| scholarly article | Q13442814 |
| P2093 | author name string | Leigh D Plant | |
| P2860 | cites work | Human TREK2, a 2P domain mechano-sensitive K+ channel with multiple regulations by polyunsaturated fatty acids, lysophospholipids, and Gs, Gi, and Gq protein-coupled receptors | Q22254402 |
| The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity | Q22337058 | ||
| A quantitative description of membrane current and its application to conduction and excitation in nerve | Q22337072 | ||
| POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES | Q22337178 | ||
| A Novel Two-pore Domain K+ Channel, TRESK, Is Localized in the Spinal Cord | Q24302058 | ||
| Crystal structure of the human two-pore domain potassium channel K2P1 | Q24303649 | ||
| Crystal structure of the human K2P TRAAK, a lipid- and mechano-sensitive K+ ion channel | Q24303662 | ||
| p11, an annexin II subunit, an auxiliary protein associated with the background K+ channel, TASK-1 | Q24305279 | ||
| TWIK-1 two-pore domain potassium channels change ion selectivity and conduct inward leak sodium currents in hypokalemia | Q24306072 | ||
| SUMOylation regulates Kv2.1 and modulates pancreatic beta-cell excitability | Q24311712 | ||
| Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I | Q24312557 | ||
| TASK, a human background K+ channel to sense external pH variations near physiological pH | Q24314854 | ||
| Phosphorylation-dependent binding of 14-3-3 proteins controls TRESK regulation | Q24318495 | ||
| TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure | Q24323355 | ||
| A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids. | Q24533254 | ||
| Cross-talk between the mechano-gated K2P channel TREK-1 and the actin cytoskeleton. | Q24539089 | ||
| Cloning, functional expression and brain localization of a novel unconventional outward rectifier K+ channel | Q24561735 | ||
| Pungent agents from Szechuan peppers excite sensory neurons by inhibiting two-pore potassium channels | Q24622936 | ||
| Interaction with 14-3-3 proteins promotes functional expression of the potassium channels TASK-1 and TASK-3 | Q24641890 | ||
| Expression pattern and functional characteristics of two novel splice variants of the two-pore-domain potassium channel TREK-2 | Q24642277 | ||
| Functional expression of the epithelial Ca(2+) channels (TRPV5 and TRPV6) requires association of the S100A10-annexin 2 complex | Q24683784 | ||
| A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. | Q27933854 | ||
| Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3 | Q28140649 | ||
| Inhalational anesthetics activate two-pore-domain background K+ channels | Q28143765 | ||
| KCNK2: reversible conversion of a hippocampal potassium leak into a voltage-dependent channel | Q28185346 | ||
| Annexin II light chain regulates sensory neuron-specific sodium channel expression | Q28202799 | ||
| TREK-1, a K+ channel involved in polymodal pain perception | Q41962937 | ||
| Crystal-induced inflammation in canine joints. I. An experimental model with quantification of the host response | Q42153566 | ||
| Block of Kcnk3 by protons. Evidence that 2-P-domain potassium channel subunits function as homodimers. | Q43612382 | ||
| KCNQ/M currents in sensory neurons: significance for pain therapy. | Q44540560 | ||
| Species-specific differences in response to anesthetics and other modulators by the K2P channel TRESK. | Q45080383 | ||
| Characterization and function of TWIK-related acid sensing K+ channels in a rat nociceptive cell | Q45110559 | ||
| Potent activation of the human tandem pore domain K channel TRESK with clinical concentrations of volatile anesthetics | Q45161464 | ||
| PIP2 hydrolysis underlies agonist-induced inhibition and regulates voltage gating of two-pore domain K+ channels. | Q45242239 | ||
| Control of the single channel conductance of K2P10.1 (TREK-2) by the amino-terminus: role of alternative translation initiation. | Q46323082 | ||
| Calcineurin inhibitor-induced headache: clinical characteristics and possible mechanisms | Q46442419 | ||
