(Q43058060)

13 November 2017

Rapid formation of amyloid from alpha-monomeric recombinant human PrP in vitro (English)

1 reference

13 November 2017

Abdessamad Tahiri-Alaoui

series ordinal

1

1 reference

PMC publication ID

2253435

13 November 2017

William James

series ordinal

2

1 reference

13 November 2017

1 March 2005

1 reference

13 November 2017

1 reference

13 November 2017

14

1 reference

13 November 2017

4

1 reference

13 November 2017

942-947

1 reference

Evidence for assembly of prions with left-handed beta-helices into trimers

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Unzipping the mysteries of amyloid fiber formation

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

The peculiar nature of unfolding of the human prion protein

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Characterization of 2'-fluoro-RNA aptamers that bind preferentially to disease-associated conformations of prion protein and inhibit conversion.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Competing intrachain interactions regulate the formation of beta-sheet fibrils in bovine PrP peptides.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Structural studies of the scrapie prion protein by electron crystallography

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Molecular biology and pathogenesis of prion diseases

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Molecular biology of prion diseases

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Methionine 129 variant of human prion protein oligomerizes more rapidly than the valine 129 variant: implications for disease susceptibility to Creutzfeldt-Jakob disease.

26 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

The mechanism of insulin action on islet amyloid polypeptide fiber formation

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Islet amyloid: phase partitioning and secondary nucleation are central to the mechanism of fibrillogenesis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Pathway complexity of prion protein assembly into amyloid

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Folding of prion protein to its native alpha-helical conformation is under kinetic control

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Scrapie prions aggregate to form amyloid-like birefringent rods

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Strain-specific prion-protein conformation determined by metal ions

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253435

Thermodynamic instability of human lambda 6 light chains: correlation with fibrillogenicity

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15741327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Kinetic intermediate in the folding of human prion protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15741327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Extremely rapid folding of the C-terminal domain of the prion protein without kinetic intermediates

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15741327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1110/PS.041000905

1 reference

13 November 2017

1 reference

PMC publication ID

2253435

13 November 2017

PubMed publication ID

15741327

1 reference

PMC publication ID

2253435