raw data-miR-206 Reduces the Severity of Motor Neuron Degeneration in the Facial Nuclei of the Brainstem in a Mouse Model of SMA
收藏NIAID Data Ecosystem2026-03-12 收录
官方服务：
资源简介：
research data of the work
应用场景：
创建时间：
2021-04-14
相关数据集
Genetic Data from MLPA Analysis in a Consanguineous Iranian Family with Spinal Muscular Atrophy (SMA)
This dataset includes raw electropherogram files (FSA format) generated by Multiplex Ligation-dependent Probe Amplification (MLPA) analysis of SMN1 and SMN2 genes in three affected members (Patients 7
Figshare2025-11-12 更新70
Additional file 1 of Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy
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
Mechanism of Mitochondrial Dysfunction in Spinal and Bulbar Muscular Atrophy [RNA-seq]. Mechanism of Mitochondrial Dysfunction in Spinal and Bulbar Muscular Atrophy [RNA-seq]
Spinal and bulbar muscular atrophy (SBMA) is a neuromuscular disorder caused by a polyglutamine expansion in the androgen receptor (AR). Previous studies have shown that transcriptional dysregulation
NIAID Data Ecosystem30
Expression data from SMA fibroblasts treated with amiloride or EIPA. Expression data from SMA fibroblasts treated with amiloride or EIPA
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
Suppression of NCALD protects against spinal muscular atrophy by restoring impaired endocytosis. Homo sapiens
Spinal muscular atrophy (SMA) is a common genetic motor neuron (MN) disease caused by low levels of the ubiquitously expressed housekeeping survival motor neuron (SMN) protein, whereas concomitant ove
NIAID Data Ecosystem30
