(Q71965164)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

author name string

H. Furukawa

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7637591

1 July 2024

T. Kitamoto

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7637591

1 July 2024

Y. Tanaka

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7637591

1 July 2024

J. Tateishi

4

1 reference

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1 July 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7637591

1 July 2024

publication date

1 June 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

22 October 2019

https://api.elsevier.com/content/article/PII:0169328X9500034P?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

https://api.elsevier.com/content/article/PII:0169328X9500034P?httpAccept=text/plain

1 July 2024

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

1 July 2024

published in

Molecular Brain Research

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

385-388

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

2

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

4

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

5

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

6

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis

1 July 2024

7

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

8

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

9

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

10

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

1 July 2024

11

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Human prion diseases with variant prion protein

1 July 2024

13

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker

1 July 2024

14

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 July 2024

15

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

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

1 July 2024

16

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

1 July 2024

Human prion diseases

17

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

1 July 2024

18

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies

1 July 2024

19

1 reference

https://api.crossref.org/works/10.1016/0169-328X(95)00034-P

1 July 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7637591%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference