Correction of tau mis-splicing caused by FTDP-17 MAPT mutations by spliceosome-mediated RNA trans- splicing

By Rodriguez-Martin Teresa   Anthony Karen   Garcia-Blanco Mariano A.   Mansfield S. Gary   Anderton Brian H.   Gallo Jean-Marc  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3266-3273

Oxford University Press

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Puromycin-sensitive aminopeptidase (PSA/NPEPPS) impedes development of neuropathology in hPSA/TAU P301L double-transgenic mice

By Kudo Lili C.   Parfenova Liubov   Ren Guijie   Vi Nancy   Hui Maria   Ma Zhongcai   Lau Kimbley   Gray Michelle   Bardag-Gorce Fawzia   Wiedau-Pazos Martina   Hui Koon-Sea   Karsten Stanislav L.  

Human Molecular Genetics, Vol. 20, Iss. 9, 2011-05 ,pp. : 1820-1833

Oxford University Press

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-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi

By Clarkson Yvonne L.   Gillespie Trudi   Perkins Emma M.   Lyndon Alastair R.   Jackson Mandy  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3634-3641

Oxford University Press

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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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Aggregation of N-terminal huntingtin is dependent on the length of its glutamine repeats

By Li S-H.   Li X-J.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 777-782

Oxford University Press

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