(Q59690434)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Allelic origin of the abnormal prion protein isoform in familial prion diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Sabina Capellari

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Lucila Autilio-Gambetti

12

object named as

L Autilio-Gambetti

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

13

P Gambetti

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

S G Chen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

P Brown

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

W Zou

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

E J Cochran

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

C L Vnencak-Jones

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

J Julien

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

C Vital

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

J Mikol

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

E Lugaresi

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

language of work or name

English

0 references

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

1009-1015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nm0997-1009

5 November 2019

exact match

0 references

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

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%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Separation and properties of cellular and scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

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%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Clinical and genetic studies of fatal familial insomnia.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Deletions in the prion protein gene are not associated with CJD.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Truncated forms of the human prion protein in normal brain and in prion diseases.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Isolation and structural studies of the intact scrapie agent protein.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Typing prion isoforms.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Regional distribution of protease-resistant prion protein in fatal familial insomnia.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Transmission of fatal familial insomnia to laboratory animals.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

First experimental transmission of fatal familial insomnia.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid proteins

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Selective labeling of sulfhydryls and disulfides on blot transfers using avidin-biotin technology: studies on purified proteins and erythrocyte membranes

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

1 reference

https://api.crossref.org/works/10.1038%2FNM0997-1009

7 January 2021

Identifiers

DOI

10.1038/NM0997-1009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9288728%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference