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

Microglial Inhibition Promotes Proliferation and Differentiation of Neural Stem Cells via STAT3/SDF-1/CXCR4 Signaling Pathway in Hypoxic-Ischemic Encephalopathy.

在缺氧缺血性脑病中,小胶质细胞抑制通过 STAT3/SDF-1/CXCR4 信号通路促进神经干细胞的增殖和分化。

Ding Ao, Duan Guiqin, Zhu Mingwei, Chen Li, Luo Jie, Tan Ting, Li Zilin, Wang Wenhui, Wang Jun, Chen Yuan, Tang Ya-Ping

Dysfunctional connectivity within hippocampal and entorhinal networks underlies early-life iron deficiency induced social recognition deficits, a preliminary study.

初步研究表明,海马和内嗅皮层网络内的功能连接障碍是早期缺铁引起的社会认知缺陷的根本原因。

Ding Ao, Tan Ting, Liu Peng, Li Xin, Zhu Mingwei, Liu Hongsheng, Wang Ying, Chen Yuan, Tang Ya-Ping

Divergent response associates with the differential amplitudes of immunity against Magnaporthe oryzae by different blast resistance genes

不同的抗稻瘟病基因对稻瘟病菌的免疫反应强度存在差异,这与这些基因的免疫反应强度不同有关。

Hassan, Beenish; Bhutto, Sadam Hussain; Yin, Xiao-Xiao; Yan, Xiu-Lian; Liao, Rong; Guo, Mao-Lin; Tang, Ya-Ping; Guo, Dai-Ming; Yang, Si-Jia; Gulzar, Faiza; Li, Yan; Zeng, Xian-Yin; Zhao, Zhi-Xue; Wang, Wen-Ming

Melatonin Enhances Blast Disease Resistance via Inducing Rice Immunity and Inhibits the Growth of the Magnaporthe Oryzae

褪黑素通过诱导水稻免疫力增强稻瘟病抗性并抑制稻瘟病菌的生长

Yang, Si-Jia; Yan, Xiu-Lian; Guo, Mao-Lin; Tang, Ya-Ping; Liao, Rong; Yin, Xiao-Xiao; Hassan, Beenish; Yuan, Ming; Zhao, Zhi-Xue; Wang, Wen-Ming

Natural variation of the MIR168a promoter influences its activity and miR168a abundance in rice

水稻中 miR168a 启动子的自然变异会影响其活性和 miR168a 的丰度。

Zhao, Zhi-Xue; Yan, Xiu-Lian; Liao, Rong; Guo, Dai-Ming; Tang, Ya-Ping; Guo, Mao-Lin; Yang, Si-Jia; Yin, Xiao-Xiao; Hassan, Beenish; Li, De-Qiang; Fan, Jing; Huang, Yan-Yan; Zhang, Ji-Wei; Wang, He; Li, Guo-Bang; Zhu, Yong; Li, Yan; Wang, Wen-Ming

A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report

FKBP10基因中一种新的复合杂合变异导致布鲁克综合征,但无先天性挛缩:病例报告

Shang, Liyuan; Shi, Weizhe; Xu, Yibo; Nong, Tianying; Li, Xia; Li, Zhaohui; Liu, Yanhan; Li, Jingchun; Tang, Ya-Ping; Zhu, Mingwei; Xu, Hongwen

The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats

GNPTAB基因中的c.1760G>C突变是导致粘脂病III型的原因,该突变会破坏大鼠体节的发育。

Nong, Tianying; Li, Jiangui; Li, Xia; Li, Yiqiang; Li, Zhaohui; Shi, Weizhe; Zhou, Qiuchan; Xu, Hongwen; Zhu, Mingwei; Tang, Ya-Ping

A novel mutation in intron 1 of Wnt1 causes developmental loss of dopaminergic neurons in midbrain and ASD-like behaviors in rats

Wnt1基因内含子1中的一种新突变导致大鼠中脑多巴胺能神经元发育丢失,并出现类似自闭症谱系障碍的行为。

Li, Yongyi; Zhu, Mingwei; Chen, Wen-Xiong; Luo, Jing; Li, Xin; Cao, Yangyang; Zheng, Meng; Ma, Shanshan; Xiao, Zhilan; Zhang, Yani; Jiang, Linyan; Wang, Xiumin; Tan, Ting; Li, Xia; Gong, Qian; Xiong, Xiaoli; Wang, Jun; Tang, Mingxi; Li, Mingtao; Tang, Ya-Ping

Cataract-causing Y204X mutation of crystallin protein CRYβB1 promotes its C-terminal degradation and higher-order oligomerization

晶状体蛋白CRYβB1的Y204X突变是导致白内障的原因,该突变促进其C端降解和高级寡聚化。

Jing, Xuping; Zhu, Mingwei; Lu, Xiaoyun; Wei, Ping; Shi, Lingyu; Zhang, Bu-Yu; Xu, Yi; Tang, Ya-Ping; Xiang, Dao-Man; Gong, Peng

A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate.

ext2 中的一种新突变通过减少硫酸乙酰肝素的合成,导致遗传性多发性外生骨疣

Xian Caixia, Zhu Mingwei, Nong Tianying, Li Yiqiang, Xie Xingmei, Li Xia, Li Jiangui, Li Jingchun, Wu Jianping, Shi Weizhe, Wei Ping, Xu Hongwen, Tang Ya-Ping