课题基金 / 基金详情

Understanding the genetic architecture and pathophysiology of focal cortical dysplasias using single nucleus RNA sequencing

Understanding the genetic architecture and pathophysiology of focal cortical dysplasias using single nucleus RNA sequencing
使用单核 RNA 测序了解局灶性皮质发育不良的遗传结构和病理生理学
批准号：
470217
负责人：
Srour Myriam
金额：
$67.43万
依托单位：
Research Institute of the McGill University Health Centre
依托单位国家：
加拿大
项目类别：
Operating Grants
财政年份：
2022
资助国家：
加拿大
项目状态：
未结题
起止时间：
2022-09-01 至 2027-09-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=470217&lang=en
关键词：
Epilepsy Mtor Pathway Neurogenetics Single Nucleus Rna Sequencing Somatic Disorders

项目摘要

项目成果

Srour Myriam的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Focal cortical dysplasia (FCD) is a developmental malformation of the cerebral cortex, composed of disorganized and abnormal neurons and glia. FCDs are the most common cause of drug-resistant epilepsy in children and adults. Antiseizure medications are us
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
The physiological, molecular and genetic mechanisms underlying lateralization of motor control
The physiological, molecular and genetic mechanisms underlying lateralization of motor control
The use of Next Generation Exome sequencing in the identification of genes responsible for rare childhood neurologic disorders
海外基金