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250 related items for PubMed ID: 9689132
41. Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration. Li J, Li T, Zhang X, Tang Y, Yang J, Le W. Neurobiol Aging; 2014 Apr; 35(4):837-46. PubMed ID: 24126158 [Abstract] [Full Text] [Related]
42. Transgenic mice with human mutant genes causing Parkinson's disease and amyotrophic lateral sclerosis provide common insight into mechanisms of motor neuron selective vulnerability to degeneration. Martin LJ. Rev Neurosci; 2007 Apr; 18(2):115-36. PubMed ID: 17593875 [Abstract] [Full Text] [Related]
43. Metallothionein expression is altered in a transgenic murine model of familial amyotrophic lateral sclerosis. Gong YH, Elliott JL. Exp Neurol; 2000 Mar; 162(1):27-36. PubMed ID: 10716886 [Abstract] [Full Text] [Related]
44. Overexpression of neurofilament subunit NF-L and NF-H extends survival of a mouse model for amyotrophic lateral sclerosis. Kong J, Xu Z. Neurosci Lett; 2000 Mar 03; 281(1):72-4. PubMed ID: 10686419 [Abstract] [Full Text] [Related]
45. 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]
46. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Tu PH, Raju P, Robinson KA, Gurney ME, Trojanowski JQ, Lee VM. Proc Natl Acad Sci U S A; 1996 Apr 02; 93(7):3155-60. PubMed ID: 8610185 [Abstract] [Full Text] [Related]
47. The human G93A-SOD1 mutation in a pre-symptomatic rat model of amyotrophic lateral sclerosis increases the vulnerability to a mild spinal cord compression. Jokic N, Yip PK, Michael-Titus A, Priestley JV, Malaspina A. BMC Genomics; 2010 Nov 15; 11():633. PubMed ID: 21078175 [Abstract] [Full Text] [Related]
49. Enhancing NAD+ Salvage Pathway Reverts the Toxicity of Primary Astrocytes Expressing Amyotrophic Lateral Sclerosis-linked Mutant Superoxide Dismutase 1 (SOD1). Harlan BA, Pehar M, Sharma DR, Beeson G, Beeson CC, Vargas MR. J Biol Chem; 2016 May 13; 291(20):10836-46. PubMed ID: 27002158 [Abstract] [Full Text] [Related]
50. Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation. Shibata N. Neuropathology; 2001 Mar 13; 21(1):82-92. PubMed ID: 11304046 [Abstract] [Full Text] [Related]
51. 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 Mar 13; 9(6):e99879. PubMed ID: 24945277 [Abstract] [Full Text] [Related]
52. Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells. Oh YK, Shin KS, Yuan J, Kang SJ. J Neurochem; 2008 Feb 13; 104(4):993-1005. PubMed ID: 18233996 [Abstract] [Full Text] [Related]
53. Ablation of proliferating microglia does not affect motor neuron degeneration in amyotrophic lateral sclerosis caused by mutant superoxide dismutase. Gowing G, Philips T, Van Wijmeersch B, Audet JN, Dewil M, Van Den Bosch L, Billiau AD, Robberecht W, Julien JP. J Neurosci; 2008 Oct 08; 28(41):10234-44. PubMed ID: 18842883 [Abstract] [Full Text] [Related]
54. Early and selective pathology of light chain neurofilament in the spinal cord and sciatic nerve of G86R mutant superoxide dismutase transgenic mice. Morrison BM, Shu IW, Wilcox AL, Gordon JW, Morrison JH. Exp Neurol; 2000 Oct 08; 165(2):207-20. PubMed ID: 10993681 [Abstract] [Full Text] [Related]
55. Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation. Kokubo Y, Kuzuhara S, Narita Y, Kikugawa K, Nakano R, Inuzuka T, Tsuji S, Watanabe M, Miyazaki T, Murayama S, Ihara Y. Arch Neurol; 1999 Dec 08; 56(12):1506-8. PubMed ID: 10593307 [Abstract] [Full Text] [Related]
56. Dysregulation of intracellular copper homeostasis is common to transgenic mice expressing human mutant superoxide dismutase-1s regardless of their copper-binding abilities. Tokuda E, Okawa E, Watanabe S, Ono S, Marklund SL. Neurobiol Dis; 2013 Jun 08; 54():308-19. PubMed ID: 23321002 [Abstract] [Full Text] [Related]
57. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1. Tokuda E, Okawa E, Watanabe S, Ono S. Hum Mol Genet; 2014 Mar 01; 23(5):1271-85. PubMed ID: 24163136 [Abstract] [Full Text] [Related]
58. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS. Robertson J, Sanelli T, Xiao S, Yang W, Horne P, Hammond R, Pioro EP, Strong MJ. Neurosci Lett; 2007 Jun 13; 420(2):128-32. PubMed ID: 17543992 [Abstract] [Full Text] [Related]
59. Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease. Nagai M, Aoki M, Miyoshi I, Kato M, Pasinelli P, Kasai N, Brown RH, Itoyama Y. J Neurosci; 2001 Dec 01; 21(23):9246-54. PubMed ID: 11717358 [Abstract] [Full Text] [Related]
60. Defective neurofilament transport in mouse models of amyotrophic lateral sclerosis: a review. Rao MV, Nixon RA. Neurochem Res; 2003 Jul 01; 28(7):1041-7. PubMed ID: 12737529 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]