FASEB SRC: The Translational Neuroimmunology Conference: From Bench to Bedside and Back

FASEB SRC:转化神经免疫学会议:从实验室到临床并返回

基本信息

项目摘要

Project Summary The purpose of this R13 proposal is to support the attendance of trainees, young investigators, and individuals historically underrepresented in science and medicine, at the 2022 FASEB Conference: Translational Neuroimmunology: From Bench to Bedside and Back. This will be the 15th biannual FASEB Neuroimmunology conference, the first having been held in 1988. The current meeting will be held August 29-September 2, 2022 at the Renaissance Asheville Hotel in Asheville, North Carolina. Neuroimmunology is one of the fastest growing fields in biomedical research. It has also been one of the most fruitful in terms of the successful translation of wet bench discoveries into impactful clinical therapies. The overall intent of this conference is to bring together the world’s leading scientists, young investigators, and trainees, who are engaged in neuroimmunology research from a broad range of perspectives, in a collegial and supportive environment. The specific goals are to: 1) provide a forum for the presentation of unpublished, cutting-edge research on immune- nervous system interactions during health and disease, by speakers from diverse backgrounds; 2) provide opportunities for both formal and informal discussions on neuroimmune pathways in health and disease, the environmental and genetic factors that influence those pathways, and efforts to translate scientific insights in neuroimmunology from “bench to bedside”; 3) support the participation of young investigators, particularly those traditionally under-represented in the field, and facilitate their integration into the broader research community in a meaningful and interactive way; (4) promote principles of rigor, transparency, and equipoise in the conduct and evaluation of research. The program is intentionally multifaceted to ensure that attendees working on different aspects of Neuroimmunology research have the opportunity to meet colleagues with complementary interests and areas of expertise, either one-on-one or in small group settings. The agenda consists of a series of sequential sessions in a single track, without competing talks, and unscheduled afternoon time to encourage informal communications. These collective features of the conference will facilitate brainstorming and mentoring in a variety of formats. A priority is to inspire women scientists, and learners and junior faculty from groups that are traditionally underrepresented in science and medicine, and to connect those individuals with role models, future mentors, and peers, thereby strengthening their commitment to Neuroimmunology research. To that end, we are introducing workshops on “How to Forge Collaborations with Clinicians and Translate Wet Bench Findings to Human Studies”; “Women and Under-represented Minorities in Neuroimmunology: Challenges and Opportunities”; and “Scientific Rigor and Transparency in Research”, as well as a career panel discussion on “Career Trajectories in Neuroimmunology”. This conference is designed to foster creative partnerships and collaborations between wet bench scientists, clinical trialists/ researchers, and clinicians who are focused on Neuroimmunology, ultimately leading to clinical advances in the field.
项目摘要 该R13提案的目的是支持培训,年轻调查人员和个人的出席 从历史上讲,科学和医学的代表性不足,在2022 Faseb会议上:翻译 神经免疫学:从长凳到床边再到背部。这将是第15次双年度FASEB神经免疫学 会议,第一次于1988年举行。当前会议将于2022年8月29日至9月2日举行 在北卡罗来纳州阿什维尔的文艺复兴时期的阿什维尔酒店。神经免疫学是最快的 生物医学研究的成长领域。就成功而言,它也是最富有成果的 将湿长凳发现转化为有影响力的临床疗法。这次会议的总体意图是 将参与的世界领先科学家,年轻调查员和学员汇集在一起 从广泛的角度来看,神经免疫学研究在合作和支持性的环境中。 具体目标是:1)提供一个论坛,以展示有关免疫的未发表的尖端研究 来自潜水员背景的演讲者在健康和疾病期间的神经系统相互作用; 2)提供 关于健康和疾病中神经免疫途径的正式和非正式讨论的机会, 影响这些途径的环境和遗传因素,并努力翻译科学见解 神经免疫学从“长凳到床边”; 3)支持年轻调查员的参与 传统上那些在该领域中代表性不足的人,并促进了它们与更广泛的研究的融合 社区以有意义的互动方式; (4)促进严格,透明度和设置的原则 研究的行为和评估。该计划是有意的,以确保与会者 从事神经免疫学研究的不同方面有机会与 完全有趣的专业知识领域,无论是一对一还是小组设置。 Agernda 由单个轨道中的一系列顺序会话组成,无需进行竞争对话,并且不定期 下午鼓励非正式通讯。会议的这些集体特征将有助于 以各种格式进行头脑风暴和心理。优先的是激发女性科学家,学习者和 传统在科学和医学中代表不足的团体的初级教师 那些具有榜样,未来导师和同伴的人,从而加强了他们对 神经免疫学研究。为此,我们正在介绍有关“如何与 临床医生并将湿的卧台调查结果转化为人类研究”;“妇女和代表性不足的少数民族 神经免疫学:挑战和机遇”;“研究中的科学严谨和透明度”,作为 以及关于“神经免疫学的职业轨迹”的职业小组讨论。这次会议是设计的 促进湿板凳科学家,临床试验者/研究人员之间的创造性伙伴关系和合作 专注于神经免疫学的临床医生,最终导致该领域的临床进展。

