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Journal Abstract Search

329 related items for PubMed ID: 29666246

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  • 3. The metal cofactor zinc and interacting membranes modulate SOD1 conformation-aggregation landscape in an in vitro ALS model.
    Sannigrahi A, Chowdhury S, Das B, Banerjee A, Halder A, Kumar A, Saleem M, Naganathan AN, Karmakar S, Chattopadhyay K.
    Elife; 2021 Apr 07; 10():. PubMed ID: 33825682
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  • 5. Nonnative SOD1 trimer is toxic to motor neurons in a model of amyotrophic lateral sclerosis.
    Proctor EA, Fee L, Tao Y, Redler RL, Fay JM, Zhang Y, Lv Z, Mercer IP, Deshmukh M, Lyubchenko YL, Dokholyan NV.
    Proc Natl Acad Sci U S A; 2016 Jan 19; 113(3):614-9. PubMed ID: 26719414
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  • 8. A copper-deficient form of mutant Cu/Zn-superoxide dismutase as an early pathological species in amyotrophic lateral sclerosis.
    Tokuda E, Nomura T, Ohara S, Watanabe S, Yamanaka K, Morisaki Y, Misawa H, Furukawa Y.
    Biochim Biophys Acta Mol Basis Dis; 2018 Jun 19; 1864(6 Pt A):2119-2130. PubMed ID: 29551730
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  • 9. Polyanion binding accelerates the formation of stable and low-toxic aggregates of ALS-linked SOD1 mutant A4V.
    Zhao D, Zhang S, Meng Y, Xiongwei D, Zhang D, Liang Y, Wang L, Liu C.
    Proteins; 2014 Dec 19; 82(12):3356-72. PubMed ID: 25220364
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  • 13. Heterodimer formation of wild-type and amyotrophic lateral sclerosis-causing mutant Cu/Zn-superoxide dismutase induces toxicity independent of protein aggregation.
    Witan H, Kern A, Koziollek-Drechsler I, Wade R, Behl C, Clement AM.
    Hum Mol Genet; 2008 May 15; 17(10):1373-85. PubMed ID: 18211954
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  • 15. Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS).
    Sangwan S, Zhao A, Adams KL, Jayson CK, Sawaya MR, Guenther EL, Pan AC, Ngo J, Moore DM, Soriaga AB, Do TD, Goldschmidt L, Nelson R, Bowers MT, Koehler CM, Shaw DE, Novitch BG, Eisenberg DS.
    Proc Natl Acad Sci U S A; 2017 Aug 15; 114(33):8770-8775. PubMed ID: 28760994
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  • 17. Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS Patients.
    Keskin I, Forsgren E, Lange DJ, Weber M, Birve A, Synofzik M, Gilthorpe JD, Andersen PM, Marklund SL.
    PLoS One; 2016 Aug 15; 11(2):e0150133. PubMed ID: 26919046
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  • 19. Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stress.
    Cookson MR, Menzies FM, Manning P, Eggett CJ, Figlewicz DA, McNeil CJ, Shaw PJ.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun 15; 3(2):75-85. PubMed ID: 12215229
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  • 20. ALS-linked misfolded SOD1 species have divergent impacts on mitochondria.
    Pickles S, Semmler S, Broom HR, Destroismaisons L, Legroux L, Arbour N, Meiering E, Cashman NR, Vande Velde C.
    Acta Neuropathol Commun; 2016 Apr 27; 4(1):43. PubMed ID: 27121871
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