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...
Asıl Yazarlar: | Murray, L, Comley, L, Thomson, D, Parkinson, N, Talbot, K, Gillingwater, T |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
2008
|
Benzer Materyaller
-
Review: neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy.
Yazar:: Murray, L, ve diğerleri
Baskı/Yayın Bilgisi: (2010) -
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy.
Yazar:: Mutsaers, C, ve diğerleri
Baskı/Yayın Bilgisi: (2011) -
Neuromuscular junction pathology is correlated with differential motor unit vulnerability in spinal and bulbar muscular atrophy
Yazar:: Elana Molotsky, ve diğerleri
Baskı/Yayın Bilgisi: (2022-07-01) -
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy.
Yazar:: Bäumer, D, ve diğerleri
Baskı/Yayın Bilgisi: (2009) -
Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy.
Yazar:: Karen K Y Ling, ve diğerleri
Baskı/Yayın Bilgisi: (2010-11-01)