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1. Full Text Synergistic effects of polyphenols and methylxanthines with leucine on AMPK/Sirtuin-mediated metabolism in muscle cells and adipocytes
by Bruckbauer, Antje and Zemel, Michael B
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e89166 - e89166
The AMPK-Sirt1 pathway is an important regulator of energy metabolism and therefore a potential target for prevention and therapy of metabolic diseases. We... 
SKELETAL-MUSCLE | RESVERATROL | ACTIVATED PROTEIN-KINASE | MITOCHONDRIAL BIOGENESIS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | NITRIC-OXIDE | AMPK | ENERGY-METABOLISM | SIRT1 ACTIVATION | ADIPOSE-TISSUE | Sirtuin 1 - metabolism | AMP-Activated Protein Kinases - metabolism | Leucine - pharmacology | Chlorogenic Acid - pharmacology | Humans | Muscle Cells - drug effects | Polyphenols - pharmacology | Caffeic Acids - pharmacology | Adipocytes - drug effects | Stilbenes - pharmacology | Valerates - pharmacology | Xanthines - pharmacology | Oxidation-Reduction - drug effects | Fatty Acids - metabolism | Ellagic Acid - pharmacology | AMP-Activated Protein Kinases - antagonists & inhibitors | Muscle Cells - metabolism | NAD - pharmacology | Phosphodiesterase Inhibitors - pharmacology | 3T3-L1 Cells | Sirtuin 1 - antagonists & inhibitors | Animals | Adipocytes - metabolism | Mice | Protein Kinase Inhibitors - pharmacology | Metabolites | Analysis | Resveratrol | Physiological aspects | Polyphenols | Amino acids | Fatty acids | Energy metabolism | Biosynthesis | Adipocytes | Leucine | Kinases | Synergism | Synergistic effects | Energy | Ellagic acid | Penicillin | Oxidation | Enzymes | Myotubes | Research & development--R&D | Oral administration | Muscles | Bioavailability | Metabolism | Mammals | Insulin | SIRT1 protein | NAD | Studies | Musculoskeletal system | Signaling | Epigallocatechin gallate | Acids | Antibiotics | Diabetes | Kinetics | Metabolic disorders | Index Medicus | Research & development | R&D
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2. Full Text Acute exposure to indoxyl sulfate impairs endothelium-dependent vasorelaxation in rat aorta
by Matsumoto, Takayuki and Matsumoto, Takayuki and Takayanagi, Keisuke and Takayanagi, Keisuke and Kojima, Mihoka and Kojima, Mihoka and Taguchi, Kumiko and Kobayashi, Tsuneo and Kobayashi, Tsuneo
International Journal of Molecular Sciences, ISSN 1661-6596, 01/2019, Volume 20, Issue 2, p. 338
Gut microbiota are emerging as potential contributors to the regulation of host homeostasis. Dysbiosis of the gut microbiota associated with increased... 
Aorta | Superoxide dismutase | Endothelial function | Keywords: aorta | Indoxyl sulfate | endothelial function | OXIDATIVE STRESS | MESENTERIC-ARTERIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | VASCULAR DYSFUNCTION | CELL-PROLIFERATION | GUT MICROBIOTA | CHEMISTRY, MULTIDISCIPLINARY | UREMIC TOXIN | indoxyl sulfate | superoxide dismutase | NITRIC-OXIDE | aorta | INDUCED RELAXATION | CHRONIC KIDNEY-DISEASE | END-PRODUCTS | Enzyme Activators - pharmacology | Norepinephrine - pharmacology | Leucine - pharmacology | Rats, Wistar | NADPH Oxidases - metabolism | Endothelium, Vascular - drug effects | Male | Nitroprusside - pharmacology | TRPV Cation Channels - metabolism | Calcium Ionophores - pharmacology | Aorta - physiopathology | Leucine - analogs & derivatives | Superoxide Dismutase - metabolism | Acetylcholine - pharmacology | Colforsin - pharmacology | Aorta - drug effects | NADPH Oxidases - antagonists & inhibitors | TRPV Cation Channels - agonists | Endothelium, Vascular - physiopathology | Enzyme Inhibitors - pharmacology | Adenylyl Cyclases - metabolism | Potassium - pharmacology | Sulfonamides - pharmacology | Calcimycin - pharmacology | Vasoconstriction - drug effects | Aorta - pathology | Indican - toxicity | Animals | Endothelium, Vascular - pathology | Vasodilation - drug effects | Index Medicus
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3. Full Text Starvation, Together with the SOS Response, Mediates High Biofilm-Specific Tolerance to the Fluoroquinolone Ofloxacin
by Bernier, Steve P and Lebeaux, David and DeFrancesco, Alicia S and Valomon, Amandine and Soubigou, Guillaume and Coppée, Jean-Yves and Ghigo, Jean-Marc and Beloin, Christophe
PLoS Genetics, ISSN 1553-7390, 01/2013, Volume 9, Issue 1, pp. e1003144 - e1003144
High levels of antibiotic tolerance are a hallmark of bacterial biofilms. In contrast to well-characterized inherited antibiotic resistance, molecular... 
