Pore dilation occurs in TRPA1 but not in TRPM8 channels

[1]  Donghee Kim,et al.  Activation of transient receptor potential A1 channels by mustard oil, tetrahydrocannabinol and Ca2+ reveals different functional channel states , 2008, Neuroscience.

[2]  P. Hajduk,et al.  Molecular Determinants of Species-Specific Activation or Blockade of TRPA1 Channels , 2008, The Journal of Neuroscience.

[3]  M. Caterina,et al.  TRPV1 shows dynamic ionic selectivity during agonist stimulation , 2008, Nature Neuroscience.

[4]  D. Julius,et al.  Fire in the hole: pore dilation of the capsaicin receptor TRPV1 , 2008, Nature Neuroscience.

[5]  Hong Ao,et al.  Activation of TRPA1 by Farnesyl Thiosalicylic Acid , 2008, Molecular Pharmacology.

[6]  Helen E. Gibson,et al.  TRPV1 Channels Mediate Long-Term Depression at Synapses on Hippocampal Interneurons , 2008, Neuron.

[7]  T. Neelands,et al.  Transient receptor potential A1 mediates an osmotically activated ion channel , 2008, The European journal of neuroscience.

[8]  E. Meacci,et al.  Pannexin 1 Is Part of the Pore Forming Unit of the P 2 x 7 Receptor Death Complex , 2008 .

[9]  Clifford J. Woolf,et al.  Inhibition of nociceptors by TRPV1-mediated entry of impermeant sodium channel blockers , 2007, Nature.

[10]  A. Basbaum,et al.  4-Hydroxynonenal, an endogenous aldehyde, causes pain and neurogenic inflammation through activation of the irritant receptor TRPA1 , 2007, Proceedings of the National Academy of Sciences.

[11]  Michael Zhao,et al.  TRPA1 mediates formalin-induced pain , 2007, Proceedings of the National Academy of Sciences.

[12]  T. Holzman,et al.  Activation of TRPA1 Channels by the Fatty Acid Amide Hydrolase Inhibitor 3′-Carbamoylbiphenyl-3-yl cyclohexylcarbamate (URB597) , 2007, Molecular Pharmacology.

[13]  J. Treanor,et al.  The Vanilloid Receptor TRPV1 Is Tonically Activated In Vivo and Involved in Body Temperature Regulation , 2007, The Journal of Neuroscience.

[14]  D. Spray,et al.  Pannexin1 is part of the pore forming unit of the P2X7 receptor death complex , 2007, FEBS letters.

[15]  Jing Xu,et al.  Utility of Large-Scale Transiently Transfected Cells for Cell-Based High-Throughput Screens to Identify Transient Receptor Potential Channel A1 (TRPA1) Antagonists , 2007, Journal of biomolecular screening.

[16]  A. Patapoutian,et al.  A role of TRPA1 in mechanical hyperalgesia is revealed by pharmacological inhibition , 2007, Molecular pain.

[17]  G. Ahern,et al.  Polyamines Are Potent Ligands for the Capsaicin Receptor TRPV1* , 2006, Journal of Biological Chemistry.

[18]  P. Steyger,et al.  TRPV1 regulators mediate gentamicin penetration of cultured kidney cells , 2005, Hearing Research.

[19]  K. Nagata,et al.  Nociceptor and Hair Cell Transducer Properties of TRPA1, a Channel for Pain and Hearing , 2005, The Journal of Neuroscience.

[20]  G. Schultz,et al.  TRPV1 Acts as Proton Channel to Induce Acidification in Nociceptive Neurons* , 2004, Journal of Biological Chemistry.

[21]  Y. Kubo,et al.  Density‐dependent changes of the pore properties of the P2X2 receptor channel , 2004, The Journal of physiology.

[22]  D. Donnelly-roberts,et al.  Mitogen-Activated Protein Kinase and Caspase Signaling Pathways Are Required for P2X7 Receptor (P2X7R)-Induced Pore Formation in Human THP-1 Cells , 2004, Journal of Pharmacology and Experimental Therapeutics.

[23]  J. T. Corwin,et al.  Lighting up the Senses: FM1-43 Loading of Sensory Cells through Nonselective Ion Channels , 2003, The Journal of Neuroscience.

[24]  Peter McIntyre,et al.  ANKTM1, a TRP-like Channel Expressed in Nociceptive Neurons, Is Activated by Cold Temperatures , 2003, Cell.

[25]  Henry A. Lester,et al.  Neuronal P2X transmitter-gated cation channels change their ion selectivity in seconds , 1999, Nature Neuroscience.

[26]  R. North,et al.  Pore dilation of neuronal P2X receptor channels , 1999, Nature Neuroscience.