| scholarly article | Q13442814 |
| P50 | author | Chung-chin Kuo | Q43190242 |
| P2093 | author name string | Ya-Chin Yang | |
| P433 | issue | 5 | |
| P304 | page(s) | 1228-1237 | |
| P577 | publication date | 2002-11-01 | |
| P1433 | published in | Molecular Pharmacology | Q1943386 |
| P1476 | title | Inhibition of Na(+) current by imipramine and related compounds: different binding kinetics as an inactivation stabilizer and as an open channel blocker | |
| P478 | volume | 62 |
| Q33918510 | A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia |
| Q30441260 | A pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profile |
| Q38040330 | Advances in targeting voltage-gated sodium channels with small molecules |
| Q36412627 | An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+. |
| Q48308933 | Antinociceptive action of carbamazepine on thermal hypersensitive pain at spinal level in a rat model of adjuvant-induced chronic inflammation |
| Q41668278 | Bupivacaine blocks N-type inactivating Kv channels in the open state: no allosteric effect on inactivation kinetics |
| Q46199353 | Characterization of voltage-gated sodium-channel blockers by electrical stimulation and fluorescence detection of membrane potential. |
| Q36410736 | Epileptic consciousness: concept and meaning of aura. |
| Q42931956 | Flufenamic acid decreases neuronal excitability through modulation of voltage-gated sodium channel gating. |
| Q35122828 | Inhibition of neuronal voltage-gated sodium channels by brilliant blue G |
| Q41952692 | Mechanism of block of hEag1 K+ channels by imipramine and astemizole |
| Q35545122 | Oxaliplatin induces hyperexcitability at motor and autonomic neuromuscular junctions through effects on voltage-gated sodium channels |
| Q35574947 | Pharmacogenomics in the treatment of epilepsy |
| Q44683069 | Potentiation of imipramine-induced antinociception by nicotine in the formalin test |
| Q39380930 | Quantitative modelling of interaction of propafenone with sodium channels in cardiac cells |
| Q38825019 | Role of Sodium Channels in Epilepsy |
| Q42088430 | SCN1A splice variants exhibit divergent sensitivity to commonly used antiepileptic drugs |
| Q42080376 | Searching for novel anti-myotonic agents: pharmacophore requirement for use-dependent block of skeletal muscle sodium channels by N-benzylated cyclic derivatives of tocainide |
| Q48274837 | State-dependent block of voltage-gated sodium channels by the casein-kinase 1 inhibitor IC261. |
| Q30866710 | State-dependent compound inhibition of Nav1.2 sodium channels using the FLIPR Vm dye: on-target and off-target effects of diverse pharmacological agents |
| Q48875355 | The antidepressant citalopram inhibits delayed rectifier outward K⁺ current in mouse cortical neurons. |
| Q34352436 | The block of CFTR by scorpion venom is state-dependent |
| Q37280509 | The external pore loop interacts with S6 and S3-S4 linker in domain 4 to assume an essential role in gating control and anticonvulsant action in the Na(+) channel |
| Q24606139 | The young brain and concussion: imaging as a biomarker for diagnosis and prognosis |
| Q40444942 | V102862 (Co 102862): a potent, broad-spectrum state-dependent blocker of mammalian voltage-gated sodium channels |
| Q48666406 | Voltage-gated Na+ channel ligands and ATP: relative molecular similarity and implications for channel function |
Search more.