<p>(A) N2aPK1 cells were exposed to 10<sup>−5</sup> dilution of strain RML scrapie PrP<sup>Sc</sup>-infected murine brain homogenate and increasing concentrations of the macropinocytosis inhibitor EIPA (25, 50 and 100 µM) for 48 hr. Infected cells were then grown on cover slips, blotted, digested with proteinase K (PK) and probed with anti-PrP antibodies (A) and Ponceau S staining (B).</p
<p>(a) Western blot analyses of the brain from wild-type and tgOv rabbits mock-infected or inoculate...
Prion diseases are rare neurodegenerative diseases, associated with a conversion of a normal cellula...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
<p>(<b>A</b>) Silver stain and Western blot analysis (using anti-PrP antibody D18) of PrP<sup>Sc</su...
<p>(A) Time dependent increase in PrP<sup>Sc</sup> in C2C12 cells. 10 µg of protein (PK−) or protein...
Mutations within a host cellular protein, PrP, have been associated with disease in the transmissibl...
<p>(A) Time course of PrP<sup>Sc</sup> accumulation. Confluent myotubes were infected by incubation ...
<p>Except for one undigested lane (−), brain samples were digested with PK (+ in panel A). All inocu...
<p>Following retrotransmission of Tg(M109)-passaged prion isolates, the biochemical characteristics ...
Prion protein (PrPC) is a protease-sensitive and soluble cell surface glycoprotein expressed in almo...
AbstractTransmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases that i...
<p>10% w/v brain homogenates (n = 3 per group) were digested with proteinase K and immunoblotted wit...
Prion diseases are characterized by the accumulation of an abnormal, proteinase K-resistant isoform ...
<p><b>a</b>. CD-1 mice were inoculated with RML and i) untreated (n = 15), ii) infused with AAV2-PrP...
The causative agent of transmissible spongiform encephalopathies (TSE) is PrPSc, an infectious, misf...
<p>(a) Western blot analyses of the brain from wild-type and tgOv rabbits mock-infected or inoculate...
Prion diseases are rare neurodegenerative diseases, associated with a conversion of a normal cellula...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
<p>(<b>A</b>) Silver stain and Western blot analysis (using anti-PrP antibody D18) of PrP<sup>Sc</su...
<p>(A) Time dependent increase in PrP<sup>Sc</sup> in C2C12 cells. 10 µg of protein (PK−) or protein...
Mutations within a host cellular protein, PrP, have been associated with disease in the transmissibl...
<p>(A) Time course of PrP<sup>Sc</sup> accumulation. Confluent myotubes were infected by incubation ...
<p>Except for one undigested lane (−), brain samples were digested with PK (+ in panel A). All inocu...
<p>Following retrotransmission of Tg(M109)-passaged prion isolates, the biochemical characteristics ...
Prion protein (PrPC) is a protease-sensitive and soluble cell surface glycoprotein expressed in almo...
AbstractTransmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases that i...
<p>10% w/v brain homogenates (n = 3 per group) were digested with proteinase K and immunoblotted wit...
Prion diseases are characterized by the accumulation of an abnormal, proteinase K-resistant isoform ...
<p><b>a</b>. CD-1 mice were inoculated with RML and i) untreated (n = 15), ii) infused with AAV2-PrP...
The causative agent of transmissible spongiform encephalopathies (TSE) is PrPSc, an infectious, misf...
<p>(a) Western blot analyses of the brain from wild-type and tgOv rabbits mock-infected or inoculate...
Prion diseases are rare neurodegenerative diseases, associated with a conversion of a normal cellula...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...