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Journal of Biological Chemistry, ISSN 0021-9258, 2017, Volume 292, Issue 50, pp. 20599 - 20612
The short neuropeptide F (sNPF) neuropeptides, closely related to vertebrate neuropeptide Y (NPY), have been suggested to exert pleiotropic effects on many... 
signaling | DROSOPHILA-MELANOGASTER | neuropeptide | BIOCHEMISTRY & MOLECULAR BIOLOGY | INSECT CELLS | Bombyx mori | ANOPHELES-GAMBIAE | FUNCTIONAL-CHARACTERIZATION | TSETSE-FLY | silkworm | N-LINKED GLYCOSYLATION | FEEDING-BEHAVIOR | G protein-coupled receptor (GPCR) | GENE-EXPRESSION | GLOSSINA-MORSITANS-MORSITANS | NEUROHORMONE GPCRS | short neuropeptide F | GTP-Binding Protein alpha Subunits, Gi-Go - agonists | Phosphorylation | Receptors, G-Protein-Coupled - metabolism | Humans | Receptors, Neuropeptide - metabolism | Receptors, G-Protein-Coupled - agonists | Recombinant Fusion Proteins - metabolism | MAP Kinase Signaling System | Spodoptera | Bombyx - metabolism | Sf9 Cells | Protein Isoforms - metabolism | Protein Isoforms - agonists | HEK293 Cells | Insect Proteins - agonists | Receptors, Neuropeptide - agonists | Neuropeptides - genetics | Insect Proteins - metabolism | Peptide Fragments - genetics | Calcium Signaling | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Down-Regulation | Gene Expression Regulation | Insect Proteins - genetics | Receptors, Neuropeptide - genetics | Recombinant Proteins - chemistry | Neuropeptides - metabolism | Recombinant Fusion Proteins - chemistry | Protein Transport | Peptide Fragments - chemistry | Animals | GTP-Binding Protein alpha Subunits, Gi-Go - antagonists & inhibitors | Insect Proteins - chemistry | Protein Processing, Post-Translational | Receptors, G-Protein-Coupled - genetics | GTP-Binding Protein alpha Subunits, Gi-Go - metabolism | Neuropeptides - chemistry | Protein Isoforms - genetics | Signal Transduction
Journal Article
PLoS Biology, ISSN 1544-9173, 12/2015, Volume 13, Issue 12, p. e1002318
Detecting danger is one of the foremost tasks for a neural system. Larval parasitoids constitute clear danger to Drosophila, as up to 80% of fly larvae become... 
ODORS | PHEROMONE | EVOLUTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGY | RECEPTOR | SPATIAL REPRESENTATION | SELECTION | MAP | AGGRESSION | PREFERENCE | FLIES | Receptors, Odorant - metabolism | Drosophila melanogaster - physiology | Olfactory Bulb - metabolism | Drosophila Proteins - agonists | Drosophila Proteins - metabolism | Wasps - metabolism | Drosophila melanogaster - genetics | Odorants | Receptors, Odorant - agonists | Terpenes - pharmacology | Protein Isoforms - metabolism | Protein Isoforms - agonists | Larva - drug effects | Behavior, Animal - drug effects | Female | Larva - genetics | Sensory Receptor Cells - metabolism | Alkaloids - pharmacology | Signal Transduction | Animals, Genetically Modified | Nerve Tissue Proteins - agonists | Mutant Proteins - metabolism | Nerve Tissue Proteins - genetics | Drosophila melanogaster - drug effects | Nerve Tissue Proteins - metabolism | Bridged Bicyclo Compounds, Heterocyclic - pharmacology | Animals | Sensory Receptor Cells - drug effects | Iridoids - pharmacology | Larva - parasitology | Receptors, Odorant - genetics | Drosophila melanogaster - parasitology | Oviposition | Pyridines - pharmacology | Drosophila Proteins - genetics | Larva - physiology | Olfactory Bulb - drug effects | Mutant Proteins - agonists | Biological Sciences | Biologi | Naturvetenskap | Natural Sciences | Zoologi | Zoology | Ligands | Behavior | Insects | Females | Neurons
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2008, Volume 105, Issue 21, pp. 7606 - 7611
Acetylcholine-binding proteins (AChBPs) from mollusks are suitable structural and functional surrogates of the nicotinic acetylcholine receptors when combined... 
