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Immunity, ISSN 1074-7613, 03/2015, Volume 42, Issue 3, pp. 443 - 456
The mechanisms underlying human natural killer (NK) cell phenotypic and functional heterogeneity are unknown. Here, we describe the emergence of diverse... 
NATURAL-KILLER-CELLS | ACTIVATION | CMV REACTIVATION | INNATE | RECEPTOR | FCR-GAMMA | DIFFERENTIATION | IMMUNOLOGY | PLZF CONTROLS | EXPRESSION | T-CELLS | Cell Proliferation | Humans | Transcription Factors - deficiency | NK Cell Lectin-Like Receptor Subfamily C - genetics | Receptors, IgG - deficiency | Intracellular Signaling Peptides and Proteins - immunology | Cytomegalovirus Infections - immunology | Gene Expression Profiling | Killer Cells, Natural - pathology | Cytomegalovirus Infections - genetics | Protein-Tyrosine Kinases - deficiency | Protein-Tyrosine Kinases - immunology | T-Lymphocytes, Cytotoxic - pathology | Intracellular Signaling Peptides and Proteins - deficiency | NK Cell Lectin-Like Receptor Subfamily C - immunology | DNA Methylation | Protein-Tyrosine Kinases - genetics | Receptors, IgG - genetics | Microarray Analysis | Antibodies - immunology | Cytomegalovirus Infections - virology | Killer Cells, Natural - immunology | Cytomegalovirus Infections - pathology | Kruppel-Like Transcription Factors - deficiency | Transcription Factors - immunology | Intracellular Signaling Peptides and Proteins - genetics | Syk Kinase | Adaptive Immunity | T-Lymphocytes, Cytotoxic - immunology | Promoter Regions, Genetic | GPI-Linked Proteins - immunology | Signal Transduction | Killer Cells, Natural - virology | T-Lymphocytes, Cytotoxic - virology | NK Cell Lectin-Like Receptor Subfamily C - deficiency | Immunophenotyping | Receptors, IgG - immunology | Transcription Factors - genetics | Killer Cells, Natural - classification | Promyelocytic Leukemia Zinc Finger Protein | Cytomegalovirus - immunology | Epigenesis, Genetic - immunology | Kruppel-Like Transcription Factors - genetics | Kruppel-Like Transcription Factors - immunology | GPI-Linked Proteins - genetics | Virus diseases | Proteins | Epigenetic inheritance | Killer cells | Immunotherapy | Genomics | Medical genetics | Cytomegalovirus infections | T cells | Methylation | Health aspects | Antigens | Flow cytometry | Cytomegalovirus | Data analysis | Biomedical research | Transplants & implants | Cytokines | Leukemia | Cytotoxicity | Infections | Kinases | Diversification | Gene expression | Experiments | Scholarships & fellowships | Lymphocytes | DNA methylation | Epigenetics | Viral infections | Immune system | Cancer | Index Medicus
Journal Article
Molecular Systems Biology, ISSN 1744-4292, 2011, Volume 7, Issue 1, pp. 525 - n/a
1 H Nuclear Magnetic Resonance spectroscopy ( 1 H NMR) is increasingly used to measure metabolite concentrations in sets of biological samples for top‐down... 
metabolome‐wide association study | top‐down systems biology | biomarker | variance decomposition | H nuclear magnetic resonance spectroscopy | metabolome-wide association study | top-down systems biology | H-1-NMR SPECTROSCOPY | METABONOMICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | NUCLEAR-MAGNETIC-RESONANCE | BIOMARKER IDENTIFICATION | ANALYTICAL REPRODUCIBILITY | SERUM | PLASMA | H-1 nuclear magnetic resonance spectroscopy | CARDIOVASCULAR-DISEASE | WIDE ASSOCIATION | HUMAN URINE | European Continental Ancestry Group - genetics | Biomarkers - urine | Twins, Monozygotic - genetics | Humans | Middle Aged | Databases, Genetic | Biomarkers - blood | Models, Statistical | Gene-Environment Interaction | Metabolome - genetics | Twins, Dizygotic - genetics | Genetic Variation | Systems Biology - methods | Sample Size | Algorithms | Nuclear Magnetic Resonance, Biomolecular - methods | Female | Aged | Research Design | Biological properties | Nuclear magnetic resonance--NMR | Variations | Population studies | Microflora | Statistical methods | Genomes | Decomposition | Epidemiology | Biological samples | Human populations | Design | Magnetic resonance spectroscopy | Biological variation | Metabolites | Mathematical analysis | Spectrum analysis | Bioindicators | Deoxyribonucleic acid--DNA | Urine | Spectroscopy | Phenotypes | Statistical analysis | Health risks | Dietary intake | Environmental factors | Genetic diversity | Metabolism | Statistics | Environmental effects | Molecular chains | Studies | Population (statistical) | Diet | Magnetic permeability | Samples | Predictions | Biomarkers | Resonance | Heritability | Variation | Twins | Index Medicus
Journal Article
Blood, ISSN 0006-4971, 04/2017, Volume 129, Issue 16, pp. 2266 - 2279
Several monogenic causes of familial myelodysplastic syndrome (MDS) have recently been identified. We studied 2 families with cytopenia, predisposition to MDS... 
