RNA-seq profiling of MED patient-derived (MATN3 T195K) and unaffected iPSC-chondrogenesis

ChEBI2026-02-12 更新2026-07-12 收录

遗传性神经疾病分子机制

干细胞软骨分化转录组学

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-16598 数据链接链接失效反馈

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资源简介：

RNA-seq profiling of MED patient-derived (MATN3 T195K) and unaffected iPSC-chondrogenesis

创建时间：

2026-02-12

mRNA Sequencing of CMT2A, CMT1A patients and Normal human fibroblasts. mRNA Sequencing of CMT2A, CMT1A patients and Normal human fibroblasts

遗传性神经疾病分子机制

RNA测序分析

We performed RNA sequencing on the 3 CMT2A-causing MFN2 mutations patient cell lines and 3 normal control lines, all cultured in galactose, we found striking transcriptional signature for CMT2A was pr

NIAID Data Ecosystem60

RNA-seq Analysis of 15q Duplication and AS Deletion DPSC derived neurons.

遗传性神经疾病分子机制

差异表达RNA分析

A major problem in studying neurogenetic syndromes is obtaining live neurons from people with these disorders. We have taken a novel approach to studying gene expression in neurons from Angelman or D

NIAID Data Ecosystem40

Additional file 2 of Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases

神经细胞蛋白质组学

遗传性神经疾病分子机制

Additional file 2: Table 2. Proteins of neuromuscular relevance expressed in human skin fibroblasts: Expression of 257 proteins is categorized according to different genetically caused diseased impact

NIAID Data Ecosystem30

RNA-seq Analysis of 15q Duplication and AS Deletion DPSC derived neurons.. Homo sapiens

遗传性神经疾病分子机制

神经元RNA-seq分析

A major problem in studying neurogenetic syndromes is obtaining live neurons from people with these disorders. We have taken a novel approach to studying gene expression in neurons from Angelman or Du

NIAID Data Ecosystem40

Exposure to the heavy metal lead induces DNA copy number alterations in zebrafish cells

重金属毒性表观遗传学

遗传性神经疾病分子机制

DNA copy number variants (CNVs) are associated with the development of complex neurological diseases and disorders including autism spectrum disorder, schizophrenia, Alzheimer’s disease, and Parkinson

NIAID Data Ecosystem30

RNA-seq profiling of MED patient-derived (MATN3 T195K) and unaffected iPSC-chondrogenesis

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