Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease. (Q43919735)

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scientific article published in October 1994

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English	Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.	scientific article published in October 1994

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

title

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

main subject

prion protein family

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Italy

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author

Mirella Salvatore

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

Maurizio Genuardi

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

Maurizio Pocchiari

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6

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Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

author name string

R Petraroli

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

C Masullo

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

M D'Alessandro

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

publication date

1 October 1994

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stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

volume

94

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

page(s)

375-379

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stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

cites work

Mice devoid of PrP are resistant to scrapie

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic structure of the human prion protein gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the PrP gene in a Tunisian family with Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hidden amyloidoses

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Considerations on a group of 13 patients with Creutzfeldt-Jakob disease in the region of Parma (Italy)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creutzfeldt-Jakob disease in Japan

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion in prion protein gene in a Moroccan family

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion in the prion protein gene in a demented patient

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and infectious prion diseases

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Codon 129 changes in the prion protein gene in Caucasians

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human pituitary growth hormone and Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CJD discrepancy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7927332

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00201596

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

Dimensions Publication ID

1048633630

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Microsoft Academic ID

2037267851

0 references

PubMed publication ID

7927332

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7927332

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927332%20AND%20SRC:MED&resulttype=core&format=json

retrieved

28 October 2019

 

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