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[会议论文] 作者:Shaobo Yang,Jiangtao Zhao,Pengfei Zong,Tieshan Wang, 来源:The 10th International Conference on Nucleus-Nucleus Collisi 年份:2009
[会议论文] 作者:Ailin Yang,Yanan Zhao,Pengfei Tu,Zhongdong Hu, 来源:第五届广州国际肿瘤学会议暨第一届中国抗癌协会肿瘤靶向治疗专业委员会年会 年份:2016
Background: Tuberous sclerosis complex(TSC)is a genetic disease with tumor formation in many different organs,including the brain,skin,heart,and kidney.TSC1 and TSC2 are tumor suppressor genes.Aberran...
[会议论文] 作者:Pengbo Zhang,Jijun Zhao,Pengfei Zheng,Jiming Chen, 来源:第13届中日双边先进能源系统和聚变裂变工程材料会议(CIS-13) 年份:2016
Fe-based alloys of bcc phase are considered as the promising structural materials in fusion reactor.Large amounts of H impurities are produced concurrently along with irradiation damage in the structu...
[会议论文] 作者:Xinmei Zhao,Pengfei Han,Ying Xiao,Wenjing Zhang,Y.James Kang, 来源:The 5th International Symposium on Metallomics(第五届金属组学国际研讨会) 年份:2015
  Depressed capillary density is associated with myocardial ischemic infarction,in which hypoxia-inducible factor 1α(HIF-1α)is increased....
[会议论文] 作者:Jun Zhang,Rui Su,Xiancheng Wang,Wenmin Li,Jianfa Zhao,Pengfei Guan,ChangqingJin, 来源:第26届国际高压科学技术大会、第8届亚洲高压科技学术会议暨第19届中国高压科学技术会议(The 26th Interna 年份:2017
In this work,a new one dimensional compound Ba9Sn3Te15 has been synthesized for the first time under high pressure and high temperature conditions....
[会议论文] 作者:Yali Jiang,Yuanyuan Wang,Junlong Zhao,Pengfei Ma,Shiqian Liang,Fei He,Liawei Liu,Hua Han,Hongyan Qin, 来源:The 1st NI-CMI Joint Conference(第一届CMI-NI免疫学国际研讨会) 年份:2015
Macrophage play critical roles in renal fibrosis, but the mechanisms of macrophages activation and function in renal fibrosis has not been fully understood.Literatures and our previous studies have sh...
[会议论文] 作者:Fei Mao,Zhaohui Li,Baoyue Zhao,Pengfei Lin,Pingting Liu,Meng Zhai,Qiji Liu,Changshun Shao,Wenjie Sun,, 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:Fei Mao,Zhaohui Li,Baoyue Zhao,Pengfei Lin,Pingting Liu,Meng Zhai,Qiji Liu,Changshun Shao,Wenjie Sun,, 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
While we previously reported heterozygous SLC33A1 p.Ser113Arg (c.339T>G) mutation as the cause for SPG42, hereditary spastic paraplegia (HSP) phenotype was recently reported to be absent in heterozygo...
[会议论文] 作者:Zhuoping Huo,Yinghong Wang,Zhizhong Ma,Shaoyang Zhao,Pengfei Tu,Ke Zhang,Xu Ma,Haixia Li,Shuyan Han,Yong, 来源:2013中国药学大会暨第十三届中国药师周 年份:2013
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