| Potassium channels opened by noradrenaline and other transmitters in excised membrane patches of guinea-pig submucosal neurones | Q46778953 | ||
| TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones. | Q46930538 | ||
| Immunohistochemical colocalization of TREK-1, TREK-2 and TRAAK with TRP channels in the trigeminal ganglion cells. | Q47839556 | ||
| Expression of TWIK-related acid sensitive K+ channels in capsaicin sensitive and insensitive cells of rat dorsal root ganglia | Q48521759 | ||
| Intracellular traffic of the K+ channels TASK-1 and TASK-3: role of N- and C-terminal sorting signals and interaction with 14-3-3 proteins | Q48729332 | ||
| Does sumoylation control K2P1/TWIK1 background K+ channels? | Q48785878 | ||
| Formation of functional heterodimers between the TASK-1 and TASK-3 two-pore domain potassium channel subunits | Q48873005 | ||
| General anesthetics hyperpolarize neurons in the vertebrate central nervous system | Q48897652 | ||
| A non-inactivating K+ current sensitive to muscarinic receptor activation in rat cultured cerebellar granule neurons. | Q49073273 | ||
| Targeting of calcineurin to an NFAT-like docking site is required for the calcium-dependent activation of the background K+ channel, TRESK. | Q50651251 | ||
| TREK-2 (K2P10.1) and TRESK (K2P18.1) are major background K+ channels in dorsal root ganglion neurons. | Q50738522 | ||
| The pH of local anesthetic solutions. | Q51865072 | ||
| pH-dependent electrophysiological effects of quinidine and lidocaine on canine cardiac purkinje fibers. | Q51869528 | ||
| Serotonin and cyclic AMP close single K+ channels in Aplysia sensory neurones. | Q52219678 | ||
| A novel oxygen-sensitive potassium current in rat carotid body type I cells. | Q52276626 | ||
| Action potentials of embryonic dorsal root ganglion neurones in Xenopus tadpoles | Q52303849 | ||
| Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel. | Q52448076 | ||
| Forward Transport of K2p3.1: mediation by 14-3-3 and COPI, modulation by p11. | Q52582531 | ||
| Voltage dependence of membrane properties of trigeminal root ganglion neurons. | Q52593631 | ||
| A G Protein Mediates the Inhibition of the Voltage-Dependent Potassium M Current by Muscarine, LHRH, Substance P and UTP in Bullfrog Sympathetic Neurons. | Q54344802 | ||
| On the resting potential of isolated frog sympathetic neurons. | Q54348359 | ||
| Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone | Q59066538 | ||
| Deletion of the background potassium channel TREK-1 results in a depression-resistant phenotype | Q60710783 | ||
| Bradykinin inhibits a potassium M-like current in rat pheochromocytoma PC12 cells | Q69749648 | ||
| Responses of adult human dorsal root ganglion neurons in culture to capsaicin and low pH | Q71578958 | ||
| Resting membrane potentials and excitability at different regions of rat dorsal root ganglion neurons in culture | Q72111217 | ||
| Potassium leak channels and the KCNK family of two-P-domain subunits | Q28205333 | ||
| Modulation of TASK-1 (Kcnk3) and TASK-3 (Kcnk9) potassium channels: volatile anesthetics and neurotransmitters share a molecular site of action | Q28206083 | ||
| Forward transport. 14-3-3 binding overcomes retention in endoplasmic reticulum by dibasic signals | Q28215227 | ||
| The two-pore domain K+ channel, TRESK, is activated by the cytoplasmic calcium signal through calcineurin | Q28246530 | ||
| Concepts in sumoylation: a decade on | Q28257220 | ||
| Crystal structure of a mammalian voltage-dependent Shaker family K+ channel | Q28260421 | ||
| Annexin II light chain p11 promotes functional expression of acid-sensing ion channel ASIC1a | Q28272902 | ||
| Molecular background of leak K+ currents: two-pore domain potassium channels | Q28279763 | ||
| Transient receptor potential cation channels in disease | Q28284143 | ||
| International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels | Q28289202 | ||
| Alterations in 5-HT1B receptor function by p11 in depression-like states | Q28290425 | ||
| The neuronal background K2P channels: focus on TREK1 | Q28294077 | ||
| Kcnkø: single, cloned potassium leak channels are multi-ion pores | Q28346209 | ||
| TASK-3, a new member of the tandem pore K(+) channel family | Q28374393 | ||
| A TRP channel that senses cold stimuli and menthol | Q28511363 | ||
| A heat-sensitive TRP channel expressed in keratinocytes | Q28512804 | ||
| The retention factor p11 confers an endoplasmic reticulum-localization signal to the potassium channel TASK-1 | Q28568568 | ||
| Hypoxic depolarization of cerebellar granule neurons by specific inhibition of TASK-1 | Q28569434 | ||
| TREK-2, a new member of the mechanosensitive tandem-pore K+ channel family | Q28571535 | ||
| Axonal transport of TREK and TRAAK potassium channels in rat sciatic nerves | Q28573535 | ||
| SUMOylation regulates kainate-receptor-mediated synaptic transmission | Q28576922 | ||
| Identification of a cold receptor reveals a general role for TRP channels in thermosensation | Q28580334 | ||
| Thermosensitivity of the two-pore domain K+ channels TREK-2 and TRAAK | Q28580851 | ||
| Synergistic interaction and the role of C-terminus in the activation of TRAAK K+ channels by pressure, free fatty acids and alkali | Q28582799 | ||
| The mechano-activated K+ channels TRAAK and TREK-1 control both warm and cold perception | Q28591983 | ||
| Cellular and Molecular Mechanisms of Pain | Q29011961 | ||
| An introduction to TRP channels | Q29615753 | ||
| TASK-1, a two-pore domain K+ channel, is modulated by multiple neurotransmitters in motoneurons | Q30305478 | ||
| The TASK-1 two-pore domain K+ channel is a molecular substrate for neuronal effects of inhalation anesthetics. | Q30306012 | ||
| Cns distribution of members of the two-pore-domain (KCNK) potassium channel family. | Q30307946 | ||
| Motoneuronal TASK channels contribute to immobilizing effects of inhalational general anesthetics | Q30433922 | ||
| Multiple ionic mechanisms mediate inhibition of rat motoneurones by inhalation anaesthetics | Q30472667 | ||
| Alternative translation initiation in rat brain yields K2P2.1 potassium channels permeable to sodium | Q30483411 | ||
| One SUMO is sufficient to silence the dimeric potassium channel K2P1 | Q30495084 | ||
| Identification and cloning of TWIK-originated similarity sequence (TOSS): a novel human 2-pore K+ channel principal subunit. | Q30708737 | ||
| TASK-3, a novel tandem pore domain acid-sensitive K+ channel. An extracellular histiding as pH sensor | Q31625560 | ||
| Cold transduction by inhibition of a background potassium conductance in rat primary sensory neurones. | Q31803977 | ||
| Mechano- or acid stimulation, two interactive modes of activation of the TREK-1 potassium channel. | Q33421003 | ||
| A phospholipid sensor controls mechanogating of the K+ channel TREK-1. | Q33432568 | ||
| Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and periphery | Q33932328 | ||
| Specificity of cold thermotransduction is determined by differential ionic channel expression | Q34113463 | ||
| A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura | Q34140189 | ||
| Cloning of two transcripts, HKT4.1a and HKT4.1b, from the human two-pore K+ channel gene KCNK4. Chromosomal localization, tissue distribution and functional expression | Q34145553 | ||
| Functional expression of TASK-1/TASK-3 heteromers in cerebellar granule cells | Q34284061 | ||
| Molecular and cellular mechanisms of general anaesthesia | Q34291163 | ||
| Functional expression of TRESK-2, a new member of the tandem-pore K+ channel family | Q34318305 | ||
| Sumoylation silences the plasma membrane leak K+ channel K2P1. | Q34410181 | ||
| Sequence and function of the two P domain potassium channels: implications of an emerging superfamily | Q34455956 | ||
| Pathways modulating neural KCNQ/M (Kv7) potassium channels | Q34464180 | ||
| Overview of molecular relationships in the voltage-gated ion channel superfamily. | Q34480285 | ||
