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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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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ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2

By Pedrini Steve   Sau Daniela   Guareschi Stefania   Bogush Marina   Brown Robert H.   Naniche Nicole   Kia Azadeh   Trotti Davide   Pasinelli Piera  

Human Molecular Genetics, Vol. 19, Iss. 15, 2010-08 ,pp. : 2974-2986

Oxford University Press

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Calcium-permeable AMPA receptors promote misfolding of mutant SOD1 protein and development of amyotrophic lateral sclerosis in a transgenic mouse model

By Tateno Minako  

Human Molecular Genetics, Vol. 13, Iss. 19, 2004-10 ,pp. : 2183-2196

Oxford University Press

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An examination of wild-type SOD1 in modulating the toxicity and aggregation of ALS-associated mutant SOD1

By Prudencio Mercedes   Durazo Armando   Whitelegge Julian P.   Borchelt David R.  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4774-4789

Oxford University Press

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