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Molecular Mechanisms of Lung Inflammation

Molecular Mechanisms of Lung Inflammation
肺部炎症的分子机制
批准号:
7595752
负责人:
Mark Damian Wewers
金额:
$24.19万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-30 至 2012-03-31

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项目成果

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中文摘要
翻译
描述(由申请人提供): 该计划的目的是培养博士后研究人员(3名博士)。(3 M.D.)培养技能,使他们成为成功的独立研究者,临床研究企业的未来领导者和下一代生物医学科学家的导师。重点将是连接免疫学,分子细胞生物学,基因组学和蛋白质组学之间的接口,以了解人类肺部疾病的病理生理学。NIH路线图倡议最近强调了这一培训计划的必要性,呼吁建立跨学科研究团队,以重新设计临床研究企业。将特别强调培训研究人员使用多学科方法来解决与肺部疾病的起源和治疗有关的基本问题。我们的培训教师是有目的地选择,以提供广泛的培训环境,跨越这个频谱,包括分子遗传学,免疫细胞功能,功能基因组学,肺上皮细胞功能,细胞信号,自由基生物学,线粒体生物学,肺和血管病理生理学。目的1.在分子生物学,免疫学,细胞信号,自由基生物学,蛋白质组学和功能基因组学方面提供足够的教学,互动和技术背景,使学员能够在这些学科之间轻松移动,并能够将他们的知识转化为对肺部疾病起源的进一步理解。目标2.开发一个创新的计划,确保学员迅速进入直接动手实验室的经验。目标3.使学员沉浸在创造性和积极的研究环境中,确保他们成功和保留的最大可能性。此外,还将提供研究伦理和哲学方面的具体培训,目的是培养具有最高水平的知识完整性的科学家。目标4.制定长期计划,鼓励妇女和少数民族从事肺部科学和研究事业,更重要的是在培训计划中建立足够的基础设施和支持系统,以确保有动力的受训者取得成功。
英文摘要
DESCRIPTION (provided by applicant): The purpose of this program is to train postdoctoral investigators (3 Ph.D. and 3 M.D.) to develop skills that will allow them to become successful independent investigators, future leaders in the clinical research enterprise and mentors for the next generation of biomedical scientists. The emphasis will be upon linking the interface between immunology, molecular cell biology, genomics, and proteomics to understand the pathophysiology of human pulmonary disease. The need for this training program was recently emphasized by the NIH Roadmap initiative, calling for building interdisciplinary research teams with the intent of re-engineering the clinical research enterprise. Particular emphasis will be placed upon training investigators to use multidisciplinary approaches in attacking fundamental problems related to origins and cures for lung disease. Our training faculty were purposefully selected to provide a wide range of training environments that cross this spectrum, including molecular genetics, immune cell function, functional genomics, lung epithelial cell function, cell signaling, free radical biology, mitochondrial biology, and lung and vascular pathophysiology. Objective 1. To provide sufficient didactic, interactive and technical background in molecular biology, immunology, cell signaling, free radical biology, proteomics, and functional genomics to allow trainees to be able to move easily between these disciplines and to be able to translate their knowledge into further understanding of the origins of pulmonary disease. Objective 2. To develop an innovative program which ensures that trainees move rapidly into direct hands-on laboratory experiences. Objective 3. To immerse the trainees in a creative and positive research environment, ensuring the greatest possibility for their success and retention. In addition, specific training will be provided in the ethics and philosophy of research with the intent of producing scientists who will operate at the highest levels of intellectual integrity. Objective 4. To develop long-range programs which encourage women and minorities to pursue careers in pulmonary science and research and more importantly to build sufficient infrastructure and support systems within the training program to ensure the success of the motivated trainee.
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会议论文
Regulation of lung host defense by inflammasome modifiers
  • 批准号:
    8048861
  • 项目类别:
  • 资助金额:
    $19.06万
  • 财政年份:
    2010
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
Regulation of lung host defense by inflammasome modifiers
  • 批准号:
    8204686
  • 项目类别:
  • 资助金额:
    $22.88万
  • 财政年份:
    2010
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
RIP2 caspase-1 signaling in macrophages
  • 批准号:
    7583471
  • 项目类别:
  • 资助金额:
    $37.5万
  • 财政年份:
    2009
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
RIP2 caspase-1 signaling in macrophages
  • 批准号:
    8024493
  • 项目类别:
  • 资助金额:
    $37.5万
  • 财政年份:
    2009
  • 负责人:
    Mark Damian Wewers
  • 依托单位:
国内基金
海外基金
Kidney injury molecular(KIM-1)介导肾小管上皮细胞自噬在糖尿病肾病肾间质纤维化中的作用
  • 批准号:
    81300605
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    23.0万元
  • 批准年份:
    2013
  • 负责人:
    唐琳
  • 依托单位:
Molecular Plant
Molecular Interaction Reconstruction of Rheumatoid Arthritis Therapies Using Clinical Data
Molecular Plant