Expression data from DM1, DM2 and Normal Adult Skeletal Muscle Biopsies

NIAID Data Ecosystem2026-03-11 收录

强直性肌营养不良转录组

骨骼肌疾病表达谱

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE7014 数据链接链接失效反馈

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资源简介：

DM1 and DM2 biopsies from patients were compared to Normal adult individuals Keywords: 3 groups of samples 10 DM1 biopsies, 20 DM2 biopsies, and 6 Normal individuals biopsies

创建时间：

2019-08-08

Expression data from normal or DM1 myoblasts. Homo sapiens

强直性肌营养不良转录组

差异基因表达分析

We are investigating the transcriptional response of changes in RNA steady-state levels between normal and DM1. We used microarrays to detail the global programme of gene expression differences in nor

NIAID Data Ecosystem40

Individual transcriptomic response to strength-training for myotonic dystrophy type 1 patients

强直性肌营养不良转录组

个体化运动干预反应

Myotonic dystrophy type 1 (DM1), the most common form of adult-onset muscular dystrophy, is caused by a CTG expansion resulting in significant transcriptomic dysregulation that leads to muscle weaknes

NIAID Data Ecosystem30

The human myotonic dystrophy type 1 transcriptome. Homo sapiens

强直性肌营养不良转录组

RNA剪接异常

Myotonic dystrophy (DM) is a highly multi-systemic disorder caused by expanded CTG/CCTG repeats. Muscle weakness, myotonia, cardiac arrhythmia, and profound fatigue are common, yet exhibit extreme var

NIAID Data Ecosystem10

RNA-seq: Analysis of differential gene expression between HD and DM1 patient lymphoblastoid cell lines (LCLs) compared to unaffected LCLs.. RNA-seq: Analysis of differential gene expression between HD and DM1 patient lymphoblastoid cell lines (LCLs) compared to unaffected LCLs.

亨廷顿病转录组

强直性肌营养不良转录组

Transcriptome from HD, DM1, and unaffected LCLs. Overall design: Data from two unaffected LCLs: GM04604 (UN-B) and GM02180 (UN-C). From three HD patient LCLs: GM02164 (HD-A), GM03620 (HD-B), and GM140

NIAID Data Ecosystem40

强直性肌营养不良转录组

皮层类器官疾病模型

Myotonic dystrophy type 1 (DM1) is a multisystem, autosomal-dominant inherited disorder caused by CTG microsatellite repeat expansions (MREs) in the 3’ untranslated region of the dystrophia myotonica-

NIAID Data Ecosystem30

Expression data from DM1, DM2 and Normal Adult Skeletal Muscle Biopsies

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