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Your search keyword '"Du, Ruo Lan"' showing total 16 results
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16 results on '"Du, Ruo Lan"'

8. Corrigendum: MicroRNA339 Targeting PDXK Improves Motor Dysfunction and Promotes Neurite Growth in the Remote Cortex Subjected to Spinal Cord Transection

Author

Xiong, Liu-Lin, primary, Qin, Yan-Xia, additional, Xiao, Qiu-Xia, additional, Jin, Yuan, additional, Al-Hawwas, Mohammed, additional, Ma, Zheng, additional, Wang, You-Cui, additional, Belegu, Visar, additional, Zhou, Xin-Fu, additional, Xue, Lu-Lu, additional, Du, Ruo-Lan, additional, Liu, Jia, additional, Bai, Xue, additional, and Wang, Ting-Hua, additional

Published
2022
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9. Corrigendum to “BDNF promotes neuronal survival after neonatal hypoxic-ischemic encephalopathy by up-regulating Stx1b and suppressing VDAC1″ [Brain Res. Bull. 174 (2021) 131–140]

Author

Xue, Lu-Lu, primary, Du, Ruo-Lan, additional, Hu, Yue, additional, Xiong, Liu-Lin, additional, Su, Zhang-Yu, additional, Ma, Zheng, additional, Tan, Ya-Xin, additional, Liu, Jia, additional, Hu, Qiao, additional, Zhu, Zhao-Qiong, additional, Liu, Xue-Zheng, additional, and Wang, Ting-Hua, additional

Published
2022
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11. Corrigendum: Vi4-miR-185-5p-Igfbp3 Network Protects the Brain From Neonatal Hypoxic Ischemic Injury via Promoting Neuron Survival and Suppressing the Cell Apoptosis

Author

Xiong, Liu-Lin, primary, Xue, Lu-Lu, additional, Du, Ruo-Lan, additional, Zhou, Hao-Li, additional, Tan, Ya-Xin, additional, Ma, Zheng, additional, Jin, Yuan, additional, Zhang, Zi-Bin, additional, Xu, Yang, additional, Hu, Qiao, additional, Bobrovskaya, Larisa, additional, Zhou, Xin-Fu, additional, Liu, Jia, additional, and Wang, Ting-Hua, additional

Published
2022
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12. Corrigendum to “LncRNA TCONS_00041002 improves neurological outcomes in neonatal rats with hypoxic-ischemic encephalopathy by inhibiting apoptosis and promoting neuron survival”

Author

Xiong, Liu-Lin, primary, Xue, Lu-Lu, additional, Du, Ruo-Lan, additional, Xu, Yang, additional, Niu, Ying-Jie, additional, Hu, Qiao, additional, Zhou, Hao-Li, additional, Liu, Fei, additional, Zhu, Zhao-Qiong, additional, Yu, Chang-Yin, additional, and Wang, Ting-Hua, additional

Published
2022
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15. Discovery of FtsZ inhibitors by virtual screening as antibacterial agents and study of the inhibition mechanismElectronic supplementary information (ESI) available. See DOI: 10.1039/d1md00249j

Author

Du, Ruo-Lan, Sun, Ning, Fung, Yik-Hong, Zheng, Yuan-Yuan, Chen, Yu-Wei, Chan, Pak-Ho, Wong, Wing-Leung, and Wong, Kwok-Yin

Abstract

Inhibition of bacterial cell division is a novel mechanistic action in the development of new antimicrobial agents. The FtsZ protein is an important antimicrobial drug target because of its essential role in bacterial cell division. In the present study, potential inhibitors of FtsZ were identified by virtual screening followed by in vivoand in vitrobioassays. One of the candidates, Dacomitinib (S2727), shows for the first time its potent inhibitory activity against the MRSA strains. The binding mode of Dacomitinib in FtsZ was analyzed by docking, and Asp199and Thr265are thought to be essential residues involved in the interactions.

Published
2022
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16. Discovery of FtsZ inhibitors by virtual screening as antibacterial agents and study of the inhibition mechanism.

Author

Du RL, Sun N, Fung YH, Zheng YY, Chen YW, Chan PH, Wong WL, and Wong KY

Abstract

Inhibition of bacterial cell division is a novel mechanistic action in the development of new antimicrobial agents. The FtsZ protein is an important antimicrobial drug target because of its essential role in bacterial cell division. In the present study, potential inhibitors of FtsZ were identified by virtual screening followed by in vivo and in vitro bioassays. One of the candidates, Dacomitinib (S2727), shows for the first time its potent inhibitory activity against the MRSA strains. The binding mode of Dacomitinib in FtsZ was analyzed by docking, and Asp 199 and Thr 265 are thought to be essential residues involved in the interactions., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Published
2021
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