INCLUSION BODY MYOPATHY ASSOPCIATED WITH APAGET DISEASE OF BONE AND FRONTOTEMPOR

与Apaget骨病和额颞叶病相关的包涵体肌病

• 批准号: 8166932
• 负责人: VIRGINIA Eunice KIMONIS
• 金额: $ 0.03万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-12-01 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8166932
• 关键词: Affect; Anxiety; Bone Diseases; Computer Retrieval of Information on Scientific Projects Database; Dementia; Disease; Funding; Genes; Genetic; Grant; Inclusion Bodies; Institution; Knowledge; Mental Depression; Myopathy; Osteitis Deformans; Questionnaires; Research; Research Personnel; Resources; Series; Source; Testing; United States National Institutes of Health; trait; Affect; Anxiety; Bone Diseases; Computer Retrieval of Information on Scientific Projects Database; Dementia; Disease; Funding; Genes; Genetic; Grant; Inclusion Bodies; Institution; Knowledge; Mental Depression; Myopathy; Osteitis Deformans; Questionnaires; Research; Research Personnel; Resources; Series; Source; Testing; United States National Institutes of Health; trait

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. Inclusion body myopathy associated with Paget s disease of the bone and/or dementia is a rare progressive autosomal dominant disorder. In this study the researchers propose to study how the knowledge of whether or not the subject has this genetic trait affects his/her levels of anxiety and depression. Subjects will be asked if they wish to be tested for this gene and a series of questionnaires and scales will be administered to test levels of anxiety and depression.

该副本是利用众多研究子项目之一 由NIH/NCRR资助的中心赠款提供的资源。子弹和 调查员（PI）可能已经从其他NIH来源获得了主要资金， 因此可以在其他清晰的条目中代表。列出的机构是 对于中心，这不一定是调查员的机构。 与骨骼和/或痴呆症Paget疾病相关的包容体肌病是一种罕见的进行性常染色体显性疾病。 在这项研究中，研究人员建议研究对受试者是否具有这种遗传特征的知识如何影响他/她的焦虑和抑郁水平。 将询问受试者是否希望对该基因进行测试，并将一系列问卷和尺度对焦虑和抑郁水平进行测试。