(Q43828081)

27 November 2017

title

Biochemical and structural studies of the prion protein polymorphism (English)

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27 November 2017

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Petchanikow C

1

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27 November 2017

Saborio GP

2

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27 November 2017

Anderes L

3

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27 November 2017

Frossard MJ

4

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27 November 2017

Olmedo MI

5

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27 November 2017

Soto C

6

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27 November 2017

language of work or name

English

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publication date

1 December 2001

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27 November 2017

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27 November 2017

volume

509

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27 November 2017

issue

3

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27 November 2017

page(s)

451-456

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Molecular biology of prion diseases

27 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

21 January 2018

1 reference

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Cell-free formation of protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

NMR structure of the mouse prion protein domain PrP(121-231)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

NMR structure of the bovine prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

NMR solution structure of the human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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/10.1016%2FS0014-5793%2801%2903147-7

Scrapie prions: a three-dimensional model of an infectious fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Pathologic conformations of prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Neurotoxicity of a prion protein fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Proposed three-dimensional structure for the cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Zone mapping of the binding domain of the rat low affinity nerve growth factor receptor by the introduction of novel N-glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Genetic influence on the structural variations of the abnormal prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

21 January 2018

1 reference

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The conformation of Alzheimer's beta peptide determines the rate of amyloid formation and its resistance to proteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Apolipoprotein E increases the fibrillogenic potential of synthetic peptides derived from Alzheimer's, gelsolin and AA amyloids

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Prion protein amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

21 January 2018

Typing prion isoforms.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Fatal familial insomnia: clinical features and molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Prion protein NMR structure and familial human spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Empirical Predictions of Protein Conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Prion protein peptides induce alpha-helix to beta-sheet conformational transitions

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Molecular genetics of transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Prion protein isoforms, a convergence of biological and structural investigations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Calculation of protein conformation from circular dichroism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Quantitative determination of helical propensities from trifluoroethanol titration curves

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Copper has differential effect on prion protein with polymorphism of position 129

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

Conformational properties of the prion octa-repeat and hydrophobic sequences

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2903147-7

10.1016/S0014-5793(01)03147-7

7 January 2021

Identifiers

DOI

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27 November 2017

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