UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

2.7 Å cryo-EM structure of ex vivo RML prion fibrils

Nature communications, 2022-07, Vol.13 (1), p.4004-11, Article 4004

2022

Volltextzugriff (PDF)

Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

The New England journal of medicine, 2017-01, Vol.376 (3), p.292-294

2017

Volltextzugriff (PDF)

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy

Nature (London), 2015-09, Vol.525 (7568), p.247-250

2015

Volltextzugriff (PDF)

Prion strains viewed through the lens of cryo-EM

Cell and tissue research, 2023-04, Vol.392 (1), p.167-178

2023

Volltextzugriff (PDF)

A structural basis for prion strain diversity

Nature chemical biology, 2023-05, Vol.19 (5), p.607-613

2023

Volltextzugriff (PDF)

A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

The New England journal of medicine, 2013-11, Vol.369 (20), p.1904-1914

2013

Volltextzugriff (PDF)

A naturally occurring variant of the human prion protein completely prevents prion disease

Nature (London), 2015-06, Vol.522 (7557), p.478-481

2015

Volltextzugriff (PDF)

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS

PLoS biology, 2020-06, Vol.18 (6), p.e3000725-e3000725

2020

Volltextzugriff (PDF)

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases

Molecular psychiatry, 2021-10, Vol.26 (10), p.5955-5966

2021

Volltextzugriff (PDF)

Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro

Scientific reports, 2019-01, Vol.9 (1), p.376-376, Article 376

2019

Volltextzugriff (PDF)

Molecular pathology of human prion disease

Acta neuropathologica, 2011-01, Vol.121 (1), p.69-77

2011

Volltextzugriff (PDF)

Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy

Scientific reports, 2022-10, Vol.12 (1), p.17198-17198, Article 17198

2022

Volltextzugriff (PDF)

Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype

Science (American Association for the Advancement of Science), 2004-12, Vol.306 (5702), p.1793-1796

2004

Volltextzugriff (PDF)

Recent Advances in Understanding Mammalian Prion Structure: A Mini Review

Frontiers in molecular neuroscience, 2019-07, Vol.12, p.169-169

2019

Volltextzugriff (PDF)

Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

Nature communications, 2014-07, Vol.5 (1), p.4347, Article 4347

2014

Volltextzugriff (PDF)

The impact of immigration on the structure of wages: Theory and evidence from Britain

Journal of the European Economic Association, 2012-02, Vol.10 (1), p.120-151

2012

Volltextzugriff (PDF)

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein

PLoS pathogens, 2013-09, Vol.9 (9), p.e1003643

2013

Volltextzugriff (PDF)

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3386-3399

2015

Volltextzugriff (PDF)

Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin

Biochemical journal, 2008-12, Vol.416 (2), p.297-305

2008

Volltextzugriff (PDF)

Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose

The Journal of infectious diseases, 2022-09, Vol.226 (5), p.933-937

2022

Volltextzugriff (PDF)

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease

JAMA neurology, 2016-04, Vol.73 (4), p.447

2016

Volltextzugriff (PDF)

Highly infectious prions are not directly neurotoxic

Proceedings of the National Academy of Sciences - PNAS, 2020-09, Vol.117 (38), p.23815-23822

2020

Volltextzugriff (PDF)

Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report

The Lancet (British edition), 2006-12, Vol.368 (9552), p.2061-2067

2006

Volltextzugriff (PDF)

Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid

PloS one, 2010-12, Vol.5 (12), p.e15679-e15679

2010

Volltextzugriff (PDF)

Amyloid-β nanotubes are associated with prion protein-dependent synaptotoxicity

Nature communications, 2013-09, Vol.4 (1), p.2416, Article 2416

2013

Volltextzugriff (PDF)

1 – 25 von 365

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(287)
Mit Volltextzugriff
(272)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(365)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

2.7 Å cryo-EM structure of ex vivo RML prion fibrils

Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy

Prion strains viewed through the lens of cryo-EM

A structural basis for prion strain diversity

A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

A naturally occurring variant of the human prion protein completely prevents prion disease

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases

Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro

Molecular pathology of human prion disease

Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy

Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype

Recent Advances in Understanding Mammalian Prion Structure: A Mini Review

Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked

The impact of immigration on the structure of wages: Theory and evidence from Britain

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin

Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and Moose

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease

Highly infectious prions are not directly neurotoxic

Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report

Isolation of proteinase K-sensitive prions using pronase E and phosphotungstic acid

Amyloid-β nanotubes are associated with prion protein-dependent synaptotoxicity

Suchergebnisse filtern