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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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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Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor

By Forsgren L.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2045-2050

Oxford University Press

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Reduction of polyglutamine toxicity by TDP-43, FUS and progranulin in Huntington's disease models

By Tauffenberger Arnaud   Chitramuthu Babykumari P.   Bateman Andrew   Bennett Hugh PJ.   Parker J. Alex  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 782-794

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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