scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1027378111 |
P356 | DOI | 10.1186/1744-8069-5-3 |
P932 | PMC publication ID | 2633278 |
P698 | PubMed publication ID | 19159452 |
P5875 | ResearchGate publication ID | 23808035 |
P2093 | author name string | Jun Chen | |
Donghee Kim | |||
Connie R Faltynek | |||
Bruce R Bianchi | |||
Philip R Kym | |||
Regina M Reilly | |||
Eric J Cavanaugh | |||
P2860 | cites work | TRPV1 channels mediate long-term depression at synapses on hippocampal interneurons | Q24644177 |
TRPA1 mediates formalin-induced pain | Q24681557 | ||
The vanilloid receptor TRPV1 is tonically activated in vivo and involved in body temperature regulation | Q28295455 | ||
ANKTM1, a TRP-like channel expressed in nociceptive neurons, is activated by cold temperatures | Q28509578 | ||
Transient receptor potential A1 mediates an osmotically activated ion channel | Q28573675 | ||
Nociceptor and hair cell transducer properties of TRPA1, a channel for pain and hearing | Q28588331 | ||
Lighting up the senses: FM1-43 loading of sensory cells through nonselective ion channels. | Q30310868 | ||
Pannexin1 is part of the pore forming unit of the P2X(7) receptor death complex | Q30479449 | ||
Utility of large-scale transiently transfected cells for cell-based high-throughput screens to identify transient receptor potential channel A1 (TRPA1) antagonists | Q30827889 | ||
Inhibition of nociceptors by TRPV1-mediated entry of impermeant sodium channel blockers | Q34698238 | ||
4-Hydroxynonenal, an endogenous aldehyde, causes pain and neurogenic inflammation through activation of the irritant receptor TRPA1 | Q35941218 | ||
Pain TRPs | Q36093784 | ||
Molecular determinants of species-specific activation or blockade of TRPA1 channels | Q39984645 | ||
TRPV1 shows dynamic ionic selectivity during agonist stimulation. | Q39994761 | ||
Polyamines are potent ligands for the capsaicin receptor TRPV1. | Q40326057 | ||
TRPV1 regulators mediate gentamicin penetration of cultured kidney cells. | Q40415348 | ||
TRPV1 acts as proton channel to induce acidification in nociceptive neurons | Q40549949 | ||
Pore dilation of neuronal P2X receptor channels | Q40960421 | ||
Neuronal P2X transmitter-gated cation channels change their ion selectivity in seconds. | Q41646184 | ||
A role of TRPA1 in mechanical hyperalgesia is revealed by pharmacological inhibition. | Q41839374 | ||
Mitogen-activated protein kinase and caspase signaling pathways are required for P2X7 receptor (P2X7R)-induced pore formation in human THP-1 cells | Q44666463 | ||
Density-dependent changes of the pore properties of the P2X2 receptor channel | Q44859237 | ||
Activation of transient receptor potential A1 channels by mustard oil, tetrahydrocannabinol and Ca2+ reveals different functional channel states | Q46565531 | ||
Fire in the hole: pore dilation of the capsaicin receptor TRPV1. | Q46626388 | ||
Activation of TRPA1 by farnesyl thiosalicylic acid | Q46825855 | ||
Activation of TRPA1 channels by the fatty acid amide hydrolase inhibitor 3'-carbamoylbiphenyl-3-yl cyclohexylcarbamate (URB597). | Q53577604 | ||
P304 | page(s) | 3 | |
P577 | publication date | 2009-01-21 | |
P1433 | published in | Molecular Pain | Q15766244 |
P1476 | title | Pore dilation occurs in TRPA1 but not in TRPM8 channels | |
P478 | volume | 5 |
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Q33775096 | Bimodal voltage dependence of TRPA1: mutations of a key pore helix residue reveal strong intrinsic voltage-dependent inactivation |
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Q38830295 | Calcium Entry Through Thermosensory Channels |
Q36236703 | Cellular permeation of large molecules mediated by TRPM8 channels |
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Q62661251 | Cinnamaldehyde inhibits L-type calcium channels in mouse ventricular cardiomyocytes and vascular smooth muscle cells |
