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增生性玻璃体视网膜病变基因治疗的研究进展 被引量：1

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摘要 随着分子生物学的发展,应用基因转移技术治疗PVR已成为可能。本文对PVR的发病机制、PVR基因治疗的理论基础以及PVR基因治疗的方法和前景进行综述。
作者 张陶然 吴雅臻
机构地区 吉林大学第二医院眼科
出处 《国外医学（眼科学分册）》 2004年第3期208-211,共4页 Foreign Medical Sciences(Section of Ophthalmology )
关键词 增生性玻璃体视网膜病变 基因治疗 研究进展 发病机制
分类号 R774.1 [医药卫生—眼科]
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  • 2La Heij EC, vande Waarenburg MP, Blaauwgeers HG, et al. Basic fibroblast growth factor, glutamine synthetase, and interleukin6 in vitreous fluid from eyes with retinal detachment complicated by proliferative vitreoretinopathy. Am J Ophthalmol, 2002,134 (3
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  • 4Stocks SZ, Taylor SM, Shiels IA, et al. Transforming growth factor-betal induces alpha-smooth muscle actin expression end fibronectin synthesis in cultured human retinal pigment epithelial cells. Clin Exp Ophthalmol, 2001,29(1) :33-37.
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  • 7Guidry C, McFarland RJ, Morris R, et al. Collagen gel contraction by cells associated with proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci, 1992,33(8) :2429-2435.
  • 8Jin M, He S, Worpel V, et al. Promotion of adhesion and migration of RPE cells to provisional extracellular matrices by TNF-alpha. Invest Ophthalmol Vis Sci, 2000,41(13) :4324-4332.
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国外医学（眼科学分册）
2004年 第3期

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