PrPSc accumulation in myocytes from sheep incubating natural scrapie. - Wikidata - awgldk - TriplyDB

PrPSc accumulation in myocytes from sheep incubating natural scrapie.

PrPSc accumulation in myocytes from sheep incubating natural scrapie.

http://www.wikidata.org/entity/Q44407386

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The synaptic pathology of alpha-synuclein aggregation in dementia with Lewy bodies, Parkinson's disease and Parkinson's disease dementia Distribution of peripheral PrP(Sc) in sheep with naturally acquired scrapie Preclinical deposition of pathological prion protein in muscle of experimentally infected primates Presence and seeding activity of pathological prion protein (PrP(TSE)) in skeletal muscles of white-tailed deer infected with chronic wasting disease Elements modulating the prion species barrier and its passage consequences Intraepithelial and interstitial deposition of pathological prion protein in kidneys of scrapie-affected sheep.The prion protein in human neuromuscular diseases.Prion infection of oral and nasal mucosa.Accumulation of pathological prion protein PrPSc in the skin of animals with experimental and natural scrapie.Detection of prion infectivity in fat tissues of scrapie-infected mice.Prions in milk from ewes incubating natural scrapie.Mouse senile amyloid fibrils deposited in skeletal muscle exhibit amyloidosis-enhancing activity Transgenic mice expressing porcine prion protein resistant to classical scrapie but susceptible to sheep bovine spongiform encephalopathy and atypical scrapie Classic scrapie in sheep with the ARR/ARR prion genotype in Germany and France.Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients Dietary Risk Factors for Sporadic Creutzfeldt-Jakob Disease: A Confirmatory Case-Control Study.Atypical/Nor98 scrapie infectivity in sheep peripheral tissues.Pathogenesis of chronic wasting disease in cervidized transgenic mice.Extraneural prion neuroinvasion without lymphoreticular system infection.PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease.Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.Impact of leucocyte depletion and prion reduction filters on TSE blood borne transmission.Medulla oblongata transcriptome changes during presymptomatic natural scrapie and their association with prion-related lesions.A lympho-follicular microenvironment is required for pathological prion protein deposition in chronically inflamed tissues from scrapie-affected sheep Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease Correlation between infectivity and disease associated prion protein in the nervous system and selected edible tissues of naturally affected scrapie sheep.Transmission of scrapie prions to primate after an extended silent incubation period.Prion infection of muscle cells in vitro Characterization of prion protein (PrP)-derived peptides that discriminate full-length PrPSc from PrPC.Classical bovine spongiform encephalopathy by transmission of H-type prion in homologous prion protein context.Current and future molecular diagnostics for prion diseases.The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies.Classical sheep transmissible spongiform encephalopathies: pathogenesis, pathological phenotypes and clinical disease.Spontaneous generation of infectious prion disease in transgenic mice.De novo prion aggregates trigger autophagy in skeletal muscle.Divergent prion strain evolution driven by PrPC expression level in transgenic mice.Role of the goat K222-PrP(C) polymorphic variant in prion infection resistance The presence of disease-associated prion protein in skeletal muscle of cattle infected with classical bovine spongiform encephalopathy.Comparison of Two US Sheep Scrapie Isolates Supports Identification as Separate Strains.Aggregation of cellular prion protein is initiated by proximity-induced dimerization.

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P2860

PrPSc accumulation in myocytes from sheep incubating natural scrapie.

http://www.wikidata.org/entity/Q44407386

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2004 nî lūn-bûn

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2004年学术文章

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2004年學術文章

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2004年學術文章

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name

PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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type

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PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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PrPSc accumulation in myocytes from sheep incubating natural scrapie.

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Nature Medicine

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PrPSc accumulation in myocytes from sheep incubating natural scrapie

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Andréoletti O

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Chabert A

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Corbière F

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Eychenne F

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Grassi J

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Lacroux C

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Laude H

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Lugan S

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Morel N

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Schelcher F

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P2860

Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp.

Prions in skeletal muscle.

Widespread PrPSc accumulation in muscles of hamsters orally infected with scrapie.

The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature.

Estimating the human health risk from possible BSE infection of the British sheep flock.

The potential size and duration of an epidemic of bovine spongiform encephalopathy in British sheep.

Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD).

Phenotyping of protein-prion (PrPsc)-accumulating cells in lymphoid and neural tissues of naturally scrapie-affected sheep by double-labeling immunohistochemistry.

Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.

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591-593

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10.1038/NM1055

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6

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10

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Guillaume Tabouret

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2004-05-23T00:00:00Z

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8550556

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15156203

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