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SCIENTIFIC REPORTS, ISSN 2045-2322, 02/2019, Volume 9, Issue 1, pp. 1824 - 15
Journal Article
Science, ISSN 0036-8075, 03/2012, Volume 335, Issue 6075, pp. 1503 - 1506
Journal Article
PLoS Pathogens, ISSN 1553-7366, 2014, Volume 10, Issue 6, pp. e1004174 - e1004174
Bacterial signaling systems are prime drug targets for combating the global health threat of antibiotic resistant bacterial infections including those caused... 
NADPH OXIDASE | ANTIBIOTICS | LYTTR DOMAIN | MODE | MICROBIOLOGY | INDUCTION | VIRULENCE | IDENTIFICATION | DISCOVERY | VIROLOGY | GENE-EXPRESSION | SKIN | PARASITOLOGY | Staphylococcus epidermidis - physiology | Skin - microbiology | Molecular Conformation | Bacterial Proteins - chemistry | Male | Promoter Regions, Genetic - drug effects | Trans-Activators - chemistry | Staphylococcal Skin Infections - immunology | Anti-Bacterial Agents - adverse effects | Macrophages - microbiology | Triazoles - therapeutic use | Bacterial Proteins - antagonists & inhibitors | Quorum Sensing - drug effects | Mice, Knockout | Macrophages - metabolism | Staphylococcus epidermidis - growth & development | Staphylococcus aureus - immunology | Anti-Bacterial Agents - pharmacology | Molecular Docking Simulation | Quinazolinones - chemistry | Mutation | Staphylococcal Skin Infections - microbiology | Triazoles - adverse effects | Staphylococcus epidermidis - drug effects | Staphylococcus aureus - physiology | Staphylococcus epidermidis - immunology | Triazoles - chemistry | Anti-Bacterial Agents - therapeutic use | Staphylococcal Skin Infections - drug therapy | Anti-Bacterial Agents - chemistry | Trans-Activators - genetics | Macrophages - immunology | Quinazolinones - pharmacology | Molecular Targeted Therapy - adverse effects | Phagocytosis - drug effects | Immunity, Innate - drug effects | Bacterial Proteins - genetics | Mice, Hairless | Drug Discovery | Triazoles - pharmacology | Animals | High-Throughput Screening Assays | Bacterial Proteins - metabolism | Genes, Reporter - drug effects | Macrophages - drug effects | Trans-Activators - metabolism | Quinazolinones - therapeutic use | Trans-Activators - antagonists & inhibitors | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Cell Line, Transformed | Quinazolinones - adverse effects | Skin - drug effects | Staphylococcus aureus infections | Physiological aspects | Development and progression | Genetic aspects | Quorum sensing | Virulence (Microbiology) | Research | Staphylococcus aureus | Index Medicus | Medical research | Bacteria | Staphylococcus infections | Bacterial infections | Antibiotics | Bacteriology
Journal Article
Nature, ISSN 0028-0836, 11/2015, Volume 527, Issue 7578, pp. 323 - 328
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2015, Volume 10, Issue 11, pp. e0142340 - e0142340
The perforant pathway projection from layer II of the entorhinal cortex to the hippocampal dentate gyrus is especially important for long-term memory... 
