Deletion of DMD exon 52 in the pig results in fulminant muscular dystrophy

ChEBI2013-08-06 更新2026-07-21 收录

基因编辑动物

杜氏肌营养不良症

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-44096 数据链接链接失效反馈

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资源简介：

Deletion of DMD exon 52 in the pig results in fulminant muscular dystrophy

创建时间：

2013-08-06

In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [WES]

基因治疗疗效评估

杜氏肌营养不良症

Duchenne muscular dystrophy (DMD) is the most common fatal genetic disease. Clustered regularly interspaced short palindromic repeat (CRISPR)-mediated gene editing is a promising strategy for permanen

NIAID Data Ecosystem110

Dataset Longitudinal alterations of gait features in children with Duchenne muscular dystrophy

步态分析

杜氏肌营养不良症

This dataset contains subject information, 3D gait analysis data (spatiotemporal, kinematic and kinetic parameters) of children with Duchenne muscular dystrophy and typically developing children. This

DataCite Commons2025-06-01 更新60

Multiomics Analysis of the mdx/mTR Mouse Model of Duchenne Muscular Dystrophy

杜氏肌营养不良症

多组学分析

This dataset contains RNA sequencing, proteomics, metabolomics, lipidomics, primer sequence, and Ingenuity Pathway Analysis data for a study evaluating differences between the transcriptome, proteome,

Zenodo2019-10-24 更新30

Cep295nl-P2A-Cre

基因编辑动物

神经科学表达谱

由国家遗传工程小鼠资源库合作共建单位江苏集萃药康生物科技有限公司利用基因编辑技术，自主研发，供应，保存。应用领域为：在成熟的精子中表达。在脑、视网膜、肺和肾中也有表达。其中脑部的大脑脑干、大脑皮层和丘脑的高度表达，在小脑和海马中表达量不及前者

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Multi-level omics analysis of gene expression in a murine model of dystrophin loss and therapeutic restoration [mRNA]

杜氏肌营养不良症

基因治疗疗效评估

Duchenne muscular dystrophy (DMD) is a classical monogenic disorder, a model disease for genomic studies and a priority candidate for regenerative medicine and gene therapy. Although the genetic cause

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Deletion of DMD exon 52 in the pig results in fulminant muscular dystrophy

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