Modulation of functional properties of laforin phosphatase by alternative splicing reveals a novel mechanism for the EPM2A gene in Lafora progressive myoclonus epilepsy

By Dubey Deepti   Ganesh Subramaniam  

Human Molecular Genetics, Vol. 17, Iss. 19, 2008-10 ,pp. : 3010-3020

Oxford University Press

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A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

By Topcu M.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 345-352

Oxford University Press

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Laforin, a dual specificity phosphatase involved in Lafora disease, regulates insulin response and whole-body energy balance in mice

By Vernia Santiago   Heredia Miguel   Criado Olga   Rodriguez de Cordoba Santiago   Garcia-Roves Pablo M.   Cansell Céline   Denis Raphael   Luquet Serge   Foufelle Fabienne   Ferre Pascal   Sanz Pascual  

Human Molecular Genetics, Vol. 20, Iss. 13, 2011-07 ,pp. : 2571-2584

Oxford University Press

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Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation

By Fernández-Sánchez Maria Elena  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3161-3171

Oxford University Press

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Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy

By Chan Elayne M.   Ackerley Cameron A.   Lohi Hannes   Ianzano Leonarda   Cortez Miguel A.   Shannon Patrick   Scherer Stephen W.   Minassian Berge A.  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1117-1129

Oxford University Press

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