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Cell reports (Cambridge), ISSN 2211-1247, 2016, Volume 16, Issue 10, pp. 2576 - 2592
The mechanisms underlying Zika virus (ZIKV)-related microcephaly and other neurodevelopment defects remain poorly understood. Here, we describe the derivation... 
NEURAL PROGENITORS | LONG-TERM | HUMAN BRAIN | ADAPTER | CENTRAL-NERVOUS-SYSTEM | INFECTION | MICE | BINDING KINASE 1 | ORGANOIDS | INNATE IMMUNITY | CELL BIOLOGY | Neocortex - pathology | Neurons - pathology | Transcription, Genetic - drug effects | Brain - embryology | Neuroglia - ultrastructure | Neuroglia - pathology | Humans | Brain - virology | Centrosome - drug effects | Gene Expression Profiling | Microcephaly - virology | Neural Stem Cells - ultrastructure | Zika Virus Infection - virology | Neural Stem Cells - immunology | Neuroepithelial Cells - immunology | Neuroprotective Agents - pharmacology | Spinal Cord - pathology | Microcephaly - pathology | Neuroepithelial Cells - virology | Nucleosides - pharmacology | Fetus - virology | Cell Death - drug effects | Phosphorylation - drug effects | Neurons - drug effects | Protein-Serine-Threonine Kinases - metabolism | Zika Virus - pathogenicity | Proto-Oncogene Proteins - metabolism | Zika Virus - ultrastructure | Neurons - virology | Virus Replication - drug effects | Neuroepithelial Cells - ultrastructure | Immunity, Innate - drug effects | Zika Virus Infection - pathology | Neural Stem Cells - virology | Zika Virus - physiology | Zika Virus - drug effects | Mitochondria - metabolism | Mitochondria - drug effects | Receptor Protein-Tyrosine Kinases - metabolism | Neural Stem Cells - enzymology | Centrosome - metabolism | Mitosis - drug effects | Brain - pathology | Protein Kinase Inhibitors - pharmacology | Neuroglia - virology | Neuroepithelial Cells - drug effects | Neurons/pathology | Zika Virus/pathogenicity | Mitochondria/metabolism | Virus Replication/drug effects | Microcephaly/pathology | Neurons/drug effects | Protein-Serine-Threonine Kinases/metabolism | Neural Stem Cells/immunology | Neuroglia/ultrastructure | Neuroepithelial Cells/drug effects | Neuroepithelial Cells/virology | Life Sciences | Brain/pathology | Zika Virus/drug effects | Brain/embryology | Mitochondria/drug effects | Fetus/virology | Neocortex/pathology | Neuroglia/pathology | Cell Death/drug effects | Mitosis/drug effects | Transcription, Genetic/drug effects | Nucleosides/pharmacology | Neural Stem Cells/enzymology | Neural Stem Cells/ultrastructure | Neuroepithelial Cells/ultrastructure | Receptor Protein-Tyrosine Kinases/metabolism | Microcephaly/virology | Proto-Oncogene Proteins/metabolism | Neuroprotective Agents/pharmacology | Zika Virus/ultrastructure | Neuroepithelial Cells/immunology | Brain/virology | Immunity, Innate/drug effects | Spinal Cord/pathology | Zika Virus/physiology | Neuroglia/virology | Microbiology and Parasitology | Zika Virus Infection/pathology | Neurons/virology | Zika Virus Infection/virology | Neural Stem Cells/virology | Centrosome/drug effects | Protein Kinase Inhibitors/pharmacology | Centrosome/metabolism | Phosphorylation/drug effects
Journal Article
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2014, Volume 146, Issue 7, pp. 1763 - 1774
Background & Aims The NACHT, LRR, and pyrin domain–containing protein 3 (NLRP3) inflammasome induces inflammation in response to organ injury, but little is... 
