Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129 (Q73067900)

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1 November 2019

title

Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129 (English)

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1 November 2019

author name string

K Young

1

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1 November 2019

H B Clark

2

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1 November 2019

P Piccardo

3

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1 November 2019

S R Dlouhy

4

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1 November 2019

B Ghetti

5

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1 November 2019

publication date

1 February 1997

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1 November 2019

published in

Molecular Brain Research

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1 November 2019

volume

44

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1 November 2019

issue

1

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1 November 2019

page(s)

147-150

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Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 November 2019

cites work

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7 January 2021

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

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7 January 2021

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

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7 January 2021

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred

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7 January 2021

Prion protein amyloidosis

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Beta-pleated sheet fibrils. A comparison of native amyloid with synthetic protein fibrils

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7 January 2021

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

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7 January 2021

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

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7 January 2021

Proposed three-dimensional structure for the cellular prion protein

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7 January 2021

A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis

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7 January 2021

Human prion diseases with variant prion protein

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165

1 reference

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7 January 2021

Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

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7 January 2021

Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2896%2900251-3

7 January 2021

10.1016/S0169-328X(96)00251-3

Identifiers

DOI

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1 November 2019

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