Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein (Q34294957)

1 August 2017

title

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

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1 August 2017

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8

Prusiner SB

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1 August 2017

7

DeArmond SJ

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1 August 2017

6

Cohen FE

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1 August 2017

Telling GC

1

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1 August 2017

Scott M

2

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1 August 2017

Mastrianni J

3

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1 August 2017

Gabizon R

4

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1 August 2017

Torchia M

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1 August 2017

language of work or name

English

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publication date

1 October 1995

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1 August 2017

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1 August 2017

volume

83

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1 August 2017

issue

1

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1 August 2017

page(s)

79-90

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Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis

1 August 2017

cites work

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

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11 October 2022

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Cell-free formation of protease-resistant prion protein.

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11 October 2022

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

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11 October 2022

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

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11 October 2022

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Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

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11 October 2022

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Role of the major heat shock proteins as molecular chaperones

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11 October 2022

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Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Mice devoid of PrP are resistant to scrapie

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease

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11 October 2022

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Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Chimeric prion protein expression in cultured cells and transgenic mice

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11 October 2022

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

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11 October 2022

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Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+]

1 reference

11 October 2022

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

1 reference

11 October 2022

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Developments in diagnosis for prion diseases

1 reference

11 October 2022

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Encephalopathy in mice produced by inoculation with scrapie brain material.

1 reference

11 October 2022

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Genetic control of nucleation and polymerization of host precursors to infectious amyloids in the transmissible amyloidoses of brain

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann‐Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Scrapie prions aggregate to form amyloid-like birefringent rods

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Experimental transmission of a Kuru-like syndrome to chimpanzees

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Inherited prion diseases and transmission to rodents

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

The neuropathology and epidemiology of bovine spongiform encephalopathy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Structural clues to prion replication

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(95)90236-8

Identifiers

DOI

10.1016/0092-8674(95)90236-8

1 reference

1 August 2017

1 reference