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Lista de obras de John Collinge

11C-PiB PET does not detect PrP-amyloid in prion disease patients including variant Creutzfeldt–Jakob disease: Figure 1

scientific article published on 08 April 2011

A 38-year-old man with a 9 month history of neurological and cognitive impairment

artículo científico publicado en 2003

A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse

artículo científico publicado en 2009

A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

artículo científico publicado en 2009

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

artículo científico publicado en 2020

A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea

artículo científico publicado en 2008

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

artículo científico publicado en 2008

A general model of prion strains and their pathogenicity

artículo científico publicado en 2007

A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase K.

artículo científico publicado en 2010

A highly specific blood test for vCJD

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromes

artículo científico publicado en 2011

A novel prion disease associated with diarrhea and autonomic neuropathy

artículo científico publicado en 2013

A novel prion protein variant in a patient with semantic dementia

artículo científico publicado en 2017

A reassessment of copper(II) binding in the full-length prion protein

artículo científico publicado en 2006

A role of cellular prion protein in programming T-cell cytokine responses in disease

artículo científico publicado en 2009

A standardized comparison of commercially available prion decontamination reagents using the Standard Steel-Binding Assay

artículo científico publicado en 2010

A systematic investigation of production of synthetic prions from recombinant prion protein

artículo científico publicado en 2015

A systematic review of prion therapeutics in experimental models

artículo científico publicado en 2006

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins

artículo científico publicado en 2009

Alterations in Ca2+-buffering in prion-null mice: association with reduced afterhyperpolarizations in CA1 hippocampal neurons.

artículo científico publicado en 2008

Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob disease

scientific article published on 12 September 2020

Alternative fates of newly formed PrPSc upon prion conversion on the plasma membrane

artículo científico publicado en 2013

Amyloid beta-protein dimers rapidly form stable synaptotoxic protofibrils

artículo científico publicado en 2010

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

artículo científico publicado en 2013

An enzyme-detergent method for effective prion decontamination of surgical steel.

artículo científico publicado en 2005

Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion protein.

artículo científico publicado en 2004

ApoE4 lowers age at onset in patients with frontotemporal dementia and tauopathy independent of amyloid-β copathology

artículo científico publicado en 2019

Ascertainment bias causes false signal of anticipation in genetic prion disease

artículo científico publicado en 2014

Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein.

artículo científico publicado en 2013

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

artículo científico publicado en 2002

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

artículo científico publicado en 2003

Behavioral and psychiatric symptoms in prion disease

artículo científico

Beta-PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91-110 that recognise native PrPSc

scientific article published on 06 September 2007

Biochemical typing of scrapie strains

artículo científico publicado en 1997

Blood test for variant Creutzfeldt-Jakob disease--reply

artículo científico publicado en 2014

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

artículo científico publicado en 2007

Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.

artículo científico publicado en 2008

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice

artículo científico publicado en 2004

Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14

scholarly article by Michael Mullan et al published 27 February 1995 in American Journal of Medical Genetics Part A

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

artículo científico publicado en 2006

Codon 129 polymorphism of the human prion protein influences the kinetics of amyloid formation

artículo científico publicado en 2006

Collinge et al. reply

artículo científico publicado en 2016

Collinge et al. reply.

artículo científico publicado en 2016

Comment on validation of diagnostic criteria for variant Creutzfeldt‐Jakob disease ⬇️

artículo científico publicado el 1 de enero de 2011

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Conformational properties of beta-PrP.

artículo científico publicado en 2009

Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

artículo científico publicado en 2011

Corrigendum to “Elongated Oligomers Assemble into Mammalian PrP Amyloid Fibrils” [J. Mol. Biol. 357 (2006) 975–985]

scholarly article published in Journal of Molecular Biology

Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman

artículo científico publicado en 2007

Definable equilibrium states in the folding of human prion protein

artículo científico publicado en 2005

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

artículo científico publicado en 2008

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay ⬇️

artículo científico publicado el 5 de febrero de 2011

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

artículo científico publicado en 2022

Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine

artículo científico publicado en 2016

Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplification

artículo científico publicado en 2010

Disease-associated prion protein elicits immunoglobulin M responses in vivo

artículo científico publicado en 2004

Disease-associated prion protein oligomers inhibit the 26S proteasome

artículo científico publicado en 2007

Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosis.

artículo científico publicado en 2005

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

artículo científico publicado en 2010

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

artículo científico publicado en 2006

Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations.

artículo científico publicado en 2006

Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis

artículo científico publicado en 2020

Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series

artículo científico publicado en 2010

Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation

artículo científico publicado en 2017

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study

scientific article published on 10 December 2010

Elongated oligomers assemble into mammalian PrP amyloid fibrils

artículo científico publicado en 2006

Enteral feeding is associated with longer survival in the advanced stages of prion disease

scientific article published on 10 September 2019

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

artículo científico publicado en 2015

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Erratum: Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

artículo científico publicado en 1991

Evaluating the causality of novel sequence variants in the prion protein gene by example

article

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

artículo científico publicado en 2015

Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation

artículo científico publicado en 2015

Ex vivo mammalian prions are formed of paired double helical prion protein fibrils.

artículo científico publicado en 2016

Exosome release from infected dendritic cells: a clue for a fast spread of prions in the periphery?

artículo científico

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein. ⬇️

artículo científico publicado en 2017

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

artículo científico publicado en 2010

Familial Creutzfeldt-Jakob Disease in an Indian Kindred

artículo científico publicado en 2019

Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases

artículo científico publicado en 2013

First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation.

artículo científico publicado en 2008

Folding kinetics of the human prion protein probed by temperature jump.

scholarly article

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown

Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology

artículo científico publicado en 2015

Frontotemporal dementia linked to chromosome 3

scientific article published on 01 January 2004

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

artículo científico publicado en 2012

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

artículo científico publicado en 2016

Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study

artículo científico publicado en 2009

Genetic susceptibility, evolution and the kuru epidemic

artículo científico publicado en 2008

Genetic variability in CLU and its association with Alzheimer's disease

artículo científico publicado en 2010

Genetics of prion disease

artículo científico publicado en 2011

Genetics of prion diseases

artículo científico publicado en 2013

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

scientific journal article

HECTD2 is associated with susceptibility to mouse and human prion disease

artículo científico publicado en 2009

HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q.

artículo científico publicado en 2009

Heterozygosity at polymorphic codon 219 in variant creutzfeldt-jakob disease

artículo científico publicado en 2010

Highly infectious prions are not directly neurotoxic

artículo científico publicado en 2020

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

scholarly article

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

artículo científico publicado en 2013

Human prion protein with valine 129 prevents expression of variant CJD phenotype

artículo científico publicado en 2004

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

artículo científico publicado en 2015

Identification and characterization of a novel mouse prion gene allele

artículo científico publicado en 2004

Identification of a Compound That Disrupts Binding of Amyloid-β to the Prion Protein Using a Novel Fluorescence-based Assay

artículo científico publicado en 2015

Identification of a gene regulatory network associated with prion replication

artículo científico publicado en 2014

Identification of clinical target areas in the brainstem of prion-infected mice

artículo científico publicado en 2015

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice

artículo científico publicado en 2002

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

scientific article published on 16 September 2020

Imaging and CSF analyses effectively distinguish CJD from its mimics

artículo científico publicado en 2017

In vitro screen of prion disease susceptibility genes using the scrapie cell assay

artículo científico publicado en 2014

Inherited mtDNA variations are not strong risk factors in human prion disease

scientific article published on 10 July 2015

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

artículo científico publicado en 2013

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors

artículo científico publicado en 2011

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

artículo científico publicado en 2006

Inhibition of proteinase K activity by copper(II) ions.

