UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 114

Sortiert nach

Potential for transmission of sporadic Creutzfeldt–Jakob disease through peripheral routes

Laboratory investigation, 2021-10, Vol.101 (10), p.1327-1330

2021

Link zum Volltext

Verfügbarkeit prüfen

The influence of PRNP polymorphisms on human prion disease susceptibility: an update

Acta neuropathologica, 2015-08, Vol.130 (2), p.159-170

2015

Link zum Volltext

Verfügbarkeit prüfen

A point mutation in GPI-attachment signal peptide accelerates the development of prion disease

Acta neuropathologica, 2023-05, Vol.145 (5), p.637-650

2023

Link zum Volltext

Verfügbarkeit prüfen

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease

Emerging infectious diseases, 2017-09, Vol.23 (9), p.1522-1530

2017

Link zum Volltext

Verfügbarkeit prüfen

Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases

Neuropathology, 2016-06, Vol.36 (3), p.305-310

2016

Link zum Volltext

Verfügbarkeit prüfen

A domain responsible for spontaneous conversion of bank vole prion protein

Brain pathology (Zurich, Switzerland), 2019-03, Vol.29 (2), p.155-163

2019

Link zum Volltext

Verfügbarkeit prüfen

Eliminating transmissibility of bovine spongiform encephalopathy by dry-heat treatment

Journal of general virology, 2020-01, Vol.101 (1), p.136-142

2020

Link zum Volltext

Verfügbarkeit prüfen

Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?

Journal of virology, 2015-04, Vol.89 (7), p.3939-3946

2015

Link zum Volltext

Verfügbarkeit prüfen

Experimental Verification of a Traceback Phenomenon in Prion Infection

Journal of Virology, 2010-04, Vol.84 (7), p.3230-3238

2010

Link zum Volltext

Verfügbarkeit prüfen

Cross-sequence Transmission of Sporadic Creutzfeldt-Jakob Disease Creates a New Prion Strain

The Journal of biological chemistry, 2007-10, Vol.282 (41), p.30022-30028

2007

Link zum Volltext

Verfügbarkeit prüfen

Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases

Neuroscience letters, 2018-03, Vol.668, p.43-47

2018

Link zum Volltext

Verfügbarkeit prüfen

Urinary excretion and blood level of prions in scrapie-infected hamsters

Journal of general virology, 2007-10, Vol.88 (10), p.2890-2898

2007

Link zum Volltext

Verfügbarkeit prüfen

Treatment of Transmissible Spongiform Encephalopathy by Intraventricular Drug Infusion in Animal Models

Journal of Virology, 2004-05, Vol.78 (10), p.4999-5006

2004

Link zum Volltext

Verfügbarkeit prüfen

Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems

Acta neuropathologica communications, 2014-03, Vol.2 (1), p.32-32, Article 32

2014

Link zum Volltext

Verfügbarkeit prüfen

Characterization of Variant Creutzfeldt-Jakob Disease Prions in Prion Protein-humanized Mice Carrying Distinct Codon 129 Genotypes

The Journal of biological chemistry, 2013-07, Vol.288 (30), p.21659-21666

2013

Link zum Volltext

Verfügbarkeit prüfen

Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits

Veterinary research (Paris), 2011-06, Vol.42 (1), p.79-79

2011

Link zum Volltext

Verfügbarkeit prüfen

Prion Replication Elicits Cytopathic Changes in Differentiated Neurosphere Cultures

Journal of Virology, 2013-08, Vol.87 (15), p.8745-8755

2013

Link zum Volltext

Verfügbarkeit prüfen

Sulfated dextrans enhance in vitro amplification of bovine spongiform encephalopathy PrP(Sc) and enable ultrasensitive detection of bovine PrP(Sc)

PloS one, 2010-10, Vol.5 (10)

2010

Link zum Volltext

Verfügbarkeit prüfen

Human Prion Protein (PrP) 219K Is Converted to PrPSc but Shows Heterozygous Inhibition in Variant Creutzfeldt-Jakob Disease Infection

