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Journal Abstract Search

177 related items for PubMed ID: 15509552

  • 1. Prion replication alters the distribution of synaptophysin and caveolin 1 in neuronal lipid rafts.
    Russelakis-Carneiro M, Hetz C, Maundrell K, Soto C.
    Am J Pathol; 2004 Nov; 165(5):1839-48. PubMed ID: 15509552
    [Abstract] [Full Text] [Related]

  • 2. Two types of detergent-insoluble, glycosphingolipid/cholesterol-rich membrane domains from isolated myelin.
    Arvanitis DN, Min W, Gong Y, Heng YM, Boggs JM.
    J Neurochem; 2005 Sep; 94(6):1696-710. PubMed ID: 16045452
    [Abstract] [Full Text] [Related]

  • 3. The prion protein requires cholesterol for cell surface localization.
    Gilch S, Kehler C, Schätzl HM.
    Mol Cell Neurosci; 2006 Feb; 31(2):346-53. PubMed ID: 16278084
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  • 4. Isolation at physiological temperature of detergent-resistant membranes with properties expected of lipid rafts: the influence of buffer composition.
    Chen X, Jen A, Warley A, Lawrence MJ, Quinn PJ, Morris RJ.
    Biochem J; 2009 Jan 15; 417(2):525-33. PubMed ID: 18831713
    [Abstract] [Full Text] [Related]

  • 5. Changes in the glycosylation pattern of prion protein in murine scrapie. Implications for the mechanism of neurodegeneration in prion diseases.
    Russelakis-Carneiro M, Saborio GP, Anderes L, Soto C.
    J Biol Chem; 2002 Sep 27; 277(39):36872-7. PubMed ID: 12130636
    [Abstract] [Full Text] [Related]

  • 6. Glypican-1 facilitates prion conversion in lipid rafts.
    Hooper NM.
    J Neurochem; 2011 Mar 27; 116(5):721-5. PubMed ID: 20681952
    [Abstract] [Full Text] [Related]

  • 7. Prion protein accumulation in lipid rafts of mouse aging brain.
    Agostini F, Dotti CG, Pérez-Cañamás A, Ledesma MD, Benetti F, Legname G.
    PLoS One; 2013 Mar 27; 8(9):e74244. PubMed ID: 24040215
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  • 8. P2X3 receptor localizes into lipid rafts in neuronal cells.
    Vacca F, Amadio S, Sancesario G, Bernardi G, Volonté C.
    J Neurosci Res; 2004 Jun 01; 76(5):653-61. PubMed ID: 15139024
    [Abstract] [Full Text] [Related]

  • 9. Virus-induced alterations of membrane lipids affect the incorporation of PrP Sc into cells.
    Avrahami D, Dayan-Amouyal Y, Tal S, Mincberg M, Davis C, Abramsky O, Gabizon R.
    J Neurosci Res; 2008 Sep 01; 86(12):2753-62. PubMed ID: 18478553
    [Abstract] [Full Text] [Related]

  • 10. Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell types.
    Kercher L, Favara C, Chan CC, Race R, Chesebro B.
    Am J Pathol; 2004 Dec 01; 165(6):2055-67. PubMed ID: 15579448
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  • 12. Correlative studies support lipid peroxidation is linked to PrP(res) propagation as an early primary pathogenic event in prion disease.
    Brazier MW, Lewis V, Ciccotosto GD, Klug GM, Lawson VA, Cappai R, Ironside JW, Masters CL, Hill AF, White AR, Collins S.
    Brain Res Bull; 2006 Jan 30; 68(5):346-54. PubMed ID: 16377442
    [Abstract] [Full Text] [Related]

  • 13. Evidence for segregation of heterologous GPI-anchored proteins into separate lipid rafts within the plasma membrane.
    Wang J, Gunning W, Kelley KM, Ratnam M.
    J Membr Biol; 2002 Sep 01; 189(1):35-43. PubMed ID: 12202950
    [Abstract] [Full Text] [Related]

  • 14. Onset of accumulation of PrPres in murine ME7 scrapie in relation to pathological and PrP immunohistochemical changes.
    Jeffrey M, Martin S, Barr J, Chong A, Fraser JR.
    J Comp Pathol; 2001 Jan 01; 124(1):20-8. PubMed ID: 11428185
    [Abstract] [Full Text] [Related]

  • 15. Translocation of cellular prion protein to non-lipid rafts protects human prion-mediated neuronal damage.
    Jeong JK, Moon MH, Lee YJ, Seol JW, Park SY.
    Int J Mol Med; 2012 Mar 01; 29(3):387-92. PubMed ID: 22179431
    [Abstract] [Full Text] [Related]

  • 16. Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice.
    Pfeifer A, Eigenbrod S, Al-Khadra S, Hofmann A, Mitteregger G, Moser M, Bertsch U, Kretzschmar H.
    J Clin Invest; 2006 Dec 01; 116(12):3204-10. PubMed ID: 17143329
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  • 18. Fibrillar prion peptide PrP(106-126) treatment induces Dab1 phosphorylation and impairs APP processing and Abeta production in cortical neurons.
    Gavín R, Ureña J, Rangel A, Pastrana MA, Requena JR, Soriano E, Aguzzi A, Del Río JA.
    Neurobiol Dis; 2008 May 01; 30(2):243-54. PubMed ID: 18374587
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  • 20. Endogenous prion protein conversion is required for prion-induced neuritic alterations and neuronal death.
    Cronier S, Carimalo J, Schaeffer B, Jaumain E, Béringue V, Miquel MC, Laude H, Peyrin JM.
    FASEB J; 2012 Sep 01; 26(9):3854-61. PubMed ID: 22661006
    [Abstract] [Full Text] [Related]

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