Matrix and Morphogenesis Conference
矩阵与形态发生会议
基本信息
- 批准号:6460073
- 负责人:
- 金额:$ 0.8万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-04-01 至 2003-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant):
Organisms undergo morphogenesis to develop structures that permit life. For
example, during embryogenesis, epithelial cells must be able to transform from
an epithelial to a fibroblast-like morphology and to migrate and proliferate.
When the process of morphogenesis goes awry, cells can transform to a
malignant phenotype. A large number of morphogenic changes are induced by
specific cell surface interactions with extracellular matrix components. The
Matrix and Morphogenesis Conference has been planned to highlight the cell-
cell and cell-matrix communications that are key players in morphogenesis.
The conference, which is to be held at the Park Plaza Hotel in Boston on April
13, 2002, is a premier meeting for scientists interested in the biochemical,
genetic, and pathological contribution of extracellular matrix to
morphogenesis. The meeting covers a broad range of topics including the role
of extracellular matrix molecules in morphogenesis, morphogenesis in a variety
of developing systems, and morphogenesis as it applies to carcinogenesis.
Talks will cover the morphogenic roles of fibrillin, SPARC, and individual
laminins. The process of cell signaling, adhesion, proteolysis, and
transformation to a malignant phenotype, will be addressed in view of their
contribution to morphogenesis. Other speakers will discuss skeletogenesis,
myogenesis, cell-cell and cell-matrix interactions. The importance of
epithelial-mesenchymal interactions will be discussed as it relates to
development, wound healing and repair, and the transformed cancer phenotype.
In addition, studies involving genetic approaches in mice will be presented to
elucidate the function of novel matrix components and to support the current
hypotheses surrounding morphogenesis. The goal of the meeting is to promote
the exchange of the most exciting and highest quality science in this research
area, and to facilitate collaborations between scientists at all levels. The
meeting will end with a banquet where new and experienced investigators are
seated together to foster discussion and networking. At the banquet, the
first woman graduate of Johns Hopkins Medical School, Dr. Elizabeth Hay, will
be honored. She has served as editor-in-chief of the journal Developmental
Biology and as chairman of the Harvard Medical School Anatomy and Cell Biology
Department. She was elected to the National Academy of Sciences in 1984. By
promoting the interactions of young scientists with the speakers, about half
of which are outstanding female role models, the conference endeavors to
encourage the careers of junior investigators. Funds are requested to
reimburse conference fees and travel expenses of invited speakers, moderators,
the honoree and organizers, and to cover audiovisual charges, and printing and
mailing costs. This meeting provides a unique opportunity for senior and
junior scientists to gather and discuss the latest and most advanced results
in the field of extracellular matrix and morphogenesis.
描述(由申请人提供):
生物体经历形态发生以发展允许生命的结构。 为
例如,在胚胎发生过程中,上皮细胞必须能够从
上皮细胞转化为成纤维细胞样形态并迁移和增殖。
当形态发生的过程出错时,细胞可以转化为
恶性表型 大量的形态发生变化是由
与细胞外基质组分的特异性细胞表面相互作用。 的
矩阵和形态发生会议已计划突出细胞-
细胞和细胞基质通信是形态发生的关键参与者。
这次会议将于4月15日在波士顿的公园广场酒店举行。
2002年13日,是对生物化学感兴趣的科学家的一次重要会议,
细胞外基质在遗传和病理方面的贡献
形态发生 会议涵盖了广泛的主题,包括
细胞外基质分子在形态发生中的作用,
和形态发生,因为它适用于致癌作用。
讲座将涵盖形态发生的作用,bepaly在线网投,和个人
层粘连蛋白。 细胞信号传导、粘附、蛋白水解和
转化为恶性表型,将根据其
对形态发生的贡献 其他演讲者将讨论骨骼发生,
肌生成、细胞-细胞和细胞-基质相互作用。 的重要性
上皮间质的相互作用将被讨论,因为它涉及到
发育、伤口愈合和修复以及转化的癌症表型。
此外,涉及小鼠遗传方法的研究将提交给
阐明新型基质组分的功能,并支持当前
围绕形态发生的假说 会议的目标是促进
在这项研究中最令人兴奋和最高质量的科学交流
这是一个重要的领域,并促进各级科学家之间的合作。 的
会议将以宴会结束,新的和有经验的研究人员将参加宴会。
坐在一起,促进讨论和网络。 在宴会上,
约翰霍普金斯医学院的第一位女毕业生伊丽莎白·海博士将
感到荣幸 她曾担任《发展》杂志的主编
生物学和哈佛医学院解剖学和细胞生物学主席
部门 1984年当选为美国国家科学院院士。 通过
促进年轻科学家与演讲者的互动,约有一半
其中有杰出的女性榜样,会议努力
鼓励初级调查员的职业生涯。 请拨资金用于
报销会议费用和受邀演讲者,主持人,
获奖者和组织者,并支付视听费用,印刷和
邮寄费用。 这次会议为高级和
年轻的科学家聚集在一起讨论最新和最先进的成果
在细胞外基质和形态发生领域。
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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MARION K GORDON其他文献
MARION K GORDON的其他文献
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{{ truncateString('MARION K GORDON', 18)}}的其他基金
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶标
- 批准号:
7933776 - 财政年份:2009
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶标
- 批准号:
7653731 - 财政年份:2008
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
7468060 - 财政年份:2007
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
8743070 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Research Project II - Vesicant-Induced Corneal Injury
研究项目 II - 起泡剂引起的角膜损伤
- 批准号:
10291227 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
8210200 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
8932579 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
8545530 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶标
- 批准号:
7235218 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
Transmembraneous collagens and matrix metalloproteinases as targets for counterme
跨膜胶原蛋白和基质金属蛋白酶作为对抗靶点
- 批准号:
8382002 - 财政年份:2006
- 资助金额:
$ 0.8万 - 项目类别:
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