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[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...
Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a exp
[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
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A common intronic variant in WDFY4 results in decreased allele-specific transcription through bindin
[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
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Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a exp
[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
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[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...
ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized lo
[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...
Homozygosity Mapping and Whole Exome Sequencing Identify Mutation in TMEM132E gene causing Nonsyndro
[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
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ErythroidKrüppel-like factor mutations are relatively morecommon in a thalassemia endemic region and
[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...
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