搜索筛选:
搜索耗时2.3792秒,为你在为你在102,285,761篇论文里面共找到 16 篇相符的论文内容
类      型:
[会议论文] 作者:Zhuohua Zhang, 来源:第三届国际神经疾病大会暨2016脑网络与脑疾病高峰论坛 年份:2016
[期刊论文] 作者:YAN ZhuoHua,ZHANG RongPing,ZHA, 来源:中国科学:化学英文版 年份:2012
在块共聚物作为溶剂蒸发时间的一个函数拍摄的答案演员组苯乙烯 /butadiene (B) 的表面化学药品结构开发用和频率产生被调查震动的光谱学(SFG ) 。块共聚物(30 wt% PS ) 在 s...
[会议论文] 作者:Ben Wu,Fangqi Ding,Zhuohua Zhang,Long Ma, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
[期刊论文] 作者:Hui Xiong,Kun Xia,Benshang Li,Guoping Zhao,Zhuohua Zhang, 来源:生物化学与生物物理学报(英文版) 年份:2009
Compelling evidences from transgenic mice, immuno-precipitation data, gene expression analysis, and func-tional heterologous expression studies supported the ro...
[会议论文] 作者:Jintao Luo,Zhaofa Xu,Zhuohua Zhang,Long Ma,Zhiping Tan, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
[会议论文] 作者:Jintao Luo,Zhaofa Xu,Zhiping Tan,Zhuohua Zhang,Long Ma, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
Methyl salicylate (MeSa) is a stress hormone released by plants under attack by pathogens or herbivores.MeSa has been shown to attract predatory insects of herbivores and repel pests.The neuromodulato...
[期刊论文] 作者:Kun Xia,Hong Ma,Hui Xiong,Qian Pan,Liangqun Huang,Danling Wang,Zhuohua Zhang, 来源:蛋白质与细胞 年份:2010
Hearing impairment (HI) affects 1/1000 children and over 2% of the aged population.We have previously reported that mutations in the gene encoding gap junction...
[会议论文] 作者:Haibo Li,Yongyi Zou,Hailong Han,Renbing Lu,Jieqiong Tan,Qian Pan,Zhuohua Zhang, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
[期刊论文] 作者:Lusi Zhang,Jie Deng,Qian Pan,Yan Zhan,Jian-Bing Fan,Kun Zhang,Zhuohua Zhang,, 来源:Journal of Genetics and Genomics 年份:2016
Parkinson disease(PD) is a progressive neurodegenerative movement disorder. Both environmental and genetic factors play important roles in PD etiology. A number...
[会议论文] 作者:Xiaoyang Gao,Yanling Teng,Jintao Luo,Liange Huang,Zhuohua Zhang,Long Ma,Min Li,Yong-Chao Ma, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
[会议论文] 作者:Xiaoyang Gao,Yanling Teng,Jintao Luo,Liange Huang,Min Li,Zhuohua Zhang,Yong-Chao Ma,Long Ma, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
Spinal muscular atrophy (SMA), the most frequent human congenital motor neuron degenerative disease, is caused by loss-of-function mutations in the highly conserved survival motor neuron gene SMN1.Mut...
[期刊论文] 作者:LI Wei-ming,YANG Xin-chun,WANG Le-feng,GE Yong-gui,WANG Hong-shi,XU Li,NI Zhuohua,ZHANG Da-peng, 来源:中华医学杂志英文版 年份:2011
[会议论文] 作者:Tongmei Zhang,Li Li,Chengyuan Tang,Zhengqing Wan,Jieqiong Tan,Ruoxi Wang,Zhuotong Zeng,Zhuohua Zhang,, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
[会议论文] 作者:Zhang,Liang Xue,Li Li,Chengyuan Tang,Zhengqing Wan,Jieqiong Tan,Ruoxi Wang,Zhuotong Zeng,Andy Tao,Zhuohua Zhang, 来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
Mutations in PINK1 cause early onset familial Parkinsons disease (PD).PINK1 is accumulated on followed by recruiting parkin to the outer membrane of damaged mitochondria to promote mitophagy.Here, we...
[会议论文] 作者:Qing Wang,Yunqi Xu,Dan Chen,Xiaobo Wei,Jinchi Liao,Xu Liu,Jing Zou,Beisha Tang,Zhuohua Zhang,Xiang Cai, 来源:第四届全国痴呆与认知障碍学术研讨会 年份:2015
[会议论文] 作者:Qing Wang,Xiaobo Wei,Jing Zou,Xu Liu,Dan Chen,Yunqi Xu,Jinchi Liao,Beisha Tang,Zhuohua Zhang,Xiang Cai, 来源:第四届全国痴呆与认知障碍学术研讨会 年份:2015
Purpose Recent evidence suggest that nerve growth factor IB(Nur77) and nuclear receptor related1(Nurr1) are differentially involved in dopaminergic neurodegeneration.Since memantinedisplayed a potent...
相关搜索: