(Q36699393)

English

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue

scientific article published on January 1995

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

prion protein family

0 references

1 reference

based on heuristic

inferred from title

author name string

H A Kretzschmar

1

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

M Neumann

2

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

D Stavrou

3

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

publication date

1 January 1995

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

89

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

96-98

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00294264

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncommon phenotype for a codon 178 mutation of the human PrP gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypic expression of different mutations in transmissible human spongiform encephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

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

https://pubmed.ncbi.nlm.nih.gov/7709737

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

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The hereditary form of Creutzfeldt-Jakob disease (the Backer family)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7709737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00294264

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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