CELLS | BACTERIAL PERSISTENCE | PSEUDOMONAS-AERUGINOSA | ESCHERICHIA-COLI | GENETICS & HEREDITY | GENE-EXPRESSION | RESISTANCE | BETA-LACTAM ANTIBIOTICS | CYSTIC-FIBROSIS | INDUCTION | STRESS | Biofilms - drug effects | Plankton - drug effects | Starvation | Drug Tolerance - genetics | Biofilms - growth & development | Amino Acids - genetics | Ofloxacin - pharmacology | Mutagenesis | Escherichia coli - genetics | Fluoroquinolones - pharmacology | SOS Response (Genetics) | DNA Transposable Elements - genetics | Plankton - genetics | Anti-Bacterial Agents - pharmacology | Drug Resistance, Bacterial - drug effects | Escherichia coli - growth & development | Drug Resistance, Bacterial - genetics | Transposons | Antibiotics | Gene mutations | Physiological aspects | Genetic aspects | Dosage and administration | Research | Drug resistance | Health aspects | Biofilms | Microbiology | E coli | Bacteria | Mutation | Carbon | Index Medicus | Ofloxacin/pharmacology | DNA Transposable Elements/genetics | Bacterial/drug effects/genetics | Anti-Bacterial Agents/pharmacology | Plankton/drug effects/genetics | Escherichia coli/genetics/growth & development | Bacteriology | Fluoroquinolones/pharmacology | Life Sciences | Microbiology and Parasitology | Biofilms/drug effects/growth & development | Drug Tolerance/genetics | Amino Acids/genetics | Drug Resistance
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4. Full Text Pain inhibition by blocking leukocytic and neuronal opioid peptidases in peripheral inflamed tissue
by Schreiter, Anja and Gore, Carmen and Labuz, Dominika and Fournie-Zaluski, Marie-Claude and Roques, Bernard P and Stein, Christoph and Machelska, Halina
FASEB Journal, ISSN 0892-6638, 12/2012, Volume 26, Issue 12, pp. 5161 - 5171
Inflammatory pain can be controlled by endogenous opioid peptides. Here we blocked the degradation of opioids in peripheral injured tissue to locally augment... 
