Neurodegenerative phenotypes in an A53T α-synuclein transgenic mouse model are independent of LRRK2

By Daher João Paulo L.   Pletnikova Olga   Biskup Saskia   Musso Alessandra   Gellhaar Sandra   Galter Dagmar   Troncoso Juan C.   Lee Michael K.   Dawson Ted M.   Dawson Valina L.   Moore Darren J.  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2420-2431

Oxford University Press

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Expansion of the Parkinson disease-associated SNCA- Rep1 allele upregulates human -synuclein in transgenic mouse brain

By Cronin Kenneth D.   Ge Dongliang   Manninger Paul   Linnertz Colton   Rossoshek Anna   Orrison Bonnie M.   Bernard David J.   El-Agnaf Omar M.A.   Schlossmacher Michael G.   Nussbaum Robert L.   Chiba-Falek Ornit  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3274-3285

Oxford University Press

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α-Synuclein accumulates in huntingtin inclusions but forms independent filaments and its deficiency attenuates early phenotype in a mouse model of Huntington's disease

By Tomás-Zapico Cristina   Díez-Zaera María   Ferrer Isidre   Gómez-Ramos Pilar   Morán María A.   Miras-Portugal M. Teresa   Díaz-Hernández Miguel   Lucas José J.  

Human Molecular Genetics, Vol. 21, Iss. 3, 2012-02 ,pp. : 495-510

Oxford University Press

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Transgenic mouse model of early-onset DYT1 dystonia

By Shashidharan P.  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 125-133

Oxford University Press

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A systematic RNAi screen reveals involvement of endocytic pathway in neuronal dysfunction in -synuclein transgenic C . elegans

By Kuwahara Tomoki   Koyama Akihiko   Koyama Shingo   Yoshina Sawako   Ren Chang-Hong   Kato Takeo   Mitani Shohei   Iwatsubo Takeshi  

Human Molecular Genetics, Vol. 17, Iss. 19, 2008-10 ,pp. : 2997-3009

Oxford University Press

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