Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

By Murray Lyndsay M.   Comley Laura H.   Thomson Derek   Parkinson Nick   Talbot Kevin   Gillingwater Thomas H.  

Human Molecular Genetics, Vol. 17, Iss. 7, 2008-04 ,pp. : 949-962

Oxford University Press

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SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

By Riessland Markus   Ackermann Bastian   Frster Anja   Jakubik Miriam   Hauke Jan   Garbes Lutz   Fritzsche Ina   Mende Ylva   Blumcke Ingmar   Hahnen Eric   Wirth Brunhilde  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1492-1506

Oxford University Press

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Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

By Minamiyama Makoto   Katsuno Masahisa   Adachi Hiroaki   Waza Masahiro   Sang Chen   Kobayashi Yasushi   Tanaka Fumiaki   Doyu Manabu   Inukai Akira   Sobue Gen  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1183-1192

Oxford University Press

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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

By Kariya Shingo   Park Gyu-Hwan   Maeno-Hikichi Yuka   Leykekhman Olga   Lutz Cathleen   Arkovitz Marc S.   Landmesser Lynn T.   Monani Umrao R.  

Human Molecular Genetics, Vol. 17, Iss. 16, 2008-08 ,pp. : 2552-2569

Oxford University Press

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Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy

By Ling Karen K. Y.   Gibbs Rebecca M.   Feng Zhihua   Ko Chien-Ping  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 185-195

Oxford University Press

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