Zhang Y - Search Results

1

Conduction slowing contributes to spontaneous ventricular arrhythmias in intrinsically active murine RyR2-P2328S hearts.

Zhang Y, Wu J, Jeevaratnam K, King JH, Guzadhur L, Ren X, Grace AA, Lei M, Huang CL, Fraser JA. Zhang Y, et al. J Cardiovasc Electrophysiol. 2013 Feb;24(2):210-8. doi: 10.1111/jce.12015. Epub 2012 Nov 6. J Cardiovasc Electrophysiol. 2013. PMID: 23131176

2

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. Zhang Y, et al. Eur J Pediatr. 2007 Sep;166(9):927-33. doi: 10.1007/s00431-006-0346-2. Epub 2006 Dec 14. Eur J Pediatr. 2007. PMID: 17171344

3

The G604S-hERG mutation alters the biophysical properties and exerts a dominant-negative effect on expression of hERG channels in HEK293 cells.

Huo J, Zhang Y, Huang N, Liu P, Huang C, Guo X, Jiang W, Zhou N, Grace A, Huang CL, Ma A. Huo J, et al. Among authors: zhang y. Pflugers Arch. 2008 Aug;456(5):917-28. doi: 10.1007/s00424-008-0454-0. Epub 2008 Apr 3. Pflugers Arch. 2008. PMID: 18386051

4

Physiological consequences of the P2328S mutation in the ryanodine receptor (RyR2) gene in genetically modified murine hearts.

Goddard CA, Ghais NS, Zhang Y, Williams AJ, Colledge WH, Grace AA, Huang CL. Goddard CA, et al. Among authors: zhang y. Acta Physiol (Oxf). 2008 Oct;194(2):123-40. doi: 10.1111/j.1748-1716.2008.01865.x. Epub 2008 Jun 28. Acta Physiol (Oxf). 2008. PMID: 18419777 Free PMC article.

5

Epac activation, altered calcium homeostasis and ventricular arrhythmogenesis in the murine heart.

Hothi SS, Gurung IS, Heathcote JC, Zhang Y, Booth SW, Skepper JN, Grace AA, Huang CL. Hothi SS, et al. Among authors: zhang y. Pflugers Arch. 2008 Nov;457(2):253-70. doi: 10.1007/s00424-008-0508-3. Epub 2008 Jul 4. Pflugers Arch. 2008. PMID: 18600344 Free PMC article.

6

Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channel.

Zhang Y, Wang T, Ma A, Zhou X, Gui J, Wan H, Shi R, Huang C, Grace AA, Huang CL, Trump D, Zhang H, Zimmer T, Lei M. Zhang Y, et al. Among authors: zhang h. Acta Physiol (Oxf). 2008 Dec;194(4):311-23. doi: 10.1111/j.1748-1716.2008.01883.x. Epub 2008 Jul 24. Acta Physiol (Oxf). 2008. PMID: 18616619 Free PMC article.

7

The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden death.

Shi R, Zhang Y, Yang C, Huang C, Zhou X, Qiang H, Grace AA, Huang CL, Ma A. Shi R, et al. Among authors: zhang y. Europace. 2008 Nov;10(11):1329-35. doi: 10.1093/europace/eun202. Epub 2008 Aug 12. Europace. 2008. PMID: 18697752 Free PMC article.

8

Arrhythmogenic actions of the Ca2+ channel agonist FPL-64716 in Langendorff-perfused murine hearts.

Ghais NS, Zhang Y, Grace AA, Huang CL. Ghais NS, et al. Among authors: zhang y. Exp Physiol. 2009 Feb;94(2):240-54. doi: 10.1113/expphysiol.2008.044669. Epub 2008 Oct 31. Exp Physiol. 2009. PMID: 18978037 Free PMC article.

9

Genetic Na+ channelopathies and sinus node dysfunction.

Lei M, Huang CL, Zhang Y. Lei M, et al. Among authors: zhang y. Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):171-8. doi: 10.1016/j.pbiomolbio.2008.10.003. Epub 2008 Nov 5. Prog Biophys Mol Biol. 2008. PMID: 19027778 Free article. Review.

10

Atrial arrhythmogenesis in wild-type and Scn5a+/delta murine hearts modelling LQT3 syndrome.

Dautova Y, Zhang Y, Sabir I, Grace AA, Huang CL. Dautova Y, et al. Among authors: zhang y. Pflugers Arch. 2009 Jul;458(3):443-57. doi: 10.1007/s00424-008-0633-z. Epub 2009 Jan 28. Pflugers Arch. 2009. PMID: 19184093 Free PMC article.

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