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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The Lafora disease gene product laforin interacts with HIRIP5, a phylogenetically conserved protein containing a NifU-like domain

By Ganesh S.  

Human Molecular Genetics, Vol. 12, Iss. 18, 2003-09 ,pp. : 2359-2368

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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Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment

By Mittal Shuchi   Dubey Deepti   Yamakawa Kazuhiro   Ganesh Subramaniam  

Human Molecular Genetics, Vol. 16, Iss. 7, 2007-04 ,pp. : 753-762

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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