Immune cells | Analgesia | Ory nerves | DEGRADING ENZYMES | NEUROGENIC INFLAMMATION | SYNOVIAL-FLUID | CATABOLIZING ENZYMES | BIOCHEMISTRY & MOLECULAR BIOLOGY | analgesia | immune cells | SPINAL-CORD | BETA-ENDORPHIN | sensory nerves | CELL BIOLOGY | RECEPTORS MEDIATING ANTINOCICEPTION | BIOLOGY | INFLAMMATORY PAIN | RAT-BRAIN | NEUTRAL ENDOPEPTIDASE ENKEPHALINASE | Leucine - pharmacology | Opioid Peptides - pharmacology | Rats, Wistar | Thiorphan - pharmacology | Opioid Peptides - immunology | Male | Enkephalin, Methionine - pharmacology | Leukocytes - enzymology | Enkephalin, Methionine - metabolism | Dose-Response Relationship, Drug | Narcotic Antagonists | Alanine - analogs & derivatives | Enkephalin, Methionine - immunology | Hindlimb - physiopathology | Inflammation - complications | Flow Cytometry | Pain - complications | Pain - enzymology | Enkephalin, Leucine - pharmacology | Antibodies - immunology | Pain Threshold - drug effects | Dynorphins - metabolism | Neurons - drug effects | Leucine - analogs & derivatives | Alanine - pharmacology | Receptors, Opioid - metabolism | Amino Acid Sequence | Enkephalin, Leucine - metabolism | Pain - prevention & control | CD13 Antigens - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Rats | Hindlimb - innervation | Enkephalin, Leucine - immunology | Neprilysin - metabolism | CD13 Antigens - metabolism | Opioid Peptides - metabolism | Antibodies - pharmacology | Dynorphins - immunology | Animals | Neurons - enzymology | Phosphinic Acids - pharmacology | Neprilysin - antagonists & inhibitors | Hindlimb - drug effects | Leukocytes - drug effects | Dynorphins - pharmacology | Inflammation - prevention & control | Inflammation - enzymology | Index Medicus
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5. Full Text Depletion of substrates for protein prenylation increases apoptosis in human periovulatory granulosa cells
by Rung, Emilia and Friberg, P. Anders and Bergh, Christina and Billig, Håkan and Institute of Clinical Sciences, Section for the Health of Women and Children and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Physiology and Sahlgrenska Academy and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa
Molecular Reproduction and Development, ISSN 1040-452X, 10/2006, Volume 73, Issue 10, pp. 1277 - 1283
Progesterone receptor (PR) stimulation promotes survival in human and rat periovulatory granulosa cells. PR antagonists, Org 31710 and RU 486, both increase... 
ovary | progesterone receptor | progesterone | ovulation | Ovary | Progesterone | Progesterone receptor | Ovulation | PHOSPHATE KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEVELOPMENTAL BIOLOGY | INDUCE APOPTOSIS | LOVASTATIN-INDUCED APOPTOSIS | CELL BIOLOGY | RAB GERANYLGERANYL TRANSFERASE | IN-VITRO | REPRODUCTIVE BIOLOGY | A REDUCTASE INHIBITORS | MESSENGER-RNA | PROGESTERONE-RECEPTOR ANTAGONISTS | MEVALONATE PATHWAY | OVARIAN FOLLICLE ATRESIA | Diterpenes - pharmacology | Protein Prenylation - drug effects | Leucine - pharmacology | Apoptosis - drug effects | Granulosa Cells - physiology | Farnesol - pharmacology | Furans - pharmacology | Humans | Cells, Cultured | Imidazoles - pharmacology | Quinolones - pharmacology | Granulosa Cells - drug effects | Granulosa Cells - metabolism | Receptors, Progesterone - antagonists & inhibitors | Hormone Antagonists - pharmacology | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology | Estrenes - pharmacology | Female | Farnesyltranstransferase - antagonists & inhibitors | Cholesterol - biosynthesis | Mifepristone - pharmacology | Leucine - analogs & derivatives | Index Medicus | MEDICIN OCH HÄLSOVETENSKAP | Granulosa Cells/drug effects/metabolism/physiology | Receptors | Farnesyltranstransferase/antagonists & inhibitors | Imidazoles/pharmacology | Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology | Progesterone/antagonists & inhibitors | Physiology | Cultured | Estrenes/pharmacology | MEDICAL AND HEALTH SCIENCES | Diterpenes/pharmacology | Farnesol/pharmacology | Hormone Antagonists/pharmacology | Fysiologi | Apoptosis/drug effects | Furans/pharmacology | Cholesterol/biosynthesis | Leucine/analogs & derivatives/pharmacology | Cells | Protein Isoprenylation/drug effects | Mifepristone/pharmacology | Quinolones/pharmacology
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6. Full Text Use of a cAMP BRET Sensor to Characterize a Novel Regulation of cAMP by the Sphingosine 1-Phosphate/G13 Pathway
by Lily I. Jiang and Julie Collins and Richard Davis and Keng-Mean Lin and Dianne DeCamp and Tamara Roach and Robert Hsueh and Robert A. Rebres and Elliott M. Ross and Ronald Taussig and Iain Fraser and Paul C. Sternweis
Journal of Biological Chemistry, ISSN 0021-9258, 04/2007, Volume 282, Issue 14, pp. 10576 - 10584
Regulation of intracellular cyclic adenosine 3 ′,5 ′-monophosphate (cAMP) is integral in mediating cell growth, cell differentiation, and immune responses... 