Gastroenterology and Hepatology | Innate Immune Response | Immune Regulation | Pancreas | Mouse Model | ACTIVATION | NLRP3 INFLAMMASOME | GPR81 | AGONISTS | GENE | TLR9 | MICE | HEPATOTOXICITY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | SEVERITY | Liver - pathology | Inflammasomes - metabolism | Receptors, G-Protein-Coupled - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Humans | Male | NF-kappa B - metabolism | Monocytes - immunology | Lipopolysaccharides | Liver - immunology | Liver - drug effects | RNA Interference | Interleukin-1beta - metabolism | Toll-Like Receptors - drug effects | Anti-Inflammatory Agents - administration & dosage | Toll-Like Receptors - metabolism | Cytoprotection | Disease Models, Animal | Galactosamine | Chemical and Drug Induced Liver Injury - prevention & control | Anti-Inflammatory Agents - pharmacology | Down-Regulation | Liver - metabolism | Injections, Intraperitoneal | Pancreas - pathology | Pancreas - metabolism | Pancreas - immunology | Toll-Like Receptor 4 - metabolism | Chemical and Drug Induced Liver Injury - immunology | Monocytes - drug effects | Macrophages - metabolism | Signal Transduction - drug effects | Chemical and Drug Induced Liver Injury - metabolism | Sodium Lactate - pharmacology | beta-Arrestins | Mice | Receptors, G-Protein-Coupled - genetics | RNA, Small Interfering - metabolism | Monocytes - metabolism | Pancreatitis - prevention & control | Arrestins - metabolism | Dose-Response Relationship, Drug | Pancreatitis - genetics | Transfection | Inflammasomes - drug effects | Sodium Lactate - administration & dosage | Pancreatitis - immunology | Chemical and Drug Induced Liver Injury - pathology | Chemical and Drug Induced Liver Injury - etiology | Macrophages - immunology | Cell Line | Immunity, Innate - drug effects | Toll-Like Receptor 4 - drug effects | Mice, Inbred C57BL | Pancreas - drug effects | Chemical and Drug Induced Liver Injury - genetics | Pancreatitis - chemically induced | Animals | Carrier Proteins - metabolism | beta-Arrestin 2 | Inflammasomes - immunology | Macrophages - drug effects | Pancreatitis - pathology | Pancreatitis - metabolism | Ceruletide | Lactates | Gastrointestinal diseases | Inflammation
Journal Article
The Plant cell, ISSN 1532-298X, 2006, Volume 18, Issue 12, pp. 3721 - 3744
We show that oomycete-derived Nep1 (for necrosis and ethylene-inducing peptide1)-like proteins (NLPs) trigger a comprehensive immune response in Arabidopsis... 
Disease resistance | Pathogens | Cell death | Genes | Innate immunity | Toxins | Cell membranes | Plants | Animal cells | Plant cells | H+-ATPASE ACTIVITY | ARABIDOPSIS-THALIANA | BIOCHEMISTRY & MOLECULAR BIOLOGY | FUSARIUM-OXYSPORUM | PLANT SCIENCES | CELL BIOLOGY | PROGRAMMED CELL-DEATH | MICROBIAL ELICITORS | GENE-EXPRESSION | HYPERSENSITIVE RESPONSE | DISEASE RESISTANCE | OLIGOPEPTIDE ELICITOR | ESSENTIAL COMPONENTS | Cell Death - radiation effects | Genes, Plant | Arabidopsis - immunology | Seedlings - microbiology | Phylogeny | Genetic Variation | Arabidopsis - radiation effects | Light | Protein Binding - drug effects | Gene Expression Regulation, Plant | Protein Binding - radiation effects | Plant Leaves - drug effects | Cell Death - drug effects | Germination - radiation effects | Plant Leaves - enzymology | Cell Membrane - drug effects | Germination - drug effects | Immunity, Innate - drug effects | Tobacco - drug effects | Plant Leaves - radiation effects | Seedlings - drug effects | Tobacco - radiation effects | Arabidopsis - genetics | Arabidopsis - microbiology | Immunity, Innate - radiation effects | Tobacco - microbiology | Fungal Proteins - pharmacology | Lipid Bilayers - metabolism | Seedlings - radiation effects | Cytoplasm - drug effects | Plant Leaves - microbiology | Fungal Proteins - metabolism | Arabidopsis thaliana | Immune response | Research | Peptides | Risk factors | Necrosis
Journal Article
Nature (London), ISSN 1476-4687, 2014, Volume 508, Issue 7494, pp. 123 - 127
Journal Article
Journal of leukocyte biology, ISSN 1938-3673, 2017, Volume 101, Issue 1, pp. 329 - 338
Intersection of innate and adaptive immunity in viral infection and implications for vaccine design... 
