• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Gene therapy: new "magic bullets" to prevent ocular scarring.

作者信息

Khaw P T, Cambrey A D, Limb G A, Daniels J T

出版信息

Br J Ophthalmol. 2002 May;86(5):490-2. doi: 10.1136/bjo.86.5.490.

DOI:10.1136/bjo.86.5.490
PMID:11973239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1771119/
Abstract
摘要

相似文献

1
Gene therapy: new "magic bullets" to prevent ocular scarring.基因疗法:预防眼部瘢痕形成的新型“神奇子弹”
Br J Ophthalmol. 2002 May;86(5):490-2. doi: 10.1136/bjo.86.5.490.
2
Ocular Gene Therapy-The Future Is Now.
Asia Pac J Ophthalmol (Phila). 2016 Jul-Aug;5(4):227-8. doi: 10.1097/APO.0000000000000216.
3
Gene Therapy for Blinding Pediatric Eye Disorders.用于致盲性小儿眼部疾病的基因治疗
Adv Pediatr. 2015 Aug;62(1):185-210. doi: 10.1016/j.yapd.2015.04.012.
4
Herpes simplex viral vectors for therapeutic gene delivery to ocular tissues. Recent breakthroughs in the molecular genetics of ocular diseases.用于将治疗性基因递送至眼组织的单纯疱疹病毒载体。眼部疾病分子遗传学的最新突破。
Invest Ophthalmol Vis Sci. 1994 May;35(6):2662-6.
5
Ocular drug delivery: molecules, cells, and genes.眼部药物递送:分子、细胞与基因
Can J Ophthalmol. 2007 Jun;42(3):447-54.
6
Nonviral ocular gene therapy: assessment and future directions.非病毒眼部基因治疗:评估与未来方向。
Curr Opin Mol Ther. 2008 Oct;10(5):456-63.
7
Development of viral vectors with optimal transgene expression for ocular gene therapies.用于眼部基因治疗的具有最佳转基因表达的病毒载体的开发。
Adv Exp Med Biol. 2008;613:113-9. doi: 10.1007/978-0-387-74904-4_12.
8
Controlling vascular endothelial growth factor: therapies for ocular diseases associated with neovascularization.控制血管内皮生长因子:治疗与新生血管形成相关的眼部疾病
Adv Exp Med Biol. 2006;572:303-7. doi: 10.1007/0-387-32442-9_42.
9
Seeing eye to eye with gene therapy.对基因治疗达成一致看法。
Mol Ther. 2012 Apr;20(4):687-8. doi: 10.1038/mt.2012.43.
10
The Ocular Gene Delivery Landscape.眼基因传递领域。
Biomolecules. 2021 Aug 1;11(8):1135. doi: 10.3390/biom11081135.

引用本文的文献

1
[Macular hole surgery with air tamponade. Does air suffice for short-term tamponade?].[黄斑裂孔手术联合空气填塞。空气用于短期填塞是否足够?]
Ophthalmologe. 2010 Nov;107(11):1043-50. doi: 10.1007/s00347-010-2171-2.

本文引用的文献

1
Cystic bleb formation and related complications in limbus- versus fornix-based conjunctival flaps in pediatric and young adult trabeculectomy with mitomycin C.在小儿及年轻成人丝裂霉素C小梁切除术中,基于角膜缘与穹窿的结膜瓣的囊肿形成及相关并发症
Ophthalmology. 2003 Nov;110(11):2192-7. doi: 10.1016/S0161-6420(03)00800-5.
2
Human antitransforming growth factor beta(2) monoclonal antibody--a new modulator of wound healing in trabeculectomy: a randomized placebo controlled clinical study.人抗转化生长因子β(2)单克隆抗体——小梁切除术中伤口愈合的新型调节剂:一项随机安慰剂对照临床研究
Ophthalmology. 2002 Mar;109(3):427-31. doi: 10.1016/s0161-6420(01)00997-6.
3
Adenoviral-mediated gene transfer to the filtering bleb in rabbits.
J Glaucoma. 2001 Dec;10(6):470-6. doi: 10.1097/00061198-200112000-00006.
4
Adjuvant 5-fluorouracil and heparin prevents proliferative vitreoretinopathy : Results from a randomized, double-blind, controlled clinical trial.辅助性5-氟尿嘧啶和肝素预防增殖性玻璃体视网膜病变:一项随机、双盲、对照临床试验的结果
Ophthalmology. 2001 Jul;108(7):1179-83. doi: 10.1016/s0161-6420(01)00589-9.
5
The Advanced Glaucoma Intervention Study (AGIS): 7. The relationship between control of intraocular pressure and visual field deterioration.The AGIS Investigators.高级青光眼干预研究(AGIS):7. 眼压控制与视野恶化之间的关系。AGIS研究人员。
Am J Ophthalmol. 2000 Oct;130(4):429-40. doi: 10.1016/s0002-9394(00)00538-9.
6
Peripheral infection with adenovirus causes unexpected long-term brain inflammation in animals injected intracranially with first-generation, but not with high-capacity, adenovirus vectors: toward realistic long-term neurological gene therapy for chronic diseases.用第一代腺病毒载体而非高容量腺病毒载体颅内注射动物后,腺病毒的外周感染会导致意外的长期脑部炎症:迈向针对慢性疾病的现实的长期神经基因治疗。
Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7482-7. doi: 10.1073/pnas.120474397.
7
Lentiviral vectors: turning a deadly foe into a therapeutic agent.慢病毒载体:将致命敌人转化为治疗剂。
Gene Ther. 2000 Jan;7(1):20-3. doi: 10.1038/sj.gt.3301105.
8
Human anti-transforming growth factor-beta2 antibody: a new glaucoma anti-scarring agent.人抗转化生长因子-β2抗体:一种新型青光眼抗瘢痕形成药物。
Invest Ophthalmol Vis Sci. 1999 Sep;40(10):2225-34.
9
Gene therapy: into the future of surgery.基因治疗:迈向外科手术的未来。
Lancet. 1999 Apr;353 Suppl 1:SI19-20. doi: 10.1016/s0140-6736(99)90224-6.
10
Effects of single, short-term exposures of human retinal pigment epithelial cells to thiotepa or 5-fluorouracil: implications for the treatment of proliferative vitreoretinopathy.硫替派或5-氟尿嘧啶单次短期暴露于人视网膜色素上皮细胞的影响:对增殖性玻璃体视网膜病变治疗的意义
Br J Ophthalmol. 1998 May;82(5):554-60. doi: 10.1136/bjo.82.5.554.