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Summary Expression Phenotypes Gene Literature (96) GO Terms (9) Nucleotides (214) Proteins (32) Interactants (464) Wiki

Papers associated with drg1

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2 paper(s) referencing morpholinos

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GiTx1(β/κ-theraphotoxin-Gi1a), a novel toxin from the venom of Brazilian tarantula Grammostola iheringi (Mygalomorphae, Theraphosidae): Isolation, structural assessments and activity on voltage-gated ion channels., Montandon GG, Cassoli JS, Peigneur S, Verano-Braga T, Santos DMD, Paiva ALB, Moraes ÉR, Kushmerick C, Borges MH, Richardson M, Pimenta AMC, Kjeldsen F, Diniz MRV, Tytgat J, Lima ME., Biochimie. September 1, 2020; 176 138-149.

Chemically Modified Derivatives of the Activator Compound Cloxyquin Exert Inhibitory Effect on TRESK (K2P18.1) Background Potassium Channel., Lengyel M, Erdélyi F, Pergel E, Bálint-Polonka Á, Dobolyi A, Bozsaki P, Dux M, Király K, Hegedűs T, Czirják G, Mátyus P, Enyedi P., Mol Pharmacol. January 1, 2019; 95 (6): 652-660.

Inhibition of Kv2.1 Potassium Channels by MiDCA1, A Pre-Synaptically Active PLA2-Type Toxin from Micrurus dumerilii carinicauda Coral Snake Venom., Schütter N, Barreto YC, Vardanyan V, Hornig S, Hyslop S, Marangoni S, Rodrigues-Simioni L, Pongs O, Dal Belo CA., Toxins (Basel). January 1, 2019; 11 (6):       

Developmentally regulated GTP-binding protein 1 modulates ciliogenesis via an interaction with Dishevelled., Lee M, Hwang YS, Yoon J, Sun J, Harned A, Nagashima K, Daar IO., J Cell Biol. January 1, 2019; 218 (8): 2659-2676.              

Identification of aurintricarboxylic acid as a potent allosteric antagonist of P2X1 and P2X3 receptors., Obrecht AS, Urban N, Schaefer M, Röse A, Kless A, Meents JE, Lampert A, Abdelrahman A, Müller CE, Schmalzing G, Hausmann R., Neuropharmacology. January 1, 2019; 158 107749.

The mechanosensitive ion channel TRAAK is localized to the mammalian node of Ranvier., Brohawn SG, Wang W, Handler A, Campbell EB, Schwarz JR, MacKinnon R., Elife. January 1, 2019; 8                     

Hyperinnervation improves Xenopus laevis limb regeneration., Mitogawa K, Makanae A, Satoh A., Dev Biol. January 1, 2018; 433 (2): 276-286.                    

The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development., Espiritu EB, Crunk AE, Bais A, Hochbaum D, Cervino AS, Phua YL, Butterworth MB, Goto T, Ho J, Hukriede NA, Cirio MC., Sci Rep. January 1, 2018; 8 (1): 16029.                                      

The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel., Stephan G, Huang L, Tang Y, Vilotti S, Fabbretti E, Yu Y, Nörenberg W, Franke H, Gölöncsér F, Sperlágh B, Dopychai A, Hausmann R, Schmalzing G, Rubini P, Illes P., Nat Commun. January 1, 2018; 9 (1): 1354.                    

A novel α-conopeptide Eu1.6 inhibits N-type (CaV2.2) calcium channels and exhibits potent analgesic activity., Liu Z, Bartels P, Sadeghi M, Du T, Dai Q, Zhu C, Yu S, Wang S, Dong M, Sun T, Guo J, Peng S, Jiang L, Adams DJ, Dai Q., Sci Rep. January 1, 2018; 8 (1): 1004.                

Direct neurotransmitter activation of voltage-gated potassium channels., Manville RW, Papanikolaou M, Abbott GW., Nat Commun. January 1, 2018; 9 (1): 1847.            

The Peptide PnPP-19, a Spider Toxin Derivative, Activates μ-Opioid Receptors and Modulates Calcium Channels., Freitas ACN, Peigneur S, Macedo FHP, Menezes-Filho JE, Millns P, Medeiros LF, Arruda MA, Cruz J, Holliday ND, Tytgat J, Hathway G, de Lima ME., Toxins (Basel). January 1, 2018; 10 (1):             

JAK-STAT pathway activation in response to spinal cord injury in regenerative and non-regenerative stages of Xenopus laevis., Tapia VS, Herrera-Rojas M, Larrain J., Regeneration (Oxf). February 1, 2017; 4 (1): 21-35.                          