Cell Line | Lysophospholipids - metabolism | Basic-Leucine Zipper Transcription Factors - metabolism | Calcium Signaling - physiology | Humans | RNA, Small Interfering - pharmacology | Prostaglandins E - pharmacology | Adrenergic beta-Agonists - pharmacology | Macrophages - metabolism | Sphingosine - analogs & derivatives | Animals | Complement C5a - pharmacology | Calcium Signaling - drug effects | Isoproterenol - pharmacology | Biosensing Techniques | Mice | Sphingosine - metabolism | Receptors, Lysosphingolipid - metabolism | Uridine Diphosphate - pharmacology | Cyclic AMP - metabolism | Immunologic Factors - pharmacology | Pertussis Toxin - pharmacology | Index Medicus
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7. Full Text TRPA1 and TRPV4 Activation in Human Odontoblasts Stimulates ATP Release
by Egbuniwe, O and Grover, S and Duggal, A.K and Mavroudis, A and Yazdi, M and Renton, T and Di Silvio, L and Grant, A.D
Journal of Dental Research, ISSN 0022-0345, 9/2014, Volume 93, Issue 9, pp. 911 - 917
The mechanism of pain in dentine hypersensitivity is poorly understood but proposed to result from the activation of dental sensory neurons in response to... 
orofacial pain | sensation | dentin | signal transduction | transient receptor potential channel | ion channels | HUMAN DENTAL-PULP | CELLS | RAT ODONTOBLASTS | SODIUM-CALCIUM EXCHANGERS | TRANSDUCTION | TOOTH-PULP | IN-VITRO | DENTISTRY, ORAL SURGERY & MEDICINE | ION-CHANNEL | MICE | EXPRESSION | Acrolein - analogs & derivatives | Transient Receptor Potential Channels - antagonists & inhibitors | Leucine - pharmacology | Capsaicin - pharmacology | Humans | Adenosine Triphosphate - secretion | Nociceptors - physiology | Sensory System Agents - pharmacology | Calcium Channels - physiology | Pyrimidinones - pharmacology | Transient Receptor Potential Channels - physiology | Cell Culture Techniques | Leucine - analogs & derivatives | Isothiocyanates - pharmacology | Acrolein - pharmacology | Cell Line | Nerve Tissue Proteins - antagonists & inhibitors | Acetanilides - pharmacology | Nerve Tissue Proteins - physiology | TRPV Cation Channels - physiology | Purines - pharmacology | Nerve Tissue Proteins - agonists | TRPV Cation Channels - agonists | Dental Pulp - cytology | TRPM Cation Channels - agonists | Sulfonamides - pharmacology | Transient Receptor Potential Channels - agonists | Culture Media, Conditioned | Calcium Signaling - drug effects | Odontoblasts - physiology | Odontoblasts - secretion | TRPA1 Cation Channel | Index Medicus | Dentistry | Research Reports
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8. Full Text The tyrosine kinase inhibitor bafetinib inhibits PAR2‐induced activation of TRPV4 channels in vitro and pain in vivo
by Grace, M S and Lieu, T and Darby, B and Abogadie, F C and Veldhuis, N and Bunnett, N W and McIntyre, P
British Journal of Pharmacology, ISSN 0007-1188, 08/2014, Volume 171, Issue 16, pp. 3881 - 3894
Background and PurposeProtease-activated receptor 2 (PAR2) is expressed on nociceptive neurons, and can sensitize transient receptor potential (TRP) ion... 
