Re-assessment of PrP(Sc) distribution in sporadic and variant CJD

scientific article (publication date: 2013)

Re-assessment of PrP(Sc) distribution in sporadic and variant CJD is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2013PLoSO...866352R
P356DOI10.1371/JOURNAL.PONE.0066352
P3181OpenCitations bibliographic resource ID2097007
P932PMC publication ID3700981
P698PubMed publication ID23843953
P5875ResearchGate publication ID248398161

P2093author name stringBinggong Chang
Richard Rubenstein
P2860cites workA report on transmissible spongiform encephalopathies and transfusion safetyQ37394382
Variant Creutzfeldt-Jakob disease in a transfusion recipient: coincidence or cause?Q37709520
Detection of infectious prions in urineQ41371006
Cellular isoform of the scrapie agent protein participates in lymphocyte activationQ41737574
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaQ43195687
Levels of infectivity in the blood throughout the incubation period of hamsters peripherally injected with scrapieQ44169038
Similar levels of infectivity in the blood of mice infected with human-derived vCJD and GSS strains of transmissible spongiform encephalopathyQ44949376
Transmission to animals of Creutzfeldt-Jakob disease from human bloodQ45346655
Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted diseaseQ48126727
Selection of specific strains in iatrogenic Creutzfeldt-Jakob diseaseQ48141679
Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob diseaseQ48152236
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.Q48297442
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report.Q48340913
Presymptomatic detection of prions in blood.Q48477099
PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brainQ48630602
PrP(Sc) detection and infectivity in semen from scrapie-infected sheepQ48666354
In vitro amplification of PrPSc derived from the brain and blood of sheep infected with scrapieQ48827827
Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.Q51037857
Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking.Q51790930
Urinary excretion and blood level of prions in scrapie-infected hamsters.Q51794689
Further studies of blood infectivity in an experimental model of transmissible spongiform encephalopathy, with an explanation of why blood components do not transmit Creutzfeldt-Jakob disease in humans.Q54068228
Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assayQ57092938
Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cellsQ64447658
Involvement of the immune system in TSE pathogenesisQ64447659
Demonstration of the Transmissible Agent in Tissue from a Pregnant Woman with Creutzfeldt–Jakob DiseaseQ68228509
Transmission of Creutzfeldt-Jakob disease from human blood and urine into miceQ69872198
Sustained viremia in experimental hamster scrapie. Brief reportQ70504979
Replication of scrapie in spleens of SCID mice follows reconstitution with wild-type mouse bone marrowQ71405658
Cerebrospinal fluidQ71748878
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteinsQ24564014
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseQ28366081
Eight prion strains have PrP(Sc) molecules with different conformationsQ29617277
Detection of CWD prions in urine and saliva of deer by transgenic mouse bioassayQ33419079
Susceptibilities of nonhuman primates to chronic wasting diseaseQ33644675
Prion diseases, blood and the immune system: concerns and realityQ33812459
Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective studyQ34059789
Sensitive detection of pathological prion protein by cyclic amplification of protein misfoldingQ34084209
A novel method for preclinical detection of PrPSc in bloodQ34107715
PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob diseaseQ34123943
Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob diseaseQ34125915
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.Q34161515
Organ distribution of prion proteins in variant Creutzfeldt-Jakob diseaseQ34188738
Prion disease detection, PMCA kinetics, and IgG in urine from sheep naturally/experimentally infected with scrapie and deer with preclinical/clinical chronic wasting diseaseQ34196340
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patientQ34339769
In vitro generation of infectious scrapie prions.Q34413661
Detection of prions in bloodQ34446509
Surround optical fiber immunoassay (SOFIA): an ultra-sensitive assay for prion protein detectionQ34981058
Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical studyQ35083260
High CJD infectivity remains after prion protein is destroyedQ35449351
Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implicationsQ36226169
Blood infectivity, processing and screening tests in transmissible spongiform encephalopathyQ36230687
Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob diseaseQ36281277
Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review studyQ36588347
Human variant Creutzfeldt-Jakob disease and sheep scrapie PrP(res) detection using seeded conversion of recombinant prion proteinQ37285506
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue7
P407language of work or nameEnglishQ1860
P304page(s)e66352
P577publication date2013-01-01
P1433published inPLOS OneQ564954
P1476titleRe-assessment of PrP(Sc) distribution in sporadic and variant CJD
P478volume8

Reverse relations

cites work (P2860)
Q35142344A novel, ultrasensitive assay for tau: potential for assessing traumatic brain injury in tissues and biofluids
Q37415429Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice
Q31095751Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease
Q55307741Are We Ready for Detecting α-Synuclein Prone to Aggregation in Patients? The Case of "Protein-Misfolding Cyclic Amplification" and "Real-Time Quaking-Induced Conversion" as Diagnostic Tools.
Q40585208Are prions transported by plasma exosomes?
Q89979817BMD42-2910, a Novel Benzoxazole Derivative, Shows a Potent Anti-prion Activity and Prolongs the Mean Survival in an Animal Model of Prion Disease
Q26739995Biomarkers for sporadic Creutzfeldt-Jakob disease
Q47984291Creutzfeldt-Jakob disease and blood transfusion: safe or not safe?
Q90597989Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases
Q34593983Development of dose-response models of Creutzfeldt-Jakob disease infection in nonhuman primates for assessing the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease
Q34355775First demonstration of transmissible spongiform encephalopathy-associated prion protein (PrPTSE) in extracellular vesicles from plasma of mice infected with mouse-adapted variant Creutzfeldt-Jakob disease by in vitro amplification.
Q42222309Genetic prion disease: no role for the immune system in disease pathogenesis?
Q92328172Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System
Q47232273Prion Strains and Transmission Barrier Phenomena
Q37363460Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients.
Q35662504Rapid and Quantitative Assay of Amyloid-Seeding Activity in Human Brains Affected with Prion Diseases
Q64943879Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans.

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