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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

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中文摘要
翻译
局灶性皮质发育不良（FCD）是一种大脑皮质发育畸形，由紊乱和异常的神经元和胶质细胞组成。非传染性疾病是儿童和成人耐药癫痫的最常见原因。抗癫痫药物就是我们
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
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