Huang C - Search Results

1

De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome.

Wang L, Meng X, Yuchi Z, Zhao Z, Xu D, Fedida D, Wang Z, Huang C. Wang L, et al. Among authors: huang c. Cell Physiol Biochem. 2015;36(6):2250-62. doi: 10.1159/000430189. Epub 2015 Jul 24. Cell Physiol Biochem. 2015. PMID: 26279430 Free article.

2

[New progress of the highly efficient siRNA design].

Xu DH, Huang C, Liu LY, Song TS. Xu DH, et al. Among authors: huang c. Yi Chuan. 2006 Nov;28(11):1457-61. doi: 10.1360/yc-006-1457. Yi Chuan. 2006. PMID: 17098718 Review. Chinese.

3

[Construction of eukaryotic expression vector of congenital long QT syndrome related HERG gene A561V mutation and its expression in HEK293 cells].

Li Y, Cui CC, Huang C, Lian JF, Zhao YH, Xue XL, Zhao XG. Li Y, et al. Among authors: huang c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Dec;23(6):627-30. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 17160940 Chinese.

4

[Functional expression of congenital long QT syndrome related HERG mutation A561V in vitro].

Li Y, Cui CC, Zhao YH, Xue XL, Zhang AF, Lian JF, Huang C. Li Y, et al. Among authors: huang c. Zhonghua Xin Xue Guan Bing Za Zhi. 2007 Feb;35(2):143-6. Zhonghua Xin Xue Guan Bing Za Zhi. 2007. PMID: 17445409 Chinese.

5

[Genetic analysis of the familial noncompaction ventricular myocardium with sick sinus syndrome].

Meng XY, Huang C, Song TS. Meng XY, et al. Among authors: huang c. Zhonghua Xin Xue Guan Bing Za Zhi. 2007 Jun;35(6):580-1. Zhonghua Xin Xue Guan Bing Za Zhi. 2007. PMID: 17711726 Chinese. No abstract available.

6

Effects of small interfering RNAs targeting MAPK1 on gene expression profile in HeLa cells as revealed by microarray analysis.

Huang C, Liu LY, Li ZF, Wang P, Ni L, Song LP, Xu DH, Song TS. Huang C, et al. Cell Biol Int. 2008 Sep;32(9):1081-90. doi: 10.1016/j.cellbi.2008.04.019. Epub 2008 May 2. Cell Biol Int. 2008. PMID: 18539490

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: huang c, huang cl. Europace. 2008 Nov;10(11):1329-35. doi: 10.1093/europace/eun202. Epub 2008 Aug 12. Europace. 2008. PMID: 18697752 Free PMC article.

8

[Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].

Shi RM, Ma AQ, Zhang YM, Yang C, Huang C, Zhou XH, Liu XH. Shi RM, et al. Among authors: huang c. Zhonghua Er Ke Za Zhi. 2009 Dec;47(12):926-30. Zhonghua Er Ke Za Zhi. 2009. PMID: 20193146 Chinese.

9

The SCN5A mutation A1180V is associated with electrocardiographic features of LQT3.

Zhang Y, Wang J, Chang S, Zhou N, Xing H, Wang L, Huang C, Ma A, Huang CL, Lei M, Fraser JA. Zhang Y, et al. Among authors: huang c, huang cl. Pediatr Cardiol. 2014 Feb;35(2):295-300. doi: 10.1007/s00246-013-0773-6. Epub 2013 Aug 21. Pediatr Cardiol. 2014. PMID: 23963187

10

MicroRNA-302b suppresses cell proliferation by targeting EGFR in human hepatocellular carcinoma SMMC-7721 cells.

Wang L, Yao J, Shi X, Hu L, Li Z, Song T, Huang C. Wang L, et al. Among authors: huang c. BMC Cancer. 2013 Oct 2;13:448. doi: 10.1186/1471-2407-13-448. BMC Cancer. 2013. Retraction in: BMC Cancer. 2024 Aug 26;24(1):1047. doi: 10.1186/s12885-024-12839-w PMID: 24083596 Free PMC article. Retracted.

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