scholarly article | Q13442814 |
P356 | DOI | 10.1016/0920-1211(95)00101-8 |
P698 | PubMed publication ID | 8739124 |
P2093 | author name string | H H Wolf | |
J Engel | |||
W Löscher | |||
H S White | |||
R Bartsch | |||
C Tober | |||
E E Polymeropoulos | |||
C Rundfeldt | |||
D Hönack | |||
A Rostock | |||
B Kutscher | |||
P433 | issue | 3 | |
P304 | page(s) | 211-223 | |
P577 | publication date | 1996-04-01 | |
P1433 | published in | Epilepsy Research | Q15746405 |
P1476 | title | D-23129: a new anticonvulsant with a broad spectrum activity in animal models of epileptic seizures. | |
P478 | volume | 23 |
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Q40745093 | Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352. |
Q43683699 | Activation of expressed KCNQ potassium currents and native neuronal M-type potassium currents by the anti-convulsant drug retigabine. |
Q34114419 | Activation of voltage-gated KCNQ/Kv7 channels by anticonvulsant retigabine attenuates mechanical allodynia of inflammatory temporomandibular joint in rats |
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Q42955356 | Anticonvulsant Effect of Antiaris toxicaria (Pers.) Lesch. (Moraceae) Aqueous Extract in Rodents |
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Q42619127 | Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions. |
Q37878206 | Basic mechanisms of antiepileptic drugs and their pharmacokinetic/pharmacodynamic interactions: an update |
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Q77893179 | Characterization of the K+ channel opening effect of the anticonvulsant retigabine in PC12 cells |
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Q38371584 | Coexpression and activation of TRPV1 suppress the activity of the KCNQ2/3 channel |
Q36498532 | Combinatorial augmentation of voltage-gated KCNQ potassium channels by chemical openers |
Q33422564 | Determination of retigabine and its acetyl metabolite in biological matrices by on-line solid-phase extraction (column switching) liquid chromatography with tandem mass spectrometry. |
Q24634116 | Discovery, Synthesis, and Structure–Activity Relationship of a Series of N -Aryl-bicyclo[2.2.1]heptane-2-carboxamides: Characterization of ML213 as a Novel KCNQ2 and KCNQ4 Potassium Channel Opener |
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Q44408542 | Effect of the KCNQ potassium channel opener retigabine on single KCNQ2/3 channels expressed in CHO cells |
Q52974740 | Effects of retigabine (D-23129) on different patterns of epileptiform activity induced by low magnesium in rat entorhinal cortex hippocampal slices. |
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Q47149739 | Flupirtine and diazepam combination terminates established status epilepticus: results in three rodent models |
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Q34458405 | Future prospects for the drug treatment of epilepsy. |
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Q42449315 | Inhibition of cAMP response element-binding protein reduces neuronal excitability and plasticity, and triggers neurodegeneration |
Q36989788 | Inside job: ligand-receptor pharmacology beneath the plasma membrane |
Q48201175 | Involvement of KCNQ2 subunits in [3H]dopamine release triggered by depolarization and pre-synaptic muscarinic receptor activation from rat striatal synaptosomes. |
Q34075106 | Is there a role for potassium channel openers in neuronal ion channel disorders? |
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Q37162392 | K+ channel modulators for the treatment of neurological disorders and autoimmune diseases |
Q46935266 | KCNQ/Kv7 channel regulation of hippocampal gamma-frequency firing in the absence of synaptic transmission. |
Q40802799 | KCNQ4 channel activation by BMS-204352 and retigabine |
Q51532244 | Kv7 (KCNQ) channel openers induce hypothermia in the mouse |
Q48472286 | Kv7/KCNQ/M-channels in rat glutamatergic hippocampal axons and their role in regulation of excitability and transmitter release. |
Q42760045 | Lack of pharmacokinetic interaction between retigabine and phenobarbitone at steady-state in healthy subjects |
Q37642003 | Management of the patient with medically refractory epilepsy. |
Q24683346 | Molecular targets for antiepileptic drug development |
Q40144001 | MrgD activation inhibits KCNQ/M-currents and contributes to enhanced neuronal excitability. |
