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1. Full Text Flavonoid galetin 3,6-dimethyl ether attenuates guinea pig ileum contraction through K+ channel activation and decrease in cytosolic calcium concentration
by Vasconcelos, Luiz H.C and Correia, Ana C. de C and Souza, Iara L.L. de and Silva, Maria da C.C and Silva, Bagnólia A. da and Paredes-Gamero, Edgar J and Santos, Bárbara V. de O and Cavalcante, Fabiana de A
European Journal of Pharmacology, ISSN 0014-2999, 11/2015, Volume 767, pp. 52 - 60
Flavonoid galetin 3,6-dimethyl ether (FGAL) has been isolated from the aerial parts of and has shown a spasmolytic effect in guinea pig ileum. Thus, we aimed... 
Potassium channels | Calcium | Flavonoid | Ileum | Galetin 3,6-dimethyl ether | LONGITUDINAL MUSCLE | PROTEIN-KINASE-C | INVOLVEMENT | CLASSIFICATION | GASTROINTESTINAL SMOOTH-MUSCLE | BAY-K-8644 | INHIBITION | SPASMOLYTIC ACTIVITY | PHARMACOLOGY & PHARMACY | RECEPTORS | Carbachol - antagonists & inhibitors | Calcium - metabolism | Muscle Cells - drug effects | Flavonoids - antagonists & inhibitors | Tetraethylammonium | Apamin - pharmacology | Ileum - drug effects | Glyburide - pharmacology | Calcium Chloride - antagonists & inhibitors | Potassium Chloride - antagonists & inhibitors | Potassium Chloride - pharmacology | Histamine Antagonists - pharmacology | Flavonoids - pharmacology | 4-Aminopyridine - pharmacology | Potassium Channel Blockers - pharmacology | Cell Survival - drug effects | Guinea Pigs | Histamine - pharmacology | Chlorides - pharmacology | 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester - pharmacology | Calcium Chloride - pharmacology | Carbachol - pharmacology | Cesium - pharmacology | Animals | Muscle Contraction - drug effects | Potassium Channels - agonists | Ileum - physiology | Index Medicus
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2. Full Text Thin Dendrites of Cerebellar Interneurons Confer Sublinear Synaptic Integration and a Gradient of Short-Term Plasticity
by Abrahamsson, Therese and Cathala, Laurence and Matsui, Ko and Shigemoto, Ryuichi and DiGregorio, David A
Neuron, ISSN 0896-6273, 03/2012, Volume 73, Issue 6, pp. 1159 - 1172
Interneurons are critical for neuronal circuit function, but how their dendritic morphologies and membrane properties influence information flow within... 
PURKINJE-CELLS | PERMEABLE AMPA RECEPTORS | POSTSYNAPTIC POTENTIALS | COINCIDENCE DETECTION | STELLATE CELLS | MOLECULAR LAYER INTERNEURONS | GRANULE CELLS | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | CA1 PYRAMIDAL NEURONS | LATERAL GENICULATE-NUCLEUS | Tetraethylammonium - pharmacology | Electric Stimulation | Age Factors | Dendrites - ultrastructure | Excitatory Postsynaptic Potentials - physiology | Neuronal Plasticity - physiology | Time Factors | Lasers | Dendrites - physiology | Statistics, Nonparametric | Indoles - pharmacology | Tetrodotoxin - pharmacology | Cadmium Chloride - pharmacology | Imaging, Three-Dimensional | Potassium Channel Blockers - pharmacology | Receptors, AMPA - metabolism | Animals, Newborn | Microscopy, Electron, Transmission | Benzodiazepines - pharmacology | Chlorides - pharmacology | Synapses - physiology | Interneurons - ultrastructure | Sodium Channel Blockers - pharmacology | Synapses - ultrastructure | Excitatory Amino Acid Antagonists - pharmacology | Biophysics | Receptors, AMPA - ultrastructure | Microscopy, Confocal | Cesium - pharmacology | Patch-Clamp Techniques | Animals | Cerebellum - cytology | Glutamates - pharmacology | Mice | Models, Neurological | In Vitro Techniques | Glutamate | Neurons | Information management | Studies | Microscopy | Cerebellum | Index Medicus | Life Sciences
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3. Full Text 5-hydroxytryptamine action in the rat olfactory bulb: In vitro electrophysiological patch-clamp recordings of juxtaglomerular and mitral cells
by Hardy, A and Palouzier-Paulignan, B and Duchamp, A and Royet, J.-P and Duchamp-Viret, P
Neuroscience, ISSN 0306-4522, 2005, Volume 131, Issue 3, pp. 717 - 731
The olfactory bulb, first relay of olfactory pathways, is densely innervated by serotoninergic centrifugal fibers originating from the raphe nuclei. Although... 
