SCOR IN CORONARY AND VASCULAR DISEASES

冠状动脉和血管疾病中的 SCOR

基本信息

  • 批准号:
    2215040
  • 负责人:
  • 金额:
    $ 197.6万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1985
  • 资助国家:
    美国
  • 起止时间:
    1985-01-01 至 1994-12-31
  • 项目状态:
    已结题

项目摘要

This is a multidisciplinary proposal to explore the fundamental pathophysiology and biochemistry of ischemic and infarcted myocardium and to implement knowledge of the pathophysiology of this disease into programs to: (1) identify those at risk of serious ischemic events and (2) examine means for improving the management of those patient manifesting ischemic heart disease. Studies of the metabolism of ischemic myocardium will utilize nuclear magnetic resonance to identify rapid changes in energy state. The importance of shape changes, relaxation characteristics of myocardium and ischemic and scarred myocardium as determinants of left ventricular function will be examined in animal models and man. The role of prostaglandins in ischemia and in the mechanism of action of cardiac active drugs will be explored. We will attempt to identify the anatomic predictors of sudden cardiac death invasively and non-invasively as well as explore risk factor profile in relationship to anatomic coronary lesions and prognosis. We will explore the therapeutic potential of a new automatic implantable defibrillator device in man. Randomized clinical intervention trials will include: (1) nitroglycerin plus propranolol in low risk patients with acute infarction (vs. placebo); (2) intraaortic balloon pumping and nitroglycerin in high risk patients with acute infarction (vs. routine therapy); (3) new vs. conventional cardiopulmonary resuscitative techniques; (4) a slow channel blocker (vs. placebo) in patients with unstable angina pectoris; (5) a membrane active anti-arrhythmic agent vs. placebo in survivors of acute infarcts assessed to be at high risk of subsequent sudden death and (6) use of perioperative agents for decreasing complications of coronary bypass surgery. Core support laboratories include: Pathology, Nuclear Cardiology, Echocardiography and Pharmacology.
这是一个多学科的建议,以探索基本病理生理学

项目成果

期刊论文数量(290)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Correction for patient and organ movement in SPECT: application to exercise thallium-201 cardiac imaging.
Regulation of myocardial glycogenolysis during post-ischemic reperfusion.
缺血后再灌注期间心肌糖原分解的调节。
  • DOI:
    10.1016/0022-2828(91)90192-o
  • 发表时间:
    1991
  • 期刊:
  • 影响因子:
    5
  • 作者:
    Kalil-Filho,R;Gerstenblith,G;Hansford,RG;Chacko,VP;Vandegaer,K;Weiss,RG
  • 通讯作者:
    Weiss,RG
Fatty acid regulation of glucose metabolism in the intact beating rat heart assessed by carbon-13 NMR spectroscopy: the critical role of pyruvate dehydrogenase.
通过碳 13 NMR 光谱评估完整跳动大鼠心脏中葡萄糖代谢的脂肪酸调节:丙酮酸脱氢酶的关键作用。
Circulatory assistance by intrathoracic pressure variations: optimization and mechanisms studied by a mathematical model in relation to experimental data.
胸腔内压力变化的循环辅助:通过与实验数据相关的数学模型研究的优化和机制。
  • DOI:
    10.1161/01.res.64.4.703
  • 发表时间:
    1989
  • 期刊:
  • 影响因子:
    20.1
  • 作者:
    Beyar,R;Halperin,HR;Tsitlik,JE;Guerci,AD;Kass,D;Weisfeldt,ML;Chandra,NC
  • 通讯作者:
    Chandra,NC
Limitations of regional myocardial thallium clearance for identification of disease in individual coronary arteries.
局部心肌铊清除率在识别个体冠状动脉疾病方面的局限性。
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Lewis C Becker其他文献

1028-169 The predictive value of parental history of coronary disease
  • DOI:
    10.1016/s0735-1097(04)91916-x
  • 发表时间:
    2004-03-03
  • 期刊:
  • 影响因子:
  • 作者:
    Pamela Ouyang;Lisa R Yanek;Daniele Fallin;Taryn F Moy;Lewis C Becker;Diane M Becker
  • 通讯作者:
    Diane M Becker
847-2 Combination aspirin and statin therapy markedly reduces C-reactive protein levels in a high-risk population without coronary disease
  • DOI:
    10.1016/s0735-1097(04)92179-1
  • 发表时间:
    2004-03-03
  • 期刊:
  • 影响因子:
  • 作者:
    Mariene S Williams;Lewis C Becker;Taryn F Moy;Lisa R Yanek;Nauder Faraday;Diane M Becker
  • 通讯作者:
    Diane M Becker

Lewis C Becker的其他文献

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{{ truncateString('Lewis C Becker', 18)}}的其他基金

Clonal Hematopoiesis in Healthy Individuals from Families with Early OnsetCoronary Artery Disease
早发冠状动脉疾病家族的健康个体的克隆性造血
  • 批准号:
    10393540
  • 财政年份:
    2019
  • 资助金额:
    $ 197.6万
  • 项目类别:
Clonal Hematopoiesis in Healthy Individuals from Families with Early OnsetCoronary Artery Disease
早发冠状动脉疾病家族的健康个体的克隆性造血
  • 批准号:
    9760677
  • 财政年份:
    2019
  • 资助金额:
    $ 197.6万
  • 项目类别:
Clonal Hematopoiesis in Healthy Individuals from Families with Early OnsetCoronary Artery Disease
早发冠状动脉疾病家族的健康个体的克隆性造血
  • 批准号:
    9923751
  • 财政年份:
    2019
  • 资助金额:
    $ 197.6万
  • 项目类别:
Gene Transcripts and Proteomics in Families with Platelet Hyperaggregation
血小板过度聚集家族的基因转录和蛋白质组学
  • 批准号:
    8696113
  • 财政年份:
    2014
  • 资助金额:
    $ 197.6万
  • 项目类别:
Gene Transcripts and Proteomics in Families with Platelet Hyperaggregation
血小板过度聚集家族的基因转录和蛋白质组学
  • 批准号:
    9258474
  • 财政年份:
    2014
  • 资助金额:
    $ 197.6万
  • 项目类别:
Gene Transcripts and Proteomics in Families with Platelet Hyperaggregation
血小板过度聚集家族的基因转录和蛋白质组学
  • 批准号:
    9039140
  • 财政年份:
    2014
  • 资助金额:
    $ 197.6万
  • 项目类别:
Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
使用 iPS 和衍生巨核细胞进行血小板聚集的功能基因组学
  • 批准号:
    8094912
  • 财政年份:
    2011
  • 资助金额:
    $ 197.6万
  • 项目类别:
Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
使用 iPS 和衍生巨核细胞进行血小板聚集的功能基因组学
  • 批准号:
    8690135
  • 财政年份:
    2011
  • 资助金额:
    $ 197.6万
  • 项目类别:
Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
使用 iPS 和衍生巨核细胞进行血小板聚集的功能基因组学
  • 批准号:
    8868161
  • 财政年份:
    2011
  • 资助金额:
    $ 197.6万
  • 项目类别:
Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
使用 iPS 和衍生巨核细胞进行血小板聚集的功能基因组学
  • 批准号:
    8294698
  • 财政年份:
    2011
  • 资助金额:
    $ 197.6万
  • 项目类别:
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