| TRAAK is a mammalian neuronal mechano-gated K+ channel. | Q34486466 | ||
| A di-acidic sequence motif enhances the surface expression of the potassium channel TASK-3. | Q34634174 | ||
| SUMO modification of cell surface Kv2.1 potassium channels regulates the activity of rat hippocampal neurons | Q34865655 | ||
| TRESK channel contribution to nociceptive sensory neurons excitability: modulation by nerve injury. | Q34984122 | ||
| Oxidative modification of M-type K(+) channels as a mechanism of cytoprotective neuronal silencing | Q35102221 | ||
| A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons | Q35118431 | ||
| SUMO modification regulates inactivation of the voltage-gated potassium channel Kv1.5. | Q35629481 | ||
| Covalent modification of a volatile anesthetic regulatory site activates TASK-3 (KCNK9) tandem-pore potassium channels | Q35776793 | ||
| TREK-1 is a heat-activated background K(+) channel | Q36246837 | ||
| Opening and closing of KCNKO potassium leak channels is tightly regulated | Q36436304 | ||
| Transient receptor potential ion channels as participants in thermosensation and thermoregulation | Q36594600 | ||
| ORK1, a potassium-selective leak channel with two pore domains cloned from Drosophila melanogaster by expression in Saccharomyces cerevisiae | Q36690601 | ||
| Nociceptor sensitization in pain pathogenesis | Q37254618 | ||
| A structural model for K2P potassium channels based on 23 pairs of interacting sites and continuum electrostatics | Q37267666 | ||
| Phosphorus nuclear magnetic resonance of perfused working rat hearts | Q39145840 | ||
| Sustained graded pain and hyperalgesia from harmless experimental tissue acidosis in human skin | Q39493670 | ||
| A specific two-pore domain potassium channel blocker defines the structure of the TASK-1 open pore | Q39777149 | ||
| P304 | page(s) | 21 | |
| P577 | publication date | 2012-03-05 | |
| P1433 | published in | Frontiers in Molecular Neuroscience | Q27721913 |
| P1476 | title | A Role for K2P Channels in the Operation of Somatosensory Nociceptors | |
| P478 | volume | 5 |
| Q37058127 | Functional analysis of a migraine-associated TRESK K+ channel mutation |
| Q41983600 | Functional significance of M-type potassium channels in nociceptive cutaneous sensory endings |
| Q48278693 | GI-530159, a novel, selective, mechanosensitive two-pore-domain potassium (K2P ) channel opener, reduces rat dorsal root ganglion neuron excitability. |
| Q30459043 | Ion channel profile of TRPM8 cold receptors reveals a role of TASK-3 potassium channels in thermosensation |
| Q57456146 | K2P channels: Emerging targets for novel analgesic drugs |
| Q34006322 | Nonmigraine-associated TRESK K+ channel variant C110R does not increase the excitability of trigeminal ganglion neurons |
| Q37623462 | Opening paths to novel analgesics: the role of potassium channels in chronic pain |
| Q46197109 | Piezo2 expression in corneal afferent neurons |
| Q37362041 | Potassium channels in peripheral pain pathways: expression, function and therapeutic potential |
| Q37502544 | TREK2 expressed selectively in IB4-binding C-fiber nociceptors hyperpolarizes their membrane potentials and limits spontaneous pain. |
| Q27021286 | Temperature sensitivity of two-pore (K2P) potassium channels |
| Q34396710 | The LQLP calcineurin docking site is a major determinant of the calcium-dependent activation of human TRESK background K+ channel |
| Q92402642 | The Role of TRESK in Discrete Sensory Neuron Populations and Somatosensory Processing |
| Q38859500 | The function and regulation of acid-sensing ion channels (ASICs) and the epithelial Na(+) channel (ENaC): IUPHAR Review 19. |
| Q37381403 | The fundamental unit of pain is the cell |
| Q26822748 | Two-pore domain potassium channels enable action potential generation in the absence of voltage-gated potassium channels |
| Q38270913 | Two-pore domain potassium channels: potential therapeutic targets for the treatment of pain |
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