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581 related items for PubMed ID: 23281774

  • 21. 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
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  • 22. A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum.
    Fasana E, Fossati M, Ruggiano A, Brambillasca S, Hoogenraad CC, Navone F, Francolini M, Borgese N.
    FASEB J; 2010 May; 24(5):1419-30. PubMed ID: 20008544
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  • 23. Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8).
    Kanekura K, Nishimoto I, Aiso S, Matsuoka M.
    J Biol Chem; 2006 Oct 06; 281(40):30223-33. PubMed ID: 16891305
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  • 24. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M, Dykes-Hoberg M, Culotta VC, Price DL, Wong PC, Rothstein JD.
    Neurobiol Dis; 2001 Dec 06; 8(6):933-41. PubMed ID: 11741389
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  • 25. VAPB interacts with and modulates the activity of ATF6.
    Gkogkas C, Middleton S, Kremer AM, Wardrope C, Hannah M, Gillingwater TH, Skehel P.
    Hum Mol Genet; 2008 Jun 01; 17(11):1517-26. PubMed ID: 18263603
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  • 26. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1.
    Bruijn LI, Houseweart MK, Kato S, Anderson KL, Anderson SD, Ohama E, Reaume AG, Scott RW, Cleveland DW.
    Science; 1998 Sep 18; 281(5384):1851-4. PubMed ID: 9743498
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  • 27. A potential role for the p75 low-affinity neurotrophin receptor in spinal motor neuron degeneration in murine and human amyotrophic lateral sclerosis.
    Lowry KS, Murray SS, McLean CA, Talman P, Mathers S, Lopes EC, Cheema SS.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Sep 18; 2(3):127-34. PubMed ID: 11771768
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  • 28. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations.
    Jeon GS, Shim YM, Lee DY, Kim JS, Kang M, Ahn SH, Shin JY, Geum D, Hong YH, Sung JJ.
    Mol Neurobiol; 2019 Mar 18; 56(3):2007-2021. PubMed ID: 29982983
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  • 29. Alterations in AQP4 expression and polarization in the course of motor neuron degeneration in SOD1G93A mice.
    Dai J, Lin W, Zheng M, Liu Q, He B, Luo C, Lu X, Pei Z, Su H, Yao X.
    Mol Med Rep; 2017 Aug 18; 16(2):1739-1746. PubMed ID: 28627708
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  • 30. Delayed disease onset and extended survival in the SOD1G93A rat model of amyotrophic lateral sclerosis after suppression of mutant SOD1 in the motor cortex.
    Thomsen GM, Gowing G, Latter J, Chen M, Vit JP, Staggenborg K, Avalos P, Alkaslasi M, Ferraiuolo L, Likhite S, Kaspar BK, Svendsen CN.
    J Neurosci; 2014 Nov 19; 34(47):15587-600. PubMed ID: 25411487
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  • 31. Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.
    Hossaini M, Cardona Cano S, van Dis V, Haasdijk ED, Hoogenraad CC, Holstege JC, Jaarsma D.
    J Neuropathol Exp Neurol; 2011 Aug 19; 70(8):662-77. PubMed ID: 21760539
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  • 32. 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
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  • 33. Muscle atrophy and motor neuron degeneration in human NEDL1 transgenic mice.
    Zhang L, Haraguchi S, Koda T, Hashimoto K, Nakagawara A.
    J Biomed Biotechnol; 2011 Oct 08; 2011():831092. PubMed ID: 20976258
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  • 34. 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 Oct 08; 18(2):115-36. PubMed ID: 17593875
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  • 35. Corticospinal motor neurons and related subcerebral projection neurons undergo early and specific neurodegeneration in hSOD1G⁹³A transgenic ALS mice.
    Ozdinler PH, Benn S, Yamamoto TH, Güzel M, Brown RH, Macklis JD.
    J Neurosci; 2011 Mar 16; 31(11):4166-77. PubMed ID: 21411657
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  • 36. Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice.
    Wong M, Martin LJ.
    Hum Mol Genet; 2010 Jun 01; 19(11):2284-302. PubMed ID: 20223753
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  • 37. Depletion of reduced glutathione enhances motor neuron degeneration in vitro and in vivo.
    Chi L, Ke Y, Luo C, Gozal D, Liu R.
    Neuroscience; 2007 Feb 09; 144(3):991-1003. PubMed ID: 17150307
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  • 38. Functional links between SQSTM1 and ALS2 in the pathogenesis of ALS: cumulative impact on the protection against mutant SOD1-mediated motor dysfunction in mice.
    Hadano S, Mitsui S, Pan L, Otomo A, Kubo M, Sato K, Ono S, Onodera W, Abe K, Chen X, Koike M, Uchiyama Y, Aoki M, Warabi E, Yamamoto M, Ishii T, Yanagawa T, Shang HF, Yoshii F.
    Hum Mol Genet; 2016 Aug 01; 25(15):3321-3340. PubMed ID: 27439389
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  • 39. Neuroprotective effect of the PACAP-ADNP axis on SOD1G93A mutant motor neuron death induced by trophic factors deprivation.
    Magrì B, D'Amico AG, Maugeri G, Morello G, La Cognata V, Saccone S, Federico C, Cavallaro S, D'Agata V.
    Neuropeptides; 2023 Dec 01; 102():102386. PubMed ID: 37856900
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  • 40. Mutant SOD1G93A triggers mitochondrial fragmentation in spinal cord motor neurons: neuroprotection by SIRT3 and PGC-1α.
    Song W, Song Y, Kincaid B, Bossy B, Bossy-Wetzel E.
    Neurobiol Dis; 2013 Mar 01; 51():72-81. PubMed ID: 22819776
    [Abstract] [Full Text] [Related]

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