(Q48592691)

English

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

scientific article published on January 1, 1992

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scholarly article

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

Creutzfeldt-Jakob disease

1 reference

based on heuristic

inferred from title

author name string

M. Miyazono

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

T. Kitamoto

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

K. Doh-ura

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

T. Iwaki

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

J. Tateishi

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1359725

18 September 2022

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1359725

18 September 2022

publication date

1 January 1992

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

Acta Neuropathologica

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

84

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

349-354

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

4

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

https://scigraph.springernature.com/pub.10.1007/bf00227660

0 references

N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

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

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

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/1359725

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/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of avidin-biotin interaction in immunoenzymatic techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of a human prion protein cDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Codon 129 changes in the prion protein gene in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel proteinaceous infectious particles cause scrapie

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CJD discrepancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular biology of prion diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1359725

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

https://pubmed.ncbi.nlm.nih.gov/1359725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00227660

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/1359725

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