MAMMALIAN TARGET | IN-VITRO | STIMULATION | MULTIDISCIPLINARY SCIENCES | MEMORY IMPAIRMENT | DISEASE | TAU | ENTORHINAL CORTEX NEURONS | TOXICITY | AUTOPHAGY | PATHOLOGY | Microglia - metabolism | Entorhinal Cortex - metabolism | Humans | tau Proteins - metabolism | Male | Hippocampus - drug effects | Neurodegenerative Diseases - drug therapy | TOR Serine-Threonine Kinases - antagonists & inhibitors | Synapses - metabolism | Dentate Gyrus - drug effects | Perforant Pathway - metabolism | Neurons - metabolism | Phosphorylation - drug effects | Neurons - drug effects | Disease Models, Animal | Synapses - drug effects | Dentate Gyrus - metabolism | Microglia - drug effects | Alzheimer Disease - drug therapy | Axons - drug effects | Axons - metabolism | Memory, Long-Term - drug effects | Entorhinal Cortex - drug effects | Neurodegenerative Diseases - metabolism | Sirolimus - pharmacology | Hippocampus - metabolism | Tauopathies - metabolism | Animals | Perforant Pathway - drug effects | Alzheimer Disease - metabolism | Mice | Tauopathies - drug therapy | TOR protein | Brain | Phosphorylation | Toxicity | Medical services | Activation | mRNA | Kinases | Autophagy | Neurotoxicity | Neurodegeneration | Rodents | Long term memory | Degeneration | Inhibition | Alzheimer's disease | Neurodegenerative diseases | Neurons | Astrocytes | Rapamycin | Inflammation | Substrates | Microglia | Pathology | Cortex (entorhinal) | Dentate gyrus | Gliosis | Inhibitors | Tau protein | Hippocampus | Phagocytosis | Synapses | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, pp. 315 - 326
Secondary damage following primary spinal cord injury extends pathology beyond the site of initial trauma, and effective management is imperative for... 
SURVIVAL | PROTEIN-KINASE-B | TYROSINE-PHOSPHATASE INHIBITION | MULTIDISCIPLINARY SCIENCES | CONTUSION INJURY | PTEN | AKT | UP-REGULATION | EXPRESSION | BRAIN | CELL-DEATH | Neuroprotective Agents - therapeutic use | Spinal Cord Injuries - drug therapy | Recovery of Function - drug effects | TOR Serine-Threonine Kinases - metabolism | Microtubule-Associated Proteins - metabolism | Cervical Vertebrae - blood supply | Protein Transport - drug effects | Autophagy - drug effects | Motor Neurons - pathology | Spinal Cord Injuries - pathology | Forelimb - physiopathology | Neuroprotective Agents - pharmacology | Spinal Cord Injuries - enzymology | Vanadium Compounds - pharmacology | Female | Phosphorylation - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Forelimb - drug effects | Motor Neurons - drug effects | Contusions - complications | Phagosomes - drug effects | Cervical Vertebrae - drug effects | Phagosomes - metabolism | Contusions - physiopathology | PTEN Phosphohydrolase - metabolism | Rats | Vanadium Compounds - therapeutic use | Enzyme Activation - drug effects | Rats, Sprague-Dawley | Contusions - drug therapy | Animals | Signal Transduction - drug effects | Models, Biological | Cervical Vertebrae - pathology | Spinal Cord Injuries - physiopathology | Spinal cord injuries | Phosphatases | TOR protein | Neuroprotection | Neurosciences | Spinal cord | Vanadium compounds | Traumatic brain injury | Central nervous system | Vanadium | Recovery of function | Homology | AKT protein | Spinal cord injury | Kinases | Phosphatase | Autophagy | Western blotting | Proteins | Rodents | Cell cycle | Bisperoxovanadium | Tumorigenesis | Research centers | Tensin | Hematology | Neurons | Rapamycin | Pharmacology | Functional analysis | Trauma | Medicine | Signaling | Injury prevention | Brain research | Insects | Immunofluorescence | Potassium | Histochemistry | Phagocytosis | Apoptosis | Index Medicus
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 10/2017, Volume 32, Issue 10, pp. 2128 - 2141
Autophagy is activated during nutritionally depleted or hypoxic conditions to facilitate cell survival. Because growth plate is an avascular and hypoxic... 