5HT | 5HT 2A receptors | 5HT 2C receptors | olfactory bulb | rat | whole-cell recordings | Olfactory bulb | receptors | Rat | Whole-cell recordings | 5HT(2A) receptors | RETROGRADE AXONAL-TRANSPORT | SEROTONERGIC MODULATION | 5HT(2C) receptors | 5-HT2A RECEPTOR | NEUROSCIENCES | CEREBRAL-CORTEX | DEFINED NEURON GROUPS | NERVE-TERMINALS | GLOMERULAR LAYER | RECIPROCAL SYNAPSES | NEONATE RAT | ACTIVATED CATION CURRENT | Free Radical Scavengers - pharmacology | Rats, Wistar | Electrophysiology | Membrane Potentials - radiation effects | Methysergide - pharmacology | Apamin - pharmacology | Serotonin - pharmacology | Patch-Clamp Techniques - methods | Mianserin - pharmacology | Neurons - classification | Olfactory Pathways - physiology | Drug Interactions | Kynurenic Acid - pharmacology | Neurons - drug effects | Nickel - pharmacology | Olfactory Pathways - drug effects | Electric Stimulation - methods | 4-Aminopyridine - pharmacology | Potassium Channel Blockers - pharmacology | Olfactory Bulb - cytology | Animals, Newborn | Membrane Potentials - drug effects | Benzodiazepines - pharmacology | Chlorides - pharmacology | Rats | Logistic Models | Excitatory Amino Acid Antagonists - pharmacology | Bicuculline - pharmacology | Membrane Potentials - physiology | Serotonin Antagonists - pharmacology | GABA Antagonists - pharmacology | Cesium - pharmacology | Animals | In Vitro Techniques | Olfactory Pathways - radiation effects | Dose-Response Relationship, Radiation | Olfactory Bulb - drug effects | Index Medicus
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4. Full Text Muscarinic modulation of TREK currents in mouse sympathetic superior cervical ganglion neurons
by Rivas‐Ramírez, P and Cadaveira‐Mosquera, A and Lamas, J. A and Reboreda, A
European Journal of Neuroscience, ISSN 0953-816X, 07/2015, Volume 42, Issue 2, pp. 1797 - 1807
Muscarinic receptors play a key role in the control of neurotransmission in the autonomic ganglia, which has mainly been ascribed to the regulation of... 
potassium channel | TREK | two‐pore domain potassium channel | PIP | muscarinic receptor | TREK-2 | Muscarinic receptor | Potassium channel | Two-pore domain potassium channel | CALCIUM CURRENT | NEUROPROTECTIVE AGENT RILUZOLE | NEUROSCIENCES | two-pore domain potassium channel | ENTORHINAL CORTEX | ACETYLCHOLINE-RECEPTORS | POLYUNSATURATED FATTY-ACIDS | COUPLED RECEPTORS | DOMAIN K+ CHANNELS | INDUCED INHIBITION | FUNCTIONAL-CHARACTERISTICS | PIP2 | KCNQ1-4 POTASSIUM CHANNELS | Potassium Channels, Tandem Pore Domain - metabolism | Oxotremorine - pharmacology | Tetraethylammonium - pharmacology | Electric Stimulation | Chlorides - pharmacology | Cholinergic Agents - pharmacology | Cells, Cultured | Male | Receptors, Muscarinic - metabolism | Sodium Channel Blockers - pharmacology | Excitatory Amino Acid Antagonists - pharmacology | Superior Cervical Ganglion - cytology | Cesium - pharmacology | Patch-Clamp Techniques | Animals | Oxotremorine - analogs & derivatives | Female | Mice | Riluzole - pharmacology | Tetrodotoxin - pharmacology | Neurons - drug effects | Potassium Channel Blockers - pharmacology | Pertussis Toxin - pharmacology | Index Medicus
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5. Full Text Sodium fluxes through nonselective cation channels in the plasma membrane of protoplasts from Arabidopsis roots
by Demidchik, Vadim and Tester, Mark
Plant Physiology, ISSN 0032-0889, 2002, Volume 128, Issue 2, pp. 379 - 387
The aim of the present work was to characterize Na(+) currents through nonselective cation channels (NSCCs) in protoplasts derived from root cells of... 
