RETINAL CELL REMODELING UTILIZING ADVANCED IMAGING TECHNOLOGY

利用先进成像技术重塑视网膜细胞

• 批准号: 8169644
• 负责人: Steven A. Fisher
• 金额: $ 2.39万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-01 至 2011-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8169644
• 关键词: Biological Assay; Cells; Cellular biology; Computer Retrieval of Information on Scientific Projects Database; Family Felidae; Funding; Goals; Grant; Imaging technology; Institution; Photoreceptors; Presynaptic Terminals; Research; Research Personnel; Resources; Retina; Retinal; Retinal Detachment; Series; Source; Synaptic plasticity; Tissues; United States National Institutes of Health; image processing; novel

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This project represents a series of related collaborative projects on retina cell biology. Our overall goal is to provide reconstructed volumes of retinal tissue, emphasizing photoreceptor synaptic terminals in a novel study of photoreceptor synaptic plasticity. The NCMIR researchers will use their image processing schema to assay the structural correlates of changes in feline photoreceptor synaptic terminals after retinal detachment and reattachment.

该子项目是利用该技术的众多研究子项目之一 资源由 NIH/NCRR 资助的中心拨款提供。子项目及 研究者 (PI) 可能已从 NIH 的另一个来源获得主要资金， 因此可以在其他 CRISP 条目中表示。列出的机构是 对于中心来说，它不一定是研究者的机构。 该项目代表了视网膜细胞生物学的一系列相关合作项目。我们的总体目标是提供视网膜组织的重建体积，在光感受器突触可塑性的新颖研究中强调光感受器突触末端。 NCMIR 研究人员将使用他们的图像处理模式来分析视网膜脱离和重新附着后猫科动物感光器突触末端变化的结构相关性。