(Q41970471)

English

Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome

scientific article published on February 1990

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

prion protein family

0 references

Creutzfeldt-Jakob disease

1 reference

based on heuristic

inferred from title

author name string

Doh-ura K

1

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Tateishi J

2

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Kitamoto T

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Sasaki H

4

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Sakaki Y

5

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

publication date

1 February 1990

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Annals of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

121-126

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Scrapie prions aggregate to form amyloid-like birefringent rods

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

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

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Dideoxy sequencing method using denatured plasmid templates

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Empirical Predictions of Protein Conformation

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene

1 reference

https://api.crossref.org/works/10.1002%2FANA.410270205

21 January 2018

Molecular cloning of a human prion protein cDNA

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1089/DNA.1986.5.315

Identifiers

10.1002/ANA.410270205

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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