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Items: 12

1.

Cloning and expression of the human kv4.3 potassium channel.

Dilks D, Ling HP, Cockett M, Sokol P, Numann R.

J Neurophysiol. 1999 Apr;81(4):1974-7.

2.

Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).

Isbrandt D, Leicher T, Waldschütz R, Zhu X, Luhmann U, Michel U, Sauter K, Pongs O.

Genomics. 2000 Mar 1;64(2):144-54.

PMID:
10729221
3.

Modulation of Kv4.3 current by accessory subunits.

Deschênes I, Tomaselli GF.

FEBS Lett. 2002 Sep 25;528(1-3):183-8.

4.

Two N-terminal domains of Kv4 K(+) channels regulate binding to and modulation by KChIP1.

Scannevin RH, Wang K, Jow F, Megules J, Kopsco DC, Edris W, Carroll KC, Lü Q, Xu W, Xu Z, Katz AH, Olland S, Lin L, Taylor M, Stahl M, Malakian K, Somers W, Mosyak L, Bowlby MR, Chanda P, Rhodes KJ.

Neuron. 2004 Feb 19;41(4):587-98.

5.

Structural basis for modulation of Kv4 K+ channels by auxiliary KChIP subunits.

Wang H, Yan Y, Liu Q, Huang Y, Shen Y, Chen L, Chen Y, Yang Q, Hao Q, Wang K, Chai J.

Nat Neurosci. 2007 Jan;10(1):32-9. Epub 2006 Dec 24. Erratum in: Nat Neurosci. 2007 Feb;10(2):263.

PMID:
17187064
6.

Kv4 potassium channels form a tripartite complex with the anchoring protein SAP97 and CaMKII in cardiac myocytes.

El-Haou S, Balse E, Neyroud N, Dilanian G, Gavillet B, Abriel H, Coulombe A, Jeromin A, Hatem SN.

Circ Res. 2009 Mar 27;104(6):758-69. doi: 10.1161/CIRCRESAHA.108.191007. Epub 2009 Feb 12.

PMID:
19213956
7.

Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome.

Giudicessi JR, Ye D, Tester DJ, Crotti L, Mugione A, Nesterenko VV, Albertson RM, Antzelevitch C, Schwartz PJ, Ackerman MJ.

Heart Rhythm. 2011 Jul;8(7):1024-32. doi: 10.1016/j.hrthm.2011.02.021. Epub 2011 Feb 22.

8.

Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death.

Giudicessi JR, Ye D, Kritzberger CJ, Nesterenko VV, Tester DJ, Antzelevitch C, Ackerman MJ.

Hum Mutat. 2012 Jun;33(6):989-97. doi: 10.1002/humu.22058. Epub 2012 Mar 27.

9.

Mutations in KCND3 cause spinocerebellar ataxia type 22.

Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW.

Ann Neurol. 2012 Dec;72(6):859-69. doi: 10.1002/ana.23701.

10.

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P, Küsters B, van de Warrenburg BP, Kremer B, Wijmenga C, Sinke RJ, Swertz MA, Kampinga HH, Boddeke E, Verbeek DS.

Ann Neurol. 2012 Dec;72(6):870-80. doi: 10.1002/ana.23700.

PMID:
23280838
11.

Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia.

Kurihara M, Ishiura H, Sasaki T, Otsuka J, Hayashi T, Terao Y, Matsukawa T, Mitsui J, Kaneko J, Nishiyama K, Doi K, Yoshimura J, Morishita S, Shimizu J, Tsuji S.

Cerebellum. 2018 Apr;17(2):237-242. doi: 10.1007/s12311-017-0883-4.

PMID:
28895081
12.

Isolation and characterization of the human gene encoding Ito: further diversity by alternative mRNA splicing.

Kong W, Po S, Yamagishi T, Ashen MD, Stetten G, Tomaselli GF.

Am J Physiol. 1998 Dec;275(6):H1963-70. doi: 10.1152/ajpheart.1998.275.6.H1963.

PMID:
9843794

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