Q33845614 | Multiple-dose, linear, dose-proportional pharmacokinetics of retigabine in healthy volunteers |
Q24644947 | Neural KCNQ (Kv7) channels |
Q92532747 | Neurobiology of organophosphate-induced seizures |
Q35683922 | Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine. |
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Q34119473 | New anti-epileptic drugs |
Q36600282 | Novel anticonvulsant drugs targeting voltage-dependent ion channels |
Q34974862 | Novel anticonvulsant medications in development |
Q37950518 | Novel medications for epilepsy |
Q36603168 | One man's side effect is another man's therapeutic opportunity: targeting Kv7 channels in smooth muscle disorders |
Q35102221 | Oxidative modification of M-type K(+) channels as a mechanism of cytoprotective neuronal silencing |
Q45143751 | Paradoxical cerebral cortical hyperexcitability following flupirtine overdose |
Q34464180 | Pathways modulating neural KCNQ/M (Kv7) potassium channels |
Q35761335 | Perspectives on treatment options for mesial temporal lobe epilepsy with hippocampal sclerosis |
Q47270986 | Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy. |
Q97420402 | Pharmacological Manipulation of K v 7 Channels as a New Therapeutic Tool for Multiple Brain Disorders |
Q34823174 | Pharmacological management of epilepsy: recent advances and future prospects |
Q51527954 | Pharmacophore modeling, 3D-QSAR, and in silico ADME prediction of N-pyridyl and pyrimidine benzamides as potent antiepileptic agents. |
Q37831297 | Pharmacotherapy of epilepsy: newly approved and developmental agents |
Q37992162 | Pharmacotherapy of the third-generation AEDs: lacosamide, retigabine and eslicarbazepine acetate |
Q24545908 | Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains |
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Q43515162 | Progress report on new antiepileptic drugs: a summary of the Fifth Eilat Conference (EILAT V). |
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Q36697501 | Retigabine |
Q37936428 | Retigabine (ezogabine): in partial-onset seizures in adults with epilepsy |
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Q73318360 | Retigabine strongly reduces repetitive firing in rat entorhinal cortex |
Q34333196 | Retigabine/Ezogabine, a KCNQ/K(V)7 channel opener: pharmacological and clinical data |
Q34415600 | Retigabine: chemical synthesis to clinical application. |
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Q34541901 | Retigabine: in partial seizures |
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Q35872543 | The Effects of the KCNQ Openers Retigabine and Flupirtine on Myotonia in Mammalian Skeletal Muscle Induced by a Chloride Channel Blocker |
Q58258271 | The Kv7 potassium channel activator retigabine decreases alcohol consumption in rats |
Q44791007 | The anti-hyperalgesic activity of retigabine is mediated by KCNQ potassium channel activation |
Q53920348 | The anticonvulsant retigabine potently suppresses epileptiform discharges in the low Ca ++ and low Mg++ model in the hippocampal slice preparation. |
Q37973378 | The mechanism of action of retigabine (ezogabine), a first-in-class K+ channel opener for the treatment of epilepsy |
Q34305846 | The mechanisms of action of commonly used antiepileptic drugs |
Q36675813 | The new KCNQ2 activator 4-Chlor-N-(6-chlor-pyridin-3-yl)-benzamid displays anticonvulsant potential. |
Q34447899 | The new anticonvulsant retigabine (D-23129) acts as an opener of K+ channels in neuronal cells |
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Q28138343 | The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits |
Q34393213 | The pharmacology of imepitoin: the first partial benzodiazepine receptor agonist developed for the treatment of epilepsy |
Q45906577 | The preclinical discovery and development of ezogabine for the treatment of epilepsy. |
Q46886423 | The role of Gilbert's syndrome and frequent NAT2 slow acetylation polymorphisms in the pharmacokinetics of retigabine |
Q37973453 | The spectrum of anticonvulsant efficacy of retigabine (ezogabine) in animal models: implications for clinical use. |
Q35593939 | The therapeutic potential of neuronal KCNQ channel modulators |
Q37994720 | The urinary safety profile and secondary renal effects of retigabine (ezogabine): a first-in-class antiepileptic drug that targets KCNQ (K(v)7) potassium channels |
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