Oxidative stress causes abnormal accumulation of familial amyotrophic lateral sclerosis-related mutant SOD1 in transgenic Caenorhabditis elegans

By Ishii N.   Oeda T.   Shimohama S.   Kitagawa N.   Kohno R.   Imura T.   Shibasaki H.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2013-2023

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

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

Oxford University Press

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SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments

By Joyce Peter  

Mammalian Genome, Vol. 22, Iss. 7-8, 2011-08 ,pp. : 420-448

Springer Publishing Company

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Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria

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Human Molecular Genetics, Vol. 21, Iss. 9, 2012-05 ,pp. : 1979-1988

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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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