CORIELL - NINDS HUMAN GENETICS RESOURCE CENTER

CORIELL - NINDS 人类遗传学资源中心

• 批准号: 10930767
• 负责人: LAURA SCHEINFELDT
• 金额: $ 150.61万
• 依托单位: CORIELL INSTITUTE FOR MEDICAL RESEARCH
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-09-30 至 2024-09-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10930767
• 关键词: Academia; Biological; Catalogs; Cell Line; Cerebrovascular Disorders; Clinical; Communities; DNA; Data; Data Set; Dedications; Diagnosis; Dystonia; Ensure; Epilepsy; Equipment and supply inventories; Funding; Genetic; Genotype; Gilles de la Tourette syndrome; Goals; Human Genetics; Individual; Industry; Infrastructure; Motor Neuron Disease; National Institute of Neurological Disorders and Stroke; Neurologic; Nonprofit Organizations; Parkinsonian Disorders; Phenotype; Policies; Process; Research Personnel; Resources; Sampling; Scientist; Standardization; Subjects Selections; System; United States National Institutes of Health; data exchange; data interoperability; data sharing; database of Genotypes and Phenotypes; genetic resource; lymphoblastoid cell line; nervous system disorder; repository; web site

"The NINDS DNA and Cell Line Repository (hereinafter “NINDS repository”), established in 2002, receives, processes, curates, stores, and distributes genetic samples and accompanying clinical and genotypic data to the scientific community. Samples are available to researchers from academia, industry, and non-profit organizations. Currently, the NINDS repository contains DNA samples, lymphoblastoid cell lines (LCL), and DNA 96-well plates (panels) from more than 51,000 well phenotyped unique individuals diagnosed with neurological disorders (cerebrovascular diseases, dystonia, epilepsy, motor neuron diseases, Parkinsonism, or Tourette syndrome), or from neurologically normal controls. These materials were collected and generated over many years from NINDS-funded studies that carefully selected subjects, and many of the samples are available in a finite quantity."

2002年成立的“ Ninds DNA和细胞系存储库（本文“ NINDS储存库”），将接收，过程，策划，存储和分发遗传样本，并分发遗传样本，并参与临床和基因型数据，向科学界提供。样本可供研究人员提供学术界，行业，行业以及非计划的colosity colosity collys collys colosity contrys conts conters。 （LCL）和DNA 96孔板（面板），来自51,000多个诊断为神经系统疾病（脑血管疾病，肌张力障碍，癫痫，癫痫，运动神经元疾病，parkinsonism或Tourette综合症）的独特个体（脑血管疾病，癫痫，运动神经元疾病），或从这些材料中进行了多个材料，该材料是毛茸茸的。许多样品都有有限的数量。”