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TranscriptomicsModeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs (RNA-Seq)
Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by mutations of the survival of motor neuron 1 (SMN1) gene. In the pathogenesis of SMA, pathological changes of the neuromuscular junction (NMJ) precede the motor neuronal loss. Therefore, it is critical to evaluate the NMJ formed by S...
ORGANISM(S): Homo sapiens 
2015-02-03 | E-GEOD-65508 | biostudies-arrayexpress
TranscriptomicsModeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs
Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by mutations of the survival of motor neuron 1 (SMN1) gene. In the pathogenesis of SMA, pathological changes of the neuromuscular junction (NMJ) precede the motor neuronal loss. Therefore, it is critical to evaluate the NMJ formed by S...
ORGANISM(S): Homo sapiens 
2015-01-31 | E-GEOD-65470 | biostudies-arrayexpress
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