Center for Redox Biology and Cardiovascular Disease

氧化还原生物学和心血管疾病中心

基本信息

项目摘要

Project Abstract Cardiovascular disease is the leading cause of death and disability in the United States with a disproportional effect on southern regions of the country. According to the 2016 America's Health Rankings Annual Report, Louisiana ranks 46/50 in cardiovascular deaths and 48/50 in heart disease placing it in the lowest categories of cardiovascular health across the nation. Moreover, for the first time in 27 years, the rate of cardiovascular deaths increased across the nation highlighting the magnitude and importance of cardiovascular research. While advances in cardiovascular treatments have been realized, many cardiovascular disease mechanisms remain poorly understood. It has become clear that changes in heart and vascular oxidative stress and antioxidant defenses, the so called `redox balance', plays critical roles in disease initiation and propagation. However, specific ways that alterations in redox biology control cellular and molecular responses leading to cardiovascular disease remains largely unknown. The Center for Cardiovascular Diseases and Sciences at LSU Health Sciences Center Shreveport has assembled investigators with state of the art knowledge and research expertise across several departments to address redox biology molecular mechanisms contributing to cardiovascular pathophysiology. The intent of this proposal is to develop and establish a COBRE Center for Redox Biology and Cardiovascular Disease with a nationally recognized enriched training environment for junior faculty that advances the competitiveness of research programs for national awards. Individual primary projects have been carefully chosen based on their relevance to the research theme, novelty of the research topic regarding redox biology and cardiovascular disease, and their potential ability to achieve program independence. The proposed projects will provide new understanding of redox biology mechanisms required for cardiac and vascular (dys)function with support from advanced, state of the art animal models and redox molecular pathology research core facilities. Research and professional development programs are also proposed that will provide continued growth and leadership in this area.
项目摘要

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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Christopher G Kevil其他文献

ICAM Cytoplasmic Tail Regulates VEGF Mediated Angiogenesis in a Redox Dependent Manner in vitro and in vivo
  • DOI:
    10.1016/j.freeradbiomed.2010.10.557
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Sibile Pardue;Eric R Reeves;Faisal Bahadur;Christopher Pattillo;Terrance J Kavanagh;Christopher G Kevil
  • 通讯作者:
    Christopher G Kevil
Sodium Nitrite Therapy Positively Augments Arteriogenesis as Monitored over Time with Serial Angiography in a Murine Model of Hind Limb Ischemia
  • DOI:
    10.1016/j.freeradbiomed.2010.10.046
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Christopher B Pattillo;Shyamal C Bir;Christopher G Kevil
  • 通讯作者:
    Christopher G Kevil
Sodium Sulfide Augments Ischemic Angiogenesis by Increasing the Activity of Hypoxia Inducible Factor-1 as well as increasing the VEGF Expression in Murine Critical Limb Ischemia
  • DOI:
    10.1016/j.freeradbiomed.2010.10.504
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Shyamal C Bir;Christopher B Pattillo;Paul McCarthy;Xinggui Shen;Gopi Krishna Kolluru;Kai Fang;Christopher G Kevil
  • 通讯作者:
    Christopher G Kevil
PSS152 - Exogenous Thiosulfate Differentially Affects Endothelial Cell Proliferation in an Oxygen Dependent Manner
  • DOI:
    10.1016/j.freeradbiomed.2013.10.571
  • 发表时间:
    2013-11-01
  • 期刊:
  • 影响因子:
  • 作者:
    Anna Leskova;Sibile Pardue;Xinggui Shen;Christopher G Kevil
  • 通讯作者:
    Christopher G Kevil
PSS225 - Nitrite regulation of Hydrogen Sulfide Metabolism in the Endothelial Cells
  • DOI:
    10.1016/j.freeradbiomed.2013.10.646
  • 发表时间:
    2013-11-01
  • 期刊:
  • 影响因子:
  • 作者:
    Sibile Pardue;Xinggui Shen;Christopher G Kevil
  • 通讯作者:
    Christopher G Kevil

Christopher G Kevil的其他文献

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{{ truncateString('Christopher G Kevil', 18)}}的其他基金

Administrative Core
行政核心
  • 批准号:
    10715403
  • 财政年份:
    2023
  • 资助金额:
    $ 26.34万
  • 项目类别:
CSE regulation of vascular remodeling
CSE对血管重塑的调节
  • 批准号:
    10630127
  • 财政年份:
    2020
  • 资助金额:
    $ 26.34万
  • 项目类别:
CSE regulation of vascular remodeling
CSE对血管重塑的调节
  • 批准号:
    10206260
  • 财政年份:
    2020
  • 资助金额:
    $ 26.34万
  • 项目类别:
CSE regulation of vascular remodeling
CSE对血管重塑的调节
  • 批准号:
    10427218
  • 财政年份:
    2020
  • 资助金额:
    $ 26.34万
  • 项目类别:
CSE regulation of vascular remodeling
CSE对血管重塑的调节
  • 批准号:
    10007007
  • 财政年份:
    2020
  • 资助金额:
    $ 26.34万
  • 项目类别:
Center for Redox Biology and Cardiovascular Disease
氧化还原生物学和心血管疾病中心
  • 批准号:
    10715402
  • 财政年份:
    2018
  • 资助金额:
    $ 26.34万
  • 项目类别:
SARS-CoV-2 Genomic Surveillance in North Louisiana
路易斯安那州北部的 SARS-CoV-2 基因组监测
  • 批准号:
    10595390
  • 财政年份:
    2018
  • 资助金额:
    $ 26.34万
  • 项目类别:
Administration and Mentorship Core
管理和指导核心
  • 批准号:
    10331748
  • 财政年份:
    2018
  • 资助金额:
    $ 26.34万
  • 项目类别:
SARS-CoV-2 Genomic Surveillance in North Louisiana
路易斯安那州北部的 SARS-CoV-2 基因组监测
  • 批准号:
    10381353
  • 财政年份:
    2018
  • 资助金额:
    $ 26.34万
  • 项目类别:
Center for Redox Biology and Cardiovascular Disease
氧化还原生物学和心血管疾病中心
  • 批准号:
    10331747
  • 财政年份:
    2018
  • 资助金额:
    $ 26.34万
  • 项目类别:

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