Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice (Q41618801)

5 October 2017

title

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

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5 October 2017

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13

Prusiner SB

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12

DeArmond SJ

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Cohen FE

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Supattapone S

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Bosque P

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Muramoto T

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Wille H

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Aagaard C

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Peretz D

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Nguyen HO

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Heinrich C

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Torchia M

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Safar J

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Scott M

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5 October 2017

language of work or name

English

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publication date

1 March 1999

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5 October 2017

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5 October 2017

volume

96

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issue

6

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5 October 2017

page(s)

869-878

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

5 October 2017

cites work

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7 January 2021

High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene

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7 January 2021

Examination of the secondary structure of proteins by deconvolved FTIR spectra

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7 January 2021

Linkage of prion protein and scrapie incubation time genes

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7 January 2021

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

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7 January 2021

Encephalopathy in mice produced by inoculation with scrapie brain material.

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7 January 2021

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

1 reference

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7 January 2021

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

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7 January 2021

Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity

1 reference

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7 January 2021

Proposed three-dimensional structure for the cellular prion protein

1 reference

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7 January 2021

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

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7 January 2021

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change

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7 January 2021

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

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7 January 2021

Recombinant scrapie-like prion protein of 106 amino acids is soluble

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7 January 2021

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix

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7 January 2021

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

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7 January 2021

Further purification and characterization of scrapie prions

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7 January 2021

Scrapie prions aggregate to form amyloid-like birefringent rods

1 reference

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7 January 2021

Purification and structural studies of a major scrapie prion protein

1 reference

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7 January 2021

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

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7 January 2021

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

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7 January 2021

Prion Protein Biology

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7 January 2021

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

1 reference

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7 January 2021

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity

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7 January 2021

Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells

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7 January 2021

Eight prion strains have PrP(Sc) molecules with different conformations

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980596-6

7 January 2021

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980596-6

7 January 2021

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

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7 January 2021

Propagation of prion strains through specific conformers of the prion protein

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7 January 2021

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

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7 January 2021

Regional mapping of prion proteins in brain

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7 January 2021

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

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7 January 2021

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980596-6

7 January 2021

Ultrastructural studies on scrapie prion protein crystals obtained from reverse micellar solutions

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980596-6

7 January 2021

10.1016/S0092-8674(00)80596-6

Identifiers

DOI

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5 October 2017

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