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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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, 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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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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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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