Search Results - "Lasmézas, C I"

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  1. 1

    Tissue distribution of bovine spongiform encephalopathy agent in primates after intravenous or oral infection by Herzog, C, Salès, N, Etchegaray, N, Charbonnier, A, Freire, S, Dormont, D, Deslys, J-P, Lasmézas, CI

    Published in The Lancet (British edition) (07-02-2004)
    “…The disease-associated form of prion protein (PrP res) has been noted in lymphoreticular tissues in patients with variant Creutzfeldt-Jakob disease (vCJD)…”
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    Journal Article
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    The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells by Rieger, Roman, Edenhofer, Frank, Lasmézas, Corinne Ida, Weiss, Stefan

    Published in Nature medicine (01-12-1997)
    “…Prions are thought to consist of infectious proteins that cause transmissible spongiform encephalopathies. According to overwhelming evidence, the pathogenic…”
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    Journal Article
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    Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals by Demaimay, R, Adjou, K T, Beringue, V, Demart, S, Lasmézas, C I, Deslys, J P, Seman, M, Dormont, D

    Published in Journal of Virology (01-12-1997)
    “…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    Immune system-dependent and -independent replication of the scrapie agent by Lasmezas, C.I. (CEA/DSV/DRM/CRSSA, Fontenay-aux-Roses, France.), Cesbron, J.Y, Deslys, J.P, Demaimay, R, Adjou, K.T, Rioux, R, Lemaire, C, Locht, C, Dormont, D

    Published in Journal of Virology (01-02-1996)
    “…Using the severe combined immunodeficiency (SCID) mouse model, we investigated the requirement of the immune system for the development of scrapie after…”
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  5. 5

    The transmissible spongiform encephalopathies by Lasmézas, C I

    “…Transmissible spongiform encephalopathies (TSEs) represent a group of neurodegenerative diseases characterised by a very long incubation period in regard to…”
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    Journal Article
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    Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis by Beringue, Vincent, Demoy, Marina, Lasmézas, Corinne I., Gouritin, Bruno, Weingarten, Colette, Deslys, Jean-Philippe, Andreux, Jean-Paul, Couvreur, Patrick, Dormont, Dominique

    Published in The Journal of pathology (01-03-2000)
    “…The involvement of spleen macrophages in the early stages of scrapie pathogenesis was studied by applying the ‘macrophage‐suicide technique’ to…”
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    Journal Article
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    BSE transmission to macaques by Lasmezas, C.I, Deslys, J.P, Demaimay, R, Adjou, I.T, Lamoury, F, Dormont, D, Robain, O, Ironside, J, Hauw, J.J

    Published in Nature (London) (27-06-1996)
    “…The recent description in the United Kingdom of a new variant of Creutzfeldt-Jacob disease (vCJD) with a unique clinicopathological presentation has raised…”
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    Journal Article
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    Role of the 37 kDa laminin receptor precursor in the life cycle of prions by Rieger, R., Lasmézas, C.I., Weiss, S.

    Published in Transfusion clinique et biologique (Paris) (01-02-1999)
    “…Prions are thought to consist of infectious proteins that cause, in the absence of detectable nucleic acid, a group of fatal neurodegenerative diseases, called…”
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    Journal Article Conference Proceeding
  10. 10

    The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein by Gauczynski, Sabine, Peyrin, Jean-Michel, Haïk, Stéphane, Leucht, Christoph, Hundt, Christoph, Rieger, Roman, Krasemann, Susanne, Deslys, Jean-Philippe, Dormont, Dominique, Lasmézas, Corinne Ida, Weiss, Stefan

    Published in The EMBO journal (01-11-2001)
    “…Recently, we identified the 37‐kDa laminin receptor precursor (LRP) as an interactor for the prion protein (PrP). Here, we show the presence of the 37‐kDa LRP…”
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    Journal Article
  11. 11

    Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein by Lasmezas, C.I. (Commissariat a l'Energie Atomique, Fontenay-aux-Roses, France.), Deslys, J.P, Robain, I, Jaegly, A, Beringue, V, Peyrin, J.M, Fournier, J.G, Hauw, J.J, Rossier, J, Dormont, D

    “…The agent responsible for transmissible spongiform encephalopathies (TSEs) is thought to be a malfolded, protease-resistant version (PrPres) of the normal…”
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  12. 12

    Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor by Hundt, Christoph, Peyrin, Jean-Michel, Haïk, Stéphane, Gauczynski, Sabine, Leucht, Christoph, Rieger, Roman, Riley, Maria Louise, Deslys, Jean-Philippe, Dormont, Dominique, Lasmézas, Corinne Ida, Weiss, Stefan

    Published in The EMBO journal (01-11-2001)
    “…Cell‐binding and internalization studies on neuronal and non‐neuronal cells have demonstrated that the 37‐kDa/67‐kDa laminin receptor (LRP/LR) acts as the…”
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    Journal Article
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    Microglial cells respond to amyloidogenic PrP peptide by the production of inflammatory cytokines by Peyrin, Jean-Michel, Lasmézas, Corinne Ida, Haïk, Stéphane, Tagliavini, Fabrizio, Salmona, Mario, Williams, Alun, Richie, Diane, Deslys, Jean-Philippe, Dormont, Dominique

    Published in Neuroreport (17-03-1999)
    “…The scrapie isoform of the prion protein (PrPres) induces neurodegeneration and gliosis in the central nervous system. These features may be reproduced in…”
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    Journal Article
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    Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy by Lasmezas, Corinne Ida, Deslys, Jean-Philippe, Demaimay, Remi, Adjou, Karim T, Hauw, Jean-Jacques, Dormont, Dominique

    Published in Journal of general virology (01-07-1996)
    “…1 Service de Neurovirologie, DSV/DRM/CRSSA, Commissariat à l'Energie Atomique, 60-68 avenue Div. Leclerc, BP 6, 92 265 Fontenay-aux-Roses Cedex, France 2…”
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    Journal Article
  17. 17

    Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junction by Gohel, C., Grigoriev, V., Escaig-Haye, F., Lasmézas, C. I., Deslys, J.-P., Langeveld, J., Akaaboune, M., Hantaï, D., Fournier, J.-G.

    Published in Journal of neuroscience research (15-01-1999)
    “…We examined the localization of the normal cellular isoform of prion protein (PrPc) in mammalian skeletal muscle. Using two anti‐PrP antibodies, the…”
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    Journal Article
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    Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues by Fournier, J G, Escaig-Haye, F, Billette de Villemeur, T, Robain, O, Lasmézas, C I, Deslys, J P, Dormont, D, Brown, P

    Published in Cell and tissue research (01-04-1998)
    “…In transmissible spongiform encephalopathies (TSE), such as scrapie in animals and Creutzfeldt-Jakob disease in humans, the central event is the conversion of…”
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    A novel generation of heparan sulfate mimetics for the treatment of prion diseases by Adjou, Karim Tarik, Simoneau, Steve, Sales, Nicole, Lamoury, Francois, Dormont, Dominique, Papy-Garcia, Dulce, Barritault, Denis, Deslys, Jean-Philippe, Lasmezas, Corinne Ida

    Published in Journal of general virology (01-09-2003)
    “…1 CEA, DSV/DRM, 18 route du Panorama, BP6, 92265 Fontenay aux Roses Cedex, France 2 OTR3 Sarl, 33 rue Pierre Brossolette, 94000 Créteil, France 3 Laboratoire…”
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