Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice (Q48963662)

17 February 2018

title

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

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17 February 2018

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6

Prusiner SB

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17 February 2018

5

DeArmond SJ

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17 February 2018

Telling GC

1

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17 February 2018

Haga T

series ordinal

2

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17 February 2018

Torchia M

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3

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17 February 2018

Tremblay P

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4

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17 February 2018

publication date

1 July 1996

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17 February 2018

published in

Genes & Development

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17 February 2018

volume

10

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17 February 2018

issue

14

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17 February 2018

page(s)

1736-1750

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17 February 2018

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

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

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Mice devoid of PrP are resistant to scrapie

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Normal development of nerve—muscle synapses in mice lacking the prion protein gene

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Structures of prion proteins and conformational models for prion diseases

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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

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

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https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

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Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

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Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

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The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system

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

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The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist

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Inherited prion diseases and transmission to rodents

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https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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Inherited prion diseases

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Spontaneous neurodegeneration in transgenic mice with mutant prion protein

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Monoclonal antibodies to the cellular and scrapie prion proteins

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

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11 October 2022

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Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

A protease-resistant protein is a structural component of the scrapie prion

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Unconventional Viruses and the Origin and Disappearance of Kuru

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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

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Prion protein is strongly immunolocalized at the postsynaptic domain of human normal neuromuscular junctions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Transmissible and non-transmissible neurodegenerative disease: similarities in age of onset and genetics in relation to aetiology

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Structural clues to prion replication

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

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

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Molecular biology of prion diseases

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Familial neurological disease associated with spongiform encephalopathy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Novel proteinaceous infectious particles cause scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1101/GAD.10.14.1736

Identifiers

DOI

10.1101/GAD.10.14.1736

1 reference

17 February 2018

1 reference

17 February 2018