A gene-targeted mouse model of P102L Gerstmann-Sträussler-Scheinker syndrome. (Q35122345)

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3 November 2019

review article

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title

A gene-targeted mouse model of P102L Gerstmann-Sträussler-Scheinker syndrome (English)

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3 November 2019

1

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3 November 2019

author name string

Jean C Manson

series ordinal

2

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3 November 2019

publication date

1 March 2003

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Clinics in laboratory medicine

3 November 2019

published in

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3 November 2019

volume

23

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3 November 2019

issue

1

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3 November 2019

page(s)

161-173

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Altering genes in animals by gene targeting

3 November 2019

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Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruent

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An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene

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The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype

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

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Spontaneous Neurodegeneration in Transgenic Mice with Prion Protein Codon 101 Proline → Leucine Substitutiona

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A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice

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A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy

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Double replacement gene targeting for the production of a series of mouse strains with different prion protein gene alterations

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Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

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7 January 2021

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12733430%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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