The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

By Young Philip J.  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2869-2877

Oxford University Press

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The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy

By Cartaud J.  

Human Molecular Genetics, Vol. 7, Iss. 12, 1998-11 ,pp. : 1927-1933

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 Schizosaccharomyces pombe protein Yab8p and a novel factor, Yip1p, share structural and functional similarity with the spinal muscular atrophy-associated proteins SMN and SIP1

By Hannus Stefan   Bühler Dirk   Romano Marta   Seraphin Bertrand   Fischer Utz  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 663-674

Oxford University Press

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Novel aminoglycosides increase SMN levels in spinal muscular atrophy fibroblasts

By Mattis Virginia   Rai Ravi   Wang Jinhua   Chang Cheng-Wei   Coady Tristan   Lorson Christian  

Human Genetics, Vol. 120, Iss. 4, 2006-11 ,pp. : 589-601

Springer Publishing Company

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