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MeSH:(NAV1.5 Voltage-Gated Sodium Channel/genetics)

3.Desmoplakin expression silencing affects cardiac voltage-gated sodium channel Nav1.5 in HL-1 cells.

Qianhuan ZHANG ; Chunyu DENG ; Fang RAO ; Xiaoying LIU ; Liping MAI ; Jiening ZHU ; Honghong TAN ; Shulin WU

Journal of Southern Medical University 2013;33(7):983-989

4.Long QT syndrome gene diagnosis by haplotype analysis.

Jiang-fang LIAN ; Chang-cong CUI ; Xiao-lin XUE ; Chen HUANG ; Han-bing CUI ; Hai-zhu ZHANG

Chinese Journal of Medical Genetics 2004;21(3):272-273

5.Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617.

Peng LIANG ; Wen-ling LIU ; Da-yi HU ; Cui-lan LI ; Wu-hua TAO ; Lei LI

Chinese Journal of Cardiology 2006;34(7):616-619

6.Single nucleotide polymorphisms of the SCN5A gene in Han Chinese and their relation with Brugada syndrome.

Jun-zhu CHEN ; Xu-dong XIE ; Xing-xiang WANG ; Ming TAO ; Yun-peng SHANG ; Xiao-gang GUO

Chinese Medical Journal 2004;117(5):652-656

7.Structure-based assessment of disease-related mutations in human voltage-gated sodium channels.

Weiyun HUANG ; Minhao LIU ; S Frank YAN ; Nieng YAN

Protein & Cell 2017;8(6):401-438

8.A simulation study for the effect of acid concentration and temperture on sick sinus syndrome.

Xiang LI ; Jiqian ZHANG ; Rui CHENG ; Yingfang JIANG ; Fei GAO

Journal of Biomedical Engineering 2013;30(4):697-703

9.Functional analysis of a novel SCN5A mutation G1712C identified in Brugada syndrome.

Yan-Yu CHEN ; Shen-Rong LIU ; Liang-Zhen XIE ; Ting-Yan ZHU ; Yi-Zhen CHEN ; Xiao-Jiang DENG ; Su-Rong MENG ; Jian PENG

Journal of Southern Medical University 2016;37(2):256-260

10.Site-directed mutagenesis and protein expression of SCN5A gene associated with congenital long QT syndrome.

Rui-Ming SHI ; Hua QIANG ; Yan-Min ZHANG ; Ai-Qun MA ; Jie GAO

Chinese Journal of Contemporary Pediatrics 2013;15(3):223-226

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