scholarly article | Q13442814 |
P50 | author | Alana M Thackray | Q89270334 |
Raymond Bujdoso | Q89270336 | ||
P2093 | author name string | Olivier Andréoletti | |
P2860 | cites work | Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response | Q26797972 |
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD | Q27324879 | ||
Mice devoid of PrP are resistant to scrapie | Q28249108 | ||
Novel proteinaceous infectious particles cause scrapie | Q29547678 | ||
Preclinical detection of variant CJD and BSE prions in blood | Q30436588 | ||
Methods to assay Drosophila behavior | Q30452184 | ||
Conserved genetic programs in insect and mammalian brain development | Q33707302 | ||
Mutational analysis of topological determinants in prion protein (PrP) and measurement of transmembrane and cytosolic PrP during prion infection | Q48219838 | ||
Preliminary observations on the pathogenesis of experimental bovine spongiform encephalopathy (BSE): an update | Q48510790 | ||
Ovine PrP transgenic Drosophila show reduced locomotor activity and decreased survival | Q48604508 | ||
Transmission of experimental kuru to the spider monkey (Ateles geoffreyi). | Q49128323 | ||
EXPERIMENTAL TRANSMISSION OF MOUSE PASSAGED SCRAPIE TO GOATS, SHEEP, RATS AND HAMSTERS. | Q51252974 | ||
Encephalopathy in mice produced by inoculation with scrapie brain material. | Q51301574 | ||
Propagation of ovine prions from "poor" transmitter scrapie isolates in ovine PrP transgenic mice | Q82697070 | ||
B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease | Q33826801 | ||
Atypical/Nor98 scrapie infectivity in sheep peripheral tissues | Q33828597 | ||
Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp. | Q33842432 | ||
Cytosolic PrP can participate in prion-mediated toxicity | Q33900238 | ||
Mouse models for studying the formation and propagation of prions | Q33931079 | ||
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding | Q34084209 | ||
A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes | Q34115787 | ||
Distinct molecular phenotypes in bovine prion diseases | Q34165722 | ||
Cases of scrapie with unusual features in Norway and designation of a new type, Nor98. | Q34228022 | ||
Experimental transmission of a Kuru-like syndrome to chimpanzees | Q34241831 | ||
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. | Q34273746 | ||
Cotranslational partitioning of nascent prion protein into multiple populations at the translocation channel | Q34274103 | ||
A transmembrane form of the prion protein in neurodegenerative disease | Q34454961 | ||
First case of chronic wasting disease in Europe in a Norwegian free-ranging reindeer | Q34540612 | ||
Infectious prions in the saliva and blood of deer with chronic wasting disease | Q34571835 | ||
Drosophila models of neurodegenerative diseases | Q34610331 | ||
A bovine cell line that can be infected by natural sheep scrapie prions | Q34856581 | ||
Prion protein biosynthesis and its emerging role in neurodegeneration | Q35094535 | ||
Prionemia and leukocyte-platelet-associated infectivity in sheep transmissible spongiform encephalopathy models. | Q35826534 | ||
Diet, metabolism and lifespan in Drosophila | Q36246979 | ||
Drosophila as a model for human neurodegenerative disease | Q36312196 | ||
Drosophila in the study of neurodegenerative disease | Q36610370 | ||
Biogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein [published errratum appears in Mol Cell Biol 1987 May;7(5):2035] | Q36835752 | ||
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease | Q36853707 | ||
Classical sheep transmissible spongiform encephalopathies: pathogenesis, pathological phenotypes and clinical disease | Q36873204 | ||
Prion disease: experimental models and reality | Q37596801 | ||
Bioassay of prion-infected blood plasma in PrP transgenic Drosophila | Q39297891 | ||
Efficient transmission of two different sheep scrapie isolates in transgenic mice expressing the ovine PrP gene | Q39606216 | ||
Role of ADAMs in the ectodomain shedding and conformational conversion of the prion protein | Q39831418 | ||
Screening of 145 anti-PrP monoclonal antibodies for their capacity to inhibit PrPSc replication in infected cells. | Q40477337 | ||
Molecular and transmission characteristics of primary-passaged ovine scrapie isolates in conventional and ovine PrP transgenic mice | Q41965529 | ||
Prion-induced toxicity in PrP transgenic Drosophila | Q43936085 | ||
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 | ||
Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor | Q46096263 | ||
Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner | Q46174770 | ||
Prion-induced and spontaneous formation of transmissible toxicity in PrP transgenic Drosophila | Q46869696 | ||
Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein | Q48099698 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | infectivity | Q1662346 |
P304 | page(s) | 595 | |
P577 | publication date | 2018-05-15 | |
P1433 | published in | F1000Research | Q27701587 |
P1476 | title | The use of PrP transgenic Drosophila to replace and reduce vertebrate hosts in the bioassay of mammalian prion infectivity | |
P478 | volume | 7 |
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