Astrocyte loss of mutant SOD1 delays ALS disease onset and progression in G85R transgenic mice

By Wang Lijun   Gutmann David H.   Roos Raymond P.  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 286-293

Oxford University Press

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Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse

By Wang Lijun   Deng Han-Xiang   Grisotti Gabriella   Zhai Hong   Siddique Teepu   Roos Raymond P.  

Human Molecular Genetics, Vol. 18, Iss. 9, 2009-05 ,pp. : 1642-1651

Oxford University Press

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A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice

By Teuling Eva   van Dis Vera   Wulf Phebe S.   Haasdijk Elize D.   Akhmanova Anna   Hoogenraad Casper C.   Jaarsma Dick  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2849-2862

Oxford University Press

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Variation in aggregation propensities among ALS-associated variants of SOD1: Correlation to human disease

By Prudencio Mercedes   Hart P. John   Borchelt David R.   Andersen Peter M.  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3217-3226

Oxford University Press

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Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice

By Turner Bradley J.   Ackerley Steven   Davies Kay E.   Talbot Kevin  

Human Molecular Genetics, Vol. 19, Iss. 5, 2010-03 ,pp. : 815-824

Oxford University Press

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