Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.
about
Oral transmissibility of prion disease is enhanced by binding to soil particlesBranched polyamines cure prion-infected neuroblastoma cellsPrionsA novel human disease with abnormal prion protein sensitive to proteaseKuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceUnraveling prion strains with cell biology and organic chemistryThe mechanism of prion strain propagationAnalysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.Insights into Mechanisms of Chronic NeurodegenerationPrion strains and amyloid polymorphism influence phenotypic variationMechanisms of protein seeding in neurodegenerative diseasesTransmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamstersThe strain-encoded relationship between PrP replication, stability and processing in neurons is predictive of the incubation period of diseaseThe physical relationship between infectivity and prion protein aggregates is strain-dependentPrion shedding from olfactory neurons into nasal secretionsSynthetic prions with novel strain-specified propertiesDe novo generation of infectious prions in vitro produces a new disease phenotypeEvidence that bank vole PrP is a universal acceptor for prionsPK-sensitive PrP is infectious and shares basic structural features with PK-resistant PrPN-Terminal Helix-Cap in α-Helix 2 Modulates β-State Misfolding in Rabbit and Hamster Prion ProteinsMolecular Structure of β-Amyloid Fibrils in Alzheimer’s Disease Brain TissueA brief history of prionsStrain-specified relative conformational stability of the scrapie prion proteinBeyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob diseaseIn situ photodegradation of incorporated polyanion does not alter prion infectivityRelationships between PrPSc stability and incubation time for United States scrapie isolates in a natural host systemBiological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prionsCorrelation analysis for the incubation period of prion diseaseIsolation of proteinase K-sensitive prions using pronase E and phosphotungstic acidAnalysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease PrionsPrions in Saccharomyces and Podospora spp.: protein-based inheritance.Structural effects of PrP polymorphisms on intra- and interspecies prion transmission.Charge neutralization of the central lysine cluster in prion protein (PrP) promotes PrP(Sc)-like folding of recombinant PrP amyloids.Prion amyloid structure explains templating: how proteins can be genes.Post-translational modifications in PrP expand the conformational diversity of prions in vivoAttachment of pathogenic prion protein to model oxide surfaces.Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.Prion replication without host adaptation during interspecies transmissions.Molecular Mechanisms of Chronic Wasting Disease Prion Propagation.Prion infection of oral and nasal mucosa.
P2860
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P2860
Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.
description
1994 nî lūn-bûn
@nan
1994 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@ast
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@en
type
label
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@ast
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@en
prefLabel
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@ast
Distinct PrP properties sugges ...... smissible mink encephalopathy.
@en
P2860
P1433
P1476
Distinct PrP properties sugges ...... nsmissible mink encephalopathy
@en
P2093
P2860
P304
P577
1994-12-01T00:00:00Z