Conserved gene regulatory module specifies lateral neural borders across bilaterians., Li Y, Zhao D, Horie T, Chen G, Bao H, Chen S, Liu W, Horie R, Liang T, Dong B, Feng Q, Tao Q, Tao Q, Liu X., Proc Natl Acad Sci U S A. January 1, 2017; 114 (31): E6352-E6360.      

Selective and state-dependent activation of TRESK (K2P 18.1) background potassium channel by cloxyquin., Lengyel M, Dobolyi A, Czirják G, Enyedi P., Br J Pharmacol. January 1, 2017; 174 (13): 2102-2113.

Evolution of Heat Sensors Drove Shifts in Thermosensation between Xenopus Species Adapted to Different Thermal Niches., Saito S, Ohkita M, Saito CT, Takahashi K, Tominaga M, Ohta T., J Biol Chem. May 20, 2016; 291 (21): 11446-59.                      

Activation of TRESK channels by the inflammatory mediator lysophosphatidic acid balances nociceptive signalling., Kollert S, Dombert B, Döring F, Wischmeyer E., Sci Rep. September 21, 2015; 5 12548.            

Resin-acid derivatives as potent electrostatic openers of voltage-gated K channels and suppressors of neuronal excitability., Ottosson NE, Wu X, Nolting A, Karlsson U, Lund PE, Ruda K, Svensson S, Konradsson P, Elinder F., Sci Rep. August 24, 2015; 5 13278.            

Less is More: Design of a Highly Stable Disulfide-Deleted Mutant of Analgesic Cyclic α-Conotoxin Vc1.1., Yu R, Seymour VA, Berecki G, Jia X, Akcan M, Adams DJ, Kaas Q, Craik DJ., Sci Rep. August 20, 2015; 5 13264.            

Regeneration inducers in limb regeneration., Satoh A, Mitogawa K, Makanae A., Dev Growth Differ. August 1, 2015; 57 (6): 421-9.  

Mesodermal origin of median fin mesenchyme and tail muscle in amphibian larvae., Taniguchi Y, Kurth T, Medeiros DM, Tazaki A, Ramm R, Epperlein HH., Sci Rep. June 18, 2015; 5 11428.                

Properties, regulation, pharmacology, and functions of the K₂p channel, TRESK., Enyedi P, Czirják G., Pflugers Arch. May 1, 2015; 467 (5): 945-58.

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

Characterization of a T-superfamily conotoxin TxVC from Conus textile that selectively targets neuronal nAChR subtypes., Wang S, Du T, Liu Z, Wang S, Wu Y, Ding J, Jiang L, Dai Q., Biochem Biophys Res Commun. November 7, 2014; 454 (1): 151-6.

A family of excitatory peptide toxins from venomous crassispirine snails: using Constellation Pharmacology to assess bioactivity., Imperial JS, Cabang AB, Song J, Raghuraman S, Gajewiak J, Watkins M, Showers-Corneli P, Fedosov A, Concepcion GP, Terlau H, Teichert RW, Olivera BM., 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, Suzuki M, Ochi H, Ikeda K, Sato S, Yamamura K, Ogino H, Ueno N, Kawakami K., BMC Biol. May 29, 2014; 12 40.                        

Dicarba α-conotoxin Vc1.1 analogues with differential selectivity for nicotinic acetylcholine and GABAB receptors., van Lierop BJ, Robinson SD, Kompella SN, Belgi A, McArthur JR, Hung A, MacRaild CA, Adams DJ, Norton RS, Robinson AJ., ACS Chem Biol. August 16, 2013; 8 (8): 1815-21.

Pharmacological fractionation of tetrodotoxin-sensitive sodium currents in rat dorsal root ganglion neurons by μ-conotoxins., Zhang MM, Wilson MJ, Gajewiak J, Rivier JE, Bulaj G, Olivera BM, Yoshikami D., Br J Pharmacol. May 1, 2013; 169 (1): 102-14.

Axonal growth towards Xenopus skin in vitro is mediated by matrix metalloproteinase activity., Tonge D, Zhu N, Lynham S, Leclere P, Snape A, Brewer A, Schlomann U, Ferdous T, Tennyson C, Bartsch JW, Ward M, Pizzey J., Eur J Neurosci. February 1, 2013; 37 (4): 519-31.                  

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

A novel µ-conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors., Favreau P, Benoit E, Hocking HG, Carlier L, D' hoedt D, Leipold E, Markgraf R, Schlumberger S, Córdova MA, Gaertner H, Paolini-Bertrand M, Hartley O, Tytgat J, Heinemann SH, Bertrand D, Boelens R, Stöcklin R, Molgó J., Br J Pharmacol. July 1, 2012; 166 (5): 1654-68.

