(Q44548848)

4 December 2017

Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease (English)

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4 December 2017

3

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4 December 2017

6

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4 December 2017

5

Pierluigi Gambetti

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4 December 2017

Wen-Quan Zou

1

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4 December 2017

Sabina Capellari

series ordinal

2

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4 December 2017

Man-Sun Sy

series ordinal

4

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4 December 2017

language of work or name

English

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publication date

12 August 2003

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Journal of Biological Chemistry

4 December 2017

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4 December 2017

278

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4 December 2017

42

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4 December 2017

40429-40436

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https://api.crossref.org/works/10.1074%2FJBC.M308550200

4 December 2017

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Nearly ubiquitous tissue distribution of the scrapie agent precursor protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Purification and properties of the cellular and scrapie hamster prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Scrapie prion protein contains a phosphatidylinositol glycolipid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Identification of a protein that purifies with the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Purification and structural studies of a major scrapie prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Separation and properties of cellular and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Genetic influence on the structural variations of the abnormal prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Partial unfolding and refolding of scrapie-associated prion protein: evidence for a critical 16-kDa C-terminal domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Strain-dependent differences in beta-sheet conformations of abnormal prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Truncated forms of the human prion protein in normal brain and in prion diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Isolation and structural studies of the intact scrapie agent protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

The glycosylphosphatidylinositol-anchored surface glycoprotein Thy-1 is a receptor for the channel-forming toxin aerolysin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

NMR solution structure of the human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Pathologic conformations of prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Folding and intrinsic stability of deletion variants of PrP(121-231), the folded C-terminal domain of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Structural studies of the scrapie prion protein by electron crystallography

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

A protease-resistant 61-residue prion peptide causes neurodegeneration in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308550200

21 January 2018

Identifiers

DOI

10.1074/JBC.M308550200

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4 December 2017

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