Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
about
Complex proteinopathy with accumulations of prion protein, hyperphosphorylated tau, α-synuclein and ubiquitin in experimental bovine spongiform encephalopathy of monkeys.11C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer's disease in the absence of known mutations retains higher levels of PIB in the basal gangliaNext generation sequencing techniques in neurological diseases: redefining clinical and molecular associations.Nonsense mutation in PRNP associated with clinical Alzheimer's diseaseProteomics analysis of amyloid and nonamyloid prion disease phenotypes reveals both common and divergent mechanisms of neuropathogenesisLevels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion diseaseSquirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathologyNew approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degenerationQuantifying prion disease penetrance using large population control cohortsDrivers: A Biologically Contextualized, Cross-Inferential View of the Epidemiology of Neurodegenerative Disorders.Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.Activation of the unfolded protein response and granulovacuolar degeneration are not common features of human prion pathology.A novel prion disease associated with diarrhea and autonomic neuropathy.Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China.Unusual cerebral vascular prion protein amyloid distribution in scrapie-infected transgenic mice expressing anchorless prion protein.Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral NeuropathyDistinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion proteinGerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.Interaction between pathogenic proteins in neurodegenerative disorders.The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease.Genetics of dementia: update and guidelines for the clinician.Review: cerebral amyloid angiopathy, prion angiopathy, CADASIL and the spectrum of protein elimination failure angiopathies (PEFA) in neurodegenerative disease with a focus on therapy.Genetics of prion diseasesA new prion disease: relationship with central and peripheral amyloidoses.Lavandula angustifolia extract improves deteriorated synaptic plasticity in an animal model of Alzheimer's disease.Hereditary Human Prion Diseases: an Update.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Conserved amyloid core structure of stop mutants of the human prion protein.Burial of the polymorphic residue 129 in amyloid fibrils of prion stop mutantsC-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178.Prion Proteins Without the Glycophosphatidylinositol Anchor: Potential Biomarkers in Neurodegenerative Diseases.Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases
P2860
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P2860
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
@en
type
label
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
@en
prefLabel
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
@en
P2093
P2860
P356
P1433
P1476
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
@en
P2093
Bernardino Ghetti
David Nochlin
Ellen J Steinbart
Gerard D Schellenberg
James A Mastrianni
James B Leverenz
Parvoneh Poorkaj
Thomas D Bird
Thomas J Montine
P2860
P304
P356
10.1002/ANA.22264
P577
2011-03-17T00:00:00Z