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Summary Anatomy Item Literature (7748) Expression Attributions Wiki
XB-ANAT-11

Papers associated with brain (and kcna1)

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Apamin structure and pharmacology revisited., Kuzmenkov AI., Front Pharmacol. January 1, 2022; 13 977440.          


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.                        


Coexpression of auxiliary Kvβ2 subunits with Kv1.1 channels is required for developmental acquisition of unique firing properties of zebrafish Mauthner cells., Watanabe T., J Neurophysiol. March 1, 2014; 111 (6): 1153-64.


Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain., Imbrici P., Am J Physiol Cell Physiol. June 1, 2011; 300 (6): C1314-22.


RNA editing of Kv1.1 channels may account for reduced ictogenic potential of 4-aminopyridine in chronic epileptic rats., Streit AK., Epilepsia. March 1, 2011; 52 (3): 645-8.


Hemitoxin, the first potassium channel toxin from the venom of the Iranian scorpion Hemiscorpius lepturus., Srairi-Abid N., FEBS J. September 1, 2008; 275 (18): 4641-50.


Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1., Imbrici P., Am J Physiol Cell Physiol. February 1, 2007; 292 (2): C778-87.


A truncated Kv1.1 protein in the brain of the megencephaly mouse: expression and interaction., Persson AS., BMC Neurosci. November 23, 2005; 6 65.          


Molecular cloning and expression of a Kv1.1-like potassium channel from the electric organ of Electrophorus electricus., Thornhill WB., J Membr Biol. November 1, 2003; 196 (1): 1-8.


KCNE4 is an inhibitory subunit to Kv1.1 and Kv1.3 potassium channels., Grunnet M., Biophys J. September 1, 2003; 85 (3): 1525-37.


Synthesis and characterization of Pi4, a scorpion toxin from Pandinus imperator that acts on K+ channels., M'Barek S., Eur J Biochem. September 1, 2003; 270 (17): 3583-92.


Early embryonic expression of ion channels and pumps in chick and Xenopus development., Rutenberg J., Dev Dyn. December 1, 2002; 225 (4): 469-84.                            


Modulation of a brain voltage-gated K+ channel by syntaxin 1A requires the physical interaction of Gbetagamma with the channel., Michaelevski I., J Biol Chem. September 20, 2002; 277 (38): 34909-17.


Characteristics of brain Kv1 channels tailored to mimic native counterparts by tandem linkage of alpha subunits: implications for K+ channelopathies., Akhtar S., J Biol Chem. May 10, 2002; 277 (19): 16376-82.


Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2)., McCormack K., J Biol Chem. April 12, 2002; 277 (15): 13219-28.


Chemical synthesis and characterization of Pi1, a scorpion toxin from Pandinus imperator active on K+ channels., Fajloun Z., Eur J Biochem. August 1, 2000; 267 (16): 5149-55.


Maurotoxin and the Kv1.1 channel: voltage-dependent binding upon enantiomerization of the scorpion toxin disulfide bridge Cys31-Cys34., Lecomte C., J Pept Res. March 1, 2000; 55 (3): 246-54.


A functional spliced-variant of beta 2 subunit of Kv1 channels in C6 glioma cells and reactive astrocytes from rat lesioned cerebellum., Akhtar S., Biochemistry. December 21, 1999; 38 (51): 16984-92.


Modal behavior of the Kv1.1 channel conferred by the Kvbeta1.1 subunit and its regulation by dephosphorylation of Kv1.1., Singer-Lahat D., Pflugers Arch. December 1, 1999; 439 (1-2): 18-26.


Distribution in rat brain of binding sites of kaliotoxin, a blocker of Kv1.1 and Kv1.3 alpha-subunits., Mourre C., J Pharmacol Exp Ther. December 1, 1999; 291 (3): 943-52.


Role of disulfide bonds in the structure and potassium channel blocking activity of ShK toxin., Pennington MW., Biochemistry. November 2, 1999; 38 (44): 14549-58.


