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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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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Dual effects of increased glycogen synthase kinase-3β activity on adult neurogenesis

By Fuster-Matanzo Almudena   Llorens-Martín María   Sirerol-Piquer María Salomé   García-Verdugo José Manuel   Avila Jesús   Hernández Félix  

Human Molecular Genetics, Vol. 22, Iss. 7, 2013-04 ,pp. : 1300-1315

Oxford University Press

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Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localization of polycystin-2 in vivo and in vitro

By Streets Andrew J.   Moon David J.   Kane Michelle E.   Obara Tomoko   Ong Albert C.M.  

Human Molecular Genetics, Vol. 15, Iss. 9, 2006-05 ,pp. : 1465-1473

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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