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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Laforin, the most common protein mutated in Lafora disease, regulates autophagy

By Aguado Carmen   Sarkar Sovan   Korolchuk Viktor I.   Criado Olga   Vernia Santiago   Boya Patricia   Sanz Pascual   de Crdoba Santiago Rodrguez   Knecht Erwin   Rubinsztein David C.  

Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2867-2876

Oxford University Press

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Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

By Ganesh Subramaniam   Agarwala Kishan Lal   Ueda Kazunori  

Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2251-2261

Oxford University Press

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Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype

By Alonso M.E.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1263-1271

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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