<p>Each group received a tracer dose (~0.14 mg/kg) of <sup>89</sup>Zr-GSK2849330 plus a dose of non-labeled GSK2849330 (0, 0.3, 1, 3, or 10 mg/kg) (panels A and B). The normalized liver uptake to blood uptake ratio (Panel C) showed a significant decrease with the increased non labeled GSK2849330 (***p<0.01 vs 0 mg/kg; <sup>##</sup>p<0.01, <sup>###</sup>p<0.001 vs 0.3 mg/kg using One-way ANOVA). The normalized tumor uptake to blood uptake ratio (Panel D) showed a significant decrease with the increased non labeled GSK2849330 from 0.3 and 1 mg/kg compared to the 10 mg/kg group (<sup>#</sup>p<0.05 vs 1 mg/kg; ** p<0.01, *** p<0.001 vs 10 mg/kg using One-way ANOVA). Data is presented as mean±SEM (<a href="http://www.plosone.org/article/info:doi...
<p><b><i>A</i></b><i>)</i> MIP and transaxial images of radioactivity (summed over 10–55 min) after ...
<p>The tracer uptake was measured ex vivo and is shown as % ID/g values with standard deviation and ...
<p>Plasma and tumour concentrations of the PI3K inhibitor GDC-0941 (GDC) (<b>A</b>) and the MEK inhi...
<p>Mice bearing BT474 tumors were treated with vehicle or GSK2110183 at 10, 30 or 100/kg (A) or GSK2...
<p>Group 1 (blocking) received 5 mg/kg of VivoTag 680-GSK28493330 24 hours post injection of GSK2849...
<p>[<b>A–D</b>] HCT116 tumour xenograft [<sup>18</sup>F]-FLT uptake over the 1 hour dynamic PET scan...
The purpose of this work was to use various molecular imaging techniques to non-invasively assess GS...
The purpose of this work was to use various molecular imaging techniques to non-invasively assess GS...
For the successful clinical advancement of exosome therapeutics, the biodistribution and pharmacokin...
<p>Mice bearing either BT474 (<i>A</i>) or SKOV3 (<i>B</i>) tumors were treated with vehicle (black ...
The present investigation focuses on the accumulative activity and absorbed dose of 89Zr in mice to ...
In Panel A, in vivo inhibition of GSK3 activity by CHIR99021 was confirmed by western blot analysis ...
<p>(A) Representative images of MDA-MB 231 xenograft nude mice showing regression in tumor volume af...
Background: The purpose of this study was to evaluate whether early changes in 3'-deoxy-3'-H-3-fluor...
One of the challenges that physicians face is the uncertainty that their therapy of choice will be e...
<p><b><i>A</i></b><i>)</i> MIP and transaxial images of radioactivity (summed over 10–55 min) after ...
<p>The tracer uptake was measured ex vivo and is shown as % ID/g values with standard deviation and ...
<p>Plasma and tumour concentrations of the PI3K inhibitor GDC-0941 (GDC) (<b>A</b>) and the MEK inhi...
<p>Mice bearing BT474 tumors were treated with vehicle or GSK2110183 at 10, 30 or 100/kg (A) or GSK2...
<p>Group 1 (blocking) received 5 mg/kg of VivoTag 680-GSK28493330 24 hours post injection of GSK2849...
<p>[<b>A–D</b>] HCT116 tumour xenograft [<sup>18</sup>F]-FLT uptake over the 1 hour dynamic PET scan...
The purpose of this work was to use various molecular imaging techniques to non-invasively assess GS...
The purpose of this work was to use various molecular imaging techniques to non-invasively assess GS...
For the successful clinical advancement of exosome therapeutics, the biodistribution and pharmacokin...
<p>Mice bearing either BT474 (<i>A</i>) or SKOV3 (<i>B</i>) tumors were treated with vehicle (black ...
The present investigation focuses on the accumulative activity and absorbed dose of 89Zr in mice to ...
In Panel A, in vivo inhibition of GSK3 activity by CHIR99021 was confirmed by western blot analysis ...
<p>(A) Representative images of MDA-MB 231 xenograft nude mice showing regression in tumor volume af...
Background: The purpose of this study was to evaluate whether early changes in 3'-deoxy-3'-H-3-fluor...
One of the challenges that physicians face is the uncertainty that their therapy of choice will be e...
<p><b><i>A</i></b><i>)</i> MIP and transaxial images of radioactivity (summed over 10–55 min) after ...
<p>The tracer uptake was measured ex vivo and is shown as % ID/g values with standard deviation and ...
<p>Plasma and tumour concentrations of the PI3K inhibitor GDC-0941 (GDC) (<b>A</b>) and the MEK inhi...