<p><b>(a)</b> Terminal disease lymph node tissue showing granular PrP-d accumulation in Tingible body macrophages (TBMS, arrowheads) and diffuse punctuate PrP-d accumulation in association with follicular dendritic cells (arrow). Bar = 50μm. <b>(b)</b> Immunogold electron microscopy of terminal disease lymph node shows PrP-d (black) in lysosomes and endo-lysosomes of TBMs. The 1A8 antibody was used for immunogold staining. Bar = 500 nm. <b>(c)</b> Terminal disease intestine showing granular PrP-d accumulation in neurons of enteric nerve plexuses. Bar = 20 μm.</p
Prion diseases are infectious neurodegenerative disorders characterized by accumulations of abnormal...
<p>Immunoblots of the two PK-treated individual brains (A) and spinal cords (B) from terminally ill ...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...
<p>Patterns of PrP-d accumulation in brains of wild-type CD-1 mice i.p. challenged with rec-Prions. ...
<p><b>(a)</b> and <b>(b)</b> show dendritic membrane invaginations (arrows) in two dendrites (D). Th...
<p>Each tissue is presented as a pair, tg44 on top and WT on the bottom. Tissue sections were staine...
<p>PrP-d, disease specific aberrant PrP deposition</p><p>SMLN, submandibular lymph node</p><p>lgLN, ...
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases. Infection by the ora...
Prior to invading the nervous system, prions frequently colonize lymphoid organs and sites of inflam...
During prion disease, cellular prion protein (PrP(C)) is refolded into a pathogenic isoform (PrP(Sc)...
SummaryPrior to invading the nervous system, prions frequently colonize lymphoid organs and sites of...
<p>TNFR1<sup>−/−</sup> mice inoculated i.p. with 6 log LD<sub>50</sub> RML6 and treated weekly with ...
Transmissible spongiform encephalopathies (TSEs) are slowly progressive and fatal neurodegenerative ...
<p><b>(A)</b> PrP-res in brain (top panel) and spleen (bottom panel) of mice that received i.p. or i...
In most prion diseases, infectivity accumulates in lymphoreticular organs early after infection. Def...
Prion diseases are infectious neurodegenerative disorders characterized by accumulations of abnormal...
<p>Immunoblots of the two PK-treated individual brains (A) and spinal cords (B) from terminally ill ...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...
<p>Patterns of PrP-d accumulation in brains of wild-type CD-1 mice i.p. challenged with rec-Prions. ...
<p><b>(a)</b> and <b>(b)</b> show dendritic membrane invaginations (arrows) in two dendrites (D). Th...
<p>Each tissue is presented as a pair, tg44 on top and WT on the bottom. Tissue sections were staine...
<p>PrP-d, disease specific aberrant PrP deposition</p><p>SMLN, submandibular lymph node</p><p>lgLN, ...
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases. Infection by the ora...
Prior to invading the nervous system, prions frequently colonize lymphoid organs and sites of inflam...
During prion disease, cellular prion protein (PrP(C)) is refolded into a pathogenic isoform (PrP(Sc)...
SummaryPrior to invading the nervous system, prions frequently colonize lymphoid organs and sites of...
<p>TNFR1<sup>−/−</sup> mice inoculated i.p. with 6 log LD<sub>50</sub> RML6 and treated weekly with ...
Transmissible spongiform encephalopathies (TSEs) are slowly progressive and fatal neurodegenerative ...
<p><b>(A)</b> PrP-res in brain (top panel) and spleen (bottom panel) of mice that received i.p. or i...
In most prion diseases, infectivity accumulates in lymphoreticular organs early after infection. Def...
Prion diseases are infectious neurodegenerative disorders characterized by accumulations of abnormal...
<p>Immunoblots of the two PK-treated individual brains (A) and spinal cords (B) from terminally ill ...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...