X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4660) 4660
Publication (775) 775
Book Chapter (53) 53
Book Review (52) 52
Conference Proceeding (26) 26
Dissertation (15) 15
Reference (6) 6
Book / eBook (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (2618) 2618
mu-opioid receptor (2298) 2298
neurosciences (1954) 1954
male (1716) 1716
index medicus (1715) 1715
pharmacology & pharmacy (1421) 1421
rats (1331) 1331
humans (1314) 1314
morphine (1153) 1153
mice (952) 952
mu-opioid receptors (848) 848
female (693) 693
receptors, opioid, mu - metabolism (672) 672
biochemistry & molecular biology (620) 620
rats, sprague-dawley (593) 593
analgesics, opioid - pharmacology (592) 592
morphine - pharmacology (590) 590
article (548) 548
dose-response relationship, drug (546) 546
pain (519) 519
mu opioid receptor (481) 481
analgesia (455) 455
receptors, opioid, mu - genetics (443) 443
brain (441) 441
narcotic antagonists - pharmacology (406) 406
receptors, opioid, mu - agonists (381) 381
rat (340) 340
neurons (330) 330
mu-opioid-receptor (328) 328
psychiatry (318) 318
rat-brain (317) 317
antinociception (307) 307
analysis (301) 301
nucleus-accumbens (301) 301
tolerance (297) 297
rats, wistar (296) 296
naloxone - pharmacology (287) 287
μ-opioid receptor (283) 283
opioids (277) 277
expression (271) 271
opioid receptors (266) 266
activation (251) 251
spinal-cord (245) 245
clinical neurology (239) 239
beta-endorphin (238) 238
binding (238) 238
adult (236) 236
neuropathic pain (236) 236
dopamine (235) 235
naltrexone - pharmacology (234) 234
time factors (231) 231
brain - metabolism (229) 229
opioid (229) 229
mice, inbred c57bl (225) 225
receptors, opioid, mu - antagonists & inhibitors (224) 224
ventral tegmental area (223) 223
addiction (218) 218
narcotics (216) 216
ligands (214) 214
cell biology (212) 212
receptors, opioid, mu - physiology (212) 212
behavioral sciences (211) 211
anesthesiology (209) 209
naloxone (208) 208
analgesics (205) 205
receptors, opioid, mu - drug effects (202) 202
central-nervous-system (201) 201
analgesics - pharmacology (199) 199
research (199) 199
nervous system (197) 197
pain - drug therapy (197) 197
desensitization (193) 193
messenger-rna (192) 192
reward (192) 192
morphine - administration & dosage (188) 188
disease models, animal (187) 187
enkephalin, ala-mephe-gly- - pharmacology (187) 187
neurology (187) 187
dependence (185) 185
analgesics, opioid - administration & dosage (184) 184
immunohistochemistry (183) 183
naltrexone (183) 183
receptors (183) 183
oligopeptides - pharmacology (181) 181
signal transduction (178) 178
care and treatment (175) 175
gene expression (173) 173
neurons - drug effects (173) 173
neurons - metabolism (173) 173
narcotics - pharmacology (172) 172
naltrexone - analogs & derivatives (170) 170
proteins (169) 169
agonist (168) 168
medicine, research & experimental (168) 168
mice, knockout (168) 168
behavior, animal - drug effects (167) 167
drug tolerance (166) 166
chemistry, medicinal (164) 164
pain measurement - drug effects (163) 163
conditioned place preference (161) 161
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4579) 4579
Chinese (42) 42
Japanese (41) 41
German (10) 10
French (8) 8
Spanish (7) 7
Korean (3) 3
Persian (1) 1
Polish (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 2007, Volume 320, Issue 1, pp. 1 - 13
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2011, Volume 108, Issue 22, pp. 9268 - 9273
Journal Article
Philosophical Transactions: Biological Sciences, ISSN 0962-8436, 12/2012, Volume 367, Issue 1607, pp. 3353 - 3363
Human tissues express cannabinoid CB₁ and CB₂ receptors that can be activated by endogenously released 'endocannabinoids' or exogenously administered compounds... 
