Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

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Analyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011.Genetic studies in human prion diseases.Three sporadic cases of Creutzfeldt-Jakob disease in China and their clinical analysis.

P2860

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P2860

Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

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http://www.wikidata.org/entity/Q39331213

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh

2012年學術文章

@zh-hant

name

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@en

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@nl

type

Item

label

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@en

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@nl

prefLabel

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@en

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@nl

P1476

Association between the PRNP 1 ...... dic Creutzfeldt-Jakob disease.

@en

P2093

Annemieke J Rozemuller

http://www.w3.org/2001/XMLSchema#string

Casper Jansen

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Gerard H Jansen

http://www.w3.org/2001/XMLSchema#string

Joanna Smoleń-Dzirba

http://www.w3.org/2001/XMLSchema#string

Jolanta Bratosiewicz-Wąsik

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Paweł P Liberski

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Tomasz J Wąsik

http://www.w3.org/2001/XMLSchema#string

Wim Spliet

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P2860

Haploview: analysis and visualization of LD and haplotype maps

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

Mice devoid of PrP are resistant to scrapie

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

Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia

Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.

Genetics of prion disease.

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease.

Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.

Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice.

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413-416

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scholarly article

P356

10.4161/PRI.21773

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2012-08-16T00:00:00Z

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22895088

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P932

3609072

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Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

about

P2860

P2860

Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932