Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

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

Papers associated with spinal ganglion (and drg1)

Limit to papers also referencing gene:
Show all spinal ganglion papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

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.


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.


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.


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.                        


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.


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.                


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.


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


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.


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.


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.


Downregulation of transient receptor potential melastatin 8 by protein kinase C-mediated dephosphorylation., Premkumar LS., J Neurosci. December 7, 2005; 25 (49): 11322-9.


Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner., Kanjhan R., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.


Sensitization and translocation of TRPV1 by insulin and IGF-I., Van Buren JJ., Mol Pain. April 27, 2005; 1 17.        


Enhancement of potency and efficacy of NADA by PKC-mediated phosphorylation of vanilloid receptor., Premkumar LS., J Neurophysiol. March 1, 2004; 91 (3): 1442-9.


Voltage-dependent priming of rat vanilloid receptor: effects of agonist and protein kinase C activation., Ahern GP., J Physiol. December 1, 2002; 545 (2): 441-51.


Single-channel properties of native and cloned rat vanilloid receptors., Premkumar LS., J Physiol. November 15, 2002; 545 (1): 107-17.


Gating properties of Na(v)1.7 and Na(v)1.8 peripheral nerve sodium channels., Vijayaragavan K., J Neurosci. October 15, 2001; 21 (20): 7909-18.


Expression of glycine receptors in rat sensory neurons vs. HEK293 cells yields different functional properties., Kung AY., Neurosci Lett. August 31, 2001; 309 (3): 202-6.


Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons., Cummins TR., J Neurosci. August 15, 2001; 21 (16): 5952-61.


The cAMP-dependent kinase pathway does not sensitize the cloned vanilloid receptor type 1 expressed in xenopus oocytes or Aplysia neurons., Lee YS., Neurosci Lett. July 7, 2000; 288 (1): 57-60.


Cloning and functional expression of novel N-type Ca(2+) channel variants., Lü Q., J Biol Chem. December 3, 1999; 274 (49): 34566-75.


A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia., Sangameswaran L., J Biol Chem. June 6, 1997; 272 (23): 14805-9.


The development of primary afferents to the lumbar spinal cord in Xenopus laevis., van Mier P., Neurosci Lett. January 11, 1988; 84 (1): 35-40.


Regulation of neuron numbers in Xenopus laevis: effects of hormonal manipulation altering size at metamorphosis., Sperry DG., J Comp Neurol. February 15, 1985; 232 (3): 287-98.


Rapid orthograde transport of 32P-labelled material in amphibian sensory axons: a multiwire proportional chamber study., Snyder RE., Can J Physiol Pharmacol. May 1, 1980; 58 (5): 513-24.

???pagination.result.page??? 1