Zhu C - Search Results

1

Interaction between mitochondrial NADH dehydrogenase subunit-2 5178 C > A and clinical risk factors on the susceptibility of essential hypertension in Chinese population.

Chen X, He XY, Zhu C, Zhang Y, Li Z, Liu Y, Zhang Y, Yin T, Li Y. Chen X, et al. Among authors: zhu c. BMC Med Genet. 2019 Jul 5;20(1):121. doi: 10.1186/s12881-019-0838-3. BMC Med Genet. 2019. PMID: 31277597 Free PMC article.

2

Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes.

Liu Y, Li Y, Gao J, Zhu C, Lan Y, Yang J, Li Z, Guan M, Chen Y. Liu Y, et al. Among authors: zhu c. BMC Med Genet. 2014 Jul 23;15:84. doi: 10.1186/1471-2350-15-84. BMC Med Genet. 2014. PMID: 25056089 Free PMC article.

3

Electrophysiological and trafficking defects of the SCN5A T353I mutation in Brugada syndrome are rescued by alpha-allocryptopine.

Zhang J, Chen Y, Yang J, Xu B, Wen Y, Xiang G, Wei G, Zhu C, Xing Y, Li Y. Zhang J, et al. Among authors: zhu c. Eur J Pharmacol. 2015 Jan 5;746:333-43. doi: 10.1016/j.ejphar.2014.09.028. Epub 2014 Sep 23. Eur J Pharmacol. 2015. PMID: 25261036

4

[Mitochondrial DNA mutation associated with hypertension in tRNA(Ile) and tRNA(Gln) genes].

Zhu C, Liu Y, Gao J, Yang J, Yin T, Lan Y, Li Z, Guan M, Li Y. Zhu C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):619-22. doi: 10.3760/cma.j.issn.1003-9406.2014.01.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297595 Chinese.

5

Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.

Liu Y, Zhu Q, Zhu C, Wang X, Yang J, Yin T, Gao J, Li Z, Ma Q, Guan M, Li Y, Chen Y. Liu Y, et al. Among authors: zhu q, zhu c. BMC Med Genomics. 2014 Dec 24;7:73. doi: 10.1186/s12920-014-0073-x. BMC Med Genomics. 2014. PMID: 25539907 Free PMC article.

6

Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.

Wu ZJ, Huang Y, Fu YC, Zhao XJ, Zhu C, Zhang Y, Xu B, Zhu QL, Li Y. Wu ZJ, et al. Among authors: zhu c, zhu ql. J Geriatr Cardiol. 2015 Jul;12(4):394-401. doi: 10.11909/j.issn.1671-5411.2015.04.002. J Geriatr Cardiol. 2015. PMID: 26346102 Free PMC article.

7

Mitochondrial tRNA mutations in Chinese hypertensive individuals.

Liu Y, Li Y, Wang X, Ma Q, Zhu C, Li Z, Yin T, Yang J, Chen Y, Guan M. Liu Y, et al. Among authors: zhu c. Mitochondrion. 2016 May;28:1-7. doi: 10.1016/j.mito.2016.02.007. Epub 2016 Feb 26. Mitochondrion. 2016. PMID: 26923935

8

Stromal Cell-Derived Factor 1 Increases Tetrodotoxin-Resistant Sodium Currents Nav1.8 and Nav1.9 in Rat Dorsal Root Ganglion Neurons via Different Mechanisms.

Qiu F, Li Y, Fu Q, Fan YY, Zhu C, Liu YH, Mi WD. Qiu F, et al. Among authors: zhu c. Neurochem Res. 2016 Jul;41(7):1587-603. doi: 10.1007/s11064-016-1873-5. Epub 2016 Apr 2. Neurochem Res. 2016. PMID: 27038931

9

Effects of allocryptopine on outward potassium current and slow delayed rectifier potassium current in rabbit myocardium.

Fu YC, Zhang Y, Tian LY, Li N, Chen X, Cai ZQ, Zhu C, Li Y. Fu YC, et al. Among authors: zhu c. J Geriatr Cardiol. 2016 May;13(4):316-25. doi: 10.11909/j.issn.1671-5411.2016.04.008. J Geriatr Cardiol. 2016. PMID: 27403141 Free PMC article.

10

Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2.

Liu L, Tian J, Lu C, Chen X, Fu Y, Xu B, Zhu C, Sun Y, Zhang Y, Zhao Y, Li Y. Liu L, et al. Among authors: zhu c. Front Physiol. 2016 Dec 27;7:650. doi: 10.3389/fphys.2016.00650. eCollection 2016. Front Physiol. 2016. PMID: 28082916 Free PMC article.

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