CAPSAICIN RECEPTOR | HEAT-EVOKED ACTIVATION | PROTEIN | CONCISE GUIDE | CATION CHANNEL | ION-CHANNEL | PHARMACOLOGY & PHARMACY | INFLAMMATORY PAIN | HYPERALGESIA | MICE | DROSOPHILA TRP | Leucine - pharmacology | Hyperalgesia - metabolism | Humans | Mice, Inbred C57BL | Receptor, PAR-2 - metabolism | TRPV Cation Channels - agonists | Morpholines - pharmacology | Male | Pyrimidines - pharmacology | Pain - metabolism | Sulfonamides - pharmacology | TRPV Cation Channels - genetics | TRPV Cation Channels - metabolism | Pyrroles - pharmacology | Receptor, PAR-2 - antagonists & inhibitors | Animals | Trypsin - pharmacology | TRPV Cation Channels - antagonists & inhibitors | HEK293 Cells | Receptor, PAR-2 - agonists | Protein Kinase Inhibitors - pharmacology | Oligopeptides - pharmacology | Leucine - analogs & derivatives | Tyrosine | Phenols | Phosphotransferases | Adenosine triphosphatase | Rodents | Index Medicus | Research Papers
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9. Full Text Protein prenylation contributes to the effects of LPS on EFS-induced responses in human isolated bronchi
by Cazzola, Mario and Calzetta, Luigino and Page, Clive P and Rinaldi, Barbara and Capuano, Annalisa and Matera, Maria Gabriella
American Journal of Respiratory Cell and Molecular Biology, ISSN 1044-1549, 10/2011, Volume 45, Issue 4, pp. 704 - 710
Rho/Ras signaling pathways may play an important role in the mechanism of LPS-induced inflammation and bronchoconstriction. In this study, we investigated the... 
EFS | Rho/Ras signaling pathways | Human bronchi | LPS | Statins | human bronchi | BIOCHEMISTRY & MOLECULAR BIOLOGY | RHO-KINASE INHIBITOR | LUNG INJURY | CONTRACTILE ACTIVITY | CELL BIOLOGY | LIPOPOLYSACCHARIDE EXPOSURE | IN-VITRO | RESPIRATORY SYSTEM | statins | NITRIC-OXIDE | INDUCED AIRWAY HYPERRESPONSIVENESS | INHALED ENDOTOXIN | TRACHEAL SMOOTH-MUSCLE | GERANYLGERANYLTRANSFERASE-I | Leucine - pharmacology | Electric Stimulation | Sesquiterpenes - metabolism | Humans | Middle Aged | Alkyl and Aryl Transferases - metabolism | Alkyl and Aryl Transferases - antagonists & inhibitors | ras Proteins - metabolism | Male | Methionine - pharmacology | Simvastatin - pharmacology | rho-Associated Kinases - antagonists & inhibitors | Bronchi - drug effects | Methionine - analogs & derivatives | Time Factors | rho-Associated Kinases - metabolism | Bronchoconstriction - drug effects | Bronchi - metabolism | Female | Leucine - analogs & derivatives | Amides - pharmacology | Protein Prenylation - drug effects | Enzyme Inhibitors - pharmacology | Imidazoles - pharmacology | Polyisoprenyl Phosphates - metabolism | Naphthalenes - pharmacology | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology | Signal Transduction - drug effects | rho GTP-Binding Proteins - metabolism | Lipopolysaccharides - pharmacology | Protein Kinase Inhibitors - pharmacology | Pyridines - pharmacology | In Vitro Techniques | Index Medicus
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10. Full Text Central antinociception induced by ketamine is mediated by endogenous opioids and μ- and δ-opioid receptors
by Pacheco, Daniela da Fonseca and Romero, Thiago Roberto Lima and Duarte, Igor Dimitri Gama
Brain Research, ISSN 0006-8993, 2014, Volume 1562, pp. 69 - 75
Abstract It is generally believed that NMDA receptor antagonism accounts for most of the anesthetic and analgesic effects of ketamine, however, it interacts at... 
Neurology | Endogenous opioid | Ketamine | Central antinociception | Naltrexone - analogs & derivatives | Receptors, Opioid, delta - metabolism | Analgesics - pharmacology | Leucine - pharmacology | Pain Perception - physiology | Male | Nociceptive Pain - drug therapy | Brain - metabolism | Dose-Response Relationship, Drug | Nociceptive Pain - metabolism | Naltrexone - pharmacology | Pain Perception - drug effects | Receptors, Opioid, delta - antagonists & inhibitors | Aminopeptidases - metabolism | Leucine - analogs & derivatives | Receptors, Opioid, kappa - antagonists & inhibitors | Receptors, Opioid, mu - metabolism | Enzyme Inhibitors - pharmacology | Receptors, Opioid, kappa - metabolism | Aminopeptidases - antagonists & inhibitors | Hot Temperature | Receptors, Opioid, mu - antagonists & inhibitors | Cinnamates - pharmacology | Opioid Peptides - metabolism | Brain - drug effects | Animals | Naloxone - pharmacology | Narcotic Antagonists - pharmacology | Mice | Morphine Derivatives - pharmacology | Ketamine - pharmacology | Index Medicus
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11. Full Text Effects of nominally selective inhibitors of the kinases PI3K, SGK1 and PKB on the insulin-dependent control of epithelial Na + absorption
by Mansley, Morag K and Wilson, Stuart M
British Journal of Pharmacology, ISSN 0007-1188, 10/2010, Volume 161, Issue 3, pp. 571 - 588
BACKGROUND AND PURPOSE Insulin-induced Na+ retention in the distal nephron may contribute to the development of oedema/hypertension in patients with type 2... 