artículo científico publicado en 2007

Interaction between prion protein and toxic amyloid β assemblies can be therapeutically targeted at multiple sites

artículo científico publicado en 2011

Introduction

Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouse

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Kuru in the 21st century--an acquired human prion disease with very long incubation periods

artículo científico publicado en 2006

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice

artículo científico publicado en 2008

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

artículo científico publicado en 2013

MRI detection of prion protein plaques in variant Creutzfeldt-Jakob disease.

artículo científico publicado en 2015

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

artículo científico publicado en 2012

Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases.

artículo científico publicado en 2010

Mapping the progression of progranulin-associated frontotemporal lobar degeneration

artículo científico publicado en 2008

Methods for Molecular Diagnosis of Human Prion Disease

artículo científico publicado en 2017

Microglial Cx3cr1 knockout reduces prion disease incubation time in mice

artículo científico publicado en 2014

Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry

artículo científico publicado en 2011

Molecular and clinical classification of human prion disease ⬇️

artículo científico publicado el 1 de enero de 2003

Molecular classification of sporadic Creutzfeldt-Jakob disease.

artículo científico publicado en 2003

Molecular diagnosis of human prion disease.

artículo científico publicado en 2008

Molecular pathology of human prion disease ⬇️

artículo científico publicado el 8 de agosto de 2010

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

artículo científico publicado en 2003

Mortuary rites of the South Fore and kuru

artículo científico publicado en 2008

Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4.

artículo científico publicado en 2006

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

artículo científico publicado en 2005

N-terminal domain of prion protein directs its oligomeric association

artículo científico publicado en 2014

Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study

artículo científico publicado en 2016

Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progression.

artículo científico publicado en 2018

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration

artículo científico publicado en 2009

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

artículo científico publicado en 2011

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

artículo científico publicado en 2012

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit

artículo científico publicado en 2010

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene

artículo científico publicado en 2008

Pathogenic human prion protein rescues PrP null phenotype in transgenic mice.

artículo científico publicado en 2004

Peripheral administration of a humanized anti-PrP antibody blocks Alzheimer's disease Aβ synaptotoxicity

artículo científico publicado en 2014

Pharmacological chaperone for the structured domain of human prion protein.

artículo científico publicado en 2010

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.

artículo científico publicado en 2006

Physical, chemical and kinetic factors affecting prion infectivity

artículo científico publicado en 2016

Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection

artículo científico publicado en 2012

Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study

artículo científico publicado en 2014

Potential human transmission of amyloid β pathology: surveillance and risks

scientific article published on 16 September 2020

PrP antibodies do not trigger mouse hippocampal neuron apoptosis

artículo científico publicado en 2012

PrP glycoforms are associated in a strain-specific ratio in native PrPSc

scientific article published on 01 September 2005

PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteins

artículo científico publicado en 2019

PrP-grafted antibodies bind certain amyloid β-protein aggregates, but do not prevent toxicity

scientific article published on 26 December 2018

PrPSc binding antibodies are potent inhibitors of prion replication in cell lines.

artículo científico publicado en 2004

Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion disease

artículo científico publicado en 2015

Predictive testing for inherited prion disease: report of 22 years experience

artículo científico publicado en 2014

Preventing prion pathogenicity by targeting the cellular prion protein

artículo científico publicado en 2009

Prion Diseases

scientific article published on 01 April 2003

Prion Protein as a Toxic Acceptor of Amyloid-β Oligomers

artículo científico publicado en 2017

Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process

scientific article published on 25 October 2019

Prion disease incubation time is not affected in mice heterozygous for a dynein mutation

artículo científico publicado en 2005

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes

scientific article published on 01 November 2006

Prion protein gene M232R variation is probably an uncommon polymorphism rather than a pathogenic mutation

scientific article published on 21 November 2011

Prion protein gene mutation detection using long-read Nanopore sequencing

artículo científico publicado en 2022

Prion strains and species barriers

artículo científico publicado en 2004

Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin-proteasome system

artículo científico publicado en 2015

Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice

artículo científico publicado en 2012

Protein conformation significantly influences immune responses to prion protein.

