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Reevaluating the role of skeletal muscle in amyotrophic lateral sclerosis pathogenesis:Insights from muscle-derived factors
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作者 Pablo Martinez Brigitte van Zundert Fernando JBustos 《Neural Regeneration Research》 2026年第7期2944-2945,共2页
Amyotrophic lateral sclerosis(ALS)is a progressive neurodegenerative disease marked by motor neuron(MN)degeneration,neuromuscular junction disruption,and muscle atrophy,ultimately leading to paralysis and death.Despit... Amyotrophic lateral sclerosis(ALS)is a progressive neurodegenerative disease marked by motor neuron(MN)degeneration,neuromuscular junction disruption,and muscle atrophy,ultimately leading to paralysis and death.Despite extensive research,no effective treatment exists,highlighting the need to elucidate mechanisms driving ALS pathogenesis.About 90%of ALS cases are sporadic ALS and lack a clear genetic cause;the remaining 10%are familial ALS,associated with mutations in over 25 genes.The most common mutations are in superoxide dismutase 1(SOD1)and C9ORF72,with rarer variants in FUS,TARDBP,TBK1,and VCP. 展开更多
关键词 amyotrophic lateral sclerosis als neurodegenerative disease elucidate mechanisms neuromuscular junction amyotrophic lateral sclerosis motor neuron muscle atrophyultimately junction disruptionand
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