Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Meifen, Xu"'
Autor:
Fan, Wu, Yue, Yuan, Zhaomin, Deng, Di, Yin, Qiufeng, Shen, Jiehua, Zeng, Yanhong, Xie, Meifen, Xu, Meiyi, Yang, Shiqiang, Jiang, Chunhuan, Zhang, Huixi, Lu, Caijun, Sun
Publikováno v:
Journal of Medical Virology. 94:4115-4124
The promotion of the booster shots against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is an open issue to be discussed. Little is known about the public intention and the influencing factors regarding the booster vaccine.
Autor:
Hanjun, Chen, Zhaoyun, Li, Lihong, Zhang, Liming, Zhang, Yaqiong, Zhang, Yichao, Wang, Meifen, Xu, Qianyi, Zhong
Publikováno v:
Annals of clinical and laboratory science. 50(4)
Triple-negative breast cancer (TNBC) is one of the most common malignant, highly heterogeneous tumors in women. MicroRNAs (miRNAs), such as miR-200c, play an important role in various types of malignant cancer, including TNBC. However, the biological
Autor:
Meifen Xu, Yiqun He, Junwei Geng, Zhi Lin, Suxue Shi, Yanzi Meng, Ling Xue, Min-Xin Guan, Han Yu, Zhongqiu Lu
Publikováno v:
Hereditas (Beijing). 36:127-134
Mitochondrial tRNA genes are the hot spots for mutations associated with essential hypertension. We report here the clinical and molecular genetic characterization of two Han Chinese pedigrees with materially inherited essential hypertension. Clinica
Publikováno v:
Hereditas (Beijing). 35:1237-1243
Dyslipidemia is defined as high levels of serum cholesterol and/or triglycerides. Dyslipidemia often leads to severe cardiovascular diseases including coronary heart disease and stroke as the first clinical manifestation, thus threatening the health
Autor:
Yanwen Qin, Ling Xue, Yiqun He, Min-Xin Guan, Jun Qin Mo, Suxue Shi, Pingping Jiang, Jiqiang He, Yangyiyi Huang, Meifen Xu
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Coronary heart disease is the leading cause of death worldwide. Mitochondrial genetic determinants for the development of this disorder remain less explored. Methods and Results We performed a clinical and genetic evaluation and mutational
Autor:
Yanchun Ji, Fuxin Zhao, Xiangjuan Meng, Jia Qu, Jinping Zhu, Xiaoling Liu, Yi Tong, Min Liang, Min-Xin Guan, Xiangtian Zhou, Feng Li, Meifen Xu, Yiqun He, Yan-Hong Sun, Jun Qin Mo, Juanjuan Zhang, Pingping Jiang
Publikováno v:
Investigative Opthalmology & Visual Science. 55:1321
PURPOSE To investigate the molecular pathogenesis of Leber's hereditary optic neuropathy (LHON) in Chinese families. METHODS A cohort of 1218 Han Chinese subjects with LHON and 316 control subjects underwent the clinical and genetic evaluation and mo
Publikováno v:
Electroencephalography and Clinical Neurophysiology. 87:S99