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Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions

Emerging infectious diseases, 2018-08, Vol.24 (8), p.1482-1489

2018

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Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner

The Journal of experimental medicine, 2017-12, Vol.214 (12), p.3481-3495

2017

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Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease

Annals of neurology, 2012-08, Vol.72 (2), p.278-285

2012

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Prion diseases

Handbook of Clinical Neurology, 2018-01, Vol.145, p.393-403

2018

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Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

The Lancet (British edition), 2004-08, Vol.364 (9433), p.527-529

2004

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Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK

Acta neuropathologica, 2017-08, Vol.134 (2), p.221-240

2017

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Human prion diseases: Molecular, cellular and population biology

Neuropathology, 2013-06, Vol.33 (3), p.221-236

Head, Mark W.

2013

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Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients

Emerging infectious diseases, 2017-06, Vol.23 (6), p.946-956

2017

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The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

PLoS pathogens, 2016-02, Vol.12 (2), p.e1005416-e1005416

2016

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Molecular barriers to zoonotic transmission of prions

Emerging infectious diseases, 2014-01, Vol.20 (1), p.88-97

2014

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Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies

Acta neuropathologica, 2019-03, Vol.137 (3), p.363-377

2019

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Sensitive and specific detection of sporadic Creutzfeldt―Jakob disease brain prion protein using real-time quaking-induced conversion

Journal of general virology, 2012-02, Vol.93 (Pt 2), p.438-449

2012

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UK Iatrogenic Creutzfeldt–Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches

Acta neuropathologica, 2017-04, Vol.133 (4), p.579-595

2017

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Uptake and Degradation of Protease-Sensitive and -Resistant Forms of Abnormal Human Prion Protein Aggregates by Human Astrocytes

The American journal of pathology, 2014-12, Vol.184 (12), p.3299-3307

2014

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Safety and effectiveness of indirect radiofrequency ablation (closure FAST) of incompetent great saphenous veins with Type I aneurysms: Long-term results radiofrequency ablation for saphenous aneurysms

Phlebology, 2023-03, Vol.38 (2), p.129-132

2023

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Variably protease-sensitive prionopathy in the UK: a retrospective review 1991―2008

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1102-1115

2013

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Variant CJD: 18 years of research and surveillance

Prion, 2014-07, Vol.8 (4), p.286-295

2014

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Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies

Neurology, 2014-06, Vol.82 (23), p.2107-2111

2014

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Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage

The American journal of pathology, 2004-07, Vol.165 (1), p.227-235

2004

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A case of variably protease-sensitive prionopathy treated with doxycyclin

Journal of neurology, neurosurgery and psychiatry, 2015-07, Vol.86 (7), p.816-818

2015

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Human Tonsil-Derived Follicular Dendritic-Like Cells are Refractory to Human Prion Infection in Vitro and Traffic Disease-Associated Prion Protein to Lysosomes

The American journal of pathology, 2014, Vol.184 (1), p.64-70

2014

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Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease

The American journal of pathology, 2006, Vol.168 (1), p.151-157

2006

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Rapid amplification of prions from variant Creutzfeldt–Jakob disease cerebrospinal fluid

The journal of pathology. Clinical research, 2018-04, Vol.4 (2), p.86-92

2018

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Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease: An Immunohistochemical, Quantitative, and Biochemical Study

The American journal of pathology, 2004-01, Vol.164 (1), p.143-153

2004

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Genotype-dependent Molecular Evolution of Sheep Bovine Spongiform Encephalopathy (BSE) Prions in Vitro Affects Their Zoonotic Potential

The Journal of biological chemistry, 2014-09, Vol.289 (38), p.26075-26088

2014

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Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions

Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease

Prion diseases

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK

Human prion diseases: Molecular, cellular and population biology

Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

Molecular barriers to zoonotic transmission of prions

Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies

Sensitive and specific detection of sporadic Creutzfeldt―Jakob disease brain prion protein using real-time quaking-induced conversion

UK Iatrogenic Creutzfeldt–Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches

Uptake and Degradation of Protease-Sensitive and -Resistant Forms of Abnormal Human Prion Protein Aggregates by Human Astrocytes

Safety and effectiveness of indirect radiofrequency ablation (closure FAST) of incompetent great saphenous veins with Type I aneurysms: Long-term results radiofrequency ablation for saphenous aneurysms

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991―2008

Variant CJD: 18 years of research and surveillance

Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies

Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage

A case of variably protease-sensitive prionopathy treated with doxycyclin

Human Tonsil-Derived Follicular Dendritic-Like Cells are Refractory to Human Prion Infection in Vitro and Traffic Disease-Associated Prion Protein to Lysosomes

Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease

Rapid amplification of prions from variant Creutzfeldt–Jakob disease cerebrospinal fluid

Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease: An Immunohistochemical, Quantitative, and Biochemical Study

Genotype-dependent Molecular Evolution of Sheep Bovine Spongiform Encephalopathy (BSE) Prions in Vitro Affects Their Zoonotic Potential

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