Mayo Center for Cell Signaling in Gastroenterology

梅奥胃肠病学细胞信号转导中心

基本信息

  • 批准号:
    8903714
  • 负责人:
  • 金额:
    $ 119.25万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2009
  • 资助国家:
    美国
  • 起止时间:
    2009-09-01 至 2019-08-31
  • 项目状态:
    已结题

项目摘要

The goal of the Mayo Clinic Center for Cell Signaling in Gastroenterology (C-SiG) is to connect discovery, translational, and patient-oriented investigators to enhance understanding and therapeutically exploit signaling pathways in gastrointestinal cells to improve the health of patients with digestive diseases. The Research Base consists of 59 scientists and $23 million (direct costs, 70% growth) in digestive disease-related funding. C-SiG members are organized into three Mechanistic Research Themes: 1) Ion channels/membrane receptors; ii) Signal transduction; and, iii) Genetics and gene regulation. Our CENTRAL HYPOTHESIS is that advances in clinical care of patients with digestive diseases requires a facilitative infrastructure supporting meaningful interactions among multidisciplinary scientists investigating cellular mechanisms, pathways and therapeutic targets to enhance rapid translation of basic discoveries into clinical trials. C-SiG's OVERALL SPECIFIC AIMS are to: i) Foster multidisciplinary research by expanding technical and collaborative capabilities of established Gl scientists and attracting investigators from other disciplines; li) Develop and implement a robust Scientific Enrichment Program that includes seminars, workshops, symposia, a visiting faculty program, mini-sabbatical, and Web-based curricula; iii) Offer specialized equipment, technologies, methodologies, reagents, and expertise to assist C-SiG members through the C-SiG Cores, including: a) State-of-the-art microscopic technology and consultative expertise (Optical Microscopy Core); b) Accelerated and expanded biospecimen acquisition, processing, and annotation (Clinical Core); c) Emerging genetic technologies and model systems (Genetics and Model Systems Core); iv) Identify and nurture new GI investigators via a peer-reviewed Pilot and Feasibility Program; v) Promote synergistic interactions between C-SiG members and other Gl investigators at Mayo and at other Gl centers to facilitate clinical trials resulting from the identification of cellular therapeutic targets; vi) Share technologies with other NIDDK centers at Mayo (e.g., PKD Center) and existing Digestive Disease Research Core Centers, especially in the Midwest (i.e.. Midwest DDRCC Alliance).
梅奥诊所胃肠病学细胞信号中心(C-SiG)的目标是将发现,

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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Nicholas F. LaRusso其他文献

Abnormalities of Chemical Tests for Copper Metabolism in Chronic Active Liver Disease: Differentiation from Wilson's Disease
  • DOI:
    10.1016/s0016-5085(76)80249-1
  • 发表时间:
    1976-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Nicholas F. LaRusso;William H.J. Summerskill;John T. McCall
  • 通讯作者:
    John T. McCall
Lysosomal enzymes in biological fluids
  • DOI:
    10.1007/bf01308425
  • 发表时间:
    1979-03-01
  • 期刊:
  • 影响因子:
    2.500
  • 作者:
    Nicholas F. LaRusso
  • 通讯作者:
    Nicholas F. LaRusso
1103 - Fluorescence-Activated Cell Sorting of Enteroendocrine Cells in Humans: Technique Validation by Mucosal Endoscopic Biopsies and Novel Progression to <em>Ex-Vivo</em> Studies
  • DOI:
    10.1016/s0016-5085(18)31118-1
  • 发表时间:
    2018-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Alison N. Bonis;Geoffrey Roberts;Gerardo Calderon;Julie Woodrum;Jeffrey Salisbury;Frank Reimann;Michael Camilleri;Nicholas F. LaRusso;Fiona Gribble;Andres Acosta
  • 通讯作者:
    Andres Acosta
Nitric oxide (NO) inhibits apoptosis in cholangiocarcinoma cells by blocking caspase 9 activation
  • DOI:
    10.1016/s0016-5085(00)85990-9
  • 发表时间:
    2000-04-01
  • 期刊:
  • 影响因子:
  • 作者:
    Natalie J. Torok;Timothy J. Kottke;Scott H. Kaufmann;Nicholas F. LaRusso;Gregory J. Gores;Mayo Clin
  • 通讯作者:
    Mayo Clin
Ursodeoxycholic acid ingestion after ileal resection
  • DOI:
    10.1007/bf01316859
  • 发表时间:
    1981-08-01
  • 期刊:
  • 影响因子:
    2.500
  • 作者:
    Nicholas F. LaRusso;Johnson L. Thistle
  • 通讯作者:
    Johnson L. Thistle

Nicholas F. LaRusso的其他文献

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{{ truncateString('Nicholas F. LaRusso', 18)}}的其他基金

Midwest DDRCC Alliance Conference (Hosted by the Mayo Clinic DDRCC)
中西部DDRCC联盟会议(由梅奥诊所DDRCC主办)
  • 批准号:
    10675868
  • 财政年份:
    2023
  • 资助金额:
    $ 119.25万
  • 项目类别:
The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
用于治疗胆管病的 TGR5 拮抗剂的开发
  • 批准号:
    10201582
  • 财政年份:
    2019
  • 资助金额:
    $ 119.25万
  • 项目类别:
The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
用于治疗胆管病的 TGR5 拮抗剂的开发
  • 批准号:
    10018484
  • 财政年份:
    2019
  • 资助金额:
    $ 119.25万
  • 项目类别:
The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
用于治疗胆管病的 TGR5 拮抗剂的开发
  • 批准号:
    10431962
  • 财政年份:
    2019
  • 资助金额:
    $ 119.25万
  • 项目类别:
Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
  • 批准号:
    7908858
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:
Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
  • 批准号:
    10630250
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:
Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
  • 批准号:
    8699451
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:
Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
  • 批准号:
    10438737
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:
Administrative Core
行政核心
  • 批准号:
    10438738
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:
Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
  • 批准号:
    8309305
  • 财政年份:
    2009
  • 资助金额:
    $ 119.25万
  • 项目类别:

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Nonlocal Variational Problems from Physical and Biological Models
物理和生物模型的非局部变分问题
  • 批准号:
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Point-of-care optical spectroscopy platform and novel ratio-metric algorithms for rapid and systematic functional characterization of biological models in vivo
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利用机器学习和云计算来测试白质在人类学习中的作用的生物模型
  • 批准号:
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便携式低成本调查点 CapCell 示波器,用于对体外和体内生物模型中的主要代谢轴和相关脉管系统进行成像和量化
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    Discovery Grants Program - Individual
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