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[期刊论文] 作者:Li Xiaoyang,Gao Pengfei,Sun Fuqiang,, 来源:Chinese Journal of Aeronautics 年份:2015
Lognormal distribution is commonly used in engineering.It is also a life distribution of important research values.For long-life products follow this distributi...
[会议论文] 作者:Wenjing Gan,Xiaoyang Gao,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
[会议论文] 作者:Xiaoyang Gao,Long Li,Guohua Wu, 来源:第六届上海国际分析化学研讨会 年份:2012
Changes in haemolymph ion concentration might represent a source of information to alter the physiological function of many tissues surrounded by the environment,since the haemolymph is the direct ext...
[会议论文] 作者:Wenjing Gan,Xiaoyang Gao,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
Pre-mRNA splicing is a key regulatory step of eukaryotic gene expression.The splicing machinery consists of five RNA-protein complexes named small nuclear ribonucleoprotein particles (snRNPs) (U 1, U2...
[会议论文] 作者:Guotai Zhou,Xiaoyang Gao,Kang Wang,Jin Peng,Xiaoshan Wu, 来源:中国晶体学会第六届学术年会暨会员代表大会 年份:2016
[会议论文] 作者:Zhiyi Cai,Shandong Li,Xiaoqin Cao,Qian Xue,Honglei Du,Xiaoyang Gao,Shiming Xie, 来源:International Conference on Nanoscience & Technology,China 2 年份:2013
Nanocrystalline (Co2FeA1)1-x(Al2O3)x soft magnetic thin films with variable large in-plane uniaxial magnetic anisotropy were prepared by an oblique sputtering, without using the field induced method o...
[会议论文] 作者:Xiaoqin Cao,Shandong Li,Zhiyi Cai,Honglei Du,Qian Xue,Xiaoyang Gao,Shiming Xie, 来源:International Conference on Nanoscience & Technology,China 2 年份:2013
The fabrication and high-frequency ferromagnetic performances of Co2FeSi Heusler alloy films were investigated.The Co2FeSi films were deposited on Si (100) single crystal substrates by the composition...
[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...
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