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[会议论文] 作者：Xiangmin Xu,
来源：第九届海内外华人神经科学家研讨会(The 9th Symposium for Chinese Neuroscientis 年份：2016
The hippocampal formation is traditionally viewed as having a feed-forward,unidirectional circuit organization which promotes propagation of excitatory processes.While the substantial forward projecti...
Petrogenetic Evolution of the Bayan Gol Ophiolite-- Geological Record of an Early Carboniferous &quo
[期刊论文] 作者：Xia Linqi,LI XiangMin,Xu Xueyi,
来源：黑龙江科技学院学报 年份：2005
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7...
Petrogenetic Evolution of the Bayan Gol Ophiolite-- Geological Record of an Early Carboniferous “Red
[期刊论文] 作者：Xia Linqi,LI XiangMin,Xu Xueyi,
来源：地质学报（英文版） 年份：2004
The Bayan Gol ophiolite fragment is a portion of the North Tianshan Early Carboniferous ophiolite belt. This ophiolite belt represents a geological record of an...
Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelog
[期刊论文] 作者：Ting Lu,Meiyi Li,Xiangmin Xu,J,
来源：国际口腔科学杂志:英文版 年份：2018
Tooth development is a complex process that involves precise and time-dependent orchestration of multiple genetic,molecular,and cellular interactions.Ameloblast...
A New Pipeline Based on Target Capture Deep Sequencing Accurately Identifies Variants of a and β Glo
[会议论文] 作者：Qiuxia Yu,Yuhua Ye,Haoli Li,Xiangmin Xu,
来源：第十四次全国医学遗传学学术会议 年份：2015
Objective: Thalassemia is one of the most common monogenic disorders worldwide and it is most prevalent hemoglobinopathy in Southern China.Accurate detectin...
A New Pipeline Based on Target Capture Deep Sequencing Accurately Identifies Variants of a and β Glo
[会议论文] 作者：Qiuxia Yu,Yuhua Ye,Haoli Li,Xiangmin Xu,
来源：第十四次全国医学遗传学学术会议 年份：2015
Objective: Thalassemia is one of the most common monogenic disorders worldwide and it is most prevalent hemoglobinopathy in Southern China.Accurate detecting disease-causing variants is the basic step...
[会议论文] 作者：Li Xiangmin,Xu Qingfeng,李向民,许清风,
来源：2012既有建筑绿色化改造关键技术研究与示范项目交流会 年份：2012
本文共进行了7根木梁粘贴CFRP板加固的对比试验研究,其中3根为对比试件,4根为粘贴CFRP片加固木梁试件.研究结果表明,粘贴CFRP板加固木梁的极限承载力有明显提高,提高幅度...
Numerical simulation of the soliton solutions for a complex modified Korteweg-de Vries equation by a
[期刊论文] 作者：Tao Xu,Guowei Zhang,Liqun Wang,Xiangmin Xu,Min Li,
来源：理论物理通讯（英文版） 年份：2021
In this paper,a Crank-Nicolson-type finite difference method is proposed for computing the soliton solutions of a complex modified Korteweg-de Vries(MKdV)equati...
[会议论文] 作者：Yuhua Ye,Yidan Liang,Lingling Hu,Qiuxia Yu,Haoli Li,Xiangmin Xu,Zhenhai Zhang,
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：Yuhua Ye,Yidan Liang,Lingling Hu,Qiuxia Yu,Haoli Li,Zhenhai Zhang,Xiangmin Xu,
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
Upstream open reading frame(uORF) is one of the post-transcriptional regulatory elements in the 5UTR, which modulates the translation levels of its downstream main coding sequence, namely main ORF(mOR...
Compound heterozygosity for KLF1 mutations associated with microcytic hypochromic anemia and remarka
[会议论文] 作者：Jiwei Huang,Dun Liu,Xiaofeng Wei,Xuan Shang,Fu Xiong,Lihua Yu,Xiangmin Xu,Xinhua Zhang,Xiaolin Yin,
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
...
Compound heterozygosity for KLF1 mutations associated with microcytic hypochromic anemia and remarka
[会议论文] 作者：Jiwei Huang,Xinhua Zhang,Dun Liu,Xiaofeng Wei,Xuan Shang,Fu Xiong,Lihua Yu,Xiaolin Yin,Xiangmin Xu,
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
KLF 1 regulates erythroid lineage commitment, globin switching, and the terminal maturation of red blood cells.Variants in human KLF1 are identified as an important causative factor that produces a wi...
Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalasse
[会议论文] 作者：Lingling Hu,Xuan Shang,Sheng Yi,Ren Cai,Zhetao Li,Cuixian Liu,Yidan Liang,Decheng Cai,Feng Zhang,Xiangmin Xu,
来源：The 2nd International Symposium on Erythrocyte Biology(2016第 年份：2016
Copy number variations (CNVs) can cause many genetic disorders and the structure analysis of unknown CNVs is important for clinical diagnosis.The human α-globin gene cluster lies close to the telomere...
Analyses of GATA4,NKX2.5 and TFAP2B genes in subjects from southern China with sporadic congenital h
[会议论文] 作者：Fu Xiong,Xuan Shang,Xiangmin Xu,Qian Li,Cuimei Zhang,Youming Chen,Ping Li,Xiaofeng Wei,Qiang Li,Wanjun,
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
Background:Congenital heart disease(CHD)is the most common birth defect in newborns in southern China.The germline mutations in GATA4,NKX2.5 and TFAP2B genes have been identified to be responsible for...
[期刊论文] 作者：Hong Yang,Feng Xiong,Yi-Ge Song,Hai-Fei Jiang,Hai-Bin Qin,Jing Zhou,Sha Lu,Steven F.Grieco,Xiangmin Xu,
来源：神经科学通报（英文版） 年份：2021
Anterograde viral tracers are powerful and essential tools for dissecting the output targets of a brain region of interest.They have been developed from herpes...
[会议论文] 作者：Dun Liu,Lihua Yu,Xiaoxia Ma,Xiaofeng Wei,Li Lin,Jiwei Huang,Xiangmin Xu,Xinhua Zhang,Ren Cai,Tizhen Yan,
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：Chengguang Zheng,Yuqiu Zhou,Qiji Liu,Xiaofeng Wei,Li Lin,Tizhen Yan,Jiwei Huang,Narla Mohandas,Xiuli An,Xiangmin Xu,
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...
Multiple STEAP3 loss-of-function heterozygous mutations identified in the Chinese population with no
[会议论文] 作者：Cai,Yuhua Ye,Yuqiu Zhou,Yunhao Liang,Feng Cheng,Xuelian Zhang,Wanjun Zhou,Narla Mohandas,Xiuli An,Xiangmin Xu,
来源：第十四次全国医学遗传学学术会议 年份：2015
A ferrireductase encoded by six-transmembrane epithelial antigen of the prostate 3 (STEAP3) has been implicated in the regulation of iron homeostasis.STEAP3 null mice exhibit congenital hypochromic an...
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