(Q48721370)

14 February 2018

title

Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients (English)

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14 February 2018

Creutzfeldt-Jakob disease

main subject

prion protein family

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patient

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1 reference

Silvestrini MC

1

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14 February 2018

Cardone F

2

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14 February 2018

Maras B

3

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14 February 2018

Pucci P

4

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14 February 2018

Barra D

5

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14 February 2018

Brunori M

6

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14 February 2018

Pocchiari M

7

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14 February 2018

language of work or name

English

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publication date

1 May 1997

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14 February 2018

published in

Nature Medicine

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14 February 2018

volume

3

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14 February 2018

issue

5

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14 February 2018

page(s)

521-525

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14 February 2018

https://api.crossref.org/works/10.1038%2FNM0597-521

1 reference

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

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

21 January 2018

1 reference

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Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

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Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

21 January 2018

1 reference

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Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

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First experimental transmission of fatal familial insomnia

21 January 2018

1 reference

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

21 January 2018

1 reference

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Biology and genetics of prion diseases

21 January 2018

1 reference

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The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies

21 January 2018

1 reference

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

21 January 2018

1 reference

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A 'unified theory' of prion propagation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

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

21 January 2018

1 reference

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Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

21 January 2018

1 reference

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NMR structure of the mouse prion protein domain PrP(121-231)

21 January 2018

1 reference

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

21 January 2018

1 reference

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Infectivity and host responses in Creutzfeldt-Jakob disease

21 January 2018

1 reference

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Detection of proteinase-resistant protein (PrP) in small brain tissue samples from Creutzfeldt-Jakob disease patients.

21 January 2018

1 reference

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Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

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

1 reference

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7 January 2021

Inherited prion diseases

1 reference

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7 January 2021

The transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Gene

1 reference

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7 January 2021

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

The nature of the scrapie agent: the virus theory

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Expression of a normal and variant Alzheimer's beta-protein gene in amyloid of hereditary cerebral hemorrhage, Dutch type: DNA and protein diagnostic assays.

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Spontaneous generation of infectious nucleating amyloids in the transmissible and nontransmissible cerebral amyloidoses

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

A kinetic model for amyloid formation in the prion diseases: importance of seeding

1 reference

https://api.crossref.org/works/10.1038%2FNM0597-521

7 January 2021

Identifiers

DOI

10.1038/NM0597-521

1 reference

14 February 2018

Dimensions Publication ID

1036157557

0 references

1 reference

14 February 2018