FAMILIAL TUMORAL CALCINOSIS | GERM-LINE | FANCONI-ANEMIA REGISTRY | HEMATOPOIETIC STEM-CELLS | IN-VIVO | SPONTANEOUS REMISSION | ACUTE MYELOID-LEUKEMIA | RETROSPECTIVE ANALYSIS | HEMATOLOGY | DETECTABLE CLONAL MOSAICISM | MYELODYSPLASTIC SYNDROMES | Cell Proliferation | Humans | Middle Aged | Pancytopenia - immunology | Male | Killer Cells, Natural - pathology | Cognitive Dysfunction - immunology | Interferon Type I - pharmacology | Myeloid Cells - immunology | Tumor Suppressor Proteins - genetics | Killer Cells, Natural - immunology | Adult | Cognitive Dysfunction - genetics | Female | Myeloid Cells - drug effects | Cognitive Dysfunction - diagnosis | B-Lymphocytes - pathology | Cognitive Dysfunction - complications | Immunologic Deficiency Syndromes - diagnosis | Immunologic Deficiency Syndromes - immunology | Child | Gene Expression | Tumor Suppressor Proteins - metabolism | Immunologic Deficiency Syndromes - complications | Pancytopenia - diagnosis | Immunophenotyping | Myelodysplastic Syndromes - complications | B-Lymphocytes - drug effects | Hematopoiesis - immunology | Myelodysplastic Syndromes - diagnosis | B-Lymphocytes - immunology | Pancytopenia - complications | Pedigree | Alleles | Immunologic Deficiency Syndromes - genetics | Heterozygote | Mosaicism | Killer Cells, Natural - drug effects | Myelodysplastic Syndromes - genetics | Mutation | Myeloid Cells - pathology | Chromosomes, Human, Pair 7 - chemistry | Pancytopenia - genetics | Myelodysplastic Syndromes - immunology | Index Medicus | Abridged Index Medicus | Myeloid Neoplasia | Clinical Medicine | Medical and Health Sciences | Hematology | Hematologi | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Journal Article
Molecular Ecology Resources, ISSN 1755-098X, 11/2008, Volume 8, Issue 6, pp. 1202 - 1211
DNA barcode sequences (a 657‐bp segment of the mtDNA cytochrome oxidase I gene, COI) were collected from 191 species (503 specimens) of Echinodermata. All five... 
Asteroidea | coxI | DNA barcode | Holothuroidea | Echinodermata | Echinoidea | Ophiuroidea | COI | Crinoidea | CoxI | BIOLOGICAL IDENTIFICATIONS | PHYLOGENY | AUSTRALIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEA | NUCLEOTIDE | EVOLUTIONARY BIOLOGY | EVOLUTION | CONSERVATION | ECOLOGY | DIVERSITY
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2011, Volume 7, Issue 9, pp. e1002270 - e1002270
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2014, Volume 111, Issue 52, pp. 18412 - 18412
Journal Article
Journal Article
Blood, ISSN 1528-0020, 02/2017, Volume 129, Issue 16, p. 2266
Several monogenic causes of familial myelodysplastic syndrome (MDS) have recently been identified. We studied two families with cytopenia, predisposition to... 
Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Klinisk medicin | Journal Article
Journal Article
Journal Article