First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases
about
Novel mutation of the PRNP gene of a clinical CJD casePrion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob diseaseThe human "prion-like" protein Doppel is expressed in both Sertoli cells and spermatozoaSporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.Genetic studies in human prion diseases.Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue DoppelAbsence of the prion protein homologue Doppel causes male sterility.Influence of the prion protein gene, Prnp, on scrapie susceptibility in sheep.Differential responses of neuronal and spermatogenic cells to the doppel cytotoxicity.Male infertility and DNA damage in Doppel knockout and prion protein/Doppel double-knockout micePRND 3'UTR polymorphism may be associated with behavioral disturbances in Alzheimer diseaseCo-clustering phenome-genome for phenotype classification and disease gene discovery.Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.Endoproteolytic processing of the mammalian prion glycoprotein family.Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease.Stability and conformational properties of doppel, a prion-like protein, and its single-disulphide mutant.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.Report about four novel mutations in the prion protein gene.Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease
P2860
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P2860
First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases
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2000 nî lūn-bûn
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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
First report of polymorphisms ...... tions for human prion diseases
@ast
First report of polymorphisms ...... tions for human prion diseases
@en
First report of polymorphisms ...... tions for human prion diseases
@nl
type
label
First report of polymorphisms ...... tions for human prion diseases
@ast
First report of polymorphisms ...... tions for human prion diseases
@en
First report of polymorphisms ...... tions for human prion diseases
@nl
prefLabel
First report of polymorphisms ...... tions for human prion diseases
@ast
First report of polymorphisms ...... tions for human prion diseases
@en
First report of polymorphisms ...... tions for human prion diseases
@nl
P2093
P1433
P1476
First report of polymorphisms ...... tions for human prion diseases
@en
P2093
J L Laplanche
J M Launay
J P Brandel
P356
10.1016/S0304-3940(00)01100-9
P407
P577
2000-06-02T00:00:00Z