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Journal Abstract Search

406 related items for PubMed ID: 26719414

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  • 24. Calcium binding to gatekeeper residues flanking aggregation-prone segments underlies non-fibrillar amyloid traits in superoxide dismutase 1 (SOD1).
    Estácio SG, Leal SS, Cristóvão JS, Faísca PF, Gomes CM.
    Biochim Biophys Acta; 2015 Feb; 1854(2):118-26. PubMed ID: 25463043
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  • 25. MS785-MS27 Reactive Misfolded/Non-Native Zn-Deficient SOD1 Species Exhibit Cytotoxicity and Adopt Heterozygous Conformations in Motor Neurons.
    Tokuda E, Sakashita Y, Tokoro N, Date A, Kosuge Y, Miyasaka T.
    Int J Mol Sci; 2024 May 21; 25(11):. PubMed ID: 38891791
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  • 26. 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 21; 119(3):335-44. PubMed ID: 20111867
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  • 30. Mechanical probes of SOD1 predict systematic trends in metal and dimer affinity of ALS-associated mutants.
    Das A, Plotkin SS.
    J Mol Biol; 2013 Mar 11; 425(5):850-74. PubMed ID: 23291526
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  • 32. Intracellular conformational alterations of mutant SOD1 and the implications for fALS-associated SOD1 mutant induced motor neuron cell death.
    Zhang F, Zhu H.
    Biochim Biophys Acta; 2006 Mar 11; 1760(3):404-14. PubMed ID: 16431026
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  • 34. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
    Jaarsma D, Haasdijk ED, Grashorn JA, Hawkins R, van Duijn W, Verspaget HW, London J, Holstege JC.
    Neurobiol Dis; 2000 Dec 11; 7(6 Pt B):623-43. PubMed ID: 11114261
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  • 35. An immunological epitope selective for pathological monomer-misfolded SOD1 in ALS.
    Rakhit R, Robertson J, Vande Velde C, Horne P, Ruth DM, Griffin J, Cleveland DW, Cashman NR, Chakrabartty A.
    Nat Med; 2007 Jun 11; 13(6):754-9. PubMed ID: 17486090
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  • 36. Superoxide Dismutase 1 (SOD1)-Derived Peptide Inhibits Amyloid Aggregation of Familial Amyotrophic Lateral Sclerosis SOD1 Mutants.
    Banerjee V, Shani T, Katzman B, Vyazmensky M, Papo N, Israelson A, Engel S.
    ACS Chem Neurosci; 2016 Nov 16; 7(11):1595-1606. PubMed ID: 27540759
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  • 37. Aberrant zinc binding to immature conformers of metal-free copper-zinc superoxide dismutase triggers amorphous aggregation.
    Leal SS, Cristóvão JS, Biesemeier A, Cardoso I, Gomes CM.
    Metallomics; 2015 Feb 16; 7(2):333-46. PubMed ID: 25554447
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  • 38. Non-native soluble oligomers of Cu/Zn superoxide dismutase (SOD1) contain a conformational epitope linked to cytotoxicity in amyotrophic lateral sclerosis (ALS).
    Redler RL, Fee L, Fay JM, Caplow M, Dokholyan NV.
    Biochemistry; 2014 Apr 15; 53(14):2423-32. PubMed ID: 24660965
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