Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition

By Hauke Jan   Riessland Markus   Lunke Sebastian   Eypoglu Ilker Y.   Blmcke Ingmar   El-Osta Assam   Wirth Brunhilde   Hahnen Eric  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 304-317

Oxford University Press

Access to resources Recommend Favorite

Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice

By Sumner Charlotte J.   Wee Claribel D.   Warsing Leigh C.   Choe Dong W.   Ng Andrew S.   Lutz Cathleen   Wagner Kathryn R.  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3145-3152

Oxford University Press

Access to resources Recommend Favorite

Stat5 constitutive activation rescues defects in spinal muscular atrophy

By Ting Chen-Hung   Lin Chiao-Wei   Wen Shin-Lan   Hsieh-Li Hsiu-Mei   Li Hung  

Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. : 499-514

Oxford University Press

Access to resources Recommend Favorite

Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice

By Heier Christopher R.   Satta Rosalba   Lutz Cathleen   DiDonato Christine J.  

Human Molecular Genetics, Vol. 19, Iss. 20, 2010-10 ,pp. : 3906-3918

Oxford University Press

Access to resources Recommend Favorite

Animal models of spinal muscular atrophy

By Monani Umrao R.  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2451-2457

Oxford University Press

Access to resources Recommend Favorite