scholarly article | Q13442814 |
P2093 | author name string | Binggong Chang | |
Richard Rubenstein | |||
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Similar levels of infectivity in the blood of mice infected with human-derived vCJD and GSS strains of transmissible spongiform encephalopathy | Q44949376 | ||
Transmission to animals of Creutzfeldt-Jakob disease from human blood | Q45346655 | ||
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Selection of specific strains in iatrogenic Creutzfeldt-Jakob disease | Q48141679 | ||
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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 brain | Q48630602 | ||
PrP(Sc) detection and infectivity in semen from scrapie-infected sheep | Q48666354 | ||
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Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. | Q51037857 | ||
Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking. | Q51790930 | ||
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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 assay | Q57092938 | ||
Scrapie replication in lymphoid tissues depends on prion protein-expressing follicular dendritic cells | Q64447658 | ||
Involvement of the immune system in TSE pathogenesis | Q64447659 | ||
Demonstration of the Transmissible Agent in Tissue from a Pregnant Woman with Creutzfeldt–Jakob Disease | Q68228509 | ||
Transmission of Creutzfeldt-Jakob disease from human blood and urine into mice | Q69872198 | ||
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Cerebrospinal fluid | Q71748878 | ||
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins | Q24564014 | ||
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease | Q28366081 | ||
Eight prion strains have PrP(Sc) molecules with different conformations | Q29617277 | ||
Detection of CWD prions in urine and saliva of deer by transgenic mouse bioassay | Q33419079 | ||
Susceptibilities of nonhuman primates to chronic wasting disease | Q33644675 | ||
Prion diseases, blood and the immune system: concerns and reality | Q33812459 | ||
Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study | Q34059789 | ||
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding | Q34084209 | ||
A novel method for preclinical detection of PrPSc in blood | Q34107715 | ||
PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease | Q34123943 | ||
Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob disease | Q34125915 | ||
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. | Q34161515 | ||
Organ distribution of prion proteins in variant Creutzfeldt-Jakob disease | Q34188738 | ||
Prion disease detection, PMCA kinetics, and IgG in urine from sheep naturally/experimentally infected with scrapie and deer with preclinical/clinical chronic wasting disease | Q34196340 | ||
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient | Q34339769 | ||
In vitro generation of infectious scrapie prions. | Q34413661 | ||
Detection of prions in blood | Q34446509 | ||
Surround optical fiber immunoassay (SOFIA): an ultra-sensitive assay for prion protein detection | Q34981058 | ||
Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study | Q35083260 | ||
High CJD infectivity remains after prion protein is destroyed | Q35449351 | ||
Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications | Q36226169 | ||
Blood infectivity, processing and screening tests in transmissible spongiform encephalopathy | Q36230687 | ||
Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease | Q36281277 | ||
Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review study | Q36588347 | ||
Human variant Creutzfeldt-Jakob disease and sheep scrapie PrP(res) detection using seeded conversion of recombinant prion protein | Q37285506 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e66352 | |
P577 | publication date | 2013-01-01 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Re-assessment of PrP(Sc) distribution in sporadic and variant CJD | |
P478 | volume | 8 |
Q35142344 | A novel, ultrasensitive assay for tau: potential for assessing traumatic brain injury in tissues and biofluids |
Q37415429 | Absence 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 |
Q31095751 | Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease |
Q55307741 | Are 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. |
Q40585208 | Are prions transported by plasma exosomes? |
Q89979817 | BMD42-2910, a Novel Benzoxazole Derivative, Shows a Potent Anti-prion Activity and Prolongs the Mean Survival in an Animal Model of Prion Disease |
Q26739995 | Biomarkers for sporadic Creutzfeldt-Jakob disease |
Q47984291 | Creutzfeldt-Jakob disease and blood transfusion: safe or not safe? |
Q90597989 | Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases |
Q34593983 | Development of dose-response models of Creutzfeldt-Jakob disease infection in nonhuman primates for assessing the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease |
Q34355775 | First 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. |
Q42222309 | Genetic prion disease: no role for the immune system in disease pathogenesis? |
Q92328172 | Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System |
Q47232273 | Prion Strains and Transmission Barrier Phenomena |
Q37363460 | Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients. |
Q35662504 | Rapid and Quantitative Assay of Amyloid-Seeding Activity in Human Brains Affected with Prion Diseases |
Q64943879 | Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans. |
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