Reduced survival motor neuron ( Smn ) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III

By Jablonka Sibylle   Schrank Bertold   Kralewski Martina   Rossoll Wilfried   Sendtner Michael  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 341-346

Oxford University Press

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The human centromeric survival motor neuron gene ( SMN2 ) rescues embryonic lethality in Smn –/– mice and results in a mouse with spinal muscular atrophy

By Monani Umrao R.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 333-339

Oxford University Press

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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

By Le Thanh T.  

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 845-857

Oxford University Press

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Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy

By Jablonka S.  

Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 497-505

Oxford University Press

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The Survival Motor Neuron Protein in Spinal Muscular Atrophy

By Coovert Daniel D.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1205-1214

Oxford University Press

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