artículo científico publicado en 2005

Putaminal diffusion tensor imaging measures predict disease severity across human prion diseases

artículo científico publicado en 2020

Quantitative EEG parameters correlate with the progression of human prion diseases

artículo científico publicado en 2016

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia

artículo científico publicado en 2014

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Rare structural genetic variation in human prion diseases

artículo científico publicado en 2015

Recombinant prion protein does not possess SOD-1 activity.

artículo científico publicado en 2005

Regional heterogeneity of cellular prion protein isoforms in the mouse brain

artículo científico publicado en 2003

Reminiscences and reflections on kuru, personal and scientific

artículo científico publicado en 2008

Removal of the glycosylphosphatidylinositol anchor from PrP(Sc) by cathepsin D does not reduce prion infectivity

artículo científico publicado en 2006

Reply to: Intrinsic Toxicity of Antibodies to the Globular Domain of the Prion Protein

scientific article published on 12 April 2018

Review. The origin of the prion agent of kuru: molecular and biological strain typing.

artículo científico publicado en 2008

Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial

artículo científico publicado en 2009

Sex effects in mouse prion disease incubation time

artículo científico publicado en 2011

Shadoo (Sprn) and prion disease incubation time in mice

artículo científico publicado en 2009

Sod1 deficiency reduces incubation time in mouse models of prion disease

artículo científico publicado en 2013

Soluble Aβ aggregates can inhibit prion propagation.

artículo científico publicado en 2017

Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease

artículo científico publicado en 2004

Species-barrier-independent prion replication in apparently resistant species.

artículo científico publicado en 2002

Spontaneous generation of mammalian prions

artículo científico publicado en 2010

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

artículo científico publicado en 2020

Structural effects of the highly protective V127 polymorphism on human prion protein

artículo científico publicado en 2020

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

artículo científico publicado en 2019

Subclinical prion infection in humans and animals ⬇️

artículo científico publicado el 1 de enero de 2003

Subclinical prion infection.

artículo científico publicado en 2003

Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms.

artículo científico publicado en 2008

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

artículo científico publicado en 2010

TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3).

artículo científico publicado en 2017

TREM2 Variants in Alzheimer's Disease

artículo científico publicado en 2013

Targeting glutamatergic and cellular prion protein mechanisms of amyloid β-mediated persistent synaptic plasticity disruption: Longitudinal studies

artículo científico publicado en 2017

Tau, prions and Aβ: the triad of neurodegeneration

artículo científico publicado en 2010

The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like form

artículo científico publicado en 2010

The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

artículo científico publicado en 2013

The Retinoic Acid Receptor Beta (Rarb) Region of Mmu14 Is Associated with Prion Disease Incubation Time in Mouse ⬇️

artículo científico publicado el 6 de diciembre de 2010

The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cells

article

The cognitive profile of prion disease: a prospective clinical and imaging study.

artículo científico publicado en 2015

The human prion protein residue 129 polymorphism lies within a cluster of epitopes for T cell recognition.

artículo científico publicado en 2006

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

artículo científico publicado en 2018

The most problematic symptoms of prion disease - an analysis of carer experiences

artículo científico publicado en 2019

The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC.

artículo científico publicado en 2004

The role of CHMP2B in frontotemporal dementia

artículo científico publicado en 2009

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

artículo científico publicado en 2015

Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone

artículo científico publicado en 2018

Typing prion isoforms

artículo científico publicado en 1997

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

artículo científico publicado en 2009

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

artículo científico publicado en 1997

Unswitched immunoglobulin M response prolongs mouse survival in prion disease.

artículo científico publicado en 2009

Update on human prion disease.

artículo científico publicado en 2007

Validation of next-generation sequencing technologies in genetic diagnosis of dementia

artículo científico publicado en 2013

Variant CJD in an individual heterozygous for PRNP codon 129

scientific article published on 01 December 2009

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

artículo científico publicado en 2017

Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein

artículo científico publicado en 2014

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study

artículo científico publicado en 2016

Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1.

artículo científico publicado en 2012

mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivo

artículo científico publicado en 2014

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