ENDOCHONDRAL OSSIFICATION | AUTOPHAGY | GROWTH PLATE CHONDROCYTES | ATG7 | ER STRESS | MATRIX | CHONDROCYTES | ENDOPLASMIC-RETICULUM STRESS | CELL-DEATH | UNFOLDED PROTEIN RESPONSE | PATHWAY | ENDOCRINOLOGY & METABOLISM | GROWTH-PLATE | BONE | DIFFERENTIATION | Chondrogenesis - drug effects | Apoptosis - drug effects | eIF-2 Kinase - metabolism | Autophagy-Related Protein 7 - metabolism | Growth Plate - embryology | Cartilage - drug effects | Autophagy - drug effects | Chondrocytes - drug effects | Gene Deletion | Phenylbutyrates - pharmacology | Tibia - growth & development | Growth Plate - ultrastructure | Chondrocytes - metabolism | Femur - growth & development | Endoplasmic Reticulum Stress - drug effects | Osteogenesis - drug effects | Cells, Cultured | Femur - drug effects | Cartilage - metabolism | Growth Plate - metabolism | Organ Specificity | Tibia - drug effects | Autophagy-Related Protein 7 - genetics | Mice, Knockout | Animals | Activating Transcription Factor 4 - metabolism | Cell Differentiation - drug effects | Chondrocytes - ultrastructure | Cell Proliferation - drug effects | Embryonic Development - drug effects | Transcription Factor CHOP - metabolism | Autophagy-Related Protein 7 - deficiency | Analysis | Stress (Physiology) | Cell proliferation | Cell survival | Growth rate | Homeostasis | Collagenase 3 | Autophagy | Ossification | Cartilage | Growth plate | Bone growth | Rodents | Chondrocytes | Hypoxia | Chondrogenesis | Stress response | Endoplasmic reticulum | Bone (endochondral) | Phenylbutyric acid | Phagocytosis | Apoptosis | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 09/2009, Volume 461, Issue 7261, pp. 282 - 286
Phagocytic removal of apoptotic cells occurs efficiently in vivo such that even in tissues with significant apoptosis, very few apoptotic cells are detectable.... 
UTP | THYMUS | RECEPTOR SUBTYPES | EPITHELIAL-CELLS | CHEMOTAXIS | INFLAMMATION | ENGULFMENT | ELEGANS | MULTIDISCIPLINARY SCIENCES | DEATH | EXTRACELLULAR NUCLEOTIDES | Uridine Triphosphate - metabolism | Monocytes - cytology | Humans | Culture Media, Conditioned - chemistry | Culture Media, Conditioned - pharmacology | Monocytes - metabolism | Receptors, Purinergic P2Y2 | Adenosine Triphosphate - pharmacology | Chemotactic Factors - pharmacology | Chemotactic Factors - metabolism | Adenosine Triphosphate - metabolism | Receptors, Purinergic P2 - genetics | Phagocytes - cytology | Cell Line | Phagocytosis - drug effects | Jurkat Cells | Phagocytes - drug effects | Mice, Inbred C57BL | Uridine Triphosphate - pharmacology | Cells, Cultured | Phagocytosis - physiology | Thymus Gland - cytology | Purinergic P2 Receptor Antagonists | Chemotaxis - drug effects | Macrophages - cytology | Phagocytes - metabolism | Monocytes - drug effects | Macrophages - metabolism | Animals | Signal Transduction - drug effects | Receptors, Purinergic P2 - metabolism | Macrophages - drug effects | Mice | Apoptosis - physiology | Macrophage Activation - drug effects | Receptors, Purinergic P2 - deficiency | Culture Media, Conditioned - metabolism | Phagocytes | Nucleotides | Research | Properties | Apoptosis | Rodents | Cells | Index Medicus
Journal Article
Journal of Immunology, ISSN 0022-1767, 07/2015, Volume 195, Issue 2, pp. 661 - 671
CD47, a self recognition marker expressed on tissue cells, interacts with immunoreceptor SIRP alpha expressed on the surface of macrophages to initiate... 
SIGNAL | IN-VITRO | PHAGOCYTOSIS | INHIBITION | CALRETICULIN | THERAPEUTIC TARGET | REGULATORY PROTEIN-ALPHA | RED-BLOOD-CELLS | NEUTROPHIL TRANSMIGRATION | IMMUNOLOGY | EXPRESSION | Spleen - immunology | Apoptosis - drug effects | Apoptosis - radiation effects | Membrane Microdomains - radiation effects | Epithelial Cells - drug effects | Humans | Protein Transport - drug effects | Spleen - drug effects | beta-Cyclodextrins - pharmacology | CD47 Antigen - immunology | Phagocytosis - radiation effects | Ultraviolet Rays | Leukocytes, Mononuclear - immunology | Leukocytes, Mononuclear - radiation effects | Macrophages - radiation effects | Receptors, Immunologic - immunology | Epithelial Cells - cytology | Binding Sites | Macrophages - immunology | CD47 Antigen - genetics | Epithelial Cells - radiation effects | Phagocytosis - drug effects | Leukocytes, Mononuclear - drug effects | Signal Transduction | Mice, Inbred C57BL | CD47 Antigen - chemistry | Gene Expression Regulation | Spleen - cytology | Macrophages - cytology | Animals | Fibroblasts - radiation effects | Membrane Microdomains - drug effects | Protein Transport - radiation effects | Epithelial Cells - immunology | Fibroblasts - drug effects | Cell Line, Tumor | Protein Binding | Fibroblasts - immunology | Leukocytes, Mononuclear - cytology | Macrophages - drug effects | Spleen - radiation effects | Antigens, Differentiation - genetics | Fibroblasts - cytology | Mice | Primary Cell Culture | Receptors, Immunologic - genetics | Antigens, Differentiation - immunology | Index Medicus | Abridged Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2012, Volume 7, Issue 5, pp. e36831 - e36831
The present study was to explore the biological responses of the newly compound, MJ-29 in murine myelomonocytic leukemia WEHI-3 cells in vitro and in vivo... 
PERMEABILITY TRANSITION PORE | IMMUNE-RESPONSE | ACUTE LYMPHOBLASTIC-LEUKEMIA | IN-VIVO | BIOLOGY | TUBULIN POLYMERIZATION | DEATH | ANTITUMOR-ACTIVITY | BINDING AGENTS | CANCER | BALB/C MICE | Leukocytes, Mononuclear - metabolism | Reactive Oxygen Species | Apoptosis - drug effects | Calcium - metabolism | Body Weight - drug effects | Male | Leukemia - metabolism | Antineoplastic Agents - administration & dosage | Antigens, CD - metabolism | Antineoplastic Agents - toxicity | Lymphocytes - immunology | Antineoplastic Agents - pharmacology | Macrophages - immunology | Quinazolinones - pharmacology | Cell Survival - drug effects | Unfolded Protein Response - drug effects | Phagocytosis - drug effects | Leukocytes, Mononuclear - drug effects | Endoplasmic Reticulum Stress - drug effects | Leukemia - drug therapy | Mitochondria - drug effects | Organ Size - drug effects | Animals | Signal Transduction - drug effects | Cell Cycle Checkpoints - drug effects | Lymphocytes - drug effects | Cell Line, Tumor | Macrophages - drug effects | Mice | Mice, Inbred BALB C | Leukemia - mortality | Chemotherapy | Immunotherapy | Leukemia | Calpain | B cells | Cancer | Apoptosis | Flow cytometry | Liver | Body weight | Red pulp | Intracellular signalling | Cytotoxicity | Macrophages | Drug resistance | Cancer therapies | Pulp | Proteins | Mitochondria | Animal tissues | Cell cycle | Life sciences | Quinazolinone | Deoxyribonucleic acid--DNA | Spleen | Stresses | Myelomonocytic leukemia | Immune response | Calcium (intracellular) | Permeability | Stress | Cytometry | Monocytes | Lymphocytes B | Infiltration | Annexin V | Viability | Endoplasmic reticulum | Pharmaceuticals | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article