Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease (Q59294063)

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13 January 2020

title

Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease (English)

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13 January 2020

4

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Young-Han Song

5

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7

Richard I Carp

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13 January 2020

author name string

Byung-Hoon Jeong

1

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13 January 2020

Nam-Ho Kim

2

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13 January 2020

Eun-Kyoung Choi

3

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Jae-Il Kim

6

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Yong-Sun Kim

8

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publication date

1 September 2005

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European Journal of Human Genetics

13 January 2020

published in

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13 January 2020

volume

13

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issue

9

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page(s)

1094-1097

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201460

13 January 2020

exact match

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cites work

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/10.1038%2FSJ.EJHG.5201460

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Polymorphism at codon 174 of the prion-like protein gene is not associated with sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Molecular analysis of prion protein gene (PRNP) in Korean patients with Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Structural and functional features of eukaryotic mRNA untranslated regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Polymorphisms of the prion protein gene (PRNP) in a Korean population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Polymorphisms within the prion (PrP) and prion-like protein (Doppel) genes in AD

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Mutation and linkage disequilibrium in human mtDNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Single nucleotide polymorphism in prohibitin 3' untranslated region and breast-cancer susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Association of resistin gene 3'-untranslated region +62G-->A polymorphism with type 2 diabetes and hypertension in a Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201460

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201460

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15986038%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

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