RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations

By Daigle J. Gavin   Lanson Nicholas A.   Smith Rebecca B.   Casci Ian   Maltare Astha   Monaghan John   Nichols Charles D.   Kryndushkin Dmitri   Shewmaker Frank   Pandey Udai Bhan  

Human Molecular Genetics, Vol. 22, Iss. 6, 2013-03 ,pp. : 1193-1205

Oxford University Press

Access to resources Recommend Favorite

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43

By Lanson Nicholas A.   Maltare Astha   King Hanna   Smith Rebecca   Kim Ji Han   Taylor J. Paul   Lloyd Thomas E.   Pandey Udai Bhan  

Human Molecular Genetics, Vol. 20, Iss. 13, 2011-07 ,pp. : 2510-2523

Oxford University Press

Access to resources Recommend Favorite

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

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite