Gong QM - Search Results

1

[The mechanistic rote of KCNH2 gene L413P and L559H mutations in long QT syndrome].

Li CL, Hu DY, Liu WL, Qi SY, Wang HT, Li L, Gong QM, Zhou ZF. Li CL, et al. Among authors: gong qm. Zhonghua Nei Ke Za Zhi. 2007 Oct;46(10):838-41. Zhonghua Nei Ke Za Zhi. 2007. PMID: 18218237 Chinese.

2

Mechanisms of pharmacological rescue of trafficking-defective hERG mutant channels in human long QT syndrome.

Gong Q, Jones MA, Zhou Z. Gong Q, et al. J Biol Chem. 2006 Feb 17;281(7):4069-74. doi: 10.1074/jbc.M511765200. Epub 2005 Dec 16. J Biol Chem. 2006. PMID: 16361248 Free PMC article.

3

Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome.

Stump MR, Gong Q, Zhou Z. Stump MR, et al. Am J Physiol Heart Circ Physiol. 2011 Jan;300(1):H312-8. doi: 10.1152/ajpheart.00818.2010. Epub 2010 Nov 5. Am J Physiol Heart Circ Physiol. 2011. PMID: 21057041 Free PMC article.

4

Isoform-specific dominant-negative effects associated with hERG1 G628S mutation in long QT syndrome.

Stump MR, Gong Q, Zhou Z. Stump MR, et al. PLoS One. 2012;7(8):e42552. doi: 10.1371/journal.pone.0042552. Epub 2012 Aug 2. PLoS One. 2012. PMID: 22876326 Free PMC article.

5

Nonsense-Mediated mRNA Decay of hERG Mutations in Long QT Syndrome.

Gong Q, Zhou Z. Gong Q, et al. Methods Mol Biol. 2018;1684:37-49. doi: 10.1007/978-1-4939-7362-0_4. Methods Mol Biol. 2018. PMID: 29058182

6

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects.

Zhou Z, Gong Q, Epstein ML, January CT. Zhou Z, et al. J Biol Chem. 1998 Aug 14;273(33):21061-6. doi: 10.1074/jbc.273.33.21061. J Biol Chem. 1998. PMID: 9694858 Free article.

7

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects.

Zhou Z, Gong Q, January CT. Zhou Z, et al. J Biol Chem. 1999 Oct 29;274(44):31123-6. doi: 10.1074/jbc.274.44.31123. J Biol Chem. 1999. PMID: 10531299 Free article.

8

Defective assembly and trafficking of mutant HERG channels with C-terminal truncations in long QT syndrome.

Gong Q, Keeney DR, Robinson JC, Zhou Z. Gong Q, et al. J Mol Cell Cardiol. 2004 Dec;37(6):1225-33. doi: 10.1016/j.yjmcc.2004.10.002. J Mol Cell Cardiol. 2004. PMID: 15572053

9

Inhibition of nonsense-mediated mRNA decay by antisense morpholino oligonucleotides restores functional expression of hERG nonsense and frameshift mutations in long-QT syndrome.

Gong Q, Stump MR, Zhou Z. Gong Q, et al. J Mol Cell Cardiol. 2011 Jan;50(1):223-9. doi: 10.1016/j.yjmcc.2010.10.022. Epub 2010 Oct 28. J Mol Cell Cardiol. 2011. PMID: 21035456 Free PMC article.

10

Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome.

Gong Q, Stump MR, Zhou Z. Gong Q, et al. Gene. 2014 Apr 15;539(2):190-7. doi: 10.1016/j.gene.2014.02.012. Epub 2014 Feb 13. Gene. 2014. PMID: 24530480 Free PMC article.

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