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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Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

By Bosco Daryl A.   Lemay Nathan   Ko Hae Kyung   Zhou Hongru   Burke Chris   Kwiatkowski Thomas J.   Sapp Peter   McKenna-Yasek Diane   Brown Robert H.   Hayward Lawrence J.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4160-4175

Oxford University Press

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Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds

By Ratovitski Tamara  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1451-1460

Oxford University Press

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The unfolded protein response in familial amyotrophic lateral sclerosis

By Wang Lijun   Popko Brian   Roos Raymond P.  

Human Molecular Genetics, Vol. 20, Iss. 5, 2011-03 ,pp. : 1008-1015

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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

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