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pädiatrie: Kinder- und Jugendmedizin hautnah, ISSN 1867-2132, 12/2015, Volume 27, Issue 6, pp. 38 - 43
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2009, Volume 360, Issue 1, pp. 32 - 43
Journal Article
Journal Article
Nature Medicine, ISSN 1078-8956, 10/2012, Volume 18, Issue 10, pp. 1550 - 1559
We found that hematopoietic cell-specific Lyn substrate 1 (HCLS1 or HS1) is highly expressed in human myeloid cells and that stimulation with granulocyte... 
FACTOR-RECEPTOR | MEDICINE, RESEARCH & EXPERIMENTAL | CELL-SPECIFIC PROTEIN-1 | HEMATOPOIETIC LINEAGE | COLONY-STIMULATING FACTOR | ENHANCER FACTOR-I | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEVERE CONGENITAL NEUTROPENIA | HS1 PROTEIN | INDUCED TYROSINE PHOSPHORYLATION | ACUTE MYELOBLASTIC-LEUKEMIA | PROXIMITY LIGATION | CELL BIOLOGY | Phosphorylation | Cell Proliferation | Humans | Leukemia, Myeloid, Acute - metabolism | Myelopoiesis - genetics | Male | Receptors, Granulocyte Colony-Stimulating Factor - genetics | Blood Proteins - metabolism | Neutropenia - congenital | RNA Interference | Blood Proteins - genetics | Base Sequence | HEK293 Cells | Female | Active Transport, Cell Nucleus | Granulocytes - metabolism | Neutropenia - genetics | Granulocyte Colony-Stimulating Factor - metabolism | Cell Line | Signal Transduction | Mice, Inbred C57BL | Lymphoid Enhancer-Binding Factor 1 - metabolism | Sequence Analysis, DNA | Mice, Knockout | Animals | Adaptor Proteins, Signal Transducing - genetics | Mice | RNA, Small Interfering | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Leukemia, Myeloid, Acute - genetics | Neutropenia - physiopathology | Genetic disorders | Granulocyte colony-stimulating factor | Physiological aspects | Genetic aspects | Research | Gene expression | Risk factors | Leucocytes | Mutagenesis | Testing laboratories | Autoimmune diseases | Leukemia | Index Medicus
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 02/2019, Volume 10, pp. 116 - 116
High frequency of acquired CSF3R (colony stimulating factor 3 receptor, granulocyte) mutations has been described in patients with severe congenital... 
COLONY-STIMULATING-FACTOR | TRANSFORMATION | CELLS | FACTOR-RECEPTOR GENE | G-CSFR mutations | pre-leukemia | ACUTE MYELOID-LEUKEMIA | IMMUNOLOGY | POINT MUTATIONS | leukemogenesis | ACTIVATING MUTATION | GRANULOPOIESIS | deep-sequencing | severe congenital neutropenia | EXPRESSION
Journal Article
NATURE MEDICINE, ISSN 1078-8956, 10/2006, Volume 12, Issue 10, pp. 1191 - 1197
We demonstrate here that lymphoid enhancer-binding factor 1 (LEF-1) mediates the proliferation, survival and differentiation of granulocyte progenitor cells.... 
COLONY-STIMULATING-FACTOR | PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MYC | ACUTE MYELOID-LEUKEMIA | BETA-CATENIN | CELL BIOLOGY | BINDING PROTEIN-ALPHA | C/EBP-ALPHA | COLORECTAL-CANCER | GENE-EXPRESSION | MUTATIONS | Bone marrow | Inhibitor drugs | Cellular biology | Gene expression | Molecular biology
Journal Article
Haematologica, ISSN 0390-6078, 07/2010, Volume 95, Issue 7, pp. 1207 - 1210
Severe congenital neutropenia a clinically and genetically heterogeneous disorder. Mutations in different genes have been described as causative for severe... 
Congenital neutropenia | HAX1 | Myelopoiesis | ELANE | GENE | ELASTASE | myelopoiesis | DISEASE | PHENOTYPE | ELA2 | congenital neutropenia | HEMATOLOGY | DEFICIENCY | Glucose-6-Phosphatase - genetics | Humans | Adaptor Proteins, Signal Transducing - genetics | Genotype | Mutation | Neutropenia - genetics | Child | Neutropenia - congenital | Index Medicus | Brief Reports
Journal Article
Nature Medicine, ISSN 1078-8956, 01/2007, Volume 13, Issue 1, pp. 38 - 45
Lysosome-related organelles have versatile functions, including protein and lipid degradation, signal transduction and protein secretion. The molecular... 
PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | GRANULE EXOCYTOSIS | COLONY-STIMULATING FACTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEVERE CONGENITAL NEUTROPENIA | MYELOID CELLS | HERMANSKY-PUDLAK-SYNDROME | CELL BIOLOGY | GRISCELLI-SYNDROME | HUMAN-NEUTROPHILS | LINKAGE ANALYSIS | CHEDIAK-HIGASHI-SYNDROME | Immunologic Deficiency Syndromes - pathology | Luciferases - metabolism | Humans | Immunoglobulin M - analysis | Neutrophils - ultrastructure | Family Health | Male | Melanocytes - metabolism | Adaptor Protein Complex 4 - genetics | Green Fluorescent Proteins - genetics | Recombinant Fusion Proteins - metabolism | Endosomes - metabolism | Luciferases - genetics | Adaptor Protein Complex 4 - deficiency | Base Sequence | Endosomes - ultrastructure | Female | Leukocyte Count | Neutrophils - metabolism | B-Lymphocytes - metabolism | B-Lymphocytes - ultrastructure | Green Fluorescent Proteins - metabolism | Microscopy, Electron, Transmission | Immunoglobulin D - analysis | Genotype | Melanocytes - ultrastructure | Adaptor Protein Complex 4 - metabolism | Linkage Disequilibrium | B-Lymphocytes - drug effects | Granulocyte Colony-Stimulating Factor - pharmacology | Point Mutation | T-Lymphocytes, Cytotoxic - metabolism | Immunologic Deficiency Syndromes - genetics | Immunologic Deficiency Syndromes - metabolism | Recombinant Fusion Proteins - genetics | Tumor Necrosis Factor Receptor Superfamily, Member 7 - analysis | T-Lymphocytes, Cytotoxic - ultrastructure | Microscopy, Fluorescence | Proteins | Signal transduction | Immunology | Mutation | Kinases | Gene expression | Index Medicus
Journal Article
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 04/2016, Volume 1370, Issue 1, pp. 119 - 125
Journal Article