Molecules | Hydrogen bonds | Atomic interactions | Drug interactions | Ligands | Agonists | Kinetics | Nicotinic receptors | Binding sites | Crystal structure | Acetylcholine-binding protein | Imidacloprid | Nicotinic receptor | Thiacloprid | SITE | DOMAIN | MULTIDISCIPLINARY SCIENCES | COMPLEXES | thiacloprid | MODEL | imidacloprid | ACETYLCHOLINE-BINDING-PROTEIN | CONFORMATIONAL-CHANGES | crystal structure | nicotinic receptor | acetylcholine-binding protein | SELECTIVITY | REVEALS | Imidazolines - metabolism | Pyridines - chemistry | Imidazoles - chemistry | Nitro Compounds - chemistry | Neonicotinoids | Crystallography, X-Ray | Nicotinic Agonists - chemistry | Nicotine - pharmacology | Aplysia | Receptors, Nicotinic - chemistry | Nitro Compounds - pharmacology | Thiazines - pharmacology | Nicotinic Agonists - pharmacology | Receptors, Nicotinic - drug effects | Bridged Bicyclo Compounds, Heterocyclic - chemistry | Imidazolines - pharmacology | Imidazoles - pharmacology | Thiazines - chemistry | Bridged Bicyclo Compounds, Heterocyclic - pharmacology | Imidazolines - chemistry | Animals | Pyridines - metabolism | Nicotine - chemistry | Protein Conformation | Pyridines - pharmacology | Evaluation | Cell receptors | Pharmacology, Experimental | Crystals | Electronegativity | Binding proteins | Properties | Structure | Index Medicus | TRYPTOPHAN | SPECIFICITY | ACETYLCHOLINE | RESOLUTION | CRYSTAL STRUCTURE | TOXICITY | INTERACTIONS | 60 APPLIED LIFE SCIENCES | FLUORESCENCE | LIGANDS | QUENCHING | AMINO ACIDS | KINETICS | ORIENTATION | EQUILIBRIUM | INTERFACES | INSECTS | AROMATICS | POSITIONING | PROTEINS | RECEPTORS | INSECTICIDES | FUNCTIONALS | Biological Sciences | Physical Sciences
Journal Article
Immunity, ISSN 1074-7613, 06/2009, Volume 30, Issue 6, pp. 789 - 801
Cellular inhibitor of apoptosis proteins (cIAPs) block apoptosis, but their physiological functions are still under investigation. Here, we report that cIAP1... 
MOLIMMUNO | CELLS | ACTIVATION | C-IAP1 | PROTEIN | DROSOPHILA IMD PATHWAY | IN-VIVO | KINASE | IMMUNOLOGY | POLYUBIQUITINATION | NF-KAPPA-B | RIP2 | Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Receptors, Pattern Recognition - immunology | Inhibitor of Apoptosis Proteins - genetics | Nod1 Signaling Adaptor Protein - agonists | Colitis - pathology | Baculoviral IAP Repeat-Containing 3 Protein | Nod1 Signaling Adaptor Protein - metabolism | Receptors, Pattern Recognition - metabolism | Signal Transduction - immunology | Receptors, Pattern Recognition - agonists | Nod2 Signaling Adaptor Protein - agonists | Inhibitor of Apoptosis Proteins - metabolism | Colitis - immunology | Receptor-Interacting Protein Serine-Threonine Kinases - immunology | Cytokines - immunology | Cytokines - metabolism | Mice, Inbred C57BL | Nod2 Signaling Adaptor Protein - immunology | Ubiquitination - immunology | Nod1 Signaling Adaptor Protein - immunology | Immunity, Innate | Mice, Knockout | Acetylmuramyl-Alanyl-Isoglutamine - pharmacology | Ubiquitin-Protein Ligases | Receptor-Interacting Protein Serine-Threonine Kinases - genetics | Animals | Apoptosis - immunology | Colitis - enzymology | Nod2 Signaling Adaptor Protein - metabolism | Signal Transduction - drug effects | Inhibitor of Apoptosis Proteins - immunology | Mice | Ubiquitin | Oligomers | Ligases | Physiological aspects | Crohn's disease | Colitis | Apoptosis | Medical research | Enzymes | Statistical analysis | Cytokines | Kinases | Proteins | Inflammatory bowel disease | Genotype & phenotype | Insects | Bacteria | Gram-negative bacteria | Chemokines | Immune system
Journal Article
Journal Article
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 05/2016, Volume 20, Issue 5, pp. 874 - 890
Pituitary adenylate cyclase‐activating polypeptide (PACAP) is a structurally endogenous peptide with many biological roles. However, little is known about its... 
apoptotic | hADSCs | proliferation | neural differentiation | maxadilan | Proliferation | Neural differentiation | Maxadilan | Apoptotic | PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | CYCLASE-ACTIVATING POLYPEPTIDE | STRESS-INDUCED APOPTOSIS | OSTEOGENIC DIFFERENTIATION | SPINAL-CORD | CHONDROGENIC DIFFERENTIATION | MESENCHYMAL STEM-CELLS | CELL BIOLOGY | ENDOTHELIAL-CELLS | RECEPTOR AGONIST | STROMAL CELLS | Caspase 9 - genetics | Caspase 9 - metabolism | Heterocyclic Compounds, 3-Ring - pharmacology | Humans | Caspase 3 - metabolism | Adipocytes - cytology | Neurons - cytology | Stem Cells - cytology | Adipocytes - drug effects | Stem Cells - metabolism | Wnt Proteins - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Cyclic AMP-Dependent Protein Kinases - genetics | Isoquinolines - pharmacology | Wnt Proteins - genetics | Pituitary Adenylate Cyclase-Activating Polypeptide - pharmacology | Caspase 3 - genetics | Neurons - metabolism | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - agonists | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - metabolism | Tetrodotoxin - pharmacology | Neurons - drug effects | Cyclic AMP-Dependent Protein Kinases - metabolism | Cell Survival - drug effects | Insect Proteins - pharmacology | Signal Transduction | Gene Expression Regulation | Sulfonamides - pharmacology | beta Catenin - metabolism | beta Catenin - genetics | Annexin A5 - metabolism | Patch-Clamp Techniques | Cell Differentiation - drug effects | Adipocytes - metabolism | Stem Cells - drug effects | Cell Proliferation - drug effects | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - genetics | Proto-Oncogene Proteins c-bcl-2 - genetics | Cell differentiation | Analysis | Proteins | Polypeptides | Kinases | Rodents | Cell cycle | Stem cells | Original
Journal Article