2014 Cornea, Biology & Pathobiology Gordon Research Conference Gordon Research Se

2014 角膜,生物学

基本信息

  • 批准号:
    8641527
  • 负责人:
  • 金额:
    $ 3万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-01-01 至 2014-12-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): This proposal requests partial support for the third Gordon Research Conference (GRC) and the first Gordon Research Seminar (GRS) on Cornea, the Biology and Pathobiology of, in Ventura, California, February, 16-21 (GRC), and February 15 -16 (GRS) 2014. The broad and long-term goal of this Cornea-GRC & GRS is to reduce corneal blindness by fostering innovation in corneal research. Researchers and trainees will be brought together to exchange data and educate one another in a GRC format (about 165 attendees including 50-60 GRS attendees) that enables cross-disciplinary discussions and collaborations. As a result, it will improve our understanding of corneal biology and pathobiology and foster development of new treatment regimens for diseases causing corneal blindness. The theme of the third GRC: Cornea, Biology and Pathobiology will be cutting edge research examining the cell lineage and cell fate of ocular surface tissues, e.g., cornea, conjunctiva, eyelid, lacrimal glands, and Meibomian glands, during development and pathogenesis. Morpho- genesis of ocular surface tissues during development involves two major cellular events: 1. the migration and differentiation of particular mesenchymal cells of neural crest origin for the formation of ocular tissue stromal, 2. differentiation of surface ectoderm into ocular surface epithelia and glands. A better understanding of the molecular and cellular mechanisms governing the orderly migration and differentiation of cells during development will aid in the design of treatment regimens for the restoration of tissue function lost by eye disease. Invited speakers represent a variety of scientific disciplines, including molecular and cellular biology, molecular genetics, biochemistry, structural biology, imaging, tissue engineering, tissue reconstruction and clinical ophthalmology. The Conference will bring together a collection of investigators who are at the forefront of ocular surface biology, and will provide opportunities fo young investigators including graduate students, post docs and early career researchers to present their work and exchange ideas with leaders in the field. Some poster presenters will be selected for short talks in GRC. The collegial atmosphere of this Conference, with programmed discussion sessions as well as opportunities for informal gatherings in the afternoons and evenings, provides an avenue for scientists from different disciplines to brainstorm and promotes cross- disciplinary collaborations in the various research areas represented. The GRS is targeted for graduate students, post-docs, early-career scientists and young faculty providing unique forum for young investigators to discuss their work in a less intimidating environment, however, in a GRC setting. The principal topic of the GRS is The Future Directions of Corneal Research which aims to give the young investigators a notion of the new trends and new directions of cornea/ocular surface tissue research to help them design and plan their future line of research. Moreover, the meeting will have a unique Session on "How to Write a Competitive Grant" followed by an open floor discussion, which is a vital step in a young investigators career.
描述(由申请人提供):本提案要求部分支持2014年2月16日至21日(GRC)和2月15日至16日(GRS)在加利福尼亚州文图拉举行的第三届戈登研究会议(GRC)和第一届戈登角膜生物学和病理生物学研讨会(GRS)。角膜grc和GRS的长远目标是通过促进角膜研究的创新来减少角膜失明。研究人员和学员将聚集在一起,以GRC形式(约165名与会者,其中包括50-60名GRS与会者)交换数据并相互教育,从而实现跨学科讨论和合作。因此,它将提高我们对角膜生物学和病理生物学的理解,并促进角膜失明疾病的新治疗方案的发展。第三届GRC的主题是:角膜、生物学和病理生物学,将对角膜、结膜、眼睑、泪腺和睑板腺等眼表组织在发育和发病过程中的细胞谱系和细胞命运进行前沿研究。眼表组织在发育过程中的形态发生涉及两个主要的细胞事件:1。神经嵴源间充质细胞在眼组织间质形成中的迁移和分化;表外胚层向眼表上皮和腺体的分化。更好地了解发育过程中控制细胞有序迁移和分化的分子和细胞机制将有助于设计治疗方案,以恢复眼病所失去的组织功能。特邀讲者代表了各个学科,包括分子和细胞生物学、分子遗传学、生物化学、结构生物学、成像、组织工程、组织重建和临床眼科学。会议将汇集一批眼表生物学前沿的研究人员,并将为年轻的研究人员提供机会,包括研究生,博士后和早期职业研究人员,展示他们的工作并与该领域的领导者交流思想。我们将挑选一些海报演讲者在GRC做简短的演讲。本次会议的学术氛围,包括安排好的讨论环节,以及下午和晚上的非正式聚会,为来自不同学科的科学家提供了一个集思广益的途径,并促进了不同研究领域的跨学科合作。GRS的目标是研究生、博士后、早期职业科学家和年轻教师,为年轻的研究人员提供了一个独特的论坛,在一个不那么吓人的环境中讨论他们的工作。GRS的主要主题是角膜研究的未来方向,旨在为年轻的研究者提供角膜/眼表组织研究的新趋势和新方向的概念,以帮助他们设计和规划他们未来的研究方向。此外,会议将有一个独特的“如何写一个有竞争力的资助”的环节,然后是一个开放的讨论,这是一个年轻的研究人员职业生涯的重要一步。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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WINSTON W KAO其他文献

WINSTON W KAO的其他文献

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{{ truncateString('WINSTON W KAO', 18)}}的其他基金

Gene Therapy of Corneal Dystrophy: Lysosomal Storage Diseases
角膜营养不良的基因治疗:溶酶体贮积病
  • 批准号:
    10203999
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Gene Therapy of Corneal Dystrophy: Lysosomal Storage Diseases
角膜营养不良的基因治疗:溶酶体贮积病
  • 批准号:
    10018871
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Cell Therapy of Corneal Diseases with Umbilical Mesenchymal Stem Cells
脐带间充质干细胞治疗角膜疾病
  • 批准号:
    8531948
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:
Cell Therapy of Corneal Diseases with Umbilical Mesenchymal Stem Cells
脐带间充质干细胞治疗角膜疾病
  • 批准号:
    8328680
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:
Cell Therapy of Corneal Diseases with Umbilical Mesenchymal Stem Cells
脐带间充质干细胞治疗角膜疾病
  • 批准号:
    8536477
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:
Cell Therapy of Corneal Diseases with Umbilical Mesenchymal Stem Cells
脐带间充质干细胞治疗角膜疾病
  • 批准号:
    8159876
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:
Cell Therapy of Corneal Diseases with Umbilical Mesenchymal Stem Cells
脐带间充质干细胞治疗角膜疾病
  • 批准号:
    8722564
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:
Structure/Function Relationship of The Lumican Gene
Lumican基因的结构/功能关系
  • 批准号:
    7486855
  • 财政年份:
    2006
  • 资助金额:
    $ 3万
  • 项目类别:
Structure/Function Relationship of The Lumican Gene
Lumican基因的结构/功能关系
  • 批准号:
    7677302
  • 财政年份:
    2006
  • 资助金额:
    $ 3万
  • 项目类别:
Structure/Function Relationship of The Lumican Gene
Lumican基因的结构/功能关系
  • 批准号:
    7289231
  • 财政年份:
    2006
  • 资助金额:
    $ 3万
  • 项目类别:

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