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

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Lack of association between 14-3-3 beta gene (YWHAB) polymorphisms and sporadic Creutzfeldt-Jakob disease (CJD).

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Q48341697-0068C18A-B57B-4F86-948D-4D496ED71A7B

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

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http://www.wikidata.org/entity/Q59294063

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im Juni 2005 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в червні 2005

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3′ UTR +28 of ...... adic Creutzfeldt–Jakob disease

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Polymorphism at 3' UTR +28 of ...... adic Creutzfeldt-Jakob disease

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Byung-Hoon Jeong

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

Eun-Kyoung Choi

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Jae-Il Kim

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Nam-Ho Kim

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Yong-Sun Kim

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P2860

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

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

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

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

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

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

Structural and functional features of eukaryotic mRNA untranslated regions.

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

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

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

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sj.ejhg.5201460

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1094-1097

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scholarly article

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10.1038/SJ.EJHG.5201460

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

P478

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Young-Han Song

Chaeyoung Lee

Richard I. Carp

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2005-09-01T00:00:00Z

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15986038

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

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P2860

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

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P1476

P2093

P2860

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P304

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P356

P433

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P50

P577

P698

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698