Characterization of a new group of vesicular transport diseases.
一组新的囊泡运输疾病的特征。
基本信息
- 批准号:304246
- 负责人:
- 金额:$ 62.42万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Operating Grants
- 财政年份:2014
- 资助国家:加拿大
- 起止时间:2014-03-01 至 2019-03-01
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The goal of our study is to better understand the neurodevelopmental disease called DOORS syndrome, not only to provide better care for the affected children, but also to better understand the physiology of the transmission of signals between neurons. DOO
我们研究的目的是为了更好地了解这种名为DOORS综合征的神经发育疾病,不仅是为了更好地照顾受影响的儿童,也是为了更好地了解神经元之间信号传递的生理学。嘟嘟
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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Campeau Philippe M其他文献
Campeau Philippe M的其他文献
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{{ truncateString('Campeau Philippe M', 18)}}的其他基金
Developmental Trajectories in ARID1B-Related Disorders - a Multi-Method Multi-Site Prospective Natural History Study
ARID1B 相关疾病的发育轨迹 - 多方法多地点前瞻性自然历史研究
- 批准号:
486840 - 财政年份:2023
- 资助金额:
$ 62.42万 - 项目类别:
Operating Grants
Identifying and understanding a new skeletal dysplasia caused by ERI1 mutations
识别和理解 ERI1 突变引起的新骨骼发育不良
- 批准号:
472627 - 财政年份:2022
- 资助金额:
$ 62.42万 - 项目类别:
Operating Grants
Role of fibronectin mutations in spondylometaphyseal dysplasia and idiopathic scoliosis.
纤连蛋白突变在脊柱干骺端发育不良和特发性脊柱侧凸中的作用。
- 批准号:
372375 - 财政年份:2017
- 资助金额:
$ 62.42万 - 项目类别:
Operating Grants
Genetic bone diseases; new genes and new treatments
遗传性骨病;
- 批准号:
375001 - 财政年份:2017
- 资助金额:
$ 62.42万 - 项目类别:
Salary Programs
Genetic bone diseases; new genes and new treatments
遗传性骨病;
- 批准号:
295781 - 财政年份:2013
- 资助金额:
$ 62.42万 - 项目类别:
Salary Programs
Phenylbutyrate use to target phosphorylation pathways in human disease
丁酸苯酯用于靶向人类疾病中的磷酸化途径
- 批准号:
248081 - 财政年份:2011
- 资助金额:
$ 62.42万 - 项目类别:
Fellowship Programs
Development of Enzyme Replacement Therapy for Urea Cycle Defects
针对尿素循环缺陷的酶替代疗法的开发
- 批准号:
173692 - 财政年份:2008
- 资助金额:
$ 62.42万 - 项目类别:
Fellowship Programs
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