首页/数据集/Detection of mitochondrial mutations through isothermal nucleic acid amplification coupled with CRISPR-Cas13a

Detection of mitochondrial mutations through isothermal nucleic acid amplification coupled with CRISPR-Cas13a

NIAID Data Ecosystem2026-03-12 收录

线粒体突变

CRISPR诊断方法

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP294257 数据链接链接失效反馈

官方服务：

资源简介：

Development of a novel method for detecting mitochondrial point mutations

应用场景：

创建时间：

2020-11-27

单细胞甲基化

线粒体突变

This is a dataset supporting the EPI-Clone manuscript: Targeted single cell methylation profiling of PBMCs was performed with the scTAMseq method.Dataset is an R Data File (RDA) with two Seurat object

DataCite Commons2025-03-04 更新70

Data_Sheet_1_Case Report: A Novel Mutation in the Mitochondrial MT-ND5 Gene Is Associated With Leber Hereditary Optic Neuropathy (LHON).pdf

遗传性视神经病变

线粒体突变

Leber hereditary optic neuropathy (LHON) is a mitochondrial disease causing severe bilateral visual loss, typically in young adults. The disorder is commonly caused by one of three primary point mutat

NIAID Data Ecosystem40

A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to Intramitochondrial Oxidation and an Inflammatory Myopathy in Dutch Shepherd Dogs

炎症性肌病

线粒体突变

Inflammatory myopathies are a group of diseases characterized by infiltration of inflammatory cells into muscle. Young dogs from a small pedigree were evaluated for muscle weakness and atrophy. Muscle

NIAID Data Ecosystem30

Detection of mitochondrial mutations through isothermal nucleic acid amplification coupled with CRISPR-Cas13a

线粒体突变

CRISPR-Cas13a

Development of a novel method for detecting mitochondrial point mutations

NIAID Data Ecosystem50

Homo sapiens Targeted Locus (Loci). Homo sapiens

线粒体突变

癌症遗传学

Studies on mutation and diversity in mitochondrial cytochrome b gene of breast & ovarian carcinoma of Central India

NIAID Data Ecosystem40