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Results: 1 to 20 of 105

Similar articles for PubMed (Select 18948620)

1.

Homozygous missense N629D hERG (KCNH2) potassium channel mutation causes developmental defects in the right ventricle and its outflow tract and embryonic lethality.

Teng GQ, Zhao X, Lees-Miller JP, Quinn FR, Li P, Rancourt DE, London B, Cross JC, Duff HJ.

Circ Res. 2008 Dec 5;103(12):1483-91. doi: 10.1161/CIRCRESAHA.108.177055. Epub 2008 Oct 23.

2.

Role of mutation and pharmacologic block of human KCNH2 in vasculogenesis and fetal mortality: partial rescue by transforming growth factor-β.

Teng G, Zhao X, Lees-Miller JP, Belke D, Shi C, Chen Y, O'Brien ER, Fedak PW, Bracey N, Cross JC, Duff HJ.

Circ Arrhythm Electrophysiol. 2015 Apr;8(2):420-8. doi: 10.1161/CIRCEP.114.001837. Epub 2015 Feb 3.

PMID:
25648353
3.
4.
5.

Prolonged repolarization and triggered activity induced by adenoviral expression of HERG N629D in cardiomyocytes derived from stem cells.

Teng G, Zhao X, Cross JC, Li P, Lees-Miller JP, Guo J, Dyck JR, Duff HJ.

Cardiovasc Res. 2004 Feb 1;61(2):268-77.

6.

Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytes.

Lin EC, Holzem KM, Anson BD, Moungey BM, Balijepalli SY, Tester DJ, Ackerman MJ, Delisle BP, Balijepalli RC, January CT.

Am J Physiol Heart Circ Physiol. 2010 Jun;298(6):H1842-9. doi: 10.1152/ajpheart.01236.2009. Epub 2010 Apr 2.

7.

C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.

Choe CU, Schulze-Bahr E, Neu A, Xu J, Zhu ZI, Sauter K, Bähring R, Priori S, Guicheney P, Mönnig G, Neapolitano C, Heidemann J, Clancy CE, Pongs O, Isbrandt D.

Hum Mol Genet. 2006 Oct 1;15(19):2888-902. Epub 2006 Aug 21.

8.

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

Paulussen AD, Raes A, Jongbloed RJ, Gilissen RA, Wilde AA, Snyders DJ, Smeets HJ, Aerssens J.

Cardiovasc Res. 2005 Aug 15;67(3):467-75.

9.

Arrhythmia phenotype in mouse models of human long QT.

Salama G, Baker L, Wolk R, Barhanin J, London B.

J Interv Card Electrophysiol. 2009 Mar;24(2):77-87. doi: 10.1007/s10840-008-9339-6. Epub 2009 Jan 16.

PMID:
19148726
10.

Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor.

McBride CM, Smith AM, Smith JL, Reloj AR, Velasco EJ, Powell J, Elayi CS, Bartos DC, Burgess DE, Delisle BP.

J Membr Biol. 2013 May;246(5):355-64. doi: 10.1007/s00232-013-9539-6. Epub 2013 Apr 2.

11.

Novel characteristics of a trafficking-defective G572R-hERG channel linked to hereditary long QT syndrome.

Lian J, Huang N, Zhou J, Ge S, Huang X, Huo J, Liu L, Xu W, Zhang S, Yang X, Zhou J, Huang C.

Can J Cardiol. 2010 Oct;26(8):417-22.

12.

Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice.

Babij P, Askew GR, Nieuwenhuijsen B, Su CM, Bridal TR, Jow B, Argentieri TM, Kulik J, DeGennaro LJ, Spinelli W, Colatsky TJ.

Circ Res. 1998 Sep 21;83(6):668-78.

13.

Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture.

Lahti AL, Kujala VJ, Chapman H, Koivisto AP, Pekkanen-Mattila M, Kerkelä E, Hyttinen J, Kontula K, Swan H, Conklin BR, Yamanaka S, Silvennoinen O, Aalto-Setälä K.

Dis Model Mech. 2012 Mar;5(2):220-30. doi: 10.1242/dmm.008409. Epub 2011 Nov 3.

14.

A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.

Zhang Y, Zhou N, Jiang W, Peng J, Wan H, Huang C, Xie Z, Huang CL, Grace AA, Ma A.

Eur J Pediatr. 2007 Sep;166(9):927-33. Epub 2006 Dec 14.

PMID:
17171344
15.

HERG-F463L potassium channels linked to long QT syndrome reduce I(Kr) current by a trafficking-deficient mechanism.

Yang HT, Sun CF, Cui CC, Xue XL, Zhang AF, Li HB, Wang DQ, Shu J.

Clin Exp Pharmacol Physiol. 2009 Aug;36(8):822-7. doi: 10.1111/j.1440-1681.2009.05150.x.

PMID:
19215240
16.

Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C.

Delisle BP, Anderson CL, Balijepalli RC, Anson BD, Kamp TJ, January CT.

J Biol Chem. 2003 Sep 12;278(37):35749-54. Epub 2003 Jul 1.

17.

Selective knockout of mouse ERG1 B potassium channel eliminates I(Kr) in adult ventricular myocytes and elicits episodes of abrupt sinus bradycardia.

Lees-Miller JP, Guo J, Somers JR, Roach DE, Sheldon RS, Rancourt DE, Duff HJ.

Mol Cell Biol. 2003 Mar;23(6):1856-62.

18.

Loss of Apaf-1 leads to partial rescue of the HAND2-null phenotype.

Aiyer AR, Honarpour N, Herz J, Srivastava D.

Dev Biol. 2005 Feb 1;278(1):155-62.

19.

Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.

Bhuiyan ZA, Momenah TS, Gong Q, Amin AS, Ghamdi SA, Carvalho JS, Homfray T, Mannens MM, Zhou Z, Wilde AA.

Heart Rhythm. 2008 Apr;5(4):553-61. doi: 10.1016/j.hrthm.2008.01.020. Epub 2008 Jan 29. Erratum in: Heart Rhythm. 2008 May;5(5):773.

20.

Ubiquitination-dependent quality control of hERG K+ channel with acquired and inherited conformational defect at the plasma membrane.

Apaja PM, Foo B, Okiyoneda T, Valinsky WC, Barriere H, Atanasiu R, Ficker E, Lukacs GL, Shrier A.

Mol Biol Cell. 2013 Dec;24(24):3787-804. doi: 10.1091/mbc.E13-07-0417. Epub 2013 Oct 23.

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