(Q48498733)

12 February 2018

title

Interaction of prion protein with small highly structured RNAs: detection and characterization of PrP-oligomers (English)

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12 February 2018

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Sara Vasan

1

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12 February 2018

Phyllus Y Mong

series ordinal

2

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12 February 2018

Abraham Grossman

series ordinal

3

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12 February 2018

publication date

1 May 2006

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12 February 2018

published in

Neurochemical Research

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12 February 2018

volume

31

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12 February 2018

issue

5

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12 February 2018

page(s)

629-637

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12 February 2018

Cellular prion protein status in sheep: tissue-specific biochemical signatures

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS11064-006-9063-5

Assembly of the full-length recombinant mouse prion protein I. Formation of soluble oligomers.

21 January 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS11064-006-9063-5

Prion diseases of humans and animals: their causes and molecular basis

21 January 2018

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12 December 2020

Structural studies of soluble oligomers of the Alzheimer beta-amyloid peptide

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12 December 2020

Formation of critical oligomers is a key event during conformational transition of recombinant syrian hamster prion protein

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12 December 2020

The peculiar nature of unfolding of the human prion protein

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12 December 2020

Oligomerization of beta-amyloid of the Alzheimer's and the Dutch-cerebral-haemorrhage types

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12 December 2020

Autocatalytic conversion of recombinant prion proteins displays a species barrier

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12 December 2020

Alzheimer's disease: the amyloid cascade hypothesis

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12 December 2020

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

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12 December 2020

Cellular prion protein neuroprotective function: implications in prion diseases

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12 December 2020

Cellular heparan sulfate participates in the metabolism of prions

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12 December 2020

Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions.

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12 December 2020

Prion protein interactions with nucleic acid: possible models for prion disease and prion function

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12 December 2020

Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis

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12 December 2020

Polymerization of murine recombinant prion protein in nucleic acid solution

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12 December 2020

Sequential generation of two structurally distinct ovine prion protein soluble oligomers displaying different biochemical reactivities

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12 December 2020

Cellular biology of prion diseases

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12 December 2020

Chaperonin-mediated de novo generation of prion protein aggregates

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12 December 2020

Shattuck lecture--neurodegenerative diseases and prions

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12 December 2020

The hypothesis of the catalytic action of nucleic acid on the conversion of prion protein

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12 December 2020

Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes

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12 December 2020

Pathway complexity of prion protein assembly into amyloid

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12 December 2020

Role of the beta-amyloid protein in Alzheimer's disease.

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12 December 2020

Prion protein conversion in vitro

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12 December 2020

Alzheimer's disease: a central role for amyloid

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12 December 2020

Oligomers on the brain: the emerging role of soluble protein aggregates in neurodegeneration

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12 December 2020

Isolation and characterization of a polymerized prion protein.

1 reference

12 December 2020

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

12 December 2020

DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation

1 reference

12 December 2020

Efficient inhibition of prion replication by PrP-Fc(2) suggests that the prion is a PrP(Sc) oligomer.

1 reference

12 December 2020

Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperone

1 reference

12 December 2020

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

12 December 2020

Small, highly structured RNAs participate in the conversion of human recombinant PrP(Sen) to PrP(Res) in vitro

1 reference

12 December 2020

Molecular mechanisms initiating amyloid beta-fibril formation in Alzheimer's disease.

1 reference

12 December 2020

Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein

1 reference

12 December 2020

Concentration and removal of prion proteins from biological solutions

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12 December 2020

The most infectious prion protein particles.

1 reference

12 December 2020

Human prion diseases: molecular and clinical aspects

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12 December 2020

pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231)

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12 December 2020

Paradigm shifts in Alzheimer's disease and other neurodegenerative disorders: the emerging role of oligomeric assemblies

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12 December 2020

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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12 December 2020

RNA molecules stimulate prion protein conversion

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12 December 2020

Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein

1 reference

12 December 2020

Identification of the heparan sulfate binding sites in the cellular prion protein

1 reference

12 December 2020

DNA-induced partial unfolding of prion protein leads to its polymerisation to amyloid

1 reference

12 December 2020

Protofibrils, pores, fibrils, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders

1 reference

12 December 2020

Prion diseases and the BSE crisis

1 reference

12 December 2020

Chaperone-supervised conversion of prion protein to its protease-resistant form

1 reference

12 December 2020

Prion protein and the transmissible spongiform encephalopathies

1 reference

12 December 2020

Molecular modelling indicates that the pathological conformations of prion proteins might be beta-helical.

1 reference

12 December 2020

Interaction of prion peptide HuPrP106-126 with nucleic acid

1 reference

12 December 2020

10.1007/S11064-006-9063-5

Identifiers

DOI

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12 February 2018

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12 February 2018