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Summary Expression Phenotypes Gene Literature (72) GO Terms (6) Nucleotides (79) Proteins (40) Interactants (59) Wiki
XB-GENEPAGE-492826

Papers associated with kcna4



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DPP10 is an inactivation modulatory protein of Kv4.3 and Kv1.4., Li HL, Qu YJ, Lu YC, Bondarenko VE, Wang S, Skerrett IM, Morales MJ., Am J Physiol Cell Physiol. November 1, 2006; 291 (5): C966-76.


Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2., Imbrici P, D'Adamo MC, Kullmann DM, Pessia M., Eur J Neurosci. December 1, 2006; 24 (11): 3073-83.


Effect of propafenone on Kv1.4 inactivation., Tian L, Jiang X, Rasmusson R, Wang S., J Physiol Biochem. December 1, 2006; 62 (4): 263-70.


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


Ginsenoside Rg3 inhibits human Kv1.4 channel currents by interacting with the Lys531 residue., Lee JH, Lee JH, Lee BH, Choi SH, Yoon IS, Pyo MK, Shin TJ, Choi WS, Lim Y, Rhim H, Won KH, Lim YW, Choe H, Kim DH, Kim YI, Nah SY., Mol Pharmacol. March 1, 2008; 73 (3): 619-26.


Effect of amiodarone on Kv1.4 channel C-type inactivation: comparison of its effects with those induced by propafenone and verapamil., Xu L, Huang C, Chen J, Jiang X, Li X, Bett GC, Rasmusson RL, Wang S., Pharmazie. June 1, 2008; 63 (6): 475-9.


Regulation of antiarrhythmic drug propafenone effects on the c-type Kv1.4 potassium channel by PHo and K+., Wang Z, Wang S, Li J, Jiang X, Wang N., J Korean Med Sci. February 1, 2009; 24 (1): 84-91.              


The effects of ginsenoside Rg(3) on human Kv1.4 channel currents without the N-terminal rapid inactivation domain., Lee JH, Lee JH, Choi SH, Lee BH, Shin TJ, Pyo MK, Hwang SH, Kim BR, Lee SM, Bae DH, Rhim H, Nah SY., Biol Pharm Bull. April 1, 2009; 32 (4): 614-8.


Multiple intermediate states precede pore block during N-type inactivation of a voltage-gated potassium channel., Prince-Carter A, Pfaffinger PJ., J Gen Physiol. July 1, 2009; 134 (1): 15-34.                              


A model of the interaction between N-type and C-type inactivation in Kv1.4 channels., Bett GC, Dinga-Madou I, Zhou Q, Bondarenko VE, Rasmusson RL., Biophys J. January 5, 2011; 100 (1): 11-21.


Effects of diltiazem and propafenone on the inactivation and recovery kinetics of fKv1.4 channel currents expressed in Xenopus oocytes., Zhang D, Wang SM, Chen H, Jiang XJ, Chao SP., Acta Pharmacol Sin. April 1, 2011; 32 (4): 465-77.                        


Sigma-1 receptor alters the kinetics of Kv1.3 voltage gated potassium channels but not the sensitivity to receptor ligands., Kinoshita M, Matsuoka Y, Suzuki T, Mirrielees J, Yang J., Brain Res. May 3, 2012; 1452 1-9.


Interaction of the S6 proline hinge with N-type and C-type inactivation in Kv1.4 channels., Bett GC, Lis A, Guo H, Liu M, Zhou Q, Rasmusson RL., Biophys J. October 3, 2012; 103 (7): 1440-50.


Effects of L-type Calcium Channel Antagonists Verapamil and Diltiazem on fKv1.4ΔN Currents in Xenopus oocytes., Chen H, Zhang D, Hua Ren J, Ping Chao S., Iran J Pharm Res. January 1, 2013; 12 (4): 855-66.            


Comparison of the effects of antiarrhythmic drugs flecainide and verapamil on fKv1.4ΔN channel currents in Xenopus oocytes., Chen H, Zhang D, Chao SP, Ren JH, Xu L, Jiang XJ, Wang SM., Acta Pharmacol Sin. February 1, 2013; 34 (2): 221-30.            


Heme impairs the ball-and-chain inactivation of potassium channels., Sahoo N, Goradia N, Ohlenschläger O, Schönherr R, Friedrich M, Plass W, Kappl R, Hoshi T, Heinemann SH., Proc Natl Acad Sci U S A. October 15, 2013; 110 (42): E4036-44.


Analysis of the interaction of tarantula toxin Jingzhaotoxin-III (β-TRTX-Cj1α) with the voltage sensor of Kv2.1 uncovers the molecular basis for cross-activities on Kv2.1 and Nav1.5 channels., Tao H, Chen JJ, Xiao YC, Wu YY, Su HB, Li D, Wang HY, Deng MC, Wang MC, Liu ZH, Liang SP., Biochemistry. October 22, 2013; 52 (42): 7439-48.


S-glutathionylation of an auxiliary subunit confers redox sensitivity to Kv4 channel inactivation., Jerng HH, Pfaffinger PJ., PLoS One. January 1, 2014; 9 (3): e93315.                      


Long-range gap junctional signaling controls oncogene-mediated tumorigenesis in Xenopus laevis embryos., Chernet BT, Fields C, Levin M., Front Physiol. January 19, 2015; 5 519.                


Expression and function of a CP339,818-sensitive K⁺ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia., Sforna L, D'Adamo MC, Servettini I, Guglielmi L, Pessia M, Franciolini F, Catacuzzeno L., J Neurophysiol. April 1, 2015; 113 (7): 2653-65.


Regulation of Human Kv1.4 Channel Activity by the Antidepressant Metergoline., Yeom HD, Lee JH., Biol Pharm Bull. January 1, 2016; 39 (6): 1069-72.


KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability., Kaya N, Alsagob M, D'Adamo MC, Al-Bakheet A, Hasan S, Muccioli M, Almutairi FB, Almass R, Aldosary M, Monies D, Mustafa OM, Alyounes B, Kenana R, Al-Zahrani J, Naim E, Binhumaid FS, Qari A, Almutairi F, Meyer B, Plageman TF, Pessia M, Colak D, Al-Owain M., J Med Genet. November 1, 2016; 53 (11): 786-792.

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