Temporal requirement for high SMN expression in SMA mice

By Le Thanh T.   McGovern Vicki L.   Alwine Isaac E.   Wang Xueyong   Massoni-Laporte Aurelie   Rich Mark M.   Burghes Arthur H.M.  

Human Molecular Genetics, Vol. 20, Iss. 18, 2011-09 ,pp. : 3578-3591

Oxford University Press

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A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype

By Gladman Jordan T.   Bebee Thomas W.   Edwards Chris   Wang Xueyong   Sahenk Zarife   Rich Mark M.   Chandler Dawn S.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4239-4252

Oxford University Press

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A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2

By Monani Umrao R.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1177-1183

Oxford University Press

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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

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Detection of the survival motor neuron (SMN) genes by FISH: further evidence for a role for SMN2 in the modulation of disease severity in SMA patients

By Vitali Tiziana   Sossi Vittorio   Tiziano Francesco   Zappata Stefania   Giuli Anna   Paravatou-Petsotas Maria   Neri Giovanni   Brahe Christina  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2525-2532

Oxford University Press

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