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Evaluation of Quinacrine Treatment for Prion Diseases

Journal of Virology, 2003-08, Vol.77 (15), p.8462-8469

2003

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Tissue distribution of bovine spongiform encephalopathy agent in primates after intravenous or oral infection

The Lancet (British edition), 2004-02, Vol.363 (9407), p.422-428

2004

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BSE transmission to macaques

Nature (London), 1996-06, Vol.381 (6585), p.743-744

1996

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The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells

Nature medicine, 1997-12, Vol.3 (12), p.1383-1388

1997

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The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

The EMBO journal, 2001-11, Vol.20 (21), p.5863-5875

2001

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Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis

The Journal of pathology, 2000-03, Vol.190 (4), p.495-502

2000

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The transmissible spongiform encephalopathies

Revue scientifique et technique (International Office of Epizootics), 2003-04, Vol.22 (1), p.23

Lasmézas, C I

2003

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Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

Science (American Association for the Advancement of Science), 1997-01, Vol.275 (5298), p.402-405

1997

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Immune system-dependent and -independent replication of the scrapie agent

Journal of Virology, 1996-02, Vol.70 (2), p.1292-1295

1996

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Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals

Journal of Virology, 1997-12, Vol.71 (12), p.9685-9689

1997

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Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

The EMBO journal, 2001-11, Vol.20 (21), p.5876-5886

2001

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Gene expression in scrapie. Cloning of a new scrapie-responsive gene and the identification of increased levels of seven other mRNA transcripts

The Journal of biological chemistry, 1998-03, Vol.273 (13), p.7691-7697

1998

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Neurotoxicity of the Putative Transmembrane Domain of the Prion Protein

Neurobiology of disease, 2000-12, Vol.7 (6), p.644-656

2000

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Early dysfunction of central 5-HT system in a murine model of bovine spongiform encephalopathy

Neuroscience, 2009-06, Vol.160 (4), p.731-743

2009

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Adaptation of the Bovine Spongiform Encephalopathy Agent to Primates and Comparison with Creutzfeldt-Jakob Disease: Implications for Human Health

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (7), p.4142-4147

2001

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New variant Creutzfeldt-Jakob disease in France

The Lancet (British edition), 1997-01, Vol.349 (9044), p.30-31

1997

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Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrP

Biological chemistry, 2003-02, Vol.384 (2), p.243-246

2003

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Role of the 37 kDa laminin receptor precursor in the life cycle of prions

Transfusion clinique et biologique (Paris), 1999-02, Vol.6 (1), p.7-16

1999

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New Insight into Abnormal Prion Protein Using Monoclonal Antibodies

Biochemical and biophysical research communications, 1999-11, Vol.265 (3), p.652-657

1999

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Une première étape dans l'identification de récepteurs cellulaires de la protéine du prion

M.S. Médecine sciences, 1998, Vol.14 (5), p.595

1998

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Microglial cells respond to amyloidogenic PrP peptide by the production of inflammatory cytokines

Neuroreport, 1999-03, Vol.10 (4), p.723-729

1999

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Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy

Journal of general virology, 1996-07, Vol.77 (7), p.1601-1609

1996

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Diagnosis of Bovine Spongiform Encephalopathy

The veterinary journal (1997), 2001-01, Vol.161 (1), p.1-4

2001

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Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues

Cell and tissue research, 1998-04, Vol.292 (1), p.77-84

1998

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Hypothèses sur les mécanismes d'action de l'amphotéricine B et de ses dérivés dans les encéphalopathies subaiguës spongiformes transmissibles

M.S. Médecine sciences, 1997, Vol.13 (6-7), p.892

1997

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Evaluation of Quinacrine Treatment for Prion Diseases

Tissue distribution of bovine spongiform encephalopathy agent in primates after intravenous or oral infection

BSE transmission to macaques

The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells

The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein

Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis

The transmissible spongiform encephalopathies

Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

Immune system-dependent and -independent replication of the scrapie agent

Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals

Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

Gene expression in scrapie. Cloning of a new scrapie-responsive gene and the identification of increased levels of seven other mRNA transcripts

Neurotoxicity of the Putative Transmembrane Domain of the Prion Protein

Early dysfunction of central 5-HT system in a murine model of bovine spongiform encephalopathy

Adaptation of the Bovine Spongiform Encephalopathy Agent to Primates and Comparison with Creutzfeldt-Jakob Disease: Implications for Human Health

New variant Creutzfeldt-Jakob disease in France

Different isoforms of the non-integrin laminin receptor are present in mouse brain and bind PrP

Role of the 37 kDa laminin receptor precursor in the life cycle of prions

New Insight into Abnormal Prion Protein Using Monoclonal Antibodies

Une première étape dans l'identification de récepteurs cellulaires de la protéine du prion

Microglial cells respond to amyloidogenic PrP peptide by the production of inflammatory cytokines

Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy

Diagnosis of Bovine Spongiform Encephalopathy

Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues

Hypothèses sur les mécanismes d'action de l'amphotéricine B et de ses dérivés dans les encéphalopathies subaiguës spongiformes transmissibles

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