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Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues

The Lancet (British edition), 2001-07, Vol.358 (9277), p.208-209

2001

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Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

Nature (London), 1997-10, Vol.389 (6650), p.498-501

1997

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Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells

Nature medicine, 1999-11, Vol.5 (11), p.1308-1312

1999

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Scrapie strain variation and mutation

British medical bulletin, 1993-10, Vol.49 (4), p.822-838

BRUCE, M. E

1993

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Comparison of the neuropathological characteristics of bovine spongiform encephalopathy (BSE) and variant Creutzfeldt-Jakob disease (vCJD) in mice

Neuropathology and applied neurobiology, 2003-06, Vol.29 (3), p.262-272

2003

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The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis

Journal of general virology, 1991-03, Vol.72 (3), p.595-603

1991

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Transmission of bovine spongiform encephalopathy and scrapie to mice

Journal of general virology, 1992-08, Vol.73 (8), p.1891-1897

1992

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Heparan Sulfate Proteoglycan Is Associated with Amyloid Plaques and Neuroanatomically Targeted PrP Pathology throughout the Incubation Period of Scrapie-Infected Mice

Experimental neurology, 1998-02, Vol.149 (2), p.447-454

1998

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Murine Scrapie Infection Causes an Abnormal Germinal Centre Reaction in the Spleen

Journal of comparative pathology, 2004-02, Vol.130 (2), p.181-194

2004

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PrP protein is associated with follicular dendritic cells of spleens and lymph nodes in uninfected and scrapie-infected mice

The Journal of pathology, 1992-12, Vol.168 (4), p.413-418

1992

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Scrapie strain variation and its implications

Current topics in microbiology and immunology, 1991, Vol.172, p.125

1991

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Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie

Nature medicine, 2001-04, Vol.7 (4), p.485-487

2001

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Straining the prion hypothesis

Nature (London), 1998-01, Vol.391 (6665), p.345-346

1998

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Biological Evidence that Scrapie Agent Has an Independent Genome

Journal of general virology, 1987-01, Vol.68 (1), p.79-89

1987

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In vivo toxicity of prion protein in murine scrapie : ultrastructural and immunogold studies

Neuropathology and applied neurobiology, 1997-04, Vol.23 (2), p.93-101

1997

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Sites of prion protein accumulation in scrapie-infected mouse spleen revealed by immuno-electron microscopy

The Journal of pathology, 2000-07, Vol.191 (3), p.323-332

2000

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Temporary inactivation of follicular dendritic cells delays neuroinvasion of scrapie

Nature medicine, 2000-07, Vol.6 (7), p.719-720

2000

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Detection of PrP in extraneural tissues

Microscopy research and technique, 2000-07, Vol.50 (1), p.40-45

2000

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Nor98-like sheep scrapie in the United Kingdom in 1989

Veterinary record, 2007-05, Vol.160 (19), p.665-666

2007

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Scrapie strains maintain biological phenotypes on propagation in a cell line in culture

The EMBO journal, 2001-07, Vol.20 (13), p.3351-3358

2001

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Morphogenesis of amyloid plaques in 87V murine scrapie

Neuropathology and applied neurobiology, 1994-12, Vol.20 (6), p.535-542

1994

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Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie

Neuroscience letters, 1989-07, Vol.102 (1), p.1-6

1989

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Severely combined immunodeficient (SCID) mice resist infection with bovine spongiform encephalopathy

Journal of general virology, 1997-10, Vol.78 (10), p.2707-2710

1997

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The immunobiology of TSE diseases

Journal of general virology, 2001-10, Vol.82 (Pt 10), p.2307-2318

2001

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Infection specific prion protein (PrP) accumulates on neuronal plasmalemma in scrapie infected mice

Neuroscience letters, 1992-11, Vol.147 (1), p.106-109

1992

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Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells

Scrapie strain variation and mutation

Comparison of the neuropathological characteristics of bovine spongiform encephalopathy (BSE) and variant Creutzfeldt-Jakob disease (vCJD) in mice

The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis

Transmission of bovine spongiform encephalopathy and scrapie to mice

Heparan Sulfate Proteoglycan Is Associated with Amyloid Plaques and Neuroanatomically Targeted PrP Pathology throughout the Incubation Period of Scrapie-Infected Mice

Murine Scrapie Infection Causes an Abnormal Germinal Centre Reaction in the Spleen

PrP protein is associated with follicular dendritic cells of spleens and lymph nodes in uninfected and scrapie-infected mice

Scrapie strain variation and its implications

Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie

Straining the prion hypothesis

Biological Evidence that Scrapie Agent Has an Independent Genome

In vivo toxicity of prion protein in murine scrapie : ultrastructural and immunogold studies

Sites of prion protein accumulation in scrapie-infected mouse spleen revealed by immuno-electron microscopy

Temporary inactivation of follicular dendritic cells delays neuroinvasion of scrapie

Detection of PrP in extraneural tissues

Nor98-like sheep scrapie in the United Kingdom in 1989

Scrapie strains maintain biological phenotypes on propagation in a cell line in culture

Morphogenesis of amyloid plaques in 87V murine scrapie

Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie

Severely combined immunodeficient (SCID) mice resist infection with bovine spongiform encephalopathy

The immunobiology of TSE diseases

Infection specific prion protein (PrP) accumulates on neuronal plasmalemma in scrapie infected mice

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