Disruption of E3 ligase NEDD4 in peripheral neurons interrupts axon outgrowth: Linkage to PTEN., Christie KJ, Martinez JA, Zochodne DW., Mol Cell Neurosci. June 1, 2012; 50 (2): 179-92.

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

Claudin-5 expression in the vasculature of the developing chick embryo., Collins MM, Baumholtz AI, Ryan AK., Gene Expr Patterns. March 1, 2012; 12 (3-4): 123-9.        

A heteromeric Texas coral snake toxin targets acid-sensing ion channels to produce pain., Bohlen CJ, Chesler AT, Sharif-Naeini R, Medzihradszky KF, Zhou S, King D, Sánchez EE, Burlingame AL, Basbaum AI, Julius D., Nature. November 17, 2011; 479 (7373): 410-4.      

Characterization of three synuclein genes in Xenopus laevis., Wang C, Wang C, Wang C, Liu Y, Chan WY, Chan SO, Grunz H, Zhao H., Dev Dyn. August 1, 2011; 240 (8): 2028-33.                

Skeletal muscle differentiation and fusion are regulated by the BAR-containing Rho-GTPase-activating protein (Rho-GAP), GRAF1., Doherty JT, Lenhart KC, Cameron MV, Mack CP, Conlon FL, Taylor JM., J Biol Chem. July 22, 2011; 286 (29): 25903-21.                    

Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors., Bosmans F, Puopolo M, Martin-Eauclaire MF, Bean BP, Swartz KJ., 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, Mandai K, Condie BG, Wickramasinghe SR, Capecchi MR, Ginty DD., Nat Neurosci. January 1, 2011; 14 (1): 31-6.          

Identification of a calcium permeable human acid-sensing ion channel 1 transcript variant., Hoagland EN, Sherwood TW, Lee KG, Walker CJ, Askwith CC., 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, Henrique D., PLoS One. December 2, 2010; 5 (12): e15459.                

Two recombinant depressant scorpion neurotoxins differentially affecting mammalian sodium channels., Yuan Y, Luo L, Peigneur S, Tytgat J, Zhu S., Toxicon. July 1, 2010; 55 (8): 1425-33.

An in vivo tethered toxin approach for the cell-autonomous inactivation of voltage-gated sodium channel currents in nociceptors., Stürzebecher AS, Hu J, Smith ES, Frahm S, Santos-Torres J, Kampfrath B, Auer S, Lewin GR, Ibañez-Tallon I., J Physiol. May 15, 2010; 588 (Pt 10): 1695-707.        

Actions of bis(7)-tacrine and tacrine on transient potassium current in rat DRG neurons and potassium current mediated by K(V)4.2 expressed in Xenopus oocyte., Li XY, Zhang J, Dai JP, Liu XM, Li ZW., Dev Biol. March 8, 2010; 1318 23-32.

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

N terminus is key to the dominant negative suppression of Ca(V)2 calcium channels: implications for episodic ataxia type 2., Page KM, Heblich F, Margas W, Pratt WS, Nieto-Rostro M, Chaggar K, Sandhu K, Davies A, Dolphin AC., J Biol Chem. January 8, 2010; 285 (2): 835-44.              

Subtype-specific regulation of P2X3 and P2X2/3 receptors by phosphoinositides in peripheral nociceptors., Mo G, Bernier LP, Zhao Q, Chabot-Doré AJ, Ase AR, Logothetis D, Cao CQ, Séguéla P., Mol Pain. January 1, 2009; 5 47.            

Analgesic alpha-conotoxins Vc1.1 and Rg1A inhibit N-type calcium channels in rat sensory neurons via GABAB receptor activation., Callaghan B, Haythornthwaite A, Berecki G, Clark RJ, Craik DJ, Adams DJ., J Neurosci. October 22, 2008; 28 (43): 10943-51.

Enhancement of axonal regeneration by in vitro conditioning and its inhibition by cyclopentenone prostaglandins., Tonge D, Chan K, Zhu N, Panjwani A, Arno M, Lynham S, Ward M, Snape A, Pizzey J., J Cell Sci. August 1, 2008; 121 (Pt 15): 2565-77.                        

Specificity, affinity and efficacy of iota-conotoxin RXIA, an agonist of voltage-gated sodium channels Na(V)1.2, 1.6 and 1.7., Fiedler B, Zhang MM, Buczek O, Azam L, Bulaj G, Norton RS, Olivera BM, Yoshikami D., Biochem Pharmacol. June 15, 2008; 75 (12): 2334-44.

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