

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Genes/CEBPEID42984ch14q11.htmlTest; Thomas, Burmeister. CEBPE (CCAAT/enhancer binding protein epsilon). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 12, p. 438-440; http://hdl.handle.net/2042/69005Test; https://doi.org/10.4267/2042/69005Test

الإتاحة: https://doi.org/10.4267/2042/69005Test
http://hdl.handle.net/2042/69005Test

المؤلفون: Michel van Houdt, Ina Schim van der Loeff, Hans Janssen, Anton T.J. Tool, Evelien G. G. Sprenkeler, Taco W. Kuijpers, Mario Abinun, Karin R. Engelhardt, Angela Grainger, Sophie Hambleton

المساهمون: Graduate School, AII - Inflammatory diseases, Paediatric Infectious Diseases / Rheumatology / Immunology, Amsterdam Reproduction & Development (AR&D)

المصدر: The Journal of Allergy and Clinical Immunology
Journal of allergy and clinical immunology, 147(6), 2381-2385.e2. Mosby Inc.
Journal of Allergy and Clinical Immunology

مصطلحات موضوعية: Cytotoxicity, Immunologic, 0301 basic medicine, Chromosomal Proteins, Non-Histone, Neutrophils, medicine.medical_treatment, CD34, Hematopoietic stem cell transplantation, 0302 clinical medicine, inborn error of immunity, Immunology and Allergy, chemotaxis, Respiratory Burst, CEBPε, CCAAT-enhancer-binding protein ε, CEBPε, biology, Brief Report, Homozygote, neutrophil-specific granule deficiency, Cell Differentiation, SMARCD2, SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 2, Pedigree, 3. Good health, lactoferrin, Chemotaxis, Leukocyte, Haematopoiesis, Phenotype, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Myeloperoxidase, Female, Myelopoiesis, Immunology, Granulopoiesis, Immunophenotyping, Sepsis, 03 medical and health sciences, medicine, Humans, SGD, Specific granule deficiency, Genetic Predisposition to Disease, business.industry, Infant, Newborn, NADPH Oxidases, medicine.disease, 030104 developmental biology, phagocyte disorder, Mutation, biology.protein, RNA Splice Sites, Bone marrow, business, Splice-site mutation, Biomarkers, Leukocyte Disorders

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac05ce09b1371fefa175acc3798493faTest
https://doi.org/10.1016/j.jaci.2020.11.025Test

المؤلفون: Mary C. Dinauer (chair, Julie A. Lekstrom-himes, David C. Dale

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://asheducationbook.hematologylibrary.org/content/2000/1/303.full.pdfTest.

مصطلحات موضوعية: NEUTROPHIL SPECIFIC GRANULE DEFICIENCY

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.318.7677Test; http://asheducationbook.hematologylibrary.org/content/2000/1/303.full.pdfTest

الإتاحة: http://asheducationbook.hematologylibrary.org/content/2000/1/303.full.pdfTest