课题基金 / 基金详情

STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS

STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
阿尔茨海默病蛋白质的结构和功能
批准号:
2771872
负责人:
JAMES J LAH
金额:
$10.72万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-09-01 至 2001-08-31

项目摘要

项目成果

JAMES J LAH的其他基金

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相关文献

中文摘要
翻译
最近发现与早发性家族性痴呆相关的基因
英文摘要
The recent identification of genes associated with early -onset familial Alzheimer's disease (FAD) opens new and exciting avenues of investigation into the pathogenesis of this devastating and incurable cause of dementia. The first gene to be identified, S182, may be responsible for many of the chromosome 14 associated cases of FAD. Subsequent reports identifying a homologous gene, STM2, implicated in chromosome 1 associated FAD are perhaps most remarkable for the fact that these two genes have begun to define a new gene family which is important in the pathogenesis of Alzheimer's disease. There are two other known members of this family which have been identified in Caenorhabditis elegans. The amino acid sequences and the putative structure of the four proteins are closely related and suggest that they may share functional similarities. In this proposal, we outline a series of experiments and hypotheses which will begin to critically analyze the function of these proteins. In Specific Aim 1, we propose the production of a series of isoform- and domain-specific antibodies to S182 and STM2. These antibodies are being designed to allow their use in addressing several specific hypotheses in subsequent Specific Aims. We present the results of some Preliminary Studies which demonstrate the successful production of the antibody to S182. In Specific Aims 2 and 3, we will exploit these antibodies to pursue questions regarding the distribution and structure of these proteins. In the final Specific Aim, we will investigate the possible functional relationship between S182 and STM2 and the C. elegans protein SPE-4. These experiments will attempt to phenotypically rescue loss of function spe-4 mutants through the introduction of human S182 and STM2 sequences. In addition to these research activities, this proposal is being submitted as part of an overall plan of training and career development. Activities are outlined over a five year period which will provide the Principal Investigator with a unique opportunity to development as a research scientist and help to insure his success in academic neurology.
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会议论文
Translation of GluN2B-selective PET radiopharmaceuticals in Alzheimers patients
  • 批准号:
    10716786
  • 项目类别:
  • 资助金额:
    $78.25万
  • 财政年份:
    2023
  • 负责人:
    JAMES J LAH
  • 依托单位:
The Emory Healthy Brain Study: Discovering Predictive Biomarkers for Alzheimer's Disease
  • 批准号:
    10348719
  • 项目类别:
  • 资助金额:
    $713.81万
  • 财政年份:
    2021
  • 负责人:
    JAMES J LAH
  • 依托单位:
The Emory Healthy Brain Study: Discovering Predictive Biomarkers for Alzheimer's Disease
  • 批准号:
    10555203
  • 项目类别:
  • 资助金额:
    $701.17万
  • 财政年份:
    2021
  • 负责人:
    JAMES J LAH
  • 依托单位:
Emory Alzheimer's Disease Research Center
  • 批准号:
    10408021
  • 项目类别:
  • 资助金额:
    $46.88万
  • 财政年份:
    2020
  • 负责人:
    JAMES J LAH
  • 依托单位:
国内基金
海外基金
犬钩虫中Caenorhabditis elegans daf同源基因的鉴定和功能研究
  • 批准号:
    30972181
  • 项目类别:
    面上项目
  • 资助金额:
    30.0万元
  • 批准年份:
    2009
  • 负责人:
    杨玉荣
  • 依托单位:
利用线虫(Caenorhabditis elegans)模型研究14-3-3蛋白在机体抵御逆境因子胁迫过程中的分子作用机制
  • 批准号:
    30771234
  • 项目类别:
    面上项目
  • 资助金额:
    30.0万元
  • 批准年份:
    2007
  • 负责人:
    王亚梅
  • 依托单位: