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

Access to resources Recommend Favorite

Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect

By Gavrilina Tatiana O.   McGovern Vicki L.   Workman Eileen   Crawford Thomas O.   Gogliotti Rocky G.   DiDonato Christine J.   Monani Umrao R.   Morris Glenn E.   Burghes Arthur H.M.  

Human Molecular Genetics, Vol. 17, Iss. 8, 2008-04 ,pp. : 1063-1075

Oxford University Press

Access to resources Recommend Favorite

The role of the SMN gene in proximal spinal muscular atrophy

By Melki J.  

Human Molecular Genetics, Vol. 7, Iss. 10, 1998-10 ,pp. : 1531-1536

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System

By Battaglia Giorgio  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1961-1971

Oxford University Press

Access to resources Recommend Favorite