Receptors | Cannabinoids | Animal models | Pain | Medical treatment | Agonists | Morphine | Drug design | Endocannabinoids | Cannabinoid receptors | And CB2 | Blood-brain barrier | Cannabinoid receptor agonists | Δ9-tetrahydrocannabinol | Cannabinoid CB1 | Therapeutic applications and strategies | blood-brain barrier | Delta-tetrahydrocannabinol | cannabinoid CB1 and CB2 receptors | CB2 RECEPTOR | LIVER-DISEASES | AMYOTROPHIC-LATERAL-SCLEROSIS | ANXIETY-LIKE BEHAVIOR | MU-OPIOID RECEPTOR | RAT FORMALIN TEST | therapeutic applications and strategies | cannabinoid receptor agonists | NEUROPATHIC PAIN | MOUSE MODEL | BIOLOGY | PENTYLENETETRAZOLE-INDUCED SEIZURE | CENTRAL-NERVOUS-SYSTEM | Endocannabinoids - metabolism | Analgesics - pharmacology | Receptor, Cannabinoid, CB2 - agonists | Cardiovascular Diseases - drug therapy | Humans | Cannabinoid Receptor Agonists - pharmacology | Neurodegenerative Diseases - drug therapy | Pain - metabolism | Receptor, Cannabinoid, CB1 - agonists | Pain - drug therapy | Cannabinoid Receptor Agonists - therapeutic use | Dronabinol - pharmacology | Analgesics - therapeutic use | Cardiovascular Diseases - metabolism | Risk Assessment | Analgesics - administration & dosage | Clinical Trials as Topic | Neurodegenerative Diseases - metabolism | Blood-Brain Barrier - drug effects | Cannabinoid Receptor Agonists - administration & dosage | Drug Discovery | Blood-Brain Barrier - metabolism | Receptor, Cannabinoid, CB1 - metabolism | Receptor, Cannabinoid, CB2 - metabolism | Animals | Dronabinol - therapeutic use | Review
Journal Article
Neuropsychopharmacology, ISSN 0893-133X, 01/2012, Volume 37, Issue 2, pp. 338 - 349
The capacity of opioids to alleviate inflammatory pain is negatively regulated by the glutamate-binding N-methyl-D-aspartate receptor (NMDAR). Increased... 
mu-opioid receptor | N-methyl-D-aspartate receptor | pain | receptor association | periaqueductal gray | analgesia | PERIAQUEDUCTAL GRAY NEURONS | G-ALPHA-SUBUNITS | PROTEIN-KINASE-C | PSYCHIATRY | D-ASPARTATE RECEPTORS | SYNAPTIC PLASTICITY | NEUROSCIENCES | NEUROPATHIC PAIN | GLUTAMATE RECEPTORS | PHARMACOLOGY & PHARMACY | DEEP BRAIN-STIMULATION | SELECTIVE-MU | ANTINOCICEPTIVE TOLERANCE | Phosphorylation - physiology | Injections, Intraventricular | Periaqueductal Gray - drug effects | Receptors, N-Methyl-D-Aspartate - metabolism | Drug Tolerance - physiology | Male | N-Methylaspartate - pharmacology | G-Protein-Coupled Receptor Kinase 2 - antagonists & inhibitors | Receptor Aggregation - drug effects | Neurons - metabolism | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Phosphorylation - drug effects | Morphine - antagonists & inhibitors | CHO Cells | Cricetinae | Protein Kinase C - physiology | Morphine - pharmacology | Pain - prevention & control | G-Protein-Coupled Receptor Kinase 2 - physiology | Receptors, Opioid, mu - metabolism | Protein Kinase C - antagonists & inhibitors | Mice, Inbred ICR | Periaqueductal Gray - metabolism | Cyclic AMP-Dependent Protein Kinases - physiology | Receptor Aggregation - physiology | Animals | Pain - physiopathology | Mice | Morphine - administration & dosage | Life Sciences | Pharmacology | Pharmaceutical sciences | signal transduction | analgesics | mouse | N-methyl--aspartate receptor | NMDA | Original | glutamate | opioids
Journal Article
Journal Article
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 11/2013, Volume 21, Issue 21, pp. 6405 - 6413
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2013, Volume 288, Issue 32, pp. 22942 - 22960
TGR5 is a G protein-coupled receptor that mediates bile acid (BA) effects on energy balance, inflammation, digestion, and sensation. The mechanisms and... 
