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Summary Anatomy Item Literature (5836) Expression Attributions Wiki
XB-ANAT-2

Papers associated with ectoderm∨derBy=4 (and gnao1)

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Blocking of the human ether-à-go-go-related gene channel by imatinib mesylate., Dong Q., Biol Pharm Bull. January 1, 2013; 36 (2): 268-75.


A natural point mutation changes both target selectivity and mechanism of action of sea anemone toxins., Peigneur S., FASEB J. December 1, 2012; 26 (12): 5141-51.


Neural crest delamination and migration: from epithelium-to-mesenchyme transition to collective cell migration., Theveneau E., Dev Biol. June 1, 2012; 366 (1): 34-54.


Split-inteins for simultaneous, site-specific conjugation of quantum dots to multiple protein targets in vivo., Charalambous A., J Nanobiotechnology. September 15, 2011; 9 37.              


Effects of the histamine H(1) receptor antagonist hydroxyzine on hERG K(+) channels and cardiac action potential duration., Lee BH., Acta Pharmacol Sin. September 1, 2011; 32 (9): 1128-37.                  


Modification of hERG1 channel gating by Cd2+., Abbruzzese J., J Gen Physiol. August 1, 2010; 136 (2): 203-24.                                        


Block of the human ether-a-go-go-related gene (hERG) K+ channel by the antidepressant desipramine., Hong HK., Biochem Biophys Res Commun. April 9, 2010; 394 (3): 536-41.


Block effect of capsaicin on hERG potassium currents is enhanced by S6 mutation at Y652., Xing J., Eur J Pharmacol. March 25, 2010; 630 (1-3): 1-9.


Block of HERG k channel by classic histamine h(1) receptor antagonist chlorpheniramine., Hong HK., Korean J Physiol Pharmacol. June 1, 2009; 13 (3): 215-20.


Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD307243)., Xu X., Mol Pharmacol. June 1, 2008; 73 (6): 1709-21.


Protriptyline block of the human ether-à-go-go-related gene (HERG) K+ channel., Jo SH., Life Sci. January 30, 2008; 82 (5-6): 331-40.


In vitro modulation of HERG channels by organochlorine solvent trichlormethane as potential explanation for proarrhythmic effects of chloroform., Scholz EP., Toxicol Lett. August 20, 2006; 165 (2): 156-66.


Blockade of HERG human K+ channels and IKr of guinea-pig cardiomyocytes by the antipsychotic drug clozapine., Lee SY., Br J Pharmacol. June 1, 2006; 148 (4): 499-509.


Inhibition of human ether-a-go-go-related gene K+ channel and IKr of guinea pig cardiomyocytes by antipsychotic drug trifluoperazine., Choi SY., J Pharmacol Exp Ther. May 1, 2005; 313 (2): 888-95.


An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.                                                                                                                                                        


Block of wild-type and inactivation-deficient human ether-a-go-go-related gene K+ channels by halofantrine., Sánchez-Chapula JA., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2004; 370 (6): 484-91.


Inhibition of human ether-a-go-go-related gene potassium channels by alpha 1-adrenoceptor antagonists prazosin, doxazosin, and terazosin., Thomas D., Naunyn Schmiedebergs Arch Pharmacol. May 1, 2004; 369 (5): 462-72.


Voltage-dependent profile of human ether-a-go-go-related gene channel block is influenced by a single residue in the S6 transmembrane domain., Sănchez-Chapula JA., Mol Pharmacol. May 1, 2003; 63 (5): 1051-8.


Molecular determinants of voltage-dependent human ether-a-go-go related gene (HERG) K+ channel block., Sánchez-Chapula JA., J Biol Chem. June 28, 2002; 277 (26): 23587-95.


Inhibition of cardiac potassium currents by pentobarbital., Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.


Molecular determinants of inactivation and dofetilide block in ether a-go-go (EAG) channels and EAG-related K(+) channels., Ficker E., Mol Pharmacol. December 1, 2001; 60 (6): 1343-8.


High-affinity blockade of human ether-a-go-go-related gene human cardiac potassium channels by the novel antiarrhythmic drug BRL-32872., Thomas D., J Pharmacol Exp Ther. May 1, 2001; 297 (2): 753-61.


Hex is a transcriptional repressor that contributes to anterior identity and suppresses Spemann organiser function., Brickman JM., Development. June 1, 2000; 127 (11): 2303-15.                    


Blockade of the HERG human cardiac K(+) channel by the antidepressant drug amitriptyline., Jo SH., Br J Pharmacol. April 1, 2000; 129 (7): 1474-80.


Regulation of deactivation by an amino terminal domain in human ether-à-go-go-related gene potassium channels., Wang J., J Gen Physiol. November 1, 1998; 112 (5): 637-47.              


Embryonic mesoderm cells spread in response to platelet-derived growth factor and signaling by phosphatidylinositol 3-kinase., Symes K., Proc Natl Acad Sci U S A. September 3, 1996; 93 (18): 9641-4.


Time, voltage and ionic concentration dependence of rectification of h-erg expressed in Xenopus oocytes., Wang S., FEBS Lett. July 1, 1996; 389 (2): 167-73.


Expression of L-type Ca2+ channel during early embryogenesis in Xenopus laevis., Drean G., Int J Dev Biol. December 1, 1995; 39 (6): 1027-32.          


Expression and potential functions of G-protein alpha subunits in embryos of Xenopus laevis., Otte AP., Development. September 1, 1992; 116 (1): 141-6.        


The organization of mesodermal pattern in Xenopus laevis: experiments using a Xenopus mesoderm-inducing factor., Cooke J., Development. December 1, 1987; 101 (4): 893-908.            

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