<p>PASA was evaluated in human urine and blood from each sCJD case and blood from vCJD-infected Tg666 mice. Following sPMCA<sub>200</sub>, samples were analyzed in triplicate by SOFIA for the presence of PrP<sup>Sc</sup>. Signal intensities from SOFIA were adjusted based on the dilution of samples throughout sPMCA<sub>200</sub>, calculated as the mean fluorescent signal±standard deviation and expressed as the signal/background ratio.</p
The emergence of variant Creutzfeldt Jakob Disease (vCJD) is considered a likely consequence of huma...
<p>Fractions were collected from the bottom of the tubes and PK-treated or untreated samples were an...
<p>Eight cynomologus macaques were intravenously challenged with vCJD brain homogenate or blood from...
<p>PASA was carried out using normal human and sCJD CSF as the source of the seeding material. Seria...
<p>Ten percent homogenates from all the normal human (N), vCJD (V), and sCJD brain tissues were prep...
<p>1/10 dilution series (in PMCA buffer) were prepared using (<b>A</b>) WBC homogenate from one Fren...
Human prion diseases are fatal neurodegenerative disorders associated with an accumulation of PrPSc ...
<p>A) Western Blot analysis for PrP<sup>Sc</sup> (frontal cortex) of vCJD, BSE and sCJD infected ani...
Variant Creutzfeldt-Jakob disease (vCJD) is a fatal neurodegenerative disorder characterised by accu...
Background: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
BACKGROUND: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
<p>A) PrP<sup>CWD</sup> was detectable by serial PMCA (sPMCA) in control and urine inocula (lanes 1 ...
<p>PrP in P2 fractions from sCJD, VPSPr and fCJD<sup>V180I</sup> was subjected to g5p-capture and tr...
<p>A) Western Blot analysis of PrP<sup>Sc</sup> from NaPTA precipitated arm and tongue tissue of sCJ...
Background: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
The emergence of variant Creutzfeldt Jakob Disease (vCJD) is considered a likely consequence of huma...
<p>Fractions were collected from the bottom of the tubes and PK-treated or untreated samples were an...
<p>Eight cynomologus macaques were intravenously challenged with vCJD brain homogenate or blood from...
<p>PASA was carried out using normal human and sCJD CSF as the source of the seeding material. Seria...
<p>Ten percent homogenates from all the normal human (N), vCJD (V), and sCJD brain tissues were prep...
<p>1/10 dilution series (in PMCA buffer) were prepared using (<b>A</b>) WBC homogenate from one Fren...
Human prion diseases are fatal neurodegenerative disorders associated with an accumulation of PrPSc ...
<p>A) Western Blot analysis for PrP<sup>Sc</sup> (frontal cortex) of vCJD, BSE and sCJD infected ani...
Variant Creutzfeldt-Jakob disease (vCJD) is a fatal neurodegenerative disorder characterised by accu...
Background: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
BACKGROUND: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
<p>A) PrP<sup>CWD</sup> was detectable by serial PMCA (sPMCA) in control and urine inocula (lanes 1 ...
<p>PrP in P2 fractions from sCJD, VPSPr and fCJD<sup>V180I</sup> was subjected to g5p-capture and tr...
<p>A) Western Blot analysis of PrP<sup>Sc</sup> from NaPTA precipitated arm and tongue tissue of sCJ...
Background: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, cha...
The emergence of variant Creutzfeldt Jakob Disease (vCJD) is considered a likely consequence of huma...
<p>Fractions were collected from the bottom of the tubes and PK-treated or untreated samples were an...
<p>Eight cynomologus macaques were intravenously challenged with vCJD brain homogenate or blood from...