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Prion Strain Mutation and Selection

Science (American Association for the Advancement of Science), 2010-05, Vol.328 (5982), p.1111-1112

Collinge, John

2010

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Depleting Neuronal PrP in Prion Infection Prevents Disease and Reverses Spongiosis

Science (American Association for the Advancement of Science), 2003-10, Vol.302 (5646), p.871-874

2003

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Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (29), p.10238-10243

2008

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Location and Properties of Metal-Binding Sites on the Human Prion Protein

Proceedings of the National Academy of Sciences - PNAS, 2001-07, Vol.98 (15), p.8531-8535

2001

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The Risk of Prion Zoonoses

Science (American Association for the Advancement of Science), 2012-01, Vol.335 (6067), p.411-413

Collinge, John

2012

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Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces

Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (9), p.3479-3483

2009

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Pharmacological chaperone for the structured domain of human prion protein

Proceedings of the National Academy of Sciences - PNAS, 2010-10, Vol.107 (41), p.17610-17615

2010

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Species-Barrier-Independent Prion Replication in Apparently Resistant Species

Proceedings of the National Academy of Sciences - PNAS, 2000-08, Vol.97 (18), p.10248-10253

2000

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A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3725

2008

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General Model of Prion Strains and Their Pathogenicity

Science (American Association for the Advancement of Science), 2007-11, Vol.318 (5852), p.930-936

2007

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Structural differences in amyloid-β fibrils from brains of nondemented elderly individuals and Alzheimer's disease patients

Proceedings of the National Academy of Sciences - PNAS, 2021-11, Vol.118 (45), p.1

2021

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Kuru Prions and Sporadic Creutzfeldt-Jakob Disease Prions Have Equivalent Transmission Properties in Transgenic and Wild-Type Mice

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (10), p.3885-3890

2008

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Spontaneous generation of mammalian prions

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (32), p.14402-14406

2010

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Folding kinetics of the human prion protein probed by temperature jump

Proceedings of the National Academy of Sciences - PNAS, 2009-04, Vol.106 (14), p.5651-5656

2009

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Mortuary rites of the South Fore and kuru

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3721

2008

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Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3755

2008

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Identification of Multiple Quantitative Trait Loci Linked to Prion Disease Incubation Period in Mice

Proceedings of the National Academy of Sciences - PNAS, 2001-05, Vol.98 (11), p.6279-6283

2001

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Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (34), p.13722-13727

2012

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Genetic susceptibility, evolution and the kuru epidemic

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3741

2008

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Dissociation of Pathological and Molecular Phenotype of Variant Creutzfeldt-Jakob Disease in Transgenic Human Prion Protein 129 Heterozygous Mice

Proceedings of the National Academy of Sciences - PNAS, 2006-07, Vol.103 (28), p.10759-10764

2006

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Review. Lessons of kuru research: background to recent studies with some personal reflections

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3689

Collinge, John

2008

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Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 1994-03, Vol.343 (1306), p.405

1994

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Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose

The Journal of infectious diseases, 2022-09, Vol.226 (5), p.933-937

2022

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Highly infectious prions are not directly neurotoxic

Proceedings of the National Academy of Sciences - PNAS, 2020-09, Vol.117 (38), p.23815-23822

2020

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The molecular biology of prion propagation

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2001-02, Vol.356 (1406), p.185

2001

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Prion Strain Mutation and Selection

Depleting Neuronal PrP in Prion Infection Prevents Disease and Reverses Spongiosis

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

Location and Properties of Metal-Binding Sites on the Human Prion Protein

The Risk of Prion Zoonoses

Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces

Pharmacological chaperone for the structured domain of human prion protein

Species-Barrier-Independent Prion Replication in Apparently Resistant Species

A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea

General Model of Prion Strains and Their Pathogenicity

Structural differences in amyloid-β fibrils from brains of nondemented elderly individuals and Alzheimer's disease patients

Kuru Prions and Sporadic Creutzfeldt-Jakob Disease Prions Have Equivalent Transmission Properties in Transgenic and Wild-Type Mice

Spontaneous generation of mammalian prions

Folding kinetics of the human prion protein probed by temperature jump

Mortuary rites of the South Fore and kuru

Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease

Identification of Multiple Quantitative Trait Loci Linked to Prion Disease Incubation Period in Mice

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

Genetic susceptibility, evolution and the kuru epidemic

Dissociation of Pathological and Molecular Phenotype of Variant Creutzfeldt-Jakob Disease in Transgenic Human Prion Protein 129 Heterozygous Mice

Review. Lessons of kuru research: background to recent studies with some personal reflections

Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier

Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose

Highly infectious prions are not directly neurotoxic

The molecular biology of prion propagation

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