The Journal of biological chemistry, 2009-02, Vol.284 (6), p.3603-3609

2009

Link zum Volltext

Verfügbarkeit prüfen

Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties

Brain pathology (Zurich, Switzerland), 2016-01, Vol.26 (1), p.95-101

2016

Link zum Volltext

Verfügbarkeit prüfen

Sulfated Dextrans Enhance In Vitro Amplification of Bovine Spongiform Encephalopathy PrPSc and Enable Ultrasensitive Detection of Bovine PrPSc

PloS one, 2010-10, Vol.5 (10), p.e13152

2010

Link zum Volltext

Verfügbarkeit prüfen

Anti-prion activity of Brilliant Blue G

PloS one, 2012-05, Vol.7 (5), p.e37896

2012

Link zum Volltext

Verfügbarkeit prüfen

Insect cell-derived cofactors become fully functional after proteinase K and heat treatment for high-fidelity amplification of glycosylphosphatidylinositol-anchored recombinant scrapie and BSE prion proteins

PloS one, 2013-12, Vol.8 (12), p.e82538-e82538

2013

Link zum Volltext

Verfügbarkeit prüfen

Subcritical Water Hydrolysis Effectively Reduces the In Vitro Seeding Activity of PrPSc but Fails to Inactivate the Infectivity of Bovine Spongiform Encephalopathy Prions

PloS one, 2015-12, Vol.10 (12), p.e0144761-e0144761

2015

Link zum Volltext

Verfügbarkeit prüfen

Prion diseases and emerging prion diseases

Current medicinal chemistry, 2008-04, Vol.15 (9), p.912

2008

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 114

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(103)
Mit Volltextzugriff
(112)

Publikationsform

Sprache

Englisch
(114)
Japanisch
(54)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Potential for transmission of sporadic Creutzfeldt–Jakob disease through peripheral routes

The influence of PRNP polymorphisms on human prion disease susceptibility: an update

A point mutation in GPI-attachment signal peptide accelerates the development of prion disease

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease

Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases

A domain responsible for spontaneous conversion of bank vole prion protein

Eliminating transmissibility of bovine spongiform encephalopathy by dry-heat treatment

Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?

Experimental Verification of a Traceback Phenomenon in Prion Infection

Cross-sequence Transmission of Sporadic Creutzfeldt-Jakob Disease Creates a New Prion Strain

Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases

Urinary excretion and blood level of prions in scrapie-infected hamsters

Treatment of Transmissible Spongiform Encephalopathy by Intraventricular Drug Infusion in Animal Models

Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems

Characterization of Variant Creutzfeldt-Jakob Disease Prions in Prion Protein-humanized Mice Carrying Distinct Codon 129 Genotypes

Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits

Prion Replication Elicits Cytopathic Changes in Differentiated Neurosphere Cultures

Sulfated dextrans enhance in vitro amplification of bovine spongiform encephalopathy PrP(Sc) and enable ultrasensitive detection of bovine PrP(Sc)

Human Prion Protein (PrP) 219K Is Converted to PrPSc but Shows Heterozygous Inhibition in Variant Creutzfeldt-Jakob Disease Infection

Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties

Sulfated Dextrans Enhance In Vitro Amplification of Bovine Spongiform Encephalopathy PrPSc and Enable Ultrasensitive Detection of Bovine PrPSc

Anti-prion activity of Brilliant Blue G

Insect cell-derived cofactors become fully functional after proteinase K and heat treatment for high-fidelity amplification of glycosylphosphatidylinositol-anchored recombinant scrapie and BSE prion proteins

Subcritical Water Hydrolysis Effectively Reduces the In Vitro Seeding Activity of PrPSc but Fails to Inactivate the Infectivity of Bovine Spongiform Encephalopathy Prions

Prion diseases and emerging prion diseases

Suchergebnisse filtern