Search Results - "Lasmézas, C I"
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Tissue distribution of bovine spongiform encephalopathy agent in primates after intravenous or oral infection
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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The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells
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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3
Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals
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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4
Immune system-dependent and -independent replication of the scrapie agent
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
The transmissible spongiform encephalopathies
Published in Revue scientifique et technique (International Office of Epizootics) (01-04-2003)“…Transmissible spongiform encephalopathies (TSEs) represent a group of neurodegenerative diseases characterised by a very long incubation period in regard to…”
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6
Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis
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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7
New variant Creutzfeldt-Jakob disease in France
Published in The Lancet (British edition) (04-01-1997)Get more information
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8
BSE transmission to macaques
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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Role of the 37 kDa laminin receptor precursor in the life cycle of prions
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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10
The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein
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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11
Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein
Published in Science (American Association for the Advancement of Science) (17-01-1997)“…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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Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor
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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Diagnosis of Bovine Spongiform Encephalopathy
Published in The veterinary journal (1997) (01-01-2001)Get full text
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14
Adaptation of the Bovine Spongiform Encephalopathy Agent to Primates and Comparison with Creutzfeldt-Jakob Disease: Implications for Human Health
Published in Proceedings of the National Academy of Sciences - PNAS (27-03-2001)“…There is substantial scientific evidence to support the notion that bovine spongiform encephalopathy (BSE) has contaminated human beings, causing variant…”
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Microglial cells respond to amyloidogenic PrP peptide by the production of inflammatory cytokines
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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Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy
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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17
Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junction
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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Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues
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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Creutzfeldt-Jakob disease
Published in The Lancet (British edition) (11-05-1996)Get more information
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A novel generation of heparan sulfate mimetics for the treatment of prion diseases
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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