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  1. 1.   ALS/FTD-Linked Mutation in FUS Suppresses Infra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS
  2. Lopez-Erauskin, Jone; Tadokoro, Takahiro; Baughn, Michael W.; Myers, Brian; McAlonis-Downes, Melissa; Chillon-Marinas, Carlos; Asiaban, Joshua N.; Artates, Jonathan; Bui, Anh T.; Vetto, Anne P.; Lee, Sandra K.; Le, Ai Vy; Sun, Ying; Jambeau, Melanie; Boubaker, Jihane; Swing, Debbie; Qiu, Jinsong; Hicks, Geoffrey G.; Ouyang, Zhengyu; Fu, Xiang-Dong; Tessarollo, Lino; Ling, Shuo-Chien; Parone, Philippe A.; Shaw, Christopher E.; Marsala, Martin; lagier-Tourenne, ClotilDe; Cleveland, Don W.; Da Cruz, Sandrine
  3. Neuron. 2018, NOV 21; 100(4): 816-+.
  1. 2.   Axonal Mitochondrial Clusters Containing Mutant SOD1 in Transgenic Models of ALS
  2. Sotelo-Silveira, J. R.; Lepanto, P.; Elizondo, V.; Horjales, S.; Palacios, F.; Martinez-Palma, L.; Marin, M.; Beckman, J. S.; Barbeito, L.
  3. Antioxidants & Redox Signaling. 2009 11(7): 1535-1546.
  1. 3.   Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA
  2. Wang, J.; Xu, G. L.; Slunt, H. H.; Gonzales, V.; Coonfield, M.; Fromholt, D.; Copeland, N. G.; Jenkins, N. A.; Borchelt, D. R.
  3. Neurobiology of Disease. 2005, DEC; 20(3): 943-952.
  1. 4.   Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature
  2. Wang, J.; Slunt, H.; Gonzales, V.; Fromholt, D.; Coonfield, M.; Copeland, N. G.; Jenkins, N. A.; Borchelt, D. R.
  3. Human Molecular Genetics. 2003 12(21): 2753-2764.
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