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Transcription profiling of mouse laser-microdissected motorneurons in a Spinal Muscular Atrophy model (SMA)

ChEBI2008-10-20 更新2026-07-21 收录

脊髓性肌萎缩症

运动神经元转录组

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-10224 数据链接链接失效反馈

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资源简介：

Transcription profiling of mouse laser-microdissected motorneurons in a Spinal Muscular Atrophy model (SMA)

应用场景：

创建时间：

2008-10-20

运动神经元转录组

肌萎缩侧索硬化症（ALS）研究

Spinal motor axons traverse large distances to innervate target muscle, and thus require local control of cellular events for proper functioning of the distal axon. To interrogate axon-specific proces

NIAID Data Ecosystem70

Spinal cord single cell Raw sequence reads of spinal muscular atrophy mouse. Mus musculus

单细胞转录组学

脊髓性肌萎缩症

We performed single-cell RNA sequencing to profile the single-cell transcriptome of the spinal cord of a type I Taiwanese SMA mouse and heterozygous mouse

NIAID Data Ecosystem50

Additional file 1 of Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy

脊髓性肌萎缩症

神经退行性疾病基因

Additional file 1: Figure S1. PLS3 overexpression suppressed pharyngeal pumping defects in smn-1(ok355) animals. Homozygous null smn-1(ok355) animals lacking smn-1 survive through early larval stages

Figshare2020-09-16 更新30

Expression data from SMA fibroblasts treated with amiloride or EIPA. Expression data from SMA fibroblasts treated with amiloride or EIPA

脊髓性肌萎缩症

SMN2

Spinal muscular atrophy (SMA) is an autosomal recessive, pediatric-onset disorder caused by the loss of spinal motor neurons thereby leading to generalized muscle atrophy. SMA is caused by the loss of

NIAID Data Ecosystem60

Munc13-1 Restoration Mitigates Presynaptic Pathology in Spinal Muscular Atrophy

脊髓性肌萎缩症

神经生物学

Data related to Manuscript "Munc13-1 Restoration Mitigates Presynaptic Pathology in Spinal Muscular Atrophy"

Figshare2025-10-01 更新40