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[期刊论文] 作者:Wanli Yang,Ruimin Qiao, 来源:中国物理B(英文版) 年份:2016
[期刊论文] 作者:Cheng Yang,Ruimin Hu,Xiaochen, 来源:中国通信:英文版 年份:2017
[期刊论文] 作者:Yang Ruimin,Deng Mingqin,Xu En, 来源:中国油气:英文版 年份:2005
As one of the lagest enterprises in China,Zhongyuan Petroleum Exploration Bureau,Sinopec (ZPEB) has become a mediumsized onshore oilfield with its exploration a...
[期刊论文] 作者:Yang Ruimin,Deng Mingqin,Xu Enxin,Zhang Guangqin, 来源:中国油气(英文版) 年份:2005
As one of the lagest enterprises in China,Zhongyuan Petroleum Exploration Bureau,Sinopec (ZPEB) has become a mediumsized onshore oilfield with its exploration...
[会议论文] 作者:Darrell W..Brann,Quan-Guang Zhang,Fang Yang,Ruimin Wang, 来源:2011第二届国际神经科技大会 年份:2011
It is well known that gender differences exist in risk and outcome of ischemic stroke.In addition, surgical menopause (long term ovariectomy) is associated with an increased risk of Alzheimers disease...
[期刊论文] 作者:Cheng Yang,Ruimin Hu,Xiaochen Wang,Yuhong Yang,Maosheng Zhang,Wei Chen, 来源:中国通信(英文版) 年份:2017
A new three-dimensional (3D) au-dio coding approach is presented to improve the spatial perceptual quality of 3D audio. Dif-ferent from other audio coding appro...
[期刊论文] 作者:Hongfeng Zhang,Yujuan Hong,Weijie Yang,Ruimin Wang,Ting Yao,Jian Wang,Ke Liu,Huilong Yuan,Chaoqun Xu,, 来源:国家科学评论:英文版 年份:2021
Loss-of-function mutations in sorting nexin 14(SNX14)cause autosomal recessive spinocerebellar ataxia 20,which is a form of early-onset cerebellar ataxia that lacks molecular mechanisms and mouse models.We generated Snx14-deficient mouse mo......
[期刊论文] 作者:Yue Gao,Shicheng Fan,Hua Li,Yiming Jiang,Xinpeng Yao,Shuguang Zhu,Xiao Yang,Ruimin Wang,Jianing Tian,, 来源:药学学报(英文版) 年份:2021
The constitutive androstane receptor(CAR,NR3I1)belongs to nuclear receptor superfamily.It was reported that CAR agonist TCPOBOP induces hepatomegaly but the und...
[期刊论文] 作者:Hongfeng Zhang,Yujuan Hong,Weijie Yang,Ruimin Wang,Ting Yao,Jian Wang,Ke Liu,Huilong Yuan,Chaoqun Xu,, 来源:国家科学评论(英文版) 年份:2021
Loss-of-function mutations in sorting nexin 14(SNX14)cause autosomal recessive spinocerebellar ataxia 20,which is a form of early-onset cerebellar ataxia that lacks molecular mechanisms and mouse models.We generated Snx1 4-deficient mouse m......
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