about
Infectivity versus Seeding in Neurodegenerative Diseases Sharing a Prion-Like MechanismEpidemiological characteristics of human prion diseasesBile Acids in Neurodegenerative DisordersHuman prion diseases: surgical lessons learned from iatrogenic prion transmissionPrionic diseases.The Malignant Protein Puzzle.Genetic studies in human prion diseases.Bovine Brain: An in vitro Translational Model in Developmental Neuroscience and Neurodegenerative ResearchLymphomatosis cerebri mimicking iatrogenic Creutzfeldt-Jakob diseasePrion protein-specific antibodies-development, modes of action and therapeutics applicationLevels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion diseaseThe Features of Genetic Prion Diseases Based on Chinese Surveillance Program.Amino acid composition predicts prion activitySelf-assembly of peptide boroxoles on cis-dihydroxylated oligoamide templates in water.Susceptibility of domestic cats to chronic wasting diseaseHow do amino acid substitutions affect the amyloidogenic properties and seeding efficiency of prion peptidesNodding syndrome in Mundri county, South Sudan: environmental, nutritional and infectious factorsRare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease.Polymorphism at 129 dictates metastable conformations of the human prion protein N-terminal β-sheet.6th International Conference on Emerging Zoonoses.Capillary electromigration based techniques in diagnostics of prion protein caused diseases.Mitochondrion-mediated cell death: dissecting yeast apoptosis for a better understanding of neurodegeneration.Proteolytic processing of the prion protein in health and disease.Natural polyphenols binding to amyloid: a broad class of compounds to treat different human amyloid diseases.Hereditary Human Prion Diseases: an Update.Significant reduction of the GLUT3 level, but not GLUT1 level, was observed in the brain tissues of several scrapie experimental animals and scrapie-infected cell lines.Genetic diversity of the prion protein gene (PRNP) coding sequence in Czech sheep and evaluation of the national breeding programme for resistance to scrapie in the Czech Republic.The Brain NO Levels and NOS Activities Ascended in the Early and Middle Stages and Descended in the Terminal Stage in Scrapie-Infected Animal Models.Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome.The copper transport-associated protein Ctr4 can form prion-like epigenetic determinants in Schizosaccharomyces pombe.Special needs populations: perioperative care of the patient with creutzfeldt-jakob disease.Aberrant alterations of the expressions and S-nitrosylation of calmodulin and the downstream factors in the brains of the rodents during scrapie infection.A patient with Creutzfeldt-Jakob disease presenting with amyotrophy: a case report.Comparative analysis of gene expression profiles between cortex and thalamus in Chinese fatal familial insomnia patients.Risks and biases in case-control studies of iatrogenic Creutzfeldt-Jakob disease.A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.What Is Our Current Understanding of PrPSc-Associated Neurotoxicity and Its Molecular Underpinnings?Unusual features of Creutzfeldt-Jakob disease followed-up in a memory clinic.Epidemiological genetics and meta-analysis of a polymorphism at codon 129 of the PRNP gene in Alzheimer's disease in Brazil.Low mood, visual hallucinations, and falls - heralding the onset of rapidly progressive probable sporadic Creutzfeldt-Jakob disease in a 73-year old: a case report.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի դեկտեմբերին 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
An overview of human prion diseases
@ast
An overview of human prion diseases
@en
An overview of human prion diseases
@nl
type
label
An overview of human prion diseases
@ast
An overview of human prion diseases
@en
An overview of human prion diseases
@nl
prefLabel
An overview of human prion diseases
@ast
An overview of human prion diseases
@en
An overview of human prion diseases
@nl
P2860
P921
P3181
P356
P1433
P1476
An overview of human prion diseases
@en
P2093
Muhammad Imran
Saqib Mahmood
P2860
P2888
P3181
P356
10.1186/1743-422X-8-559
P407
P5008
P577
2011-12-24T00:00:00Z
P6179
1024084748