SIMD ANNUAL MEETING--CONFERENCE GRANT

SIMD 年会--会议补助金

基本信息

  • 批准号:
    2805212
  • 负责人:
  • 金额:
    $ 0.7万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1999
  • 资助国家:
    美国
  • 起止时间:
    1999-03-01 至 2000-02-29
  • 项目状态:
    已结题

项目摘要

This application is on behalf of the Society for Inherited Metabolic Disorders (SIMD) to request travel support to permit young US investigators to attend the annual meeting of the SIMD in Lake Lanier, Georgia, March 13-15, 1999. Inborn errors of intermediary metabolism (IEMs) are increasingly recognized as causal to mental retardation, neuromuscular disease, cardiac disorders, hepatic and renal dysfunction, arthritis, diabetes, growth failure, and blindness. These conditions strike infants and young children and thus affect young families. Research into the causes and mechanisms of these inborn errors of metabolism improved diagnosis and has led to effective treatment for many of these conditions, but there is much left to do. This research has also led to substantive increases in our knowledge of the basic science of intermediary metabolism, signal transduction, central nervous system function, intracellular targeting, and basic genetic mechanisms. This increase in knowledge is essential to maintain progress in innovative therapies for these severe disorders. For the US to remain pre-eminent in this important area of research and clinical application, it is essential that young investigators have the opportunity to participate in the SIMD meeting, where they can share their work and contribute to new collaborative projects. The unparalleled advances in the understanding of the molecular and genetic basis of IEMs and the continuing application of this knowledge to clinical situations demands the participation, development, and encouragement of young US investigators.
本申请是代表遗传代谢学会提交的

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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Margretta Seashore其他文献

Margretta Seashore的其他文献

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{{ truncateString('Margretta Seashore', 18)}}的其他基金

DIAGNOSIS OF INBORN ERRORS OF METABOLISM IN INFANTS AND CHILDREN
婴儿和儿童先天性代谢缺陷的诊断
  • 批准号:
    6309772
  • 财政年份:
    1999
  • 资助金额:
    $ 0.7万
  • 项目类别:
SODIUM PHENYLBUTYRATE TREATMENT OF INBORN ERRORS OF AMMONIA METABOLISM
苯丁酸钠治疗先天性氨代谢缺陷
  • 批准号:
    6309732
  • 财政年份:
    1999
  • 资助金额:
    $ 0.7万
  • 项目类别:
GENE THERAPY OF CANAVAN DISEASE
卡纳万病的基因治疗
  • 批准号:
    6265832
  • 财政年份:
    1998
  • 资助金额:
    $ 0.7万
  • 项目类别:
SODIUM PHENYLBUTYRATE TREATMENT OF INBORN ERRORS OF AMMONIA METABOLISM
苯丁酸钠治疗先天性氨代谢缺陷
  • 批准号:
    6122578
  • 财政年份:
    1998
  • 资助金额:
    $ 0.7万
  • 项目类别:
GENE THERAPY OF CANAVAN DISEASE--RETREATMENT
卡纳万病的基因治疗——治疗
  • 批准号:
    6265833
  • 财政年份:
    1998
  • 资助金额:
    $ 0.7万
  • 项目类别:
DIAGNOSIS OF INBORN ERRORS OF METABOLISM IN INFANTS AND CHILDREN
婴儿和儿童先天性代谢缺陷的诊断
  • 批准号:
    6122598
  • 财政年份:
    1998
  • 资助金额:
    $ 0.7万
  • 项目类别:
DIAGNOSIS OF INBORN ERRORS OF METABOLISM IN INFANTS AND CHILDREN
婴儿和儿童先天性代谢缺陷的诊断
  • 批准号:
    6253640
  • 财政年份:
    1997
  • 资助金额:
    $ 0.7万
  • 项目类别:
SODIUM PHENYLBUTYRATE TREATMENT OF INBORN ERRORS OF AMMONIA METABOLISM
苯丁酸钠治疗先天性氨代谢缺陷
  • 批准号:
    6282613
  • 财政年份:
    1997
  • 资助金额:
    $ 0.7万
  • 项目类别:
SODIUM PHENYLBUTYRATE TREATMENT OF INBORN ERRORS OF AMMONIA METABOLISM
苯丁酸钠治疗先天性氨代谢缺陷
  • 批准号:
    6253610
  • 财政年份:
    1997
  • 资助金额:
    $ 0.7万
  • 项目类别:
DIAGNOSIS OF INBORN ERRORS OF METABOLISM IN INFANTS AND CHILDREN
婴儿和儿童先天性代谢缺陷的诊断
  • 批准号:
    6282633
  • 财政年份:
    1997
  • 资助金额:
    $ 0.7万
  • 项目类别:
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