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PUBMED FOR HANDHELDS

Journal Abstract Search


665 related items for PubMed ID: 27551074

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  • 23. 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; 7(6 Pt B):623-43. PubMed ID: 11114261
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  • 26. TNF receptor-associated factor 6 interacts with ALS-linked misfolded superoxide dismutase 1 and promotes aggregation.
    Semmler S, Gagné M, Garg P, Pickles SR, Baudouin C, Hamon-Keromen E, Destroismaisons L, Khalfallah Y, Chaineau M, Caron E, Bayne AN, Trempe JF, Cashman NR, Star AT, Haqqani AS, Durcan TM, Meiering EM, Robertson J, Grandvaux N, Plotkin SS, McBride HM, Vande Velde C.
    J Biol Chem; 2020 Mar 20; 295(12):3808-3825. PubMed ID: 32029478
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  • 27. ALS-linked mutant SOD1 proteins promote Aβ aggregates in ALS through direct interaction with Aβ.
    Jang JY, Cho H, Park HY, Rhim H, Kang S.
    Biochem Biophys Res Commun; 2017 Nov 04; 493(1):697-707. PubMed ID: 28864422
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  • 30. Wild-type Cu/Zn-superoxide dismutase is misfolded in cerebrospinal fluid of sporadic amyotrophic lateral sclerosis.
    Tokuda E, Takei YI, Ohara S, Fujiwara N, Hozumi I, Furukawa Y.
    Mol Neurodegener; 2019 Nov 19; 14(1):42. PubMed ID: 31744522
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  • 31. Extracellular wildtype and mutant SOD1 induces ER-Golgi pathology characteristic of amyotrophic lateral sclerosis in neuronal cells.
    Sundaramoorthy V, Walker AK, Yerbury J, Soo KY, Farg MA, Hoang V, Zeineddine R, Spencer D, Atkin JD.
    Cell Mol Life Sci; 2013 Nov 19; 70(21):4181-95. PubMed ID: 23765103
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  • 32. Protein disulphide isomerase is associated with mutant SOD1 in canine degenerative myelopathy.
    Chang RC, Parakh S, Coates JR, Long S, Atkin JD.
    Neuroreport; 2019 Jan 02; 30(1):8-13. PubMed ID: 30422940
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  • 33. Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosis.
    Medinas DB, Rozas P, Martínez Traub F, Woehlbier U, Brown RH, Bosco DA, Hetz C.
    Proc Natl Acad Sci U S A; 2018 Aug 07; 115(32):8209-8214. PubMed ID: 30038021
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  • 34. Immunodetection of disease-associated conformers of mutant cu/zn superoxide dismutase 1 selectively expressed in degenerating neurons in amyotrophic lateral sclerosis.
    Sábado J, Casanovas A, Hernández S, Piedrafita L, Hereu M, Esquerda JE.
    J Neuropathol Exp Neurol; 2013 Jul 07; 72(7):646-61. PubMed ID: 23771221
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  • 35. Early upregulation of cytosolic phospholipase A2α in motor neurons is induced by misfolded SOD1 in a mouse model of amyotrophic lateral sclerosis.
    Malada Edelstein YF, Solomonov Y, Hadad N, Alfahel L, Israelson A, Levy R.
    J Neuroinflammation; 2021 Nov 25; 18(1):274. PubMed ID: 34823547
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  • 36. The Timing and Extent of Motor Neuron Vulnerability in ALS Correlates with Accumulation of Misfolded SOD1 Protein in the Cortex and in the Spinal Cord.
    Genc B, Gozutok O, Kocak N, Ozdinler PH.
    Cells; 2020 Feb 22; 9(2):. PubMed ID: 32098365
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  • 38. Enhancing mitochondrial calcium buffering capacity reduces aggregation of misfolded SOD1 and motor neuron cell death without extending survival in mouse models of inherited amyotrophic lateral sclerosis.
    Parone PA, Da Cruz S, Han JS, McAlonis-Downes M, Vetto AP, Lee SK, Tseng E, Cleveland DW.
    J Neurosci; 2013 Mar 13; 33(11):4657-71. PubMed ID: 23486940
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  • 39. Aberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosis.
    Pokrishevsky E, Grad LI, Yousefi M, Wang J, Mackenzie IR, Cashman NR.
    PLoS One; 2012 Mar 13; 7(4):e35050. PubMed ID: 22493728
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  • 40. A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis.
    Maier M, Welt T, Wirth F, Montrasio F, Preisig D, McAfoose J, Vieira FG, Kulic L, Späni C, Stehle T, Perrin S, Weber M, Hock C, Nitsch RM, Grimm J.
    Sci Transl Med; 2018 Dec 05; 10(470):. PubMed ID: 30518612
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