T lymphocytes | natural killer cells | viruses | immunity | Viruses | Natural killer cells | Immunity | NATURAL-KILLER-CELLS | DENDRITIC CELLS | PROTECTION | SUBSETS | IMMUNOLOGY | CELL BIOLOGY | ADAPTIVE IMMUNITY | NK CELLS | INFLAMMATION | INFECTION | DIFFERENTIATION | HEMATOLOGY | HEPATITIS-C | Antiviral Agents - immunology | Cell Count | Chemokine CXCL9 - biosynthesis | Integrin alpha1 - metabolism | Male | Interferon-gamma - metabolism | Antigens, CD - metabolism | Epitopes - immunology | Chemotactic Factors - pharmacology | Killer Cells, Natural - immunology | Dendritic Cells - drug effects | Female | Cell Membrane - metabolism | Cell Membrane - drug effects | Dendritic Cells - metabolism | NK Cell Lectin-Like Receptor Subfamily C - metabolism | Immunity, Innate - drug effects | NK Cell Lectin-Like Receptor Subfamily C - deficiency | Integrin alpha Chains - metabolism | Lymphocytes - cytology | Animals | Cross-Priming - immunology | CD8-Positive T-Lymphocytes - drug effects | Lymphocytes - drug effects | Liver - cytology | Mice | Adenoviridae - metabolism | CD8-Positive T-Lymphocytes - immunology | Cell proliferation | Antiviral agents | Lymphoid cells | Immune response | Transcription | CD8 antigen | Liver | Priming | Infections | Lymphocytes T | Adaptive immunity | Vaccines | Recruitment | NKG2 antigen | Signaling | CD103 antigen | Hepatocytes | Lymphocytes | γ-Interferon | Interferon | Viral infections | Inflammation, Extracellular Mediators, & Effector Molecules
Journal Article
Nature (London), ISSN 1476-4687, 2017, Volume 549, Issue 7671, pp. 282 - 286
The type 2 cytokines interleukin (IL)-4, IL-5, IL-9 and IL-13 have important roles in stimulating innate and adaptive immune responses that are required for resistance to helminth infection, promotion of allergic inflammation, metabolic... 
CRTH2 | CYTOKINES | IMMUNE INTERACTIONS | RECEPTORS | MULTIDISCIPLINARY SCIENCES | Inflammation - chemically induced | Inflammation - pathology | Eosinophils - drug effects | Pneumonia - pathology | Interleukin-13 - immunology | Male | Adoptive Transfer | Nippostrongylus - immunology | Receptors, Neurotransmitter - genetics | Eosinophils - immunology | Gastrointestinal Tract - immunology | Lymphocytes - immunology | Pneumonia - chemically induced | Neuropeptides - pharmacology | Interleukin-9 - metabolism | Pneumonia - immunology | Female | GTP-Binding Protein alpha Subunits, Gq-G11 - metabolism | Gastrointestinal Tract - innervation | Cytokines - immunology | Cytokines - metabolism | Immunity, Innate - drug effects | Cholinergic Neurons - metabolism | Interleukin-5 - metabolism | Neuropeptides - metabolism | Inflammation - immunology | Lymphocytes - cytology | Cholinergic Neurons - drug effects | Interleukin-13 - metabolism | Interleukin-5 - immunology | Receptors, Neurotransmitter - deficiency | Animals | Signal Transduction - drug effects | Lymphocytes - drug effects | Gastrointestinal Tract - cytology | Mice | Receptors, Neurotransmitter - metabolism | Eosinophils - cytology | Interleukin-9 - immunology | Genomics | Mucosa | Interleukin | Homeostasis | Nervous system | Neuropeptides | Activation | Small intestine | Antiinfectives and antibacterials | Proteins | Cell activation | Microorganisms | Enteric nervous system | Interleukin 5 | Immune system | Interleukin 9 | Lymphoid cells | Immune response | Cytokines | Neurons | Hypersensitivity | Gastrointestinal tract | Inflammation | Interleukin 13 | Signaling | Lungs | Ligands | In vitro methods and tests | Neuromedin
Journal Article