Identification of residues in dendrotoxin K responsible for its discrimination between neuronal K+ channels containing Kv1.1 and 1.2 alpha subunits., Wang FC., Eur J Biochem. July 1, 1999; 263 (1): 222-9.


Fast inactivation of a brain K+ channel composed of Kv1.1 and Kvbeta1.1 subunits modulated by G protein beta gamma subunits., Jing J., EMBO J. March 1, 1999; 18 (5): 1245-56.


Open channel block and open channel destabilization: contrasting effects of phenol, TEA+ and local anaesthetics on Kv1.1 K+ channels., Elliott AA., Toxicol Lett. November 23, 1998; 100-101 277-85.


Selective peptide antagonist of the class E calcium channel from the venom of the tarantula Hysterocrates gigas., Newcomb R., Biochemistry. November 3, 1998; 37 (44): 15353-62.


A snake toxin inhibitor of inward rectifier potassium channel ROMK1., Imredy JP., Biochemistry. October 20, 1998; 37 (42): 14867-74.


Site directed mutants of Noxiustoxin reveal specific interactions with potassium channels., Martínez F., FEBS Lett. June 16, 1998; 429 (3): 381-4.


Activation of a metabotropic glutamate receptor and protein kinase C reduce the extent of inactivation of the K+ channel Kv1.1/Kvbeta1.1 via dephosphorylation of Kv1.1., Levy M., J Biol Chem. March 13, 1998; 273 (11): 6495-502.


kappa-Conotoxin PVIIA is a peptide inhibiting the shaker K+ channel., Shon KJ., J Biol Chem. January 2, 1998; 273 (1): 33-8.


A cellular model for long QT syndrome. Trapping of heteromultimeric complexes consisting of truncated Kv1.1 potassium channel polypeptides and native Kv1.4 and Kv1.5 channels in the endoplasmic reticulum., Folco E., J Biol Chem. October 17, 1997; 272 (42): 26505-10.


Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channels., Kharrat R., FEBS Lett. April 14, 1997; 406 (3): 284-90.


A potassium-channel toxin from the sea anemone Bunodosoma granulifera, an inhibitor for Kv1 channels. Revision of the amino acid sequence, disulfide-bridge assignment, chemical synthesis, and biological activity., Cotton J., Eur J Biochem. February 15, 1997; 244 (1): 192-202.


Phosphorylation of a K+ channel alpha subunit modulates the inactivation conferred by a beta subunit. Involvement of cytoskeleton., Levin G., J Biol Chem. November 15, 1996; 271 (46): 29321-8.


Functional characterization of Kv channel beta-subunits from rat brain., Heinemann SH., J Physiol. June 15, 1996; 493 ( Pt 3) 625-33.


Molecular cloning of a glibenclamide-sensitive, voltage-gated potassium channel expressed in rabbit kidney., Yao X., J Clin Invest. June 1, 1996; 97 (11): 2525-33.


Mechanism of action of the epileptogenic drug pentylenetetrazol on a cloned neuronal potassium channel., Madeja M., Dev Biol. May 25, 1996; 722 (1-2): 59-70.


Xenopus spinal neurons express Kv2 potassium channel transcripts during embryonic development., Burger C., J Neurosci. February 15, 1996; 16 (4): 1412-21.          


A novel beta subunit increases rate of inactivation of specific voltage-gated potassium channel alpha subunits., Morales MJ., J Biol Chem. March 17, 1995; 270 (11): 6272-7.


Primary sensory neurons express a Shaker-like potassium channel gene., Ribera AB., J Neurosci. November 1, 1993; 13 (11): 4988-96.                


The potassium channel MBK1 (Kv1.1) is expressed in the mouse retina., Klumpp DJ., Cell Mol Neurobiol. December 1, 1991; 11 (6): 611-22.

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