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Journal Abstract Search


227 related items for PubMed ID: 30399166

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  • 4. Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS.
    Ayers JI, Diamond J, Sari A, Fromholt S, Galaleldeen A, Ostrow LW, Glass JD, Hart PJ, Borchelt DR.
    Acta Neuropathol; 2016 Dec; 132(6):827-840. PubMed ID: 27704280
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  • 13. Tryptophan residue 32 in human Cu-Zn superoxide dismutase modulates prion-like propagation and strain selection.
    Crown A, McAlary L, Fagerli E, Brown H, Yerbury JJ, Galaleldeen A, Cashman NR, Borchelt DR, Ayers JI.
    PLoS One; 2020 Dec; 15(1):e0227655. PubMed ID: 31999698
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  • 16. Characterization of the activity, aggregation, and toxicity of heterodimers of WT and ALS-associated mutant Sod1.
    Brasil AA, de Carvalho MDC, Gerhardt E, Queiroz DD, Pereira MD, Outeiro TF, Eleutherio ECA.
    Proc Natl Acad Sci U S A; 2019 Dec 17; 116(51):25991-26000. PubMed ID: 31796595
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  • 18. 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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  • 19. Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.
    Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A.
    Acta Neuropathol; 2010 Mar 27; 119(3):335-44. PubMed ID: 20111867
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  • 20. An analysis of interactions between fluorescently-tagged mutant and wild-type SOD1 in intracellular inclusions.
    Qualls DA, Crosby K, Brown H, Borchelt DR.
    PLoS One; 2013 Mar 27; 8(12):e83981. PubMed ID: 24391857
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