Immunobiology of Trauma

创伤免疫生物学

基本信息

  • 批准号:
    9217919
  • 负责人:
  • 金额:
    $ 15.57万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2010
  • 资助国家:
    美国
  • 起止时间:
    2010-07-01 至 2022-06-30
  • 项目状态:
    已结题

项目摘要

This T32 grant, GM86308, Immunobiology of Trauma will provide the appropriate training and mentoring to create the next generation of physician scientists. Physician-scientists are a critical element of the workforce necessary to improve the health of patients. Injuries and deaths from traumatic injury represented the major cause of death and impaired function among people under the age of 44. This morbidity and mortality creates a disproportionate drain on healthcare resources due to the typical young age of the trauma patient. Additionally, new advances in identifying the scope of chronic traumatic encephalopathy (football players’ brain injury) show the need for increased investment in the basic science of trauma. Trauma disproportionately affects underserved minority patients resulting in healthcare disparities further emphasizing the role trauma plays in the health of our country. This revision of our competing renewal will build on the success of the prior five years of funding. These successes include effective recruitment of minority physicians into the program, 6 national awards to our T32 fellows, and 23 papers either published or in press. Since the original renewal submission in 2015 an additional 11 papers have been published or are in press. There are important innovations in this competing renewal which developing new evaluation tools developed by the recently funded BU Clinical Science and Translational Institute and a newly NIH funded mentoring program for minority students, among others. Some of the significant changes in the new application include a restructuring of the executive committee to include members with active funding and labs, development of clear training objectives, and expansion of the training faculty to include investigators focusing on traumatic brain injury. This grant specifically requests funding for two postdoctoral fellows for two years of training, a formula which has proven successful during the prior funding. The Executive Committee works closely with the individual trainees to identify labs whose research matches the interests of the trainees. All of our prior trainees have been drawn from the residency programs at Boston Medical Center, the largest safety net hospital in New England. There is exceptional institutional commitment manifest by the support for the recruitment and retention of minority physicians and trainees with disabilities. It should be noted that only one of our 10 trainees has completed their clinical training, and it is not possible to document successful physician scientists completing our program. However, we have prepared our trainees for academic careers by mentoring their science such that they have already been successful as documented by the numerous national awards and published multiple manuscripts in the peer reviewed literature.
这项T32拨款,GM86308,创伤免疫生物学将提供适当的培训和

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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Daniel G. Remick其他文献

Biphasic production of IL-8 in lipopolysaccharide (LPS)-stimulated human whole blood. Separation of LPS- and cytokine-stimulated components using anti-tumor necrosis factor and anti-IL-1 antibodies.
脂多糖 (LPS) 刺激的人全血中双相产生 IL-8。
  • DOI:
  • 发表时间:
    1992
  • 期刊:
  • 影响因子:
    4.4
  • 作者:
    L. Deforge;J. Kenney;M. Jones;Jeffrey S. Warren;Daniel G. Remick
  • 通讯作者:
    Daniel G. Remick
The biological activity of lipopolyscaccharide binding protein is determined by concentration
  • DOI:
    10.1016/s0016-5085(00)86238-1
  • 发表时间:
    2000-04-01
  • 期刊:
  • 影响因子:
  • 作者:
    Richard D. Klein;Andrew C. Schook;Alireza Schook;William H. Alarcon;Lars Steinstraesser;Hongyu Zhang;Stewart C. Wang;Daniel G. Remick;Grace L. Su
  • 通讯作者:
    Grace L. Su
Nitric oxide regulation of IL-8 expression in human endothelial cells.
一氧化氮对人内皮细胞 IL-8 表达的调节。
Tumor necrosis factor inhibitors for the treatment of asthma
  • DOI:
    10.1007/s11882-007-0013-3
  • 发表时间:
    2007-03-01
  • 期刊:
  • 影响因子:
    4.600
  • 作者:
    Jiyoun Kim;Daniel G. Remick
  • 通讯作者:
    Daniel G. Remick
Intratracheal administration of endotoxin and cytokines. VII. The soluble interleukin-1 receptor and the soluble tumor necrosis factor receptor II (p80) inhibit acute inflammation.
气管内施用内毒素和细胞因子。
  • DOI:
    10.1006/clin.1994.1117
  • 发表时间:
    1994
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Thomas R. Ulich;Eunhee S. Yi;Songmei Yin;Craig A. Smith;Daniel G. Remick
  • 通讯作者:
    Daniel G. Remick

Daniel G. Remick的其他文献

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{{ truncateString('Daniel G. Remick', 18)}}的其他基金

Mechanisms of improved organ function following sepsis treatment with vitamin c, thiamine and hydrocortisone (triple therapy)
维生素 C、硫胺素和氢化可的松治疗败血症后改善器官功能的机制(三联疗法)
  • 批准号:
    9978302
  • 财政年份:
    2020
  • 资助金额:
    $ 15.57万
  • 项目类别:
Mechanisms of augmented host defenses after mild brain injury
轻度脑损伤后增强宿主防御的机制
  • 批准号:
    9246802
  • 财政年份:
    2017
  • 资助金额:
    $ 15.57万
  • 项目类别:
Mechanisms of phagocytic cell defects induced by inhibitory IgG
抑制性IgG诱导吞噬细胞缺陷的机制
  • 批准号:
    8751338
  • 财政年份:
    2014
  • 资助金额:
    $ 15.57万
  • 项目类别:
Adenosine and Oxygen Modulate Antimicrobial Defenses
腺苷和氧调节抗菌防御
  • 批准号:
    8338793
  • 财政年份:
    2011
  • 资助金额:
    $ 15.57万
  • 项目类别:
Adenosine and Oxygen Modulate Antimicrobial Defenses
腺苷和氧调节抗菌防御
  • 批准号:
    8085386
  • 财政年份:
    2011
  • 资助金额:
    $ 15.57万
  • 项目类别:
Adenosine and Oxygen Modulate Antimicrobial Defenses
腺苷和氧调节抗菌防御
  • 批准号:
    8478144
  • 财政年份:
    2011
  • 资助金额:
    $ 15.57万
  • 项目类别:
Adenosine and Oxygen Modulate Antimicrobial Defenses
腺苷和氧调节抗菌防御
  • 批准号:
    8668080
  • 财政年份:
    2011
  • 资助金额:
    $ 15.57万
  • 项目类别:
Immunobiology of Trauma
创伤免疫生物学
  • 批准号:
    8280447
  • 财政年份:
    2010
  • 资助金额:
    $ 15.57万
  • 项目类别:
Immunobiology of Trauma
创伤免疫生物学
  • 批准号:
    8501538
  • 财政年份:
    2010
  • 资助金额:
    $ 15.57万
  • 项目类别:
Immunobiology of Trauma
创伤免疫生物学
  • 批准号:
    8101150
  • 财政年份:
    2010
  • 资助金额:
    $ 15.57万
  • 项目类别:

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