日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The baroreflex afferent pathway plays a critical role in H(2)S-mediated autonomic control of blood pressure regulation under physiological and hypertensive conditions.

在生理和高血压条件下,压力反射传入通路在 H(2)S 介导的自主神经控制血压调节中起着至关重要的作用

Li Ying, Feng Yan, Liu Li, Li Xue, Li Xin-Yu, Sun Xun, Li Ke-Xin, Zha Rong-Rong, Wang Hong-Dan, Zhang Meng-di, Fan Xiong-Xiong, Wu Di, Fan Yao, Zhang Hao-Cheng, Qiao Guo-Fen, Li Bai-Yan

Establishment of Functional Liver Spheroids From Human Hepatocyte-Derived Liver Progenitor-Like Cells for Cell Therapy

从人类肝细胞衍生的肝祖细胞样细胞建立功能性肝球体用于细胞治疗

Wen-Ming Liu, Xu Zhou, Cai-Yang Chen, Dong-Dong Lv, Wei-Jian Huang, Yuan Peng, Hong-Ping Wu, Yi Chen, Dan Tang, Li-Na Guo, Xiu-Li Wang, Hong-Dan Zhang, Xiao-Hua Liu, Li-Qun Yang, Wei-Feng Yu, He-Xin Yan

Investigating the characteristics of echocardiogram, surgical treatment, chromosome and prognosis for fetal right heart enlargement: A STROBE-compliant article

探讨胎儿右心扩大的超声心动图特征、手术治疗、染色体及预后:一篇符合STROBE标准的文章

Liu, Lin; Wang, Hong-Dan; Cui, Cun-Ying; Yao, Hui-Mei; Huang, Lei; Li, Tao; Fan, Tai-Bing; Peng, Bang-Tian; Zhang, Lian-Zhong

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.

通过全基因组DNA甲基化研究检测胎儿表观遗传生物标志物,用于无创产前诊断

Wang Hong-Dan, Liu Lin, Zhao Hui-Ru, Hou Qiao-Fang, Yan Jing-Bin, Shi Wei-Li, Guo Qian-Nan, Wang Li, Liao Shi-Xiu, Zhu Bo-Feng

Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication

对四个患有 1q21.1 微缺失或微重复的家族进行临床和分子细胞遗传学分析

Wang, Hong-Dan; Liu, Lin; Wu, Dong; Li, Tao; Cui, Cun-Ying; Zhang, Lian-Zhong; Wang, Cheng-Zeng

Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report

中国一例携带新生DMD基因突变的家庭的产前诊断:病例报告

Li, Tao; Zhang, Zhao-Jing; Ma, Xin; Lv, Xue; Xiao, Hai; Guo, Qian-Nan; Liu, Hong-Yan; Wang, Hong-Dan; Wu, Dong; Lou, Gui-Yu; Wang, Xin; Zhang, Chao-Yang; Liao, Shi-Xiu

Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot.

全外显子组测序在8名患有孤立性法洛四联症的中国儿童中发现了新的突变。

Liu Lin, Wang Hong-Dan, Cui Cun-Ying, Qin Yun-Yun, Fan Tai-Bing, Peng Bang-Tian, Zhang Lian-Zhong, Wang Cheng-Zeng

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

唐氏综合征胎儿海马中miRNA和mRNA表达谱的整合分析

Shi, Wei-Li; Liu, Zhong-Zhen; Wang, Hong-Dan; Wu, Dong; Zhang, Hui; Xiao, Hai; Chu, Yan; Hou, Qiao-Fang; Liao, Shi-Xiu

Genetic polymorphism analyses of 30 InDels in Chinese Xibe ethnic group and its population genetic differentiations with other groups

对中国锡伯族人群中30个插入/缺失突变(InDel)进行遗传多态性分析,并探讨其与其他人群的群体遗传分化。

Meng, Hao-Tian; Zhang, Yu-Dang; Shen, Chun-Mei; Yuan, Guo-Lian; Yang, Chun-Hua; Jin, Rui; Yan, Jiang-Wei; Wang, Hong-Dan; Liu, Wen-Juan; Jing, Hang; Zhu, Bo-Feng

DNA methylation study of fetus genome through a genome-wide analysis

通过全基因组分析研究胎儿基因组的DNA甲基化

Wang, Hong-Dan; Hou, Qiao-Fang; Guo, Qian-Nan; Li, Tao; Wu, Dong; Zhang, Xian-Ping; Chu, Yan; He, Miao; Xiao, Hai; Guo, Liang-Jie; Yang, Ke; Liao, Shi-Xiu; Zhu, Bo-Feng