Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations

Autor Zhu, Yao-Bin, Luo, Jie-Wei, Jiang, Fen, Liu, Gui
Vydáno v Mol Med Rep (2018)

N,N′-Bis(4-nitro­phen­yl)biphenyl-2,2′-dicarboxamide

Autor Wang, Gui-Yu, Qin, Da-Bin, Guo, Li-Hui, Luo, Jie-Wei
Vydáno 2010

Bis(3-bromo­methyl-2-meth­oxy-1-naphth­yl)methane

Autor Luo, Jie-Wei, Zhou, Li, He, Rui, Wang, Gui-Yu, Qin, Da-Bin
Vydáno 2008

N,N′-Bis(2-methoxy­phen­yl)biphenyl-2,2′-dicarboxamide

Autor Wang, Gui-Yu, Li, Di, Qin, Da-Bin, Luo, Jie-Wei, Guo, Li-Hui
Vydáno 2008

9,10-Bis{2-[1-(2-pyridylmeth­yl)imidazolium-3-yl]eth­oxy}anthracene bis(hexa­fluoridophosphate)

Autor Guo, Li-Hui, Qin, Da-Bin, Gu, Shao-Jin, Wang, Gui-Yu, Luo, Jie-Wei
Vydáno 2007

Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing

Autor Lin, Xin-Fu, Luo, Jie-Wei, Liu, Gui, Zhu, Yao-Bin, Jin, Zhao, Lin, Xing
Vydáno v Mol Med Rep (2018)

Association of Tongue Bacterial Flora and Subtypes of Liver-Fire Hyperactivity Syndrome in Hypertensive Patients

Autor Luo, Jie-wei, Lin, Cong-huai, Zhu, Yao-bin, Zheng, Xing-yu, Wu, Yong-xi, Chen, Wei-wei, Yang, Xiao
Vydáno v Evid Based Complement Alternat Med (2018)

Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

Autor Chen, Li, Wang, Han-Lu, Zhu, Yao-Bin, Jin, Zhao, Huang, Jian-Bin, Lin, Xin-Fu, Luo, Jie-Wei, Fang, Zhu-Ting
Vydáno v Cell Death Dis (2020)

Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype

Autor Xie, Li-jun, Ruan, Dan-dan, Zhang, Jian-hui, Li, Yi, Chen, Li, Yan, Mao-lin, Yu, Ming-dian, Luo, Jie-wei, Zhang, Hui-zhen
Vydáno v Can J Gastroenterol Hepatol (2021)

The Construction of Unsmooth Pulse Images in Traditional Chinese Medicine Based on Wave Intensity Technology

Autor Luo, Jie-wei, Guo, Si-wei, Cao, Shuang-shuang, Lin, Ning, Ye, Zhen-sheng, Wei, Shi-chao, Zheng, Xing-yu, Guo, Miao-miao, Meng, Xiao-rong, Huang, Fang-meng
Vydáno v Evid Based Complement Alternat Med (2016)

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis

Autor Ruan, Dan-Dan, Gan, Yu-Mian, Lu, Tao, Yang, Xiao, Zhu, Yao-Bin, Yu, Qing-Hua, Liao, Li-Sheng, Lin, Ning, Qian, Xin, Luo, Jie-Wei, Tang, Fa-Qiang
Vydáno v World J Clin Cases (2020)

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

Autor Zhang, Jian-hui, Ruan, Dan-dan, Hu, Ya-nan, Ruan, Xing-lin, Zhu, Yao-bin, Yang, Xiao, Wu, Jia-bin, Lin, Xin-fu, Luo, Jie-wei, Tang, Fa-qiang
Vydáno v Biomed Res Int (2021)