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Summary Anatomy Item Literature (128) Expression Attributions Wiki
XB-ANAT-208

Papers associated with spinal ganglion

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Regenerative Potential of Injured Spinal Cord in the Light of Epigenetic Regulation and Modulation., Gupta S., Cells. June 22, 2023; 12 (13):       


The Tunicate Metabolite 2-(3,5-Diiodo-4-methoxyphenyl)ethan-1-amine Targets Ion Channels of Vertebrate Sensory Neurons., Paguigan ND., ACS Chem Biol. September 17, 2021; 16 (9): 1654-1662.


Identification and classification of a new TRPM3 variant (γ subtype)., Uchida K., J Physiol Sci. July 1, 2019; 69 (4): 623-634.              


Structural basis of TRPA1 inhibition by HC-030031 utilizing species-specific differences., Gupta R., Sci Rep. November 22, 2016; 6 37460.                    


Polyunsaturated fatty acids are potent openers of human M-channels expressed in Xenopus laevis oocytes., Liin SI., Acta Physiol (Oxf). September 1, 2016; 218 (1): 28-37.


Formation of Functional Heterodimers by TREK-1 and TREK-2 Two-pore Domain Potassium Channel Subunits., Lengyel M., J Biol Chem. June 24, 2016; 291 (26): 13649-61.


PnPP-19, a Synthetic and Nontoxic Peptide Designed from a Phoneutria nigriventer Toxin, Potentiates Erectile Function via NO/cGMP., Silva CN., J Urol. November 1, 2015; 194 (5): 1481-90.


Differential sensitivity of TREK-1, TREK-2 and TRAAK background potassium channels to the polycationic dye ruthenium red., Braun G., Br J Pharmacol. April 1, 2015; 172 (7): 1728-38.


Activation of TRPV1 channels inhibits mechanosensitive Piezo channel activity by depleting membrane phosphoinositides., Borbiro I., Sci Signal. February 10, 2015; 8 (363): ra15.


A family of excitatory peptide toxins from venomous crassispirine snails: using Constellation Pharmacology to assess bioactivity., Imperial JS., Toxicon. October 1, 2014; 89 45-54.


Subtype-specific mechanisms for functional interaction between α6β4* nicotinic acetylcholine receptors and P2X receptors., Limapichat W., Mol Pharmacol. September 1, 2014; 86 (3): 263-74.


Effects of arginine 10 to lysine substitution on ω-conotoxin CVIE and CVIF block of Cav2.2 channels., Berecki G., Br J Pharmacol. July 1, 2014; 171 (13): 3313-27.


Six1 is a key regulator of the developmental and evolutionary architecture of sensory neurons in craniates., Yajima H., BMC Biol. May 29, 2014; 12 40.                        


Isolation, synthesis and characterization of ω-TRTX-Cc1a, a novel tarantula venom peptide that selectively targets L-type Cav channels., Klint JK., Biochem Pharmacol. May 15, 2014; 89 (2): 276-86.


Functional characterization of zebrafish K2P18.1 (TRESK) two-pore-domain K+ channels., Rahm AK., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2014; 387 (3): 291-300.


Abelson phosphorylation of CLASP2 modulates its association with microtubules and actin., Engel U., Cytoskeleton (Hoboken). March 1, 2014; 71 (3): 195-209.                


Loss of Extended Synaptotagmins ESyt2 and ESyt3 does not affect mouse development or viability, but in vitro cell migration and survival under stress are affected., Herdman C., Cell Cycle. January 1, 2014; 13 (16): 2616-25.            


Pharmacological fractionation of tetrodotoxin-sensitive sodium currents in rat dorsal root ganglion neurons by μ-conotoxins., Zhang MM., Br J Pharmacol. May 1, 2013; 169 (1): 102-14.


Modeling-independent elucidation of inactivation pathways in recombinant and native A-type Kv channels., Fineberg JD., J Gen Physiol. November 1, 2012; 140 (5): 513-27.                      


Inhibition of voltage-gated Na(+) currents in sensory neurones by the sea anemone toxin APETx2., Blanchard MG., Br J Pharmacol. April 1, 2012; 165 (7): 2167-77.


Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus., Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.                


Molecular cloning and functional characterization of Xenopus tropicalis frog transient receptor potential vanilloid 1 reveal its functional evolution for heat, acid, and capsaicin sensitivities in terrestrial vertebrates., Ohkita M., J Biol Chem. January 20, 2012; 287 (4): 2388-97.


Mammalian growth cone turning assays identify distinct cell signalling mechanisms that underlie axon growth, guidance and regeneration., Murray AJ., Methods Mol Biol. January 1, 2012; 846 167-78.


