Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive childhood form of motor neuron disease. Previous studies have highlighted nerve- and muscle-specific events in SMA, including atrophy of muscle fibres and post-synaptic motor endplates, loss of lower motor neuron cell bodies and...
المؤلفون الرئيسيون: | Murray, L, Comley, L, Thomson, D, Parkinson, N, Talbot, K, Gillingwater, T |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2008
|
مواد مشابهة
-
Review: neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy.
حسب: Murray, L, وآخرون
منشور في: (2010) -
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy.
حسب: Mutsaers, C, وآخرون
منشور في: (2011) -
Neuromuscular junction pathology is correlated with differential motor unit vulnerability in spinal and bulbar muscular atrophy
حسب: Elana Molotsky, وآخرون
منشور في: (2022-07-01) -
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy.
حسب: Bäumer, D, وآخرون
منشور في: (2009) -
Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy.
حسب: Karen K Y Ling, وآخرون
منشور في: (2010-11-01)