Potassium - metabolism | Protoplasts - physiology | Cations - metabolism | Sodium - metabolism | Rubidium - pharmacology | Cations - pharmacology | Lithium - metabolism | Potassium Chloride - pharmacology | Rubidium - metabolism | Membrane Potentials - drug effects | Plant Roots - metabolism | Lithium - pharmacology | Arabidopsis - cytology | Biological Transport, Active - drug effects | Plant Roots - cytology | Calcium Channel Blockers - pharmacology | Potassium - pharmacology | Protoplasts - drug effects | Arabidopsis - metabolism | Cesium - metabolism | Tetraethylammonium Compounds - pharmacology | Cesium - pharmacology | Patch-Clamp Techniques | Ion Channels - metabolism | Cell Membrane Permeability - drug effects | Quaternary Ammonium Compounds - metabolism | Ion Transport - physiology | Quaternary Ammonium Compounds - pharmacology
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6. Full Text Sodium-activated potassium channels are functionally coupled to persistent sodium currents
by Hage, Travis A and Salkoff, Lawrence
Journal of Neuroscience, ISSN 0270-6474, 02/2012, Volume 32, Issue 8, pp. 2714 - 2721
We report a novel coupled system of sodium-activated potassium currents (I-KNa) and persistent sodium currents (I-NaP), the components of which are widely... 
CELLS | K-NA CHANNELS | CA2 | RAT OLFACTORY-BULB | NEURONS | OUTWARD CURRENT | SLICK | NEUROSCIENCES | FAMILY | Tetraethylammonium - pharmacology | Electric Stimulation | Potassium Channels - physiology | Male | Sodium - metabolism | Ion Channel Gating - physiology | Neurons - physiology | Sodium Channels - metabolism | Female | Tetrodotoxin - pharmacology | Neurons - drug effects | Potassium Channel Blockers - pharmacology | Olfactory Bulb - cytology | Animals, Newborn | Membrane Potentials - drug effects | Sodium - pharmacology | Chlorides - pharmacology | Cells, Cultured | Rats | Sodium Channel Blockers - pharmacology | Biophysics | Ions - metabolism | Membrane Potentials - physiology | Potassium Channels - drug effects | Veratridine - pharmacology | Cesium - pharmacology | Patch-Clamp Techniques | Animals | Ion Channel Gating - genetics | Aminopyridines - pharmacology | Ion Channel Gating - drug effects | Index Medicus
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7. Full Text Dopamine D4 receptor excitation of lateral habenula neurons via multiple cellular mechanisms
by Good, Cameron H and Wang, Huikun and Chen, Yuan-Hao and Mejias-Aponte, Carlos A and Hoffman, Alexander F and Lupica, Carl R
Journal of Neuroscience, ISSN 0270-6474, 2013, Volume 33, Issue 43, pp. 16853 - 16864
Glutamatergic lateral habenula (LHb) output communicates negative motivational valence to ventral tegmental area (VTA) dopamine (DA) neurons via activation of... 
Receptors, Dopamine D4 - agonists | gamma-Aminobutyric Acid - metabolism | Male | Pedunculopontine Tegmental Nucleus - physiology | Receptors, Dopamine D4 - antagonists & inhibitors | Ventral Tegmental Area - cytology | Ventral Tegmental Area - physiology | Synaptic Transmission | Action Potentials | Neurons - physiology | Neurons - metabolism | Neurons - drug effects | Pedunculopontine Tegmental Nucleus - cytology | Habenula - physiology | Dopamine Agonists - pharmacology | Habenula - metabolism | Dopamine Uptake Inhibitors - pharmacology | Amphetamine - pharmacology | Dopamine - pharmacology | Rats | Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - antagonists & inhibitors | Piperazines - pharmacology | Rats, Sprague-Dawley | Cocaine - pharmacology | Cesium - pharmacology | Feedback, Physiological | Animals | Habenula - cytology | Dopamine Antagonists - pharmacology | Receptors, Dopamine D4 - metabolism | Glutamic Acid - metabolism | Index Medicus
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8. Full Text CALCIUM ANTAGONIST PROPERTY OF CPU228, A DOFETILIDE DERIVATIVE, CONTRIBUTES TO ITS LOW INCIDENCE OF TORSADES DE POINTES IN RABBITS
by Huang, Zhi-Jiang and Dai, De-Zai and Li, Na and Na, Tao and Ji, Min and Dai, Yin
Clinical and Experimental Pharmacology and Physiology, ISSN 0305-1870, 04/2007, Volume 34, Issue 4, pp. 310 - 317
SUMMARY • Torsades de pointes (TDP) is a severe adverse effect during the clinical use of dofetilide, a selective blocker of the rapid component of the delayed... 
