Phenotypic variability in human prion diseases

Prions

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The same prion strain causes vCJD and BSE

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Eight prion strains have PrPSc molecules with different conformations

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Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome

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Mortality from Creutzfeldt–Jakob disease and related disorders in Europe, Australia, and Canada

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BSE prions propagate as either variant CJD‐like or sporadic CJD‐like prion strains in transgenic mice expressing human prion protein

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Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt–Jakob Disease

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Genetic influence on the structural variations of the abnormal prion protein

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SUBACUTE SPONGIFORM ENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE): THE NATURE AND PROGRESSION OF SPONGIFORM CHANGE

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Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies

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Strain-specific prion-protein conformation determined by metal ions

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Diagnosis of human prion disease

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Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype

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Decreased interleukin-10 and increased interleukin-12p40 mRNA are associated with disease activity and characterize different disease stages in multiple sclerosis

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TSE strain variation

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Mutations of the Prion Protein Gene

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Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage

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Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

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Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann–Sträussler–Scheinker disease

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Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders

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Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrP Sc in the same brain

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Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity

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Identification of multiple quantitative trait loci linked to prion disease incubation period in mice

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Neuroprotective functions of prion protein

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Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease

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Trafficking, turnover and membrane topology of PrP

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Mapping the early steps in the pH-induced conformational conversion of the prion protein

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Laboratory diagnosis of variant Creutzfeldt–Jakob disease

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Effects of Different Experimental Conditions on the PrPSc Core Generated by Protease Digestion

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An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-Jakob disease)

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Prion protein heterogeneity in sporadic but not variant Creutzfeldt–Jakob disease: U.K. cases 1991–2002

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The Original Gerstmann‐Sträussler‐Scheinker Family of Austria: Divergent Clinicopathological Phenotypes but Constant PrP Genotype

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Molecular Pathology of Fatal Familial Insomnia

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Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease

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Changing a single amino acid in the N‐terminus of murine PrP alters TSE incubation time across three species barriers

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Immunohistochemistry for the Prion Protein: Comparison of Different Monoclonal Antibodies in Human Prion Disease Subtypes

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Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK

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Glycosylation and prion protein

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Subcellular Localization of Disease-Associated Prion Protein in the Human Brain

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Creutzfeldt-Jakob disease in United Kingdom patients treated with human pituitary growth hormone

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Hereditary prion protein amyloidoses

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Novel Differences between Two Human Prion Strains Revealed by Two-dimensional Gel Electrophoresis

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Association of an 11–12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt–Jakob disease and other prion diseases

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Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt–Jakob disease

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Untitled work

Khan (2000) · doi:10.1002/1531-8249(200008)48:2

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

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Prion-like mechanisms in neurodegenerative diseases

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Loss of Homeostatic Microglia Signature in Prion Diseases

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Discussion on pathogenesis levels of hypertension

Wang, Q. (2007) · Zhongyi-yao xuebao

Classification of FABP isoforms and tissues based on quantitative evaluation of transcript levels of these isoforms in various rat tissues

Yamamoto, T., Yamamoto, A., Watanabe, M., Matsuo, T., Yamazaki, N., Kataoka, M., Terada, H., & Shinohara, Y. (2009) · Biotechnology Letters · doi:10.1007/s10529-009-0065-7 · Cited by 39 · see citing works

Functional Roles of the α Isoforms of the Na,K‐ATPase

Lingrel, J. B., Moseley, A. E., Dostanic, I., et al. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07214.x · Cited by 100 · see citing works

Relative expression of TAp73 and ΔNp73 isoforms

Conforti, F., Yang, A. L., Agostini, M., et al. (2012) · Aging · doi:10.18632/aging.100441 · Cited by 32 · see citing works