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编号:10924654
细甘草甜素下调基质金属蛋白酶组织抑制因子-1基因的表达
http://www.100md.com 王巧侠,成 军,郭 江,李文凡,魏红山
甘草甜素;基质金属蛋白酶组织抑制因子-1;抗纤维化,王巧侠,,军,郭江,魏红山,,李文凡,王巧侠,通讯作者:,Glycyrrhizindo
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     王巧侠,兰州大学临床医学院 甘肃省兰州市 730000

    成军, 郭江, 魏红山,北京地坛医院传染病研究所 北京市 100011

    李文凡, 甘肃省人民医院消化科 甘肃省兰州市 730000

    王巧侠, 女, 1975-03-29生, 陕西省西安市人, 汉族, 住院医师, 兰州大学2003级传染病学硕士研究生, 主要从事慢性肝脏疾病发病机制的研究.

    国家自然科学基金攻关项目,No. C03011402,No. C30070689

    军队九五科技攻关项目,No. 98D063

    军队回国留学人员启动基金项目,No. 98H038

    军队十五科技攻关青年基金项目,No. 01Q138

    军队十五科技攻关面上项目,No. 01MB135

    通讯作者:成军, 100011, 北京市东城区安外大街地坛公园13号, 北京地坛医院传染病研究所. cj@genetherapy.com.cn

    电话:010-64481639 传真:010-64281540

    收稿日期:2005-07-05 接受日期:2005-07-08

    Glycyrrhizin down-regulates expression of tissue inhibitor of metalloproteinases-1

    Qiao-Xia Wang, Jun Cheng, Jiang Guo, Wen-Fan Li, Hong-Shan Wei

    Qiao-Xia Wang, Lanzhou University, Lanzhou 730000, Gansu Province, China

    Jun Cheng, Jiang Guo, Hong-Shan Wei, Institute of Infectious Diseases, Ditan Hospital, Beijing 100011, China

    Wen-Fan Li, Department of Gastroenterology, The People’s Hospital of Gansu Province, Lanzhou 730000, Gansu Province, China

    Supported by National Natural Science Foundation, No. C03011402, No. C30070689; Returned Scholarship of General Logistics Department of Chinese PLA, No. 98H038; the Key Technology Research and Development Program of Chinese PLA during the 9th Five-Year Plan Period, No. 98D063; the Key Technology Research and Development Program of Chinese PLA for Distinguished Young Scholars during the 10th Five-Year Plan Period, No. 01Q138; and the Scientific Research Program of Chinese PLA during the 10th Five-Year Plan Period, No. 01MB135

    Correspondence to: Dr. Jun Cheng, Anwai Street, Dongcheng District, Institute of Infectious Diseases, 13 Ditan Park, Ditan Hospital, Beijing 100011, China. cj@genetherapy.com.cn

    Received: 2005-07-05 Accepted: 2005-07-08

    Abstract

    AIM: To investigate the regulatory effect of glycyrrhizin on the tissue inhibitor of metalloproteinases-1(TIMP-1) expression and to explore its anti-fibrosis mechanism ......

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