Actions of Tefluthrin on Rat Na(v)1.7 Voltage-Gated Sodium Channels Expressed in Xenopus Oocytes., Tan J., Pestic Biochem Physiol. September 1, 2011; 101 (1): 21-26.


Activation characteristics of transient receptor potential ankyrin 1 and its role in nociception., Raisinghani M., Am J Physiol Cell Physiol. September 1, 2011; 301 (3): C587-600.


Characterization of three synuclein genes in Xenopus laevis., Wang C, Wang C, Wang C., Dev Dyn. August 1, 2011; 240 (8): 2028-33.                


Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors., Bosmans F., J Gen Physiol. July 1, 2011; 138 (1): 59-72.                  


An evolving NGF-Hoxd1 signaling pathway mediates development of divergent neural circuits in vertebrates., Guo T., Nat Neurosci. January 1, 2011; 14 (1): 31-6.          


Identification of a calcium permeable human acid-sensing ion channel 1 transcript variant., Hoagland EN., J Biol Chem. December 31, 2010; 285 (53): 41852-62.


HES6-1 and HES6-2 function through different mechanisms during neuronal differentiation., Vilas-Boas F., PLoS One. December 2, 2010; 5 (12): e15459.                


Phyla- and Subtype-Selectivity of CgNa, a Na Channel Toxin from the Venom of the Giant Caribbean Sea Anemone Condylactis Gigantea., Billen B., Front Pharmacol. November 23, 2010; 1 133.        


Activation of ADF/cofilin mediates attractive growth cone turning toward nerve growth factor and netrin-1., Marsick BM., Dev Neurobiol. July 1, 2010; 70 (8): 565-88.


[Inhibition of Jingzhaotoxin-V on Kv4.3 channel]., Cai LJ., Sheng Li Xue Bao. June 25, 2010; 62 (3): 255-60.


Selective potentiation of homomeric P2X2 ionotropic ATP receptors by a fast non-genomic action of progesterone., De Roo M., Neuropharmacology. March 1, 2010; 58 (3): 569-77.


Analgesic (omega)-conotoxins CVIE and CVIF selectively and voltage-dependently block recombinant and native N-type calcium channels., Berecki G., Mol Pharmacol. February 1, 2010; 77 (2): 139-48.


Enhanced activation of the transient receptor potential channel TRPA1 by ajoene, an allicin derivative., Yassaka RT., Neurosci Res. January 1, 2010; 66 (1): 99-105.


U-shaped dose-dependent effects of BmK AS, a unique scorpion polypeptide toxin, on voltage-gated sodium channels., Zhu MM., Br J Pharmacol. December 1, 2009; 158 (8): 1895-903.


Subtype-specific regulation of P2X3 and P2X2/3 receptors by phosphoinositides in peripheral nociceptors., Mo G., Mol Pain. August 11, 2009; 5 47.            


Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.                


TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones., Dobler T., J Physiol. December 15, 2007; 585 (Pt 3): 867-79.


Structure/function characterization of micro-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels., Zhang MM., J Biol Chem. October 19, 2007; 282 (42): 30699-706.


Neural MMP-28 expression precedes myelination during development and peripheral nerve repair., Werner SR., Dev Dyn. October 1, 2007; 236 (10): 2852-64.              


Characterization of voltage-and Ca2+-activated K+ channels in rat dorsal root ganglion neurons., Li W., J Cell Physiol. August 1, 2007; 212 (2): 348-57.


The rat vanilloid receptor splice variant VR.5'sv blocks TRPV1 activation., Eilers H., Neuroreport. July 2, 2007; 18 (10): 969-73.


Regeneration of neural crest derivatives in the Xenopus tadpole tail., Lin G., BMC Dev Biol. May 24, 2007; 7 56.                    


Isolation and structure-activity of mu-conotoxin TIIIA, a potent inhibitor of tetrodotoxin-sensitive voltage-gated sodium channels., Lewis RJ., Mol Pharmacol. March 1, 2007; 71 (3): 676-85.


Isolation and characterization of Jingzhaotoxin-V, a novel neurotoxin from the venom of the spider Chilobrachys jingzhao., Zeng X., Toxicon. March 1, 2007; 49 (3): 388-99.


Omega-conotoxin CVIB differentially inhibits native and recombinant N- and P/Q-type calcium channels., Motin L., Eur J Neurosci. January 1, 2007; 25 (2): 435-44.


Immunohistochemical localization of calbindin-D28k and calretinin in the spinal cord of Xenopus laevis., Morona R., J Comp Neurol. February 10, 2006; 494 (5): 763-83.


Alpha-RgIA: a novel conotoxin that specifically and potently blocks the alpha9alpha10 nAChR., Ellison M., Biochemistry. February 7, 2006; 45 (5): 1511-7.

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