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Journal Abstract Search

197 related items for PubMed ID: 7862672

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  • 3. 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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  • 4. Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice.
    Borchelt DR, Wong PC, Becher MW, Pardo CA, Lee MK, Xu ZS, Thinakaran G, Jenkins NA, Copeland NG, Sisodia SS, Cleveland DW, Price DL, Hoffman PN.
    Neurobiol Dis; 1998 Jul; 5(1):27-35. PubMed ID: 9702785
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  • 5. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria.
    Wong PC, Pardo CA, Borchelt DR, Lee MK, Copeland NG, Jenkins NA, Sisodia SS, Cleveland DW, Price DL.
    Neuron; 1995 Jun; 14(6):1105-16. PubMed ID: 7605627
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  • 6. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
    Kobayakawa Y, Sakumi K, Kajitani K, Kadoya T, Horie H, Kira J, Nakabeppu Y.
    Neuropathol Appl Neurobiol; 2015 Feb; 41(2):227-44. PubMed ID: 24707896
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  • 7. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
    Nakano R.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
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  • 8. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
    Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, Tsujino A, Nishizawa M, Kakita A, Takahashi H.
    Acta Neuropathol; 2007 May; 113(5):535-42. PubMed ID: 17333220
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  • 9. The copper chaperone CCS is abundant in neurons and astrocytes in human and rodent brain.
    Rothstein JD, Dykes-Hoberg M, Corson LB, Becker M, Cleveland DW, Price DL, Culotta VC, Wong PC.
    J Neurochem; 1999 Jan; 72(1):422-9. PubMed ID: 9886096
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  • 10. 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; 72(7):646-61. PubMed ID: 23771221
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  • 11. Mouse motor neuron disease caused by truncated SOD1 with or without C-terminal modification.
    Watanabe Y, Yasui K, Nakano T, Doi K, Fukada Y, Kitayama M, Ishimoto M, Kurihara S, Kawashima M, Fukuda H, Adachi Y, Inoue T, Nakashima K.
    Brain Res Mol Brain Res; 2005 Apr 27; 135(1-2):12-20. PubMed ID: 15857664
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  • 12. Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathology.
    Wang L, Sharma K, Deng HX, Siddique T, Grisotti G, Liu E, Roos RP.
    Neurobiol Dis; 2008 Mar 27; 29(3):400-8. PubMed ID: 18054242
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  • 13. Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
    Clement AM, Nguyen MD, Roberts EA, Garcia ML, Boillée S, Rule M, McMahon AP, Doucette W, Siwek D, Ferrante RJ, Brown RH, Julien JP, Goldstein LS, Cleveland DW.
    Science; 2003 Oct 03; 302(5642):113-7. PubMed ID: 14526083
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  • 16. 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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  • 17. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
    Kato S, Saito M, Hirano A, Ohama E.
    Histol Histopathol; 1999 Jul 01; 14(3):973-89. PubMed ID: 10425565
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  • 18. Inhibition of p38 mitogen activated protein kinase activation and mutant SOD1(G93A)-induced motor neuron death.
    Dewil M, dela Cruz VF, Van Den Bosch L, Robberecht W.
    Neurobiol Dis; 2007 May 01; 26(2):332-41. PubMed ID: 17346981
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  • 19. Therapeutic benefits of putrescine-modified catalase in a transgenic mouse model of familial amyotrophic lateral sclerosis.
    Reinholz MM, Merkle CM, Poduslo JF.
    Exp Neurol; 1999 Sep 01; 159(1):204-16. PubMed ID: 10486188
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  • 20. Assessment of metal concentrations in the SOD1G93A mouse model of amyotrophic lateral sclerosis and its potential role in muscular denervation, with particular focus on muscle tissue.
    Enge TG, Ecroyd H, Jolley DF, Yerbury JJ, Kalmar B, Dosseto A.
    Mol Cell Neurosci; 2018 Apr 01; 88():319-329. PubMed ID: 29524628
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