Akti-1/2 | epithelial Na | GSK650394A | PI103 | kinase inhibitors | channel | cortical collecting duct | GDC-0941 | ACTIVATION | SODIUM-TRANSPORT | PHOSPHORYLATION | SERUM | AKT | ENAC | IDENTIFICATION | A6 CELLS | CHANNEL | PHARMACOLOGY & PHARMACY | epithelial Na+ channel | LEUCINE-ZIPPER PROTEIN | Epithelial Cells - metabolism | Epithelial Cells - drug effects | Furans - pharmacology | Phosphatidylinositol 3-Kinases - metabolism | Sodium - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Quinoxalines - pharmacology | Epithelial Cells - physiology | Immediate-Early Proteins - metabolism | Absorption | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Ion Transport - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Protein-Serine-Threonine Kinases - metabolism | Kidney Tubules, Collecting - drug effects | Membrane Potentials - drug effects | Insulin - pharmacology | Cells, Cultured | Pyrimidines - pharmacology | Membrane Potentials - physiology | Sulfonamides - pharmacology | Indazoles - pharmacology | Bridged Bicyclo Compounds, Heterocyclic - pharmacology | Animals | Androstadienes - pharmacology | Benzoates - pharmacology | Mice | Pyridines - pharmacology | Benzylamines - pharmacology | Immediate-Early Proteins - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | Kinases | Insulin | Index Medicus | Research Papers | 2 | Akti-1
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12. Full Text Effect of Phosphoric Acid on the Degradation of Human Dentin Matrix
by Tezvergil-Mutluay, A and Mutluay, M and Seseogullari-Dirihan, R and Agee, K.A and Key, W.O and Scheffel, D.L.S and Breschi, L and Mazzoni, A and Tjäderhane, L and Nishitani, Y and Tay, F.R and Pashley, D.H
Journal of Dental Research, ISSN 0022-0345, 1/2013, Volume 92, Issue 1, pp. 87 - 91
This study determined if dentin proteases are denatured by phosphoric acid (PA) used in etch-and-rinse dentin adhesives. Dentin beams were completely... 
collagen | demineralized | bonding | cathepsins | MMPs | ACTIVATION | DENTISTRY, ORAL SURGERY & MEDICINE | METALLOPROTEINASES | BINDING | Enzyme Activators - pharmacology | Leucine - pharmacology | Phenylmercuric Acetate - pharmacology | Dipeptides - pharmacology | Humans | Peptide Hydrolases - drug effects | Enzyme Precursors - drug effects | Materials Testing | Collagenases - drug effects | Phosphoric Acids - pharmacology | Matrix Metalloproteinase Inhibitors - pharmacology | Dentin - enzymology | Dentin - drug effects | Time Factors | Matrix Metalloproteinases - drug effects | Cysteine Proteinase Inhibitors - pharmacology | Protein Denaturation | Phenylmercuric Acetate - analogs & derivatives | Sulfhydryl Reagents - pharmacology | Collagen Type I - analysis | Leucine - analogs & derivatives | Peptides - analysis | Cathepsins - antagonists & inhibitors | Index Medicus | Dentistry | Research Reports
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13. Full Text Discovery, synthesis, and molecular pharmacology of selective positive allosteric modulators of the δ-opioid receptor
by Burford, Neil T and Livingston, Kathryn E and Canals, Meritxell and Ryan, Molly R and Budenholzer, Lauren M. L and Han, Ying and Shang, Yi and Herbst, John J and OConnell, Jonathan and Banks, Martyn and Zhang, Litao and Filizola, Marta and Bassoni, Daniel L and Wehrman, Tom S and Christopoulos, Arthur and Traynor, John R and Gerritz, Samuel W and