Q30975374 | Comparative effects of heterologous TRPV1 and TRPM8 expression in rat hippocampal neurons |
Q41815881 | Comparison of the transport of QX-314 through TRPA1, TRPM8, and TRPV1 channels |
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Q43067153 | Dynamic changes in the TRPA1 selectivity filter lead to progressive but reversible pore dilation |
Q31109965 | Effect of cholesterol depletion on the pore dilation of TRPV1. |
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Q41876734 | Genetic Method for Labeling Electrically Coupled Cells: Application to Retina |
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Q42906393 | Honey Bee Thermal/Chemical Sensor, AmHsTRPA, Reveals Neofunctionalization and Loss of Transient Receptor Potential Channel Genes |
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Q36770939 | Permeation and block of TRPV1 channels by the cationic lidocaine derivative QX-314 |
Q36806245 | Phenotyping the function of TRPV1-expressing sensory neurons by targeted axonal silencing |
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Q47128203 | Potential Mechanisms Underlying Inflammation-Enhanced Aminoglycoside-Induced Cochleotoxicity. |
Q37835328 | Properties and therapeutic potential of transient receptor potential channels with putative roles in adversity: focus on TRPC5, TRPM2 and TRPA1. |
Q33883232 | Properties of the TRPML3 channel pore and its stable expansion by the Varitint-Waddler-causing mutation |
Q35126683 | Role of the outer pore domain in transient receptor potential vanilloid 1 dynamic permeability to large cations |
Q57144860 | Selective cold pain inhibition by targeted block of TRPM8-expressing neurons with quaternary lidocaine derivative QX-314 |
Q36438795 | Selectively targeting pain in the trigeminal system |
Q34089246 | Structure-functional intimacies of transient receptor potential channels |
Q30505420 | TRPA1 channels regulate astrocyte resting calcium and inhibitory synapse efficacy through GAT-3 |
Q44840215 | TRPA1 contributes to specific mechanically activated currents and sensory neuron mechanical hypersensitivity. |
Q28482501 | TRPA1 mediates mechanical sensitization in nociceptors during inflammation |
Q37638751 | TRPA1 modulators in preclinical development |
Q38686108 | TRPing on the pore phenomenon: what do we know about transient receptor potential ion channel-related pore dilation up to now? |
Q37362053 | Targeting Pain-evoking Transient Receptor Potential Channels for the Treatment of Pain |
Q37860361 | Targeting of sodium channel blockers into nociceptors to produce long-duration analgesia: a systematic study and review |
Q36185728 | The Outer Pore and Selectivity Filter of TRPA1 |
Q93046959 | The Preclinical Pharmacological Study of a Novel Long-Acting Local Anesthetic, a Fixed-Dose Combination of QX-OH/Levobupivacaine, in Rats |
Q37791280 | The Role of Transient Receptor Potential Cation Channels in Ca2+ Signaling |
Q34175932 | The dynamic TRPA1 channel: a suitable pharmacological pain target? |
Q34709039 | The pore properties of human nociceptor channel TRPA1 evaluated in single channel recordings |
Q38045749 | The transient receptor potential channel TRPA1: from gene to pathophysiology |
Q37800508 | Transient receptor potential ankyrin 1: emerging pharmacology and indications for cardiovascular biology |
Q26849317 | Transient receptor potential channels as drug targets: from the science of basic research to the art of medicine |
Q52765711 | Transient receptor potential vanilloid 4 (TRPV4) channel as a target of crotamiton and its bimodal effects. |
Q34618888 | Voltage- and temperature-dependent activation of TRPV3 channels is potentiated by receptor-mediated PI(4,5)P2 hydrolysis |
Q28484900 | Xanthurenic acid binds to neuronal G-protein-coupled receptors that secondarily activate cationic channels in the cell line NCB-20 |