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Journal Abstract Search

534 related items for PubMed ID: 15983830

  • 21. Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice.
    Turner BJ, Alfazema N, Sheean RK, Sleigh JN, Davies KE, Horne MK, Talbot K.
    Neurobiol Aging; 2014 Apr; 35(4):906-15. PubMed ID: 24210254
    [Abstract] [Full Text] [Related]

  • 22. Systemic overexpression of SQSTM1/p62 accelerates disease onset in a SOD1H46R-expressing ALS mouse model.
    Mitsui S, Otomo A, Nozaki M, Ono S, Sato K, Shirakawa R, Adachi H, Aoki M, Sobue G, Shang HF, Hadano S.
    Mol Brain; 2018 May 29; 11(1):30. PubMed ID: 29843805
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  • 24. Rodent Models of Amyotrophic Lateral Sclerosis.
    Philips T, Rothstein JD.
    Curr Protoc Pharmacol; 2015 Jun 01; 69():5.67.1-5.67.21. PubMed ID: 26344214
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  • 27. Reductions of docosahexaenoic acid-containing phosphatidylcholine levels in the anterior horn of an ALS mouse model.
    Arima H, Omura T, Hayasaka T, Masaki N, Hanada M, Xu D, Banno T, Kobayashi K, Takeuchi H, Kadomatsu K, Matsuyama Y, Setou M.
    Neuroscience; 2015 Jun 25; 297():127-36. PubMed ID: 25841322
    [Abstract] [Full Text] [Related]

  • 28. Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosis.
    Deitch JS, Alexander GM, Bensinger A, Yang S, Jiang JT, Heiman-Patterson TD.
    PLoS One; 2014 Jun 25; 9(6):e99879. PubMed ID: 24945277
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  • 29. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
    Turner BJ, Bäumer D, Parkinson NJ, Scaber J, Ansorge O, Talbot K.
    BMC Neurosci; 2008 Oct 28; 9():104. PubMed ID: 18957104
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  • 30. Amyotrophic lateral sclerosis model derived from human embryonic stem cells overexpressing mutant superoxide dismutase 1.
    Wada T, Goparaju SK, Tooi N, Inoue H, Takahashi R, Nakatsuji N, Aiba K.
    Stem Cells Transl Med; 2012 May 28; 1(5):396-402. PubMed ID: 23197818
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  • 31. Diverse expression of selected SMN complex proteins in humans with sporadic amyotrophic lateral sclerosis and in a transgenic rat model of familial form of the disease.
    Rafałowska J, Sulejczak D, Chrapusta SJ, Gadamski R, Dziewulska D.
    PLoS One; 2014 May 28; 9(8):e104614. PubMed ID: 25122454
    [Abstract] [Full Text] [Related]

  • 32. 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 28; 132(6):827-840. PubMed ID: 27704280
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  • 33. Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALS.
    Hall ED, Andrus PK, Oostveen JA, Fleck TJ, Gurney ME.
    J Neurosci Res; 1998 Jul 01; 53(1):66-77. PubMed ID: 9670993
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  • 34. Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis.
    Menzies FM, Grierson AJ, Cookson MR, Heath PR, Tomkins J, Figlewicz DA, Ince PG, Shaw PJ.
    J Neurochem; 2002 Sep 01; 82(5):1118-28. PubMed ID: 12358759
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  • 35. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
    Kato S, Sumi-Akamaru H, Fujimura H, Sakoda S, Kato M, Hirano A, Takikawa M, Ohama E.
    Acta Neuropathol; 2001 Sep 01; 102(3):233-8. PubMed ID: 11585247
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  • 36. Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis.
    Stieber A, Gonatas JO, Gonatas NK.
    J Neurol Sci; 2000 Aug 15; 177(2):114-23. PubMed ID: 10980307
    [Abstract] [Full Text] [Related]

  • 37. Aberrant enteric neuromuscular system and dysbiosis in amyotrophic lateral sclerosis.
    Zhang Y, Ogbu D, Garrett S, Xia Y, Sun J.
    Gut Microbes; 2021 Aug 15; 13(1):1996848. PubMed ID: 34812107
    [Abstract] [Full Text] [Related]

  • 38. Activation of STAT3 and inhibitory effects of pioglitazone on STAT3 activity in a mouse model of SOD1-mutated amyotrophic lateral sclerosis.
    Shibata N, Yamamoto T, Hiroi A, Omi Y, Kato Y, Kobayashi M.
    Neuropathology; 2010 Aug 15; 30(4):353-60. PubMed ID: 19925559
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  • 39. Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis.
    Turner BJ, Atkin JD, Farg MA, Zang DW, Rembach A, Lopes EC, Patch JD, Hill AF, Cheema SS.
    J Neurosci; 2005 Jan 05; 25(1):108-17. PubMed ID: 15634772
    [Abstract] [Full Text] [Related]

  • 40. Ferroptosis mediates selective motor neuron death in amyotrophic lateral sclerosis.
    Wang T, Tomas D, Perera ND, Cuic B, Luikinga S, Viden A, Barton SK, McLean CA, Samson AL, Southon A, Bush AI, Murphy JM, Turner BJ.
    Cell Death Differ; 2022 Jun 05; 29(6):1187-1198. PubMed ID: 34857917
    [Abstract] [Full Text] [Related]

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