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编号:11581718
基因芯片技术检测西藏拉萨地区的乙型肝炎病毒基因型
http://www.100md.com 曹占良, 高英堂, 刘 霜, 景 丽, 吉 宗, 刘 彤, 刘持佳, 杜 智
乙型肝炎病毒;基因型;基因芯片;序列分析,曹占良,刘持佳,高英堂,景丽,刘彤,杜智,刘霜,吉宗,曹占良,通讯作者:,DetectionofHBVgenotypesinLhasabygenechip,Zhan-LiangCao,Chi-Jia
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     曹占良, 刘持佳, 武警医学院附属医院检验科 天津市 300162

    高英堂, 景丽, 刘彤, 杜智, 天津市第三中心医院 天津市人工细胞重点实验室 天津市 300170

    刘霜, 天津市人民医院检验科 天津市 300120

    吉宗, 武警西藏总队医院检验科 西藏自治区拉萨市 850000

    曹占良, 2002年第三军医大学本科毕业, 学士学位, 副主任技师. 主要从事免疫、生化检验工作.

    天津市科委攻关项目, No. 05YFSZSF02500

    武警医学院院级科研基金项目, No. WY2004-15

    通讯作者: 高英堂, 300170, 天津市河东区津塘路83号, 天津市第三中心医院. gaoyt816@163.com

    电话: 022-84112148

    收稿日期: 2007-08-09 修回日期: 2007-10-30

    Detection of HBV genotypes in Lhasa by gene chip

    Zhan-Liang Cao, Ying-Tang Gao, Shuang Liu, Li Jing, Zong Ji, Tong Liu, Chi-Jia Liu, Zhi Du

    Zhan-Liang Cao, Chi-Jia Liu, Department of Laboratory, Affiliated Hospital of Medical College of Chinese People′s Armed Police Force, Tianjin 300162, China

    Ying-Tang Gao, Li Jing, Tong Liu, Zhi Du, Artificial Cells Key Lab of Tianjin, Tianjin Third Central Hospital, Tianjin 300170, China

    Shuang Liu, Department of Laboratory, Tianjin People's Hospital, Tianjin 300120, China

    Zong Ji, Department of Laboratory, Tibet Corps Hospital of Chinese Armed Police Forces, Lhasa 850000, Tibet Autonomous Region, China

    Supported by: the Key Research Project of the Science Committee of Tianjin, No. 05YFSZSF02500; Science Foundation of Medical College of Chinese People′s Armed Police Force, No. WY2004-15

    Correspondence to: Dr. Ying-Tang Gao, Artificial Cells Key Lab of Tianjin, Tianjin Third Central Hospital, 83 Jintang Road, Hedong District, Tianjin 300170, China. gaoyt816@163.com

    Received: 2007-08-09 Revised: 2007-10-30

    

    Abstract


    AIM: To investigate the distribution and characteristics of HBV genotypes in Lhasa.

    METHODS: A total of 92 serum samples were collected from chronic hepatitis patients in Lhasa infected with HBV. Oligonucleotide probes were designed according to the DNA sequences from GenBank and used to prepare the genotyping chip. The fragments of HBV S gene were amplified using nested PCR ......

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