SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy

By Wishart Thomas M.   Huang Jack P.-W.   Murray Lyndsay M.   Lamont Douglas J.   Mutsaers Chantal A.   Ross Jenny   Geldsetzer Pascal   Ansorge Olaf   Talbot Kevin   Parson Simon H.   Gillingwater Thomas H.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4216-4228

Oxford University Press

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Restoration of SMN to Emx-1 expressing cortical neurons is not sufficient to provide benefit to a severe mouse model of Spinal Muscular Atrophy

By Taylor Alexander   Glascock Jacqueline   Rose Ferrill   Lutz Cathleen   Lorson Christian  

Transgenic Research, Vol. 22, Iss. 5, 2013-10 ,pp. : 1029-1036

Springer Publishing Company

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Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy

By Butchbach Matthew E.R.   Singh Jasbir   orsteinsdttir Margrt   Saieva Luciano   Slominski Elzbieta   Thurmond John   Andrsson Thorkell   Zhang Jun   Edwards Jonathan D.   Simard Louise R.   Pellizzoni Livio   Jarecki Jill   Burghes Arthur H.M.   Gurney Mark E.  

Human Molecular Genetics, Vol. 19, Iss. 3, 2010-02 ,pp. : 454-467

Oxford University Press

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Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

By Frugier Tony   Tiziano Francesco D.   Cifuentes-Diaz Carmen   Miniou Pierre   Roblot Natacha   Dierich Andrée   Le Meur Marianne   Melki Judith  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 849-858

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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