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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Benjamin M Segal其他文献

Benjamin M Segal的其他文献

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{{ truncateString('Benjamin M Segal', 18)}}的其他基金

Arginase-1 and iNOS expressing CNS myeloid cell subsets in EAE and MS
EAE 和 MS 中表达精氨酸酶 1 和 iNOS 的 CNS 骨髓细胞亚群
  • 批准号:
    10221066
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
A novel inflammatory cell with neuroprotective and neuroregenerative properties
一种具有神经保护和神经再生特性的新型炎症细胞
  • 批准号:
    10391439
  • 财政年份:
    2018
  • 资助金额:
    $ 3万
  • 项目类别:
A novel inflammatory cell with neuroprotective and neuroregenerative properties
一种具有神经保护和神经再生特性的新型炎症细胞
  • 批准号:
    9900003
  • 财政年份:
    2018
  • 资助金额:
    $ 3万
  • 项目类别:
The mechanism of action of Granulocyte Macrophage-Colony Stimulating Factor in an animal model of Multiple Sclerosis
粒细胞巨噬细胞集落刺激因子在多发性硬化症动物模型中的作用机制
  • 批准号:
    9392704
  • 财政年份:
    2017
  • 资助金额:
    $ 3万
  • 项目类别:
Immune mediated regeneration of retinal ganglion cell axons following optic nerve trauma
视神经损伤后免疫介导的视网膜神经节细胞轴突再生
  • 批准号:
    10017241
  • 财政年份:
    2017
  • 资助金额:
    $ 3万
  • 项目类别:
Immune mediated regeneration of retinal ganglion cell axons following optic nerve trauma
视神经损伤后免疫介导的视网膜神经节细胞轴突再生
  • 批准号:
    9390608
  • 财政年份:
    2017
  • 资助金额:
    $ 3万
  • 项目类别:
Nogo Receptors as Therapeutic Targets in a Model of Multiple Sclerosis
Nogo 受体作为多发性硬化症模型的治疗靶点
  • 批准号:
    8774166
  • 财政年份:
    2013
  • 资助金额:
    $ 3万
  • 项目类别:
Nogo Receptors as Therapeutic Targets in a Model of Multiple Sclerosis
Nogo 受体作为多发性硬化症模型的治疗靶点
  • 批准号:
    8441391
  • 财政年份:
    2013
  • 资助金额:
    $ 3万
  • 项目类别:
Nogo Receptors as Therapeutic Targets in a Model of Multiple Sclerosis
Nogo 受体作为多发性硬化症模型的治疗靶点
  • 批准号:
    8625179
  • 财政年份:
    2013
  • 资助金额:
    $ 3万
  • 项目类别:
Preclinical studies of a MADCAM-Fc fusion protein in multiple sclerosis
MADCAM-Fc 融合蛋白治疗多发性硬化症的临床前研究
  • 批准号:
    8934116
  • 财政年份:
    2011
  • 资助金额:
    $ 3万
  • 项目类别:

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