P30 Center Core Grant for Vision Research

P30 中心视觉研究核心资助

基本信息

项目摘要

ABSTRACT Animal Analysis Core Vision research requires the use of various animal models to investigate the mechanisms of visual development and degeneration, the pathogenesis of blinding infection and inflammation, and the efficacy of vision-saving therapeutics. The Live Animal Imaging and Functional Analysis Core at the University of Oklahoma Health Sciences Center is responsible for providing vision researchers with state-of-the-art instrumentation in the physiology and function of vision in small animal models of development, degeneration, infection, and inflammation. These Cores support vision research on 16 NEI-funded R01 grants and other vision-related projects at OUHSC in two different locations within vivaria, which allows in/out privileges. More than 40 ocular disease models and more than 70 genetically altered mouse lines are currently being analyzed with electrophysiological, genotyping, functional analysis, microscopy, and other support equipment in expanded research areas renovated specifically for this use. The instrumentation provided by this Core includes electroretinography (in vivo and ex vivo), optical coherence tomography, fundoscopy, optokinetics, laser photocoagulation, tonometry, indirect ophthalmoscopy, and slit lamp and biomicroscopic imaging. Environmental housing also includes equipment for light damage, dark rearing, hypoxia/hyperoxia, controlled humidity, and glaucoma models. Genotyping provides accurate data for breeding transgenic animals for vision research. Our Systems Managers are highly skilled in training personnel, assisting with experiments and data analysis, and maintaining core equipment to a quality standard. As such, this Core consolidates and provides instrumentation and expertise which would otherwise be too expensive or logistically difficult for vision researchers across campus to easily access. As in the previous funding period, this Core is motivated and committed to providing an effective, efficient, user-friendly, and high-quality research environment for all vision researchers at OUHSC.

项目成果

期刊论文数量(0)
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专利数量(0)

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Raju VS Rajala其他文献

Raju VS Rajala的其他文献

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{{ truncateString('Raju VS Rajala', 18)}}的其他基金

Regulators of Photoreceptor Aerobic Glycolysis in Retinal Health and Disease
视网膜健康和疾病中光感受器有氧糖酵解的调节因子
  • 批准号:
    10717825
  • 财政年份:
    2023
  • 资助金额:
    $ 29.49万
  • 项目类别:
Neuroprotection Mechanism for Photoreceptors
光感受器的神经保护机制
  • 批准号:
    10428577
  • 财政年份:
    2019
  • 资助金额:
    $ 29.49万
  • 项目类别:
Neuroprotection Mechanism for Photoreceptors
光感受器的神经保护机制
  • 批准号:
    10183260
  • 财政年份:
    2019
  • 资助金额:
    $ 29.49万
  • 项目类别:
Neuroprotection Mechanism for Photoreceptors
光感受器的神经保护机制
  • 批准号:
    10006824
  • 财政年份:
    2019
  • 资助金额:
    $ 29.49万
  • 项目类别:
Mechanistic studies on obesity-deteriorated glucose and lipid metabolisms
肥胖导致糖脂代谢恶化的机制研究
  • 批准号:
    8874215
  • 财政年份:
    2013
  • 资助金额:
    $ 29.49万
  • 项目类别:
P30 Center Core Grant for Vision Research
P30 中心视觉研究核心资助
  • 批准号:
    10272005
  • 财政年份:
    2011
  • 资助金额:
    $ 29.49万
  • 项目类别:
P30 Center Core Grant for Vision Research
P30 中心视觉研究核心资助
  • 批准号:
    10696213
  • 财政年份:
    2011
  • 资助金额:
    $ 29.49万
  • 项目类别:
COBRE: INSULIN RECEPTOR SIGNALING IN DIABETIC RETINOPATHY
COBRE:糖尿病视网膜病变中的胰岛素受体信号传导
  • 批准号:
    7720534
  • 财政年份:
    2008
  • 资助金额:
    $ 29.49万
  • 项目类别:
COBRE: INSULIN RECEPTOR SIGNALING IN DIABETIC RETINOPATHY
COBRE:糖尿病视网膜病变中的胰岛素受体信号传导
  • 批准号:
    7610500
  • 财政年份:
    2007
  • 资助金额:
    $ 29.49万
  • 项目类别:
COBRE: INSULIN RECEPTOR SIGNALING IN RETINA
COBRE:视网膜中的胰岛素受体信号传导
  • 批准号:
    7381939
  • 财政年份:
    2006
  • 资助金额:
    $ 29.49万
  • 项目类别:

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GUMC斑马鱼共享资源水生栖息地现代化项目
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揭开高致病性流感病毒出现的谜团
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感染史是阿尔茨海默病年龄相关炎症的决定因素
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