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Summary Expression Gene Literature (57) GO Terms (12) Nucleotides (15) Proteins (5) Interactants (385) Wiki
XB-GENEPAGE-952448

Papers associated with kcnd2

Search for kcnd2 morpholinos using Textpresso

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1 paper(s) referencing morpholinos

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Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel., Drabkin M, Zilberberg N, Menahem S, Mulla W, Halperin D, Yogev Y, Wormser O, Perez Y, Kadir R, Etzion Y, Katz A, Birk OS., Circ Genom Precis Med. November 1, 2018; 11 (11): e002293.


Kv4.2 autism and epilepsy mutation enhances inactivation of closed channels but impairs access to inactivated state after opening., Lin MA, Cannon SC, Papazian DM., Proc Natl Acad Sci U S A. January 1, 2018; 115 (15): E3559-E3568.


Genesis of the vertebrate FoxP subfamily member genes occurred during two ancestral whole genome duplication events., Song X, Tang Y, Wang Y., Gene. August 22, 2016; 588 (2): 156-62.


Intra- and Intersubunit Dynamic Binding in Kv4.2 Channel Closed-State Inactivation., Wollberg J, Bähring R., Biophys J. January 5, 2016; 110 (1): 157-75.


Kv4.2 and accessory dipeptidyl peptidase-like protein 10 (DPP10) subunit preferentially form a 4:2 (Kv4.2:DPP10) channel complex., Kitazawa M, Kubo Y, Nakajo K., J Biol Chem. September 11, 2015; 290 (37): 22724-33.


The stoichiometry and biophysical properties of the Kv4 potassium channel complex with K+ channel-interacting protein (KChIP) subunits are variable, depending on the relative expression level., Kitazawa M, Kubo Y, Nakajo K., J Biol Chem. June 20, 2014; 289 (25): 17597-609.


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.                    


Homology model and targeted mutagenesis identify critical residues for arachidonic acid inhibition of Kv4 channels., Heler R, Bell JK, Boland LM., Channels (Austin). March 1, 2013; 7 (2): 74-84.              


Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1., Aidery P, Kisselbach J, Schweizer PA, Becker R, Katus HA, Thomas D., Gene. December 10, 2012; 511 (1): 26-33.        


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.                      


Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1., Bonnard C, Strobl AC, Shboul M, Lee H, Merriman B, Nelson SF, Ababneh OH, Uz E, Güran T, Kayserili H, Hamamy H, Reversade B., Nat Genet. May 13, 2012; 44 (6): 709-13.    


Incorporation of DPP6a and DPP6K variants in ternary Kv4 channel complex reconstitutes properties of A-type K current in rat cerebellar granule cells., Jerng HH, Pfaffinger PJ., PLoS One. January 1, 2012; 7 (6): e38205.              


Effect of NIP-142 on potassium channel alpha-subunits Kv1.5, Kv4.2 and Kv4.3, and mouse atrial repolarization., Tanaka H, Namekata I, Hamaguchi S, Kawamura T, Masuda H, Tanaka Y, Iida-Tanaka N, Takahara A., Biol Pharm Bull. January 1, 2010; 33 (1): 138-41.


A novel N-terminal motif of dipeptidyl peptidase-like proteins produces rapid inactivation of KV4.2 channels by a pore-blocking mechanism., Jerng HH, Dougherty K, Covarrubias M, Pfaffinger PJ., Channels (Austin). November 1, 2009; 3 (6): 448-61.


Inhibitory effects of polyunsaturated fatty acids on Kv4/KChIP potassium channels., Boland LM, Drzewiecki MM, Timoney G, Casey E., Am J Physiol Cell Physiol. May 1, 2009; 296 (5): C1003-14.


The dipeptidyl-peptidase-like protein DPP6 determines the unitary conductance of neuronal Kv4.2 channels., Kaulin YA, De Santiago-Castillo JA, Rocha CA, Nadal MS, Rudy B, Covarrubias M., J Neurosci. March 11, 2009; 29 (10): 3242-51.


Kv4.2 is a locus for PKC and ERK/MAPK cross-talk., Schrader LA, Ren Y, Cheng F, Bui D, Sweatt JD, Anderson AE., Biochem J. February 1, 2009; 417 (3): 705-15.


Dynamic coupling of voltage sensor and gate involved in closed-state inactivation of kv4.2 channels., Barghaan J, Bähring R., J Gen Physiol. February 1, 2009; 133 (2): 205-24.                    


I SA channel complexes include four subunits each of DPP6 and Kv4.2., Soh H, Goldstein SA., J Biol Chem. May 30, 2008; 283 (22): 15072-7.


Jingzhaotoxin-XII, a gating modifier specific for Kv4.1 channels., Yuan C, Liao Z, Zeng X, Dai L, Kuang F, Liang S., Toxicon. October 1, 2007; 50 (5): 646-52.

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