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find Author "李光辉" 3 results
  • The Interpretation of Guidelines for the Management of Candidiasis from Infectious Diseases Society of America 2009

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  • AN INVESTIGATION OF APPROACHES OF TRANSPLANTAITION OF RETINAL PIGMENT EPITHELIUM

    PURPOSE:To investigate the approaches for transplanting retinal pigment epithelium. METHODS,Retinal pigment epithelial eells(RPR)of pigmented rabbits' eyes prepared by rotalne preparation of our institute,were transphmted in 18 unpigmemed rabbits'eyes.Eight eyes were undergone outer approach, i.e., transplanting the RPR cells to the subretinal space of recipient eyes by way of perforating sclera and choroid;while 10 eyes were undergone internal approach by way of the routine procedure of vitrectomy with making artificial localized retinal delachment. Light and transmisskm electrone microscopy examination were done at 10th, goth, 40th and 90th day after the operation. RESULTS: In internal approach group,tbe operated eyes,revealed no difference in thickness of the neural retinal layer in transplanted and non-transplanted area 40 days after operation tinder light microscope. Transmission electrone microscopy revealed postoperatively the transplanted RPE cells attached to the Brucb's membrane and the outer segments of photoreeeplive ceils located at a normal position at the 40th dayland the secondary lysozymes with engulfed outer segment were found in the Iransplamed cells at the 90th day. Tbe outer approached operations in eight eyes were failed owing to ehoroid hemorrhage or perforation of retina. CONCLUSION:The internal appraach procedure is much effebtive and practical for transplantation of RPE cells. (Chin J Ocul Fundus Dis,1997,13:160-162)

    Release date:2016-09-02 06:12 Export PDF Favorites Scan
  • 腺相关病毒载体在视网膜色素变性基因治疗中的应用研究进展

    基因治疗是视网膜色素变性(RP)治疗研究的热点之一。经动物实验及临床试验证实, 腺相关病毒(AAV)载体因其无致病性、宿主范围广、转染和表达效率高、目的基因长期表达等优点成为视网膜疾病基因治疗的重要载体。但如何建立安全有效的基因治疗导入系统是目前临床需要首要解决的问题。此外, 由于基因的导向性和表达的调控性较为局限, 也限制了AAV载体介导的基因治疗在临床的广泛应用。进一步深入研究AAV的病毒生物学基础, 设计更多的组织特异性启动子以提高AAV载体的转染效率、靶向能力和安全性将为RP基因治疗带来新的曙光。

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