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Stat5 constitutive activation rescues defects in spinal muscular atrophy
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C Madocsai et al.
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The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation
F Gabanella et al.
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SMNΔ7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN
TT Le et al.
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Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons
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A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy
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L Fan et al.
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Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model
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An intrinsic distinction in neuromuscular junction assembly and maintenance in different skeletal muscles
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Modulation of survival motor neuron pre-mRNA splicing by inhibition of alternative 3′ splice site pairing
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