anti-arrhythmic agents | torsades de pointes | CPU228 | cytosolic calcium concentration | L-type calcium current | delayed rectifier potassium channel | L‐type calcium current | anti‐arrhythmic agents | Cytosolic calcium concentration | Anti-arrhythmic agents | Torsades de pointes | Delayed rectifier potassium channel | ARRHYTHMIAS | PHYSIOLOGY | MYOCARDIAL-INFARCTION | MYOCYTES | INTRACELLULAR CALCIUM | HEART-FAILURE | PROLONGATION | GUINEA-PIG | III ANTIARRHYTHMIC AGENT | LEFT-VENTRICULAR DYSFUNCTION | DRONEDARONE | PHARMACOLOGY & PHARMACY | Myocardial Contraction - drug effects | Long QT Syndrome - chemically induced | Male | Long QT Syndrome - physiopathology | Dose-Response Relationship, Drug | Heart Rate - drug effects | Electrocardiography | Female | Potassium Channels, Inwardly Rectifying - antagonists & inhibitors | Molecular Structure | Methoxamine - toxicity | Torsades de Pointes - physiopathology | Torsades de Pointes - prevention & control | Refractory Period, Electrophysiological - drug effects | Membrane Potentials - drug effects | Naphthalenes - chemistry | Methoxamine - administration & dosage | Rabbits | Long QT Syndrome - prevention & control | Guinea Pigs | Phenethylamines - pharmacology | Sulfonamides - chemistry | Torsades de Pointes - chemically induced | Phenethylamines - chemistry | Rats | Calcium Channels, L-Type - physiology | Calcium Channel Blockers - pharmacology | Sulfonamides - pharmacology | Rats, Sprague-Dawley | Naphthalenes - pharmacology | Algorithms | Animals | Myocytes, Cardiac - drug effects | Myocytes, Cardiac - physiology | Potassium Channels, Inwardly Rectifying - physiology | Calcium Channel Blockers - chemistry | Calcium, metabolism | Collagen Type II | Egtazic Acid, pharmacology | Myocytes, Cardiac, drug effects | Calcium, analysis | Myocardial Contraction, drug effects | Depression, Chemical | Tetraethylammonium Compounds, pharmacology | Aniline Compounds, pharmacology | Delayed Rectifier Potassium Channels, physiology | Heart Ventricles | Xanthenes, pharmacology | Electrocardiography, drug effects | Delayed Rectifier Potassium Channels, antagonists and inhibitors | Torsades de Pointes, physiopathology | Phenethylamines, pharmacology | Calcimycin, pharmacology | Cesium, pharmacology | Patch-Clamp Techniques | Poloxamer, pharmacology | Calcium Channels, L-Type, physiology | Sulfonamides, pharmacology | Chlorides, pharmacology | Verapamil, pharmacology | Propranolol, pharmacology | Antihypertensive drugs | Index Medicus
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9. Full Text Repeated Cocaine Administration Increases Voltage-Sensitive Calcium Currents in Response to Membrane Depolarization in Medial Prefrontal Cortex Pyramidal Neurons
by Nasif, Fernando J and Hu, Xiu-Ti and White, Francis J
Journal of Neuroscience, ISSN 0270-6474, 04/2005, Volume 25, Issue 14, pp. 3674 - 3679
The medial prefrontal cortex ( mPFC) plays a critical role in cocaine addiction. However, evidence to elucidate how the mPFC is functionally involved in... 
