(Q44549108)

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N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro

scientific article published on 20 July 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

4 December 2017

N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

prion protein family

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author name string

Lawson VA

1

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Priola SA

2

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Wehrly K

3

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Chesebro B

4

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

language of work or name

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publication date

20 July 2001

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Europe PubMed Central

PubMed publication ID

4 December 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

4 December 2017

276

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

35265-35271

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Separation and properties of cellular and scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Specific proteins associated with Creutzfeldt-Jakob disease and scrapie share antigenic and carbohydrate determinants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Solution structure of Syrian hamster prion protein rPrP(90-231).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Purification and structural studies of a major scrapie prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Non-genetic propagation of strain-specific properties of scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Susceptibility of sheep for scrapie as assessed by in vitro conversion of nine naturally occurring variants of PrP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Characterization of scrapie infection in mouse neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Characterization of monoclonal antibodies reactive with murine leukemia viruses: Use in analysis of strains of friend MCF and friend ecotropic murine leukemia virus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Abnormal properties of prion protein with insertional mutations in different cell types

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Prions and related neurological diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Molecular genetics of transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Identification of an epitope in the C terminus of normal prion protein whose expression is modulated by binding events in the N terminus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103799200

21 January 2018

Identifiers

10.1074/JBC.M103799200

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

ResearchGate publication ID

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