AMINO ACID INTERRELATIONSHIPS IN HUMAN METABOLIC DISEASE: INBORN ERRORS

人类代谢疾病中氨基酸的相互关系：先天性错误

• 批准号: 7724869
• 负责人: WILLIAM L. NYHAN
• 金额: $ 0.27万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-12-01 至 2008-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7724869
• 关键词: Amino Acids; Computer Retrieval of Information on Scientific Projects Database; Defect; Funding; Grant; Human; Inborn Errors of Metabolism; Inborn Genetic Diseases; Institution; Metabolic; Metabolic Diseases; Molecular; Research; Research Personnel; Resources; Source; United States National Institutes of Health; therapy development

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The objective of this research is the definition of new inborn errors of metabolism, the discovery of their fundamental molecular defects and the elucidation of metabolic abnormalities relevant to the development of therapy.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 本研究的目的是定义新的先天性代谢缺陷，发现其基本的分子缺陷，并阐明与治疗发展相关的代谢异常。