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Prions and associated diseases
LE WE PMID CA
Prions and associated diseases2282Prion

Alzheimer s disease

Amyloidosis

Autophagy

BCL2

Beclin1

Caspase12

Chronic wasting disease

Dendrimer

ERS UFR (Diseases)

ERS UFR (Toxikologie)

Familial mediterranean fever

Filamin A

GPI anchor

Hsp104

Hsp40

HSP70

Insomnia

Nervous system (Neurodegeneration)

Polyamines

Prions and associated diseases

Reticulon3

Tau

Tunneling nanotube

1991  
1
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1991  
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2002  
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Prion; the unconventional slow infectious agent.
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Molecular biology of prion protein and its first homologous protein.
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1998  
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Bovine spongiform encephalopathy and new variant Creutzfeldt-Jakob disease.
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Psychiatric manifestations of Creutzfeldt-Jakob disease: a 25-year analysis.
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2009  
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The transcellular spread of cytosolic amyloids, prions, and prionoids.
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2006  
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New insights into prion structure and toxicity.
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2007  
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Neurotoxic species in prion disease: a role for PrP isoforms?
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2006  
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Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis.
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2005  
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2004  
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PrPc on the road: trafficking of the cellular prion protein.
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2003  
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Cellular prion protein function in copper homeostasis and redox signalling at the synapse.
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2002  
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Mayhem of the multiple mechanisms: modelling neurodegeneration in prion disease.
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1999  
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Cellular biology of prion diseases.
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2002  
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Current perspectives on bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease.
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2007  
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Prions and prion diseases: fundamentals and mechanistic details.
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2006  
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2002  
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[12353659] Dev Immunol 9(1): 19-27 (2002)
2006  
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The role of the cellular prion protein in the immune system.
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2003  
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Variant Creutzfeldt-Jakob disease: pathology, epidemiology, and public health implications.
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2009  
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Prion variants, species barriers, generation and propagation.
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2008  
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Chemical and biophysical insights into the propagation of prion strains.
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2010  
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Emergence and natural selection of drug-resistant prions.
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2008  
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Review. The origin of the prion agent of kuru: molecular and biological strain typing.
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2008  
32
Review. Understanding kuru: the contribution of anthropology and medicine.
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2008  
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Review. The epidemiology of kuru: monitoring the epidemic from its peak to its end.
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2008  
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2008  
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Review. Lessons of kuru research: background to recent studies with some personal reflections.
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2008  
36
Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease.
[18849282] Philos Trans R Soc Lond B Biol Sci 363(1510): 3685-7 (2008)
2008  
37
Review. The changing face of kuru: a personal perspective.
[18672465] Philos Trans R Soc Lond B Biol Sci 363(1510): 3679-84 (2008)
2001  
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2001  
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2001  
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2000  
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Scrapie infections initiated at varying doses: an analysis of 117 titration experiments.
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2010  
42
The role of GPI-anchored PrP C in mediating the neurotoxic effect of scrapie prions in neurons.
[19767655] Curr Issues Mol Biol 12(2): 119-27 (2010)
2010  
43
Targeting of the prion protein to the cytosol: mechanisms and consequences.
[19767654] Curr Issues Mol Biol 12(2): 109-18 (2010)
2010  
44
Prion protein and metal interaction: physiological and pathological implications.
[19767653] Curr Issues Mol Biol 12(2): 99-107 (2010)
2010  
45
Autophagy, prion infection and their mutual interactions.
[19767652] Curr Issues Mol Biol 12(2): 87-97 (2010)
2010  
46
Prion neurotoxicity: insights from prion protein mutants.
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1999  
47
Cell biological studies of the prion protein.
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2008  
48
Physiology of the prion protein.
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1991  
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2008  
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Prion diseases: from protein to cell pathology.
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1995  
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Etiology and pathogenesis of prion diseases.
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2006  
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Emerging pharmacotherapies for Creutzfeldt-Jakob disease.
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2005  
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Human prion diseases: molecular and clinical aspects.
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1999  
55
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting.
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2004  
56
Prions in control of cell glycosylation.
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1990  
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2006  
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Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
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2006  
59
A systematic review of prion therapeutics in experimental models.
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1999  
60
How to improve the clinical diagnosis of Creutzfeldt-Jakob disease.
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2000  
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Pathogenesis of prion diseases: a progress report.
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2006  
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2002  
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A critical review of the nature of the spongiform encephalopathy agent: protein theory versus virus theory.
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2001  
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Lingering doubts about spongiform encephalopathy and Creutzfeldt-Jakob disease.
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2001  
65
A critical review of atypical cerebellum-type Creutzfeldt-Jakob disease: its relationship to "new variant" CJD and bovine spongiform encephalopathy.
[11444099] Exp Biol Med (Maywood) 226(7): 629-39 (2001)
2009  
66
Transmissible mink encephalopathy - review of the etiology of a rare prion disease.
[19618341] Folia Neuropathol 47(2): 195-204 (2009)
2009  
67
Cannibalism, kuru and anthropology.
[19618336] Folia Neuropathol 47(2): 138-44 (2009)
2009  
68
Kuru and D. Carleton Gajdusek: a close encounter.
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2009  
69
Thoughts on mammalian prion strains.
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2009  
70
Reflections on a half-century in the field of transmissible spongiform encephalopathy.
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2008  
71
Prion diseases: a riddle wrapped in a mystery inside an enigma.
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2008  
72
Cell death and autophagy in prion diseases (transmissible spongiform encephalopathies).
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2006  
73
Variant CJD (vCJD) and bovine spongiform encephalopathy (BSE): 10 and 20 years on: part 2.
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2006  
74
Variant CJD (vCJD) and bovine spongiform encephalopathy (BSE): 10 and 20 years on: part 1.
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2005  
75
Neurodegeneration and oxidative stress: prion disease results from loss of antioxidant defence.
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2004  
76
Prions: proteins as genes and infectious entities.
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2005  
77
Unraveling prion structures and biological functions.
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2005  
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Prions and the blood and immune systems.
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1997  
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Human prion diseases and bovine spongiform encephalopathy (BSE).
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A structural overview of the vertebrate prion proteins.
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Cellular prion protein: on the road for functions.
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1999  
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Prion protein interconversions and the transmissible spongiform encephalopathies.
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1994  
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Diffusion-weighted MR imaging of early-stage Creutzfeldt-Jakob disease: typical and atypical manifestations.
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Molecular pathology of human prion diseases.
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2001  
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Insights into the physiological function of cellular prion protein.
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2001  
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Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public health.
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Prion diseases: a dual view of the prion hypothesis as seen from a distance.
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122
The tubulovesicular structures - the ultrastructural hallmark for all prion diseases.
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Molecular pathology of human prion disease.
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Molecular biology and pathology of prion strains in sporadic human prion diseases.
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2011  
125
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.
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Tau, prions and Aβ: the triad of neurodegeneration.
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Prion protein misfolding and disease.
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2007  
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2007  
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2011  
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Self-propagation and transmission of misfolded mutant SOD1: prion or prion-like phenomenon?
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A new kind of prion: a modified protein necessary for its own modification.
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2009  
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Prions: protein aggregation and infectious diseases.
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2010  
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Redox control of prion and disease pathogenesis.
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Self management of fatal familial insomnia. Part 1: what is FFI?
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Neuroimaging findings in human prion disease.
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The prion hypothesis: from biological anomaly to basic regulatory mechanism.
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Prion-like transmission of protein aggregates in neurodegenerative diseases.
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A general model of prion strains and their pathogenicity.
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2008  
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Physiological role of the cellular prion protein.
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Cell models of prion infection.
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2008  
146
Cellular pathogenesis in prion diseases.
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2008  
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A prion disease of cervids: chronic wasting disease.
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2008  
148
Misfolding of the prion protein: linking biophysical and biological approaches.
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2008  
149
Prion agent diversity and species barrier.
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2007  
150
Fourth case of transfusion-associated vCJD infection in the United Kingdom.
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2011  
151
Reticulon 3 attenuates the clearance of cytosolic prion aggregates via inhibiting autophagy.
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2011  
152
Abnormal calcium homeostasis and protein folding stress at the ER: A common factor in familial and infectious prion disorders.
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2008  
153
Reduced translocation of nascent prion protein during ER stress contributes to neurodegeneration.
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2008  
154
Endoplasmic reticulum stress, PrP trafficking, and neurodegeneration.
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2003  
155
Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.
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2011  
156
An overview of animal prion diseases.
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2005  
157
2008  
158
A histopathologic and immunohistochemical review of archived UK caprine scrapie cases.
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2010  
159
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
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2003  
160
The epidemics of bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: current status and future prospects.
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2009  
161
Cellular prion protein mediates the toxicity of beta-amyloid oligomers: implications for Alzheimer disease.
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2009  
162
Rapid fracture healing in a patient with inherited prion disease.
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2010  
163
Rapidly progressive Creutzfeldt-Jakob disease in patients with Familial Mediterranean Fever.
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2006  
164
Prion diseases in humans: an update.
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2007  
165
2009  
166
Complex polyamines: unique prion disaggregating compounds.
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2004  
167
2010  
168
Prions: En route from structural models to structures.
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2010  
169
Insights into prion protein function from atomistic simulations.
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2007  
170
Prion and nonprion amyloids: a comparison inspired by the yeast Sup35 protein.
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2009  
171
The expanding realm of prion phenomena in neurodegenerative disease.
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2009  
172
Tunnelling nanotubes: a highway for prion spreading?
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2009  
173
Prion propagation by Hsp40 molecular chaperones.
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2009  
174
Influence of Hsp70s and their regulators on yeast prion propagation.
[19556854] Prion 3(2): 65-73 (2009)
2008  
175
Insights into intragenic and extragenic effectors of prion propagation using chimeric prion proteins.
[19098443] Prion 2(2): 45-7 (2008)
2008  
176
Prion interference with multiple prion isolates.
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2008  
177
The peculiar interaction between mammalian prion protein and RNA.
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2008  
178
Prion infection: seeded fibrillization or more?
[19098436] Prion 2(2): 67-72 (2008)
2008  
179
New insights into prion biology from the novel [SWI+] system.
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2008  
180
Prion proteostasis: Hsp104 meets its supporting cast.
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2009  
181
Prion neurodegeneration: starts and stops at the synapse.
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2009  
182
Prion protein and Alzheimer disease.
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2009  
183
De novo mammalian prion synthesis.
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2009  
184
Therapy for prion diseases: Insights from the use of RNA interference.
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2009  
185
The role of the prion protein membrane anchor in prion infection.
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PrPs: Proteins with a purpose: Lessons from the zebrafish.
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Prion diseases and their biochemical mechanisms.
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Binding of pro-prion to filamin A: by design or an unfortunate blunder.
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Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.
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2011  
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Aerosols transmit prions to immunocompetent and immunodeficient mice.
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Prions of fungi: inherited structures and biological roles.
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Beta-amyloid oligomers and cellular prion protein in Alzheimer's disease.
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2008  
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Protein inheritance (prions) based on parallel in-register beta-sheet amyloid structures.
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Prion protein: orchestrating neurotrophic activities.
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2002  
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Molecular genetics of transmissible spongiform encephalopathies: an introduction.
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Genomic and post-genomic analyses of human prion diseases.
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197
Copper and the prion protein: methods, structures, function, and disease.
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2002  
198
The role of dimerization in prion replication.
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199
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[12683358] Can Commun Dis Rep 28 Suppl 5(-): 1-84 (2002)
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200
Neuroinvasion in prion diseases: the roles of ascending neural infection and blood dissemination.
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2009  
201
The consequences of pathogenic mutations to the human prion protein.
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2009  
202
2009  
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Copper binding extrinsic to the octarepeat region in the prion protein.
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2010  
204
Immunomodulation for prion and prion-related diseases.
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Prion amyloid structure explains templating: how proteins can be genes.
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206
Review: contribution of transgenic models to understanding human prion disease.
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Prion hypothesis: the end of the controversy?
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