Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism

By Charbonnier F.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1825-1829

Oxford University Press

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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

By Cruts Marc   Rademakers Rosa   van der Zee Julie   Dermaut Bart   de Pooter Tim   de Rijk Peter   Del-Favero Jurgen   van Broeckhoven Christine  

Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1753-1762

Oxford University Press

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Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalance

By López-Menéndez Celia   Gamir-Morralla Andrea   Jurado-Arjona Jerónimo   Higuero Alonso M.   Campanero Miguel R.   Ferrer Isidro   Hernández Félix   Ávila Jesús   Díaz-Guerra Margarita   Iglesias Teresa  

Human Molecular Genetics, Vol. 22, Iss. 3, 2013-02 ,pp. : 466-482

Oxford University Press

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MSUT2 is a determinant of susceptibility to tau neurotoxicity

By Guthrie Chris R.   Greenup Lynne   Leverenz James B.   Kraemer Brian C.  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 1989-1999

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Tau's role in the developing brain: implications for intellectual disability

By Sapir Tamar   Frotscher Michael   Levy Talia   Mandelkow Eva-Maria   Reiner Orly  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1681-1692

Oxford University Press

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