Patch clamp | Medial prefrontal cortex | current | Cocaine | Psychostimulant | plateau potential | DENDRITES | SYSTEM | LOCALIZATION | patch clamp | ACTIVATION | medial prefrontal cortex | cocaine | CA2+ CHANNELS | BEHAVIORAL SENSITIZATION | NUCLEUS-ACCUMBENS NEURONS | NEUROSCIENCES | psychostimulant | GLUTAMATE | DOPAMINE | RAT NEOCORTICAL NEURONS | Ca2+ current | Ca2+ plateau potential | Tetraethylammonium - pharmacology | Calcium - metabolism | Male | Membrane Potentials - radiation effects | Patch-Clamp Techniques - methods | Calcium Channels - physiology | Drug Interactions | Prefrontal Cortex - drug effects | Time Factors | Pyramidal Cells - drug effects | Kynurenic Acid - pharmacology | Tetrodotoxin - pharmacology | Cadmium Chloride - pharmacology | Electric Stimulation - methods | Potassium Channel Blockers - pharmacology | Membrane Potentials - drug effects | Nifedipine - pharmacology | Drug Administration Schedule | Chlorides - pharmacology | Rats | Sodium Channel Blockers - pharmacology | Excitatory Amino Acid Antagonists - pharmacology | Calcium Channel Blockers - pharmacology | Membrane Potentials - physiology | Prefrontal Cortex - cytology | Rats, Sprague-Dawley | Dopamine Uptake Inhibitors - administration & dosage | GABA Antagonists - pharmacology | Cocaine - administration & dosage | Cesium - pharmacology | Animals | In Vitro Techniques | Dose-Response Relationship, Radiation | Index Medicus | Brief Communications
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10. Full Text A novel mechanism for the anticonvulsant effect of furosemide in rat hippocampus in vitro
by Uwera, Josiane and Nedergaard, Steen and Andreasen, Mogens
Brain Research, ISSN 0006-8993, 2015, Volume 1625, pp. 1 - 8
Abstract Though both in vivo and in vitro studies have demonstrated an anticonvulsant effect of the loop diuretic furosemide, the precise mechanism behind this... 
Neurology | pHi | NKCC1 | Seizure | KCC2 | Furosemide | Cl−/HCO−3-exchanger | HCO | exchanger | CATION-CHLORIDE COTRANSPORTERS | Cl-/HCO3--exchanger | ASTROCYTES | NEUROSCIENCES | EXTRACELLULAR-SPACE | SEIZURES | EPILEPTIFORM ACTIVITY | CL-COTRANSPORTER | pH(i) | EPILEPSY | DIURETICS | BRAIN | Electric Stimulation | Rats, Wistar | 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology | Chlorides - pharmacology | Sodium Potassium Chloride Symporter Inhibitors - pharmacology | Rats | Male | Hippocampus - drug effects | Hippocampus - cytology | Anticonvulsants - pharmacology | Bumetanide - pharmacology | Dose-Response Relationship, Drug | Cesium - pharmacology | Patch-Clamp Techniques | Animals | Thioglycolates - pharmacology | Statistics, Nonparametric | Thiazoles - pharmacology | Furosemide - pharmacology | In Vitro Techniques | Neurons - drug effects | Action Potentials - drug effects | GABA | Brain | Anticonvulsants | Epilepsy | Seizures (Medicine) | Index Medicus
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11. Full Text Extrasynaptic Release of GABA by Retinal Dopaminergic Neurons
by Hajime Hirasawa and Michelino Puopolo and Elio Raviola
Journal of Neurophysiology, ISSN 0022-3077, 07/2009, Volume 102, Issue 1, pp. 146 - 158
GABA release by dopaminergic amacrine (DA) cells of the mouse retina was detected by measuring Cl− currents generated by isolated perikarya in response to... 
