These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


374 related items for PubMed ID: 11732268

  • 1. [Superoxide dismutase-1 (SOD-1) gene mutation-dependent mechanisms of neural degeneration in amyotrophic lateral sclerosis].
    Iłzecka J.
    Neurol Neurochir Pol; 2001; 35(3):461-9. PubMed ID: 11732268
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Toxicity from different SOD1 mutants dysregulates the complement system and the neuronal regenerative response in ALS motor neurons.
    Lobsiger CS, Boillée S, Cleveland DW.
    Proc Natl Acad Sci U S A; 2007 May 01; 104(18):7319-26. PubMed ID: 17463094
    [Abstract] [Full Text] [Related]

  • 5. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
    Nakano R.
    Rinsho Shinkeigaku; 1995 Dec 01; 35(12):1546-8. PubMed ID: 8752459
    [Abstract] [Full Text] [Related]

  • 6. Imbalanced excitatory to inhibitory synaptic input precedes motor neuron degeneration in an animal model of amyotrophic lateral sclerosis.
    Schütz B.
    Neurobiol Dis; 2005 Oct 01; 20(1):131-40. PubMed ID: 16137574
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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 01; 104(4):993-1005. PubMed ID: 18233996
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 7(6 Pt B):623-43. PubMed ID: 11114261
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
    Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX.
    Science; 1994 Jun 17; 264(5166):1772-5. PubMed ID: 8209258
    [Abstract] [Full Text] [Related]

  • 18. Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS.
    Kirby J, Halligan E, Baptista MJ, Allen S, Heath PR, Holden H, Barber SC, Loynes CA, Wood-Allum CA, Lunec J, Shaw PJ.
    Brain; 2005 Jul 17; 128(Pt 7):1686-706. PubMed ID: 15872021
    [Abstract] [Full Text] [Related]

  • 19. Molecular approaches to amyotrophic lateral sclerosis.
    Smith RG, Appel SH.
    Annu Rev Med; 1995 Jul 17; 46():133-45. PubMed ID: 7598450
    [Abstract] [Full Text] [Related]

  • 20. Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis.
    Ripps ME, Huntley GW, Hof PR, Morrison JH, Gordon JW.
    Proc Natl Acad Sci U S A; 1995 Jan 31; 92(3):689-93. PubMed ID: 7846037
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 19.