(Q48088772)

English

Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro.

scientific article published on 21 January 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro. (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

prion protein family

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Victoria A. Lawson

object named as

Victoria A Lawson

1

0 references

Kimberly Meade-White

3

object named as

Kimberly Meade-White

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

Suzette A Priola

2

object named as

Suzette A Priola

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

5

object named as

Bruce Chesebro

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

author name string

McKinley Lawson

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

language of work or name

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publication date

21 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

279

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

14

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

13689-13695

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

Separation and properties of cellular and scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Purification and structural studies of a major scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Scrapie strain variation and mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Molecular classification of sporadic Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

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.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

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.M303697200

21 January 2018

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

21 January 2018

Evidence that the Transmission of One Source of Scrapie Agent to Hamsters Involves Separation of Agent Strains from a Mixture

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Subclinical scrapie infection in a resistant species: persistence, replication, and adaptation of infectivity during four passages

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humans

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

21 January 2018

Identification of two prion protein regions that modify scrapie incubation time

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Copper coordination in the full-length, recombinant prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Location and properties of metal-binding sites on the human prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

21 January 2018

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

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.M303697200

21 January 2018

Neurotoxicity of a prion protein fragment.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Toxicity of novel C-terminal prion protein fragments and peptides harbouring disease-related C-terminal mutations.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Species-barrier-independent prion replication in apparently resistant species

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Molecular genetics of transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Mouse cortical cells lacking cellular PrP survive in culture with a neurotoxic PrP fragment

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M303697200

21 January 2018

Identifiers

10.1074/JBC.M303697200

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/14736880

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