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444 related items for PubMed ID: 15294873

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content.
    De Vos KJ, Chapman AL, Tennant ME, Manser C, Tudor EL, Lau KF, Brownlees J, Ackerley S, Shaw PJ, McLoughlin DM, Shaw CE, Leigh PN, Miller CCJ, Grierson AJ.
    Hum Mol Genet; 2007 Nov 15; 16(22):2720-2728. PubMed ID: 17725983
    [Abstract] [Full Text] [Related]

  • 23. Neuronal over-expression of chromogranin A accelerates disease onset in a mouse model of ALS.
    Ezzi SA, Larivière R, Urushitani M, Julien JP.
    J Neurochem; 2010 Dec 15; 115(5):1102-11. PubMed ID: 20807312
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  • 25. Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS.
    Higgins CM, Jung C, Ding H, Xu Z.
    J Neurosci; 2002 Mar 15; 22(6):RC215. PubMed ID: 11886899
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  • 28. Early decrease of redox factor-1 in spinal motor neurons of presymptomatic transgenic mice with a mutant SOD1 gene.
    Manabe Y, Warita H, Murakami T, Shiote M, Hayashi T, Nagano I, Shoji M, Abe K.
    Brain Res; 2001 Oct 05; 915(1):104-7. PubMed ID: 11578626
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  • 29. Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.
    Wang J, Xu G, Slunt HH, Gonzales V, Coonfield M, Fromholt D, Copeland NG, Jenkins NA, Borchelt DR.
    Neurobiol Dis; 2005 Dec 05; 20(3):943-52. PubMed ID: 16046140
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  • 30. 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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  • 31. The cellular mRNA expression of GABA and glutamate receptors in spinal motor neurons of SOD1 mice.
    Petri S, Schmalbach S, Grosskreutz J, Krampfl K, Grothe C, Dengler R, Van Den Bosch L, Robberecht W, Bufler J.
    J Neurol Sci; 2005 Nov 15; 238(1-2):25-30. PubMed ID: 16087196
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  • 32. Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation.
    Shibata N.
    Neuropathology; 2001 Mar 15; 21(1):82-92. PubMed ID: 11304046
    [Abstract] [Full Text] [Related]

  • 33. Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: mechanistic relationship and differential sensitivity to intervention.
    Tradewell ML, Cooper LA, Minotti S, Durham HD.
    Neurobiol Dis; 2011 Jun 15; 42(3):265-75. PubMed ID: 21296666
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  • 34. 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
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  • 35. A cysteine residue affects the conformational state and neuronal toxicity of mutant SOD1 in mice: relevance to the pathogenesis of ALS.
    Nagano S, Takahashi Y, Yamamoto K, Masutani H, Fujiwara N, Urushitani M, Araki T.
    Hum Mol Genet; 2015 Jun 15; 24(12):3427-39. PubMed ID: 25762155
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  • 36. Appearance of phagocytic microglia adjacent to motoneurons in spinal cord tissue from a presymptomatic transgenic rat model of amyotrophic lateral sclerosis.
    Sanagi T, Yuasa S, Nakamura Y, Suzuki E, Aoki M, Warita H, Itoyama Y, Uchino S, Kohsaka S, Ohsawa K.
    J Neurosci Res; 2010 Sep 15; 88(12):2736-46. PubMed ID: 20648658
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  • 37. Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.
    Atkin JD, Farg MA, Turner BJ, Tomas D, Lysaght JA, Nunan J, Rembach A, Nagley P, Beart PM, Cheema SS, Horne MK.
    J Biol Chem; 2006 Oct 06; 281(40):30152-65. PubMed ID: 16847061
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  • 38. Loss of glial fibrillary acidic protein marginally accelerates disease progression in a SOD1(H46R) transgenic mouse model of ALS.
    Yoshii Y, Otomo A, Pan L, Ohtsuka M, Hadano S.
    Neurosci Res; 2011 Jul 06; 70(3):321-9. PubMed ID: 21453731
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  • 39. [ALS and excitatory amino acid].
    Aizawa H, Kwak S.
    Brain Nerve; 2007 Oct 06; 59(10):1117-27. PubMed ID: 17969352
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  • 40. Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis.
    Urushitani M, Kurisu J, Tsukita K, Takahashi R.
    J Neurochem; 2002 Dec 06; 83(5):1030-42. PubMed ID: 12437574
    [Abstract] [Full Text] [Related]

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