GROWTH-FACTOR RECEPTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | GPBAR1 TGR5 | DEPENDENT ENDOCYTOSIS | PROTEIN-COUPLED RECEPTORS | RESONANCE ENERGY-TRANSFER | KINASE ACTIVATION | MU-OPIOID RECEPTOR | BETA-ADRENERGIC RECEPTOR | ACTIVATED RECEPTOR-2 | EGF RECEPTOR | Cholagogues and Choleretics - pharmacology | Phenylalanine - analogs & derivatives | Receptors, G-Protein-Coupled - metabolism | Membrane Microdomains - metabolism | Phenylalanine - pharmacology | Humans | ErbB Receptors - genetics | Oleanolic Acid - pharmacology | Arrestins - genetics | Protein Transport - physiology | Protein Transport - drug effects | G-Protein-Coupled Receptor Kinase 2 - genetics | G-Protein-Coupled Receptor Kinase 2 - metabolism | Arrestins - metabolism | beta-Cyclodextrins - pharmacology | Endosomes - metabolism | Mitogen-Activated Protein Kinase 1 - genetics | HEK293 Cells | Antineoplastic Agents - pharmacology | Cyclic AMP - genetics | Cyclic AMP - metabolism | ErbB Receptors - antagonists & inhibitors | ErbB Receptors - metabolism | Endosomes - genetics | Mitogen-Activated Protein Kinase 3 - genetics | Endocytosis - drug effects | Enzyme Inhibitors - pharmacology | Thiophenes - pharmacology | Tyrphostins - pharmacology | Endocytosis - physiology | Arrestins - antagonists & inhibitors | G-Protein-Coupled Receptor Kinase 5 - metabolism | Deoxycholic Acid - pharmacology | Mitogen-Activated Protein Kinase 3 - metabolism | beta-Arrestin 2 | beta-Arrestin 1 | beta-Arrestins | Receptors, G-Protein-Coupled - genetics | Quinazolines - pharmacology | G-Protein-Coupled Receptor Kinase 5 - genetics | Membrane Microdomains - genetics | Mitogen-Activated Protein Kinase 1 - metabolism | Lipid Raft | Bile Acid | Endocytosis | G Protein-coupled Receptors (GPCR) | Arrestin | Signal Transduction
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 9/2011, Volume 68, Issue 17, pp. 2933 - 2949
A series of pharmacological and physiological studies have demonstrated the functional cross-regulation between MOR and NMDAR. These receptors coexist at... 
Life Sciences | Biochemistry, general | Analgesia | Life Sciences, general | Mu-opioid receptor | Histidine triad nucleotide-binding protein 1 | Glutamate N -methyl- d -aspartate receptor | Regulator of G-protein signaling RGSZ2 protein | Receptor desensitization | Biomedicine general | PKCγ | Cell Biology | Glutamate N-methyl-d-aspartate receptor | G-ALPHA-SUBUNITS | PERIAQUEDUCTAL GRAY NEURONS | RAT | PHOSPHORYLATION | DESENSITIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTISENSE OLIGODEOXYNUCLEOTIDES | KINASE-C | Glutamate N-methyl-D-aspartate receptor | CELL BIOLOGY | INDUCED ANALGESIA | MORPHINE-TOLERANCE | IN-VIVO | PKC gamma | Protein Structure, Tertiary | RGS Proteins - genetics | Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors | Morphine - pharmacology | Signal Transduction | Receptors, Opioid, mu - metabolism | Receptors, N-Methyl-D-Aspartate - metabolism | Male | Protein Kinase C - antagonists & inhibitors | Nerve Tissue Proteins - genetics | Mice, Knockout | Nerve Tissue Proteins - metabolism | Nerve Tissue Proteins - chemistry | Animals | Protein Kinase C - metabolism | RGS Proteins - chemistry | Protein Binding | RGS Proteins - metabolism | Mice | Dimerization | Physiological aspects | Methyl aspartate | Morphine | Histidine | Glutamate | Proteins | Pharmacology | Analgesics | Molecular biology | Protein kinase C | Mesencephalon | Opioid receptors | Glutamic acid receptors (ionotropic) | Neurons | Opioid receptors (type mu) | N-Methyl-D-aspartic acid receptors | Glutamic acid receptors | Pain | Drug tolerance
Journal Article