Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis

By Farg Manal A.   Soo Kai Y.   Warraich Sadaf T.   Sundaramoorthy Vinod   Blair Ian P.   Atkin Julie D.  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 717-728

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

By Mórotz Gábor M.   De Vos Kurt J.   Vagnoni Alessio   Ackerley Steven   Shaw Christopher E.   Miller Christopher C.J.  

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

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite