(Q37863713)

24 August 2017

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title

Prions and protein-folding diseases (English)

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24 August 2017

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1

E Norrby

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24 August 2017

language of work or name

English

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publication date

12 May 2011

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Journal of Internal Medicine

24 August 2017

published in

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24 August 2017

volume

270

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24 August 2017

issue

1

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24 August 2017

page(s)

1-14

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Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Experimental transmission of a Kuru-like syndrome to chimpanzees

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Kuru in the 21st century--an acquired human prion disease with very long incubation periods

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Lack of evidence of transfusion transmission of Creutzfeldt-Jakob disease in a US surveillance study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Purification and structural studies of a major scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Scrapie infectivity is independent of amyloid staining properties of the N-terminally truncated prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Deadly conformations--protein misfolding in prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prion diseases are efficiently transmitted by blood transfusion in sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Creutzfeldt-Jakob disease: reflections on the risk from blood product therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Evidence for case-to-case transmission of Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

A new variant of Creutzfeldt-Jakob disease in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Effectiveness of leucoreduction for removal of infectivity of transmissible spongiform encephalopathies from blood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Does the agent of scrapie replicate without nucleic acid?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Self-replication and scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

A new liquid intravenous immunoglobulin with three dedicated virus reduction steps: virus and prion reduction capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prion safety of transfusion plasma and plasma-derivatives typically used for prophylactic treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Reduction of transmissible spongiform encephalopathy infectivity from human red blood cells with prion protein affinity ligands

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prion removal effect of a specific affinity ligand introduced into the manufacturing process of the pharmaceutical quality solvent/detergent (S/D)-treated plasma OctaplasLG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Biochemical quality of the pharmaceutically licensed plasma OctaplasLG after implementation of a novel prion protein (PrPSc) removal technology and reduction of the solvent/detergent (S/D) process time

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Mammalian prion biology: one century of evolving concepts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prions: protein aggregation and infectious diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prions and their partners in crime

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Physiological role of the cellular prion protein (PrPc): protein profiling study in two cell culture systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Physiology of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Cellular prion protein mediates impairment of synaptic plasticity by amyloid-beta oligomers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Axonal prion protein is required for peripheral myelin maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Emerging principles of conformation-based prion inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prion domains: sequences, structures and interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Prions, protein homeostasis, and phenotypic diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Darwinian evolution of prions in cell culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Crucial role for prion protein membrane anchoring in the neuroinvasion and neural spread of prion infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Structure of the cross-beta spine of amyloid-like fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Atomic structures of amyloid cross-beta spines reveal varied steric zippers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Molecular mechanisms for protein-encoded inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Genes contributing to prion pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

In vitro generation of infectious scrapie prions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Formation of native prions from minimal components in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

De novo generation of infectious prions in vitro produces a new disease phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Generating a prion with bacterially expressed recombinant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Molecular properties of complexes formed between the prion protein and synthetic peptides.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Synthetic mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Design and construction of diverse mammalian prion strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Protease-sensitive synthetic prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Spontaneous generation of mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

The prion's elusive reason for being

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Induction of cerebral beta-amyloidosis: intracerebral versus systemic Abeta inoculation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Transmission and spreading of tauopathy in transgenic mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Protein fibrils in nature can enhance amyloid protein A amyloidosis in mice: Cross-seeding as a disease mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Is Parkinson's disease a prion disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Islet amyloid and type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Aplysia CPEB can form prion-like multimers in sensory neurons that contribute to long-term facilitation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Beyond the prion principle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

Epigenetics in the Extreme: Prions and the Inheritance of Environmentally Acquired Traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2011.02387.X

10.1111/J.1365-2796.2011.02387.X

21 January 2018

Identifiers

DOI

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release_czap7qxhhvcubm6vg5k3r2g2zm

24 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/czap7qxhhvcubm6vg5k3r2g2zm

mapped directly with Wikidata item

24 November 2022

based on heuristic

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