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上海交通大学医学院研究生导师简介 王学锋

上海交通大学 免费考研网/2013-01-10

基本信息
导师姓名: 王学锋 专业代码: 100208
性别: 专业名称: 临床检验诊断学
培养单位: 瑞金医院 三级学科/
专业领域:
未设
导师类型: 博士生导师 专业学位导师:
联系方式: wangxuefeng6336@hotmail.com 上海瑞金二路197号
研究方向 (点击浏览详细信息)
出血病与血栓病诊治,临床输血
社会任职
中国医师协会输血分会副会长
中华医学会血液学会血栓与止血学组副组长
中华医学会检验分会血液学和体液学专家委员会副主任
中国输血协会理事
全国临床输血委员会常务委员
科研项目
项目编号项目名称课题来源起止时间科研经费承担职责
30870942凝血因子Ⅷ His99Arg突变蛋白的分子发病机制研究国家自然基金委,面上项目2009-01~~2011-1233万元null
学术论文 (#为通讯作者,*为共同第一作者)

1、Xue-Feng Wang*, Pei-Pei Jin, Tong Zhou, Ya-Peng Zhao, Qiu-Lan Ding, Deng-Bin Wang,Guang-Ming Zhao,Jing-Dai,Hong-Li Wang, and Hai-Liang. MR Molecular Imaging of Thrombus:Development and Application of a Gd-based Novel Contrast Agent Targeting to P-selectin. Clinical and Applied Thrombosis/Hemostasis,2010;16(2):177-183
2、Wang X*, Lu Y,Ding Q,Dai J,Xi X,Wang H. Haemophilia A in two unrelated females due to F8 gene inversions combined with skewed inactivation of X chromosome. THROMBOSIS AND HAEMOSTASIS,2009;101: 775-778
3、 H. CHEN, X. WANG*, X. SU, F. YANG, Y. LU, G. XU, J. DAI, Q. DING, X. XI and H. WANG. Identification of a novel splicing mutation in the fibrinogen Aa chain gene leading to in a Chinese pedigree. HAEMOPHILIA,2009;15:394-397
4、 H. CHEN, X. WANG*, X. SU, F. YANG, Y. LU, G. XU, J. DAI, Q. DING, X. XI and H. WANG. Identification of a novel splicing mutation in the fibrinogen Aa chain gene leading to in a Chinese pedigree. HAEMOPHILIA,2009;15:394-397
5、T. YU,X. WANG*, Q. DING, Q. FU, J. DAI,Y. LU, X. XI and H. WANG . Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree. HAEMOPHILIA,2009;15, 1262–1266
6、JING WANG, XUEFENG WANG *, JING DAI, QIULAN DING, QIHUA FU, HONGLI WANG,LISONG SHEN and DAO LI. A case of factor XI deficiency caused by compound heterozygous F11 gene mutation. HAEMOPHILIA,2009; 15, 603–606
7、PEI-PEI JIN, XUE-FENG WANG.QIU-LAN DING*,QI-HUA FU, XIAO-HONG CAI, LI-SONG SHEN AND HONG-LI WANGWANG,LISONG SHEN and DAO LI. Ser234Leu missense mutation in the A 1 domain of factor V causing moderate faxtor V deficiency in a Chinese family mutation. Pathology,2009;41(6):566-571
8、Yeling Lu,Xuefeng Wang*, Qiulan Ding,Jing Dai,Xiaodong Xi,Hongli Wang. Recombination in a Chinese haemophilia A familywith skewed inactivation of X chromosome. PATHOLOGY,2008;40: 635-638
9、Xiaohong Cai,Xuefeng Wang*,Qiulan Ding,Qihua Fu,Hongli Wang. Factor V C1149G and 5609-10INSCGTGGTT causing factor V deficiency: Molecular characterization by in-vitro expression. THROMBOSIS AND HAEMOSTASIS,2007;98: 683-685


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