搜索筛选:
搜索耗时0.0806秒,为你在为你在102,285,761篇论文里面共找到 10 篇相符的论文内容
类      型:
[期刊论文] 作者:Qin Hu,Panpan Hao,Qiji Liu,Mei, 来源:中国科学:生命科学英文版 年份:2019
Epidemiological research has revealed a galaxy of biomarkers, such as genes, molecules or traits, which are associated with increased risk of atherosclerotic ca...
[会议论文] 作者:Xiaohan Zhao,Baichun Jiang,Huili Hu,Fei Mao,Jun Mi,Zhaohui Li,Qiji Liu,Changshun Shao,Yaoqin Gong, 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:Hailing Zhao,Wangling Yang,Rongfang Qiu,Jiangxia Li,Qian Xin,Xue Wang,Yapei Feng,Yaoqin Gong,Qiji Liu, 来源:2012年中国青年遗传学家论坛 年份:2012
[会议论文] 作者:Xiaohan Zhao,Baichun Jiang,Huili Hu,Fei Mao,Jun Mi,Zhaohui Li,Qiji Liu,Changshun Shao,Yaoqin Gong, 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
CUL4A and CUL4B are closely related cullin family members and can each assemble a CulIin-R1NG E3 ligase complex (CRL) and participate in a variety of biological processes.While the CRLs formed by the...
[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:Xiaochun Ma,Rongfang Qiu,Jie Dang,Jiangxia Li,Shan Shan,Qian Xin,Xianli Bian,Chengwei Zou,Yaoqin Gong,Qiji Liu, 来源:第十四次全国医学遗传学学术会议 年份:2015
ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) is a universally confirmed susceptibility gene for asthma and has recently emerged as a crucial modulator in lipid metabolism, inflammation and end...
[会议论文] 作者:Jiangxia Li,Yaoqin Gong,Qiji Liu,Xiaohan Zhao,Qian Xin,Shan Shan,Baichun Jiang,Rongfang Qiu,Hailing Zhao, 来源:中华医学会2012年医学遗传学年会暨全国第十一次医学遗传学学术会议 年份:2012
In this report,we identified a homozygous missense mutation in a novel gene,TMEM132E (transmembrane protein 132E),in a chinese consanguineous family with nonsyndromic hearing loss using whole exome se...
[会议论文] 作者:Xiaofeng Wei,Li Lin,Jiwei Huang,Xiangmin Xu,Xinhua Zhang,Ren Cai,Tizhen Yan,Chengguang Zheng,Yuqiu Zhou,Qiji Liu, 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:Dun Liu,Xinhua Zhang,Lihua Yu,Ren Cai,Xiaoxia Ma,Chengguang Zheng,Yuqiu Zhou,Qiji Liu,Xiaofeng Wei,Li, 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 human Krǖppel-like factor 1 (KLF1) have recently been reported to be responsible for increased fetal hemoglobin (HbF) and hemoglobin A2 (HbA2).As increased HbF and HbA2 levels are importa...
相关搜索: