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11 in total

1. A high-throughput screening method for small-molecule inhibitors of the aberrant mutant SOD1 and dynein complex interaction.

Authors: Xiaohu Tang; Kathleen I Seyb; Mickey Huang; Eli R Schuman; Ping Shi; Haining Zhu; Marcie A Glicksman
Journal: J Biomol Screen Date: 2011-12-01

Review 2. Oxidative stress and nitration in neurodegeneration: cause, effect, or association?

Authors: Harry Ischiropoulos; Joseph S Beckman
Journal: J Clin Invest Date: 2003-01 Impact factor: 14.808

Review 3. A role for copper in the toxicity of zinc-deficient superoxide dismutase to motor neurons in amyotrophic lateral sclerosis.

Authors: Kari A Trumbull; Joseph S Beckman
Journal: Antioxid Redox Signal Date: 2009-07 Impact factor: 8.401

4. Dysregulation of the proteasome increases the toxicity of ALS-linked mutant SOD1.

Authors: Akira Kitamura; Noriko Inada; Hiroshi Kubota; Gen Matsumoto; Masataka Kinjo; Richard I Morimoto; Kazuhiro Nagata
Journal: Genes Cells Date: 2014-01-23 Impact factor: 1.891

5. Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state.

Authors: Mikael J Lindberg; Lena Tibell; Mikael Oliveberg
Journal: Proc Natl Acad Sci U S A Date: 2002-12-13 Impact factor: 11.205

10. Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus.

Authors: Yongwang Zhong; Jiou Wang; Mark J Henderson; Peixin Yang; Brian M Hagen; Teepu Siddique; Bruce E Vogel; Han-Xiang Deng; Shengyun Fang
Journal: Elife Date: 2017-05-02 Impact factor: 8.140

Toxicity of ALS-linked SOD1 mutants.

1. A high-throughput screening method for small-molecule inhibitors of the aberrant mutant SOD1 and dynein complex interaction.

Review 2. Oxidative stress and nitration in neurodegeneration: cause, effect, or association?

Review 3. A role for copper in the toxicity of zinc-deficient superoxide dismutase to motor neurons in amyotrophic lateral sclerosis.

4. Dysregulation of the proteasome increases the toxicity of ALS-linked mutant SOD1.

5. Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state.

Review 6. RNA-binding proteins with prion-like domains in ALS and FTLD-U.

Review 7. Misfolded proteins, endoplasmic reticulum stress and neurodegeneration.

Review 8. The human G93A-superoxide dismutase-1 mutation, mitochondrial glutathione and apoptotic cell death.

9. Direct and indirect mechanisms for wild-type SOD1 to enhance the toxicity of mutant SOD1 in bigenic transgenic mice.

10. Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus.