Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. (Q54154878)

25 May 2018

title

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. (English)

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4

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Emmanuel A. Asante

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Péter Lantos

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object named as

Lantos PL

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author name string

Collinge J

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Palmer MS

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Sidle KC

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Gowland I

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Meads J

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Bradley R

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Doey LJ

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language of work or name

English

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publication date

1 December 1995

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25 May 2018

published in

Nature

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volume

378

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issue

6559

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page(s)

779-783

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https://scigraph.springernature.com/pub.10.1038/378779a0

exact match

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cites work

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine

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Molecular biology of prion diseases

21 January 2018

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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

Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier

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7 January 2021

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

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

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Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

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Transmission of fatal familial insomnia to laboratory animals.

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

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7 January 2021

Mice devoid of PrP are resistant to scrapie

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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 is necessary for normal synaptic function.

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7 January 2021

Bovine spongiform encephalopathy: a neuropathological perspective

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7 January 2021

Transmission of bovine spongiform encephalopathy to mice

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7 January 2021

Transmission of bovine spongiform encephalopathy and scrapie to mice.

1 reference

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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7 January 2021

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

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7 January 2021

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

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7 January 2021

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

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7 January 2021

Linkage of prion protein and scrapie incubation time genes

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7 January 2021

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

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7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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7 January 2021

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

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7 January 2021

Decontamination studies with the agents of bovine spongiform encephalopathy and scrapie

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7 January 2021

Prion protein immunocytochemistry helps to establish the true incidence of prion diseases

1 reference

7 January 2021

Identifiers

DOI

10.1038/378779A0

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25 May 2018

Dimensions Publication ID

1030595894

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25 May 2018