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5篇 您的检索式：作者名="Gong Chengbin"

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		题名	作者	年代	出处	被引量
	1	A New Simple Route to N-Substituted 2-Aminoethylphosphonic Acids 显示文摘	Fu Xiangkai Gong Chengbin Ma Xuebing	1998	Synth Commun1998，28，14：	2
	2	The fabrication of a photoresponsive molecularly imprinted polymer for the photoregulated uptake and release of caffeine 显示文摘	Gong Chengbin Michael Lam Hon Wah Yu Hongxia	2006	Advanced Functional Materials2006，16，13：	1
	3	A New Simple Route to N-Substituted 2-Aminoethylphosphonic Acids 显示文摘	Fu Xiangkai Gong Chengbin Ma Xuebing	1998	Synth Co mmun1998，28，14：	1
	4	A new simple route to N-substituted 2-aminoethylphonic acids显示文摘	Fu XlangKai Gong Chengbin Ma Xuebing	1998	Synth Commun1998，28，14：	1
	5	Developmental Temporal Patterns and Molecular Network Features in the Transcriptome of Rat Spinal Cord显示文摘The molecular network features of spinal cord development that are integral to tissue engineering remain poorly understood in placental mammals,especially in terms of their relationships with vital biological processes such as regeneration.Here,using a large-scale temporal transcriptomic analysis of rat spinal cord from the embryonic stage to adulthood,we show that fluctuating RNA expression levels reflect highly active transcriptional regulation,which may initiate spinal cord patterning.We also demonstrate that microRNAs(miRNAs)and transcriptional factors exhibit a mosaic profile based on their expression patterns,while differential alternative splicing events reveal that alternative splicing may be a driving force for the development of the node of Ranvier.Our study also supports the existence of a negative correlation between innate immunity and intrinsic growth capacity.Epigenetic modifications appear to perform their respective regulatory functions at different stages of development,while guanine nucleotidebinding protein(G protein)-coupled receptors(including olfactory receptors(ORs))may perform pleiotropic roles in axonal growth.This study provides a valuable resource for investigating spinal cord development and complements the increasing number of single-cell datasets.These findings also provide a genetic basis for the development of novel tissue engineering strategies.	Jian Yang Lili Zhao Sheng Yi Fei Ding Yumin Yang Yan Liu Yongjun Wang Mei Liu Chengbin Xue Lian Xu Leilei Gong Xinghui Wang Yu Zhang Bin Yu Guo-li Ming Xiaosong Gu	2021	Engineering2021，7，11：	0

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