IN-VITRO | PHYSIOLOGY | AMACRINE CELLS | SECRETORY VESICLES | TYROSINE-HYDROXYLASE | IMMUNOHISTOCHEMICAL LOCALIZATION | GLUTAMATERGIC SYNAPSES | SYNAPTIC-TRANSMISSION | RAT RETINA | RECEPTORS | MAMMALIAN RETINA | NEUROSCIENCES | Tyrosine 3-Monooxygenase - metabolism | gamma-Aminobutyric Acid - metabolism | Pyridazines - pharmacology | Exocytosis - physiology | Exocytosis - drug effects | Patch-Clamp Techniques - methods | Synapsins - metabolism | Dose-Response Relationship, Drug | Synapses - metabolism | Retina - cytology | Macrolides - pharmacology | Neurons - metabolism | Tetrodotoxin - pharmacology | Neurons - drug effects | Electric Stimulation - methods | Dopamine - metabolism | Membrane Potentials - drug effects | Synapses - drug effects | Calcium - pharmacology | Chlorides - pharmacology | Mice, Inbred C57BL | Cells, Cultured | Enzyme Inhibitors - pharmacology | Cadmium - pharmacology | gamma-Aminobutyric Acid - pharmacology | Sodium Channel Blockers - pharmacology | Membrane Potentials - physiology | GABA Antagonists - pharmacology | Cesium - pharmacology | Animals | Models, Biological | Mice | Index Medicus
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12. Full Text The stress protein heat shock cognate 70 (Hsc70) inhibits the Transient Receptor Potential Vanilloid type 1 (TRPV1) channel
by Iftinca, Mircea and Flynn, Robyn and Basso, Lilian and Melo, Helvira and Aboushousha, Reem and Taylor, Lauren and Altier, Christophe
Molecular Pain, ISSN 1744-8069, 8/2016, Volume 12, p. 174480691666394
Background Specialized cellular defense mechanisms prevent damage from chemical, biological, and physical hazards. The heat shock proteins have been recognized... 
heat shock cognate 70 | ATPase | transient receptor potential vanilloid type 1 channel | rho-associated protein kinase | cell stress | HSP70 | INVOLVEMENT | TRAFFICKING | INDUCED HYPERSENSITIVITY | KINASE-C | NEUROSCIENCES | CELL-DEATH | CAPSAICIN RECEPTOR | PAIN | IN-VIVO | EXPRESSION | Inflammation - chemically induced | Freund's Adjuvant - toxicity | Antibiotics, Antineoplastic - pharmacology | Gene Expression - drug effects | Capsaicin - pharmacology | HSC70 Heat-Shock Proteins - metabolism | Humans | Guanidines - pharmacology | Ganglia, Spinal - cytology | Pain - metabolism | TRPV Cation Channels - metabolism | Inflammation - drug therapy | HEK293 Cells | Pain - etiology | Neurons - metabolism | Neurons - drug effects | Potassium Channel Blockers - pharmacology | HSC70 Heat-Shock Proteins - genetics | Alkaloids - pharmacology | Chlorides - pharmacology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Quinolizines - pharmacology | Pain - pathology | TRPV Cation Channels - genetics | Cesium - pharmacology | Animals | Anthelmintics - pharmacology | Mice | Ganglia, Spinal - drug effects | Index Medicus
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13. Full Text Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel
by Meadows, H.J and Randall, A.D
Neuropharmacology, ISSN 0028-3908, 2001, Volume 40, Issue 4, pp. 551 - 559
Human TASK-3 (hTASK-3) is a recently identified member of the two-pore domain potassium channel (2PDKC) family which in man is predominantly expressed in the... 
Human | Potassium channel | Membrane potential | LOCALIZATION | TANDEM | NEUROSCIENCES | MEMBER | FAMILY | MECANOSENSITIVE K+ CHANNEL | CLONING | membrane potential | potassium channel | POLYUNSATURATED FATTY-ACIDS | PHARMACOLOGY & PHARMACY | human | EXPRESSION | SUBUNIT | Xenopus | Tetraethylammonium - pharmacology | Potassium Channels, Tandem Pore Domain | Tetradecanoylphorbol Acetate - pharmacology | Humans | Potassium Channels - physiology | Dose-Response Relationship, Drug | Glyburide - pharmacology | Time Factors | Oocytes - drug effects | Female | Acids - pharmacology | Halothane - pharmacology | Membrane Potentials - drug effects | Cell Line | Gene Expression | Pregnanediones - pharmacology | Chlorides - pharmacology | Colforsin - pharmacology | Potassium - pharmacology | Potassium Channels - drug effects | 1-Methyl-3-isobutylxanthine - pharmacology | Barium Compounds - pharmacology | Potassium Channels - genetics | Cesium - pharmacology | Animals | Oocytes - physiology | Bupivacaine - pharmacology | Kinetics | TASK-3 protein | Index Medicus
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