Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease. - Wikidata - wikimedia - TriplyDB

Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease.

Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q37452196

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B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C).Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation Molecular pathogenesis of sporadic prion diseases in man.Identification of misfolded proteins in body fluids for the diagnosis of prion diseases.Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection Prion disease tempo determined by host-dependent substrate reduction.Artificial strain of human prions created in vitro.

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Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q37452196

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

@en

Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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LABINVEST.2009.30

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Laboratory Investigation

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Prion proteins in subpopulatio ...... dic Creutzfeldt-Jakob disease.

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Amy Kuo

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Camille Deering

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Ed M Choi

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Jiri G Safar

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Kristen Pomeroy

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Michael D Geschwind

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

Mice devoid of PrP are resistant to scrapie

Novel proteinaceous infectious particles cause scrapie

Eight prion strains have PrP(Sc) molecules with different conformations

Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein.

The T cell surface--how well do we know it?

Diagnosis of human prion disease

Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice.

Organ distribution of prion proteins in variant Creutzfeldt-Jakob disease.

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.

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labinvest.2009.30

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624-635

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scholarly article

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10.1038/LABINVEST.2009.30

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6

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89

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Stanley B. Prusiner

Bruce L. Miller

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2009-06-01T00:00:00Z

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24419539

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19434060

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Prion protein family

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2786774

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