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Journal of Neuroscience, ISSN 0270-6474, 12/2004, Volume 24, Issue 48, pp. 10846 - 10857
The specification and organization of glutamatergic synaptic transmission require the coordinated interaction among glutamate receptors and their synaptic... 
Homer | CREB | Fos | Glutamate | PSD-95 | Elk-1 | SYNAPTIC PROTEINS | INTRACELLULAR CALCIUM | ELEMENT-BINDING PROTEIN | DEPENDENT PATHWAY | NEUROSCIENCES | SHANK FAMILY | POSTSYNAPTIC DENSITY PROTEINS | IONOTROPIC GLUTAMATE RECEPTORS | EARLY GENE-EXPRESSION | CULTURED STRIATAL NEURONS | RYANODINE RECEPTOR-TYPE-1 | glutamate | Disks Large Homolog 4 Protein | Calcium - metabolism | Sodium - metabolism | Corpus Striatum - cytology | Cell Nucleus - physiology | N-Methylaspartate - pharmacology | DNA-Binding Proteins - metabolism | Phospholipase C beta | Protein Processing, Post-Translational - drug effects | Homer Scaffolding Proteins | Neurons - physiology | Indoles - pharmacology | Transcription, Genetic | Ion Transport | Phosphorylation - drug effects | Calcium Signaling | Isoenzymes - physiology | Carrier Proteins - physiology | Proto-Oncogene Proteins - metabolism | Nerve Tissue Proteins - physiology | ets-Domain Protein Elk-1 | Protein Kinase C - physiology | Mitogen-Activated Protein Kinase 1 - physiology | Synapses - physiology | Intracellular Signaling Peptides and Proteins | Rats | Excitatory Amino Acid Agonists - pharmacology | Protein Kinase C - antagonists & inhibitors | Maleimides | Receptors, N-Methyl-D-Aspartate - physiology | Diglycerides - physiology | Mitogen-Activated Protein Kinase 3 - physiology | Protein Interaction Mapping | Gene Expression Regulation - drug effects | Membrane Proteins | Transcription Factors - metabolism | Methoxyhydroxyphenylglycol - analogs & derivatives | Methoxyhydroxyphenylglycol - pharmacology | Animals | Signal Transduction - drug effects | Neurons - enzymology | Receptors, N-Methyl-D-Aspartate - agonists | Cyclic AMP Response Element-Binding Protein - metabolism | Signal Transduction - physiology | Enzyme Activation | Carbazoles - pharmacology | Type C Phospholipases - physiology | Index Medicus | Behavioral | Cognitive | Systems
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 9, pp. e73064 - e73064
Inhibitor of DNA binding 2 (ID2) is a helix-loop-helix transcriptional repressor rhythmically expressed in many adult tissues. Our earlier studies have... 
METABOLIC SYNDROME | OBESITY | MULTIDISCIPLINARY SCIENCES | RESISTANCE | FAT | ADIPOCYTE DIFFERENTIATION | REGULATES ADIPOGENESIS | EXPRESSION PROFILES | AGED RATS | MOLECULAR CLOCK | MICE LACKING | Motor Activity - physiology | Male | Muscle, Skeletal - metabolism | Body Weight - genetics | Eating - physiology | Diglycerides - metabolism | Inhibitor of Differentiation Protein 2 - deficiency | Insulin Resistance - physiology | Gene Deletion | Inhibitor of Differentiation Protein 2 - genetics | Female | Biological Transport - genetics | Glucose Tolerance Test | Cell Size | Sex Characteristics | Circadian Rhythm | Adipocytes - pathology | Eating - genetics | Adipose Tissue, Brown - pathology | Feeding Behavior - physiology | Aging - pathology | Motor Activity - genetics | Adipocytes, White - pathology | Animals | Aging - physiology | Homeostasis - physiology | Insulin Resistance - genetics | Glucose - metabolism | Adipose Tissue, Brown - metabolism | Biological Transport - physiology | Mice | Muscle, Skeletal - pathology | Body Weight - physiology | Homeostasis - genetics | Aging - metabolism | Adipose tissues | Glucose metabolism | Muscles | Physiological aspects | Genetic aspects | Research | Insulin | Adipose tissue | Transcription | Id2 protein | Liver | Diacylglycerol | Sex | Glucose | Adipocytes | Mouse devices | Rodents | Animal tissues | Working conditions | Helix-loop-helix proteins | Lipid metabolism | Adipose tissue (brown) | Locomotor activity | Deoxyribonucleic acid--DNA | Adipogenesis | Circadian rhythms | Feeding behavior | Diabetes mellitus | Sexual behavior | Circadian rhythm | Gene expression | Metabolism | Body weight gain | Ablation | Skeletal muscle | Feeding | Shift work | Glucose tolerance | Energy balance | Sensitivity | Thermogenesis | Body mass | Insulin resistance | Sensitivity enhancement | Females | Metabolic disorders | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
The Journal of Physiology, ISSN 0022-3751, 05/2009, Volume 587, Issue 10, pp. 2275 - 2298
Journal Article
The Journal of Physiology, ISSN 0022-3751, 12/2016, Volume 594, Issue 23, pp. 7027 - 7047
Candesartan, an inverse agonist of the type 1 angiotensin II receptor (AT 1 R), causes a concentration‐dependent inhibition of pressure‐dependent myogenic tone... 
type 1 angiotensin II receptor | cytoskeleton | mechanotransduction | actin stress fibres | vascular smooth muscle cell signalling | myogenic response | protein kinase C | RHO-ASSOCIATED KINASE | INTRAVASCULAR PRESSURE | PHYSIOLOGY | CEREBRAL PARENCHYMAL ARTERIOLES | RESISTANCE ARTERIES | PROTEIN-COUPLED RECEPTORS | MYOSIN PHOSPHORYLATION | STRETCH-ACTIVATION | CYTOSKELETON REORGANIZATION | NEUROSCIENCES | VASCULAR SMOOTH-MUSCLE | LIGHT-CHAIN PHOSPHORYLATION | Arterioles - physiology | Antihypertensive Agents - pharmacology | Receptor, Angiotensin, Type 1 - physiology | Tetrazoles - pharmacology | Captopril - pharmacology | Maleimides - pharmacology | Male | Angiotensin II Type 1 Receptor Blockers - pharmacology | Muscle Development | Receptor, Angiotensin, Type 1 - genetics | Diglycerides - pharmacology | Indoles - pharmacology | Muscle Fibers, Skeletal - physiology | Vasoconstrictor Agents - pharmacology | Protein Kinase C - physiology | Abdominal Muscles - physiology | Cells, Cultured | Losartan - pharmacology | Imidazoles - pharmacology | Protein Kinase C - antagonists & inhibitors | Arterioles - drug effects | Pressure | Rats, Sprague-Dawley | Vasoconstriction - drug effects | Animals | Benzimidazoles - pharmacology | Pyridines - pharmacology | Actins - physiology | Atomic force microscopy | Actin | Angiotensin | Polymerization | Muscles | G proteins | Muscle proteins | Protein kinases | Arteries | Membrane proteins | Index Medicus | Cardiovascular Physiology | Skeletal Muscle | Cardiovascular | Research Paper
Journal Article
Journal Article
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 06/2006, Volume 79, Issue 6, pp. 1369 - 1380
Macrophage‐derived chemokine [CC chemokine ligand 22 (CCL22)] and thymus‐ and activation‐regulated chemokine (CCL17) mediate cellular effects, principally by... 
PKC | signaling | chemokines | chemotaxis | Signaling chemotaxis | Chemokines | PROTEIN-KINASE-C | MACROPHAGE-DERIVED CHEMOKINE | CELL MIGRATION | IMMUNOLOGY | PHOSPHOINOSITIDE 3-KINASE | VASCULAR ENDOTHELIUM | ACTIVATION-REGULATED CHEMOKINE | CELL BIOLOGY | SIGNAL-TRANSDUCTION | INTEGRIN ACTIVATION | PKC-DELTA | IN-VIVO | HEMATOLOGY | Phosphorylation | Recombinant Fusion Proteins - pharmacology | Calcium Signaling - physiology | Humans | Chemokine CCL22 | Cell Line, Tumor - drug effects | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Th2 Cells - drug effects | Calcium Channels - physiology | Calcium - physiology | Chemotaxis - physiology | Protein Processing, Post-Translational - drug effects | T-Lymphocytes - drug effects | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Acetophenones - pharmacology | Cell Line, Tumor - physiology | Inositol 1,4,5-Trisphosphate Receptors | Indoles - pharmacology | Benzopyrans - pharmacology | Chromones - pharmacology | Pertussis Toxin - pharmacology | Phosphatidylinositol Diacylglycerol-Lyase - antagonists & inhibitors | Catalytic Domain | Chemokine CCL17 | Morpholines - pharmacology | Receptors, Cytoplasmic and Nuclear - physiology | Th2 Cells - cytology | Inositol 1,4,5-Trisphosphate - physiology | Chemotaxis - drug effects | Leukemia-Lymphoma, Adult T-Cell - pathology | Phosphatidylinositol Diacylglycerol-Lyase - physiology | Diglycerides - physiology | Protein Processing, Post-Translational - physiology | Pyrroles - pharmacology | Receptors, Chemokine - physiology | Chemokines, CC - physiology | T-Lymphocytes - cytology | Calcium Signaling - drug effects | Cell Line, Tumor - cytology | Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors | Chemokines, CC - genetics | Phosphothreonine - chemistry | Phosphatidylinositol 3-Kinases - physiology | Receptors, CCR4 | Index Medicus
Journal Article
Neuron, ISSN 0896-6273, 2006, Volume 49, Issue 3, pp. 409 - 420
Journal Article