UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 199

Sortiert nach

Prion Strain Mutation and Selection

Science (American Association for the Advancement of Science), 2010-05, Vol.328 (5982), p.1111-1112

Collinge, John

2010

Link zum Volltext

Verfügbarkeit prüfen

Mammalian prions and their wider relevance in neurodegenerative diseases

Nature (London), 2016-11, Vol.539 (7628), p.217-226

Collinge, John

2016

Link zum Volltext

Verfügbarkeit prüfen

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

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

2022

Link zum Volltext

Verfügbarkeit prüfen

Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

Nature (London), 2011-02, Vol.470 (7335), p.540-542

2011

Link zum Volltext

Verfügbarkeit prüfen

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

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

2015

Link zum Volltext

Verfügbarkeit prüfen

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases

Scientific reports, 2021-03, Vol.11 (1), p.5231-5231, Article 5231

2021

Link zum Volltext

Verfügbarkeit prüfen

Prion protein gene mutation detection using long-read Nanopore sequencing

Scientific reports, 2022-05, Vol.12 (1), p.8284-8284, Article 8284

2022

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibody

Scientific reports, 2022-06, Vol.12 (1), p.9493-12, Article 9493

2022

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Two mouse models of Alzheimer’s disease accumulate amyloid at different rates and have distinct Aβ oligomer profiles unaltered by ablation of cellular prion protein

PloS one, 2023-11, Vol.18 (11), p.e0294465-e0294465

2023

Link zum Volltext

Verfügbarkeit prüfen

Depleting Neuronal PrP in Prion Infection Prevents Disease and Reverses Spongiosis

Science (American Association for the Advancement of Science), 2003-10, Vol.302 (5646), p.871-874

2003

Link zum Volltext

Verfügbarkeit prüfen

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (29), p.10238-10243

2008

Link zum Volltext

Verfügbarkeit prüfen

The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature

PloS one, 2018-01, Vol.13 (1), p.e0190818-e0190818

2018

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis

Nature communications, 2020-08, Vol.11 (1), p.3960-3960, Article 3960

2020

Link zum Volltext

Verfügbarkeit prüfen

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

Nature (London), 2003-03, Vol.422 (6927), p.80-83

2003

Link zum Volltext

Verfügbarkeit prüfen

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis

PloS one, 2010-05, Vol.5 (5), p.e10627

2010

Link zum Volltext

Verfügbarkeit prüfen

A novel and rapid method for obtaining high titre intact prion strains from mammalian brain

Scientific reports, 2015-05, Vol.5 (1), p.10062-10062, Article 10062

2015

Link zum Volltext

Verfügbarkeit prüfen

Location and Properties of Metal-Binding Sites on the Human Prion Protein

Proceedings of the National Academy of Sciences - PNAS, 2001-07, Vol.98 (15), p.8531-8535

2001

Link zum Volltext

Verfügbarkeit prüfen

The Risk of Prion Zoonoses

Science (American Association for the Advancement of Science), 2012-01, Vol.335 (6067), p.411-413

Collinge, John

2012

Link zum Volltext

Verfügbarkeit prüfen

Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces

Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (9), p.3479-3483

2009

Link zum Volltext

Verfügbarkeit prüfen

Pharmacological chaperone for the structured domain of human prion protein

Proceedings of the National Academy of Sciences - PNAS, 2010-10, Vol.107 (41), p.17610-17615

2010

Link zum Volltext

Verfügbarkeit prüfen

Species-Barrier-Independent Prion Replication in Apparently Resistant Species

Proceedings of the National Academy of Sciences - PNAS, 2000-08, Vol.97 (18), p.10248-10253

2000

Link zum Volltext

Verfügbarkeit prüfen

Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypes

Nature (London), 2017-01, Vol.541 (7636), p.217-221

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 199

Suche als RSS-Feed

Aktive Filter

KollektionElsevier ScienceDirect Journals Complete

Zeitschrift / SerieNeurobiology Of Aging

ThemaLife Sciences & Biomedicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(172)
Mit Volltextzugriff
(165)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(67)
Science & Technology - Other Topics
(65)
Humans
(64)
Multidisciplinary Sciences
(64)
Animals
(54)
Prions
(43)
Mice
(40)
Creutzfeldt-Jakob Disease
(37)
Proteins
(26)
Neurology
(25)
Multidisciplinary
(24)
Prions - Metabolism
(24)
Prion Diseases
(21)
Biological And Medical Sciences
(20)
Prions - Genetics
(20)
Male
(19)
Prion Protein
(19)
Female
(18)
Mice, Transgenic
(17)
Mutation
(17)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Prion Strain Mutation and Selection

Mammalian prions and their wider relevance in neurodegenerative diseases

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

Prion propagation and toxicity in vivo occur in two distinct mechanistic phases

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

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases

Prion protein gene mutation detection using long-read Nanopore sequencing

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

A high-content neuron imaging assay demonstrates inhibition of prion disease-associated neurotoxicity by an anti-prion protein antibody

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

Two mouse models of Alzheimer’s disease accumulate amyloid at different rates and have distinct Aβ oligomer profiles unaltered by ablation of cellular prion protein

Depleting Neuronal PrP in Prion Infection Prevents Disease and Reverses Spongiosis

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease

The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature

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

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis

A novel and rapid method for obtaining high titre intact prion strains from mammalian brain

Location and Properties of Metal-Binding Sites on the Human Prion Protein

The Risk of Prion Zoonoses

Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces

Pharmacological chaperone for the structured domain of human prion protein

Species-Barrier-Independent Prion Replication in Apparently Resistant Species

Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypes

Aktive Filter

Suchergebnisse filtern