<p>A, B, RAW 264.7 and Maf-KDO proliferation in the presence of different concentrations of FK866, monitored by measuring the increase in protein mass at different intervals over a 24 or 72 hour period. Data represent means of three independent experiments performed in triplicate. C, RAW 264.7 cell viability in the presence of 10 nM FK866. The appearance of the fluorescent apoptosis-specific pSIVA signal was recorded over time and the total pSIVA pixel area was determined per frame using Fiji Imaging software and plotted against time. Lines represent averages from one experiment performed in triplicate. (N.S., not significant; unpaired t-test).</p
Contains fulltext : 135974.pdf (publisher's version ) (Open Access)Functional morp...
<p>(<b>A</b>) Time-course of cell viability of mock-treated or <i>C. neoformans</i>-infected (KN99α)...
<p>PMA stimulated THP1 cells were stimulated with 20 μg/ml Rv3416 or 15 μg/ml Nef or both for 24h or...
<p>Proliferation was monitored for 24 hours in the presence of LPS and expressed as the increase in ...
<p>A. HUVEC were grown to confluence in 96-well tissue culture plates. Media was removed from the we...
<p>A, PHA-stimulated PBLs were treated (or not) with 33 nM FK866 in the presence or absence of 10 mM...
<p>(a) Percentage of apoptosis in control N expressing cells analyzed by flow cytometry after PI sta...
<p><b>A</b>. Double staining of BMMC with 7-AAD and APC-Annexin V (upper panel), and its quantitativ...
<p>Representative multichannel images are shown for apoptotic DNA fragmentation (green staining) and...
<p>Cells were incubated for 24 hours with 100 µM NAD<sup>+</sup>, 100 µM NMN or 50 µM NADP<sup>+</su...
<p>Panel A - rHP986 induced Fas expression on the surface of differentiated macrophages as quantifie...
<p>(<b>A</b>) THP-1 cells were infected with <i>MTB</i> H37Rv for 4 and 8 days with or without BAY, ...
<p>J774A.1 cells were infected with A) the <i>F</i>. <i>novicida</i> U112 parent strain, <i>kpsF</i>...
<p>(A) HCT 116 cells were treated with FKC at the indicated concentrations for 48 hours, and subsequ...
<p>Apoptosis assay was used to analyze (A) N87 or (C) Calu-3 cells after DVD-Ig proteins, mAbs, or c...
Contains fulltext : 135974.pdf (publisher's version ) (Open Access)Functional morp...
<p>(<b>A</b>) Time-course of cell viability of mock-treated or <i>C. neoformans</i>-infected (KN99α)...
<p>PMA stimulated THP1 cells were stimulated with 20 μg/ml Rv3416 or 15 μg/ml Nef or both for 24h or...
<p>Proliferation was monitored for 24 hours in the presence of LPS and expressed as the increase in ...
<p>A. HUVEC were grown to confluence in 96-well tissue culture plates. Media was removed from the we...
<p>A, PHA-stimulated PBLs were treated (or not) with 33 nM FK866 in the presence or absence of 10 mM...
<p>(a) Percentage of apoptosis in control N expressing cells analyzed by flow cytometry after PI sta...
<p><b>A</b>. Double staining of BMMC with 7-AAD and APC-Annexin V (upper panel), and its quantitativ...
<p>Representative multichannel images are shown for apoptotic DNA fragmentation (green staining) and...
<p>Cells were incubated for 24 hours with 100 µM NAD<sup>+</sup>, 100 µM NMN or 50 µM NADP<sup>+</su...
<p>Panel A - rHP986 induced Fas expression on the surface of differentiated macrophages as quantifie...
<p>(<b>A</b>) THP-1 cells were infected with <i>MTB</i> H37Rv for 4 and 8 days with or without BAY, ...
<p>J774A.1 cells were infected with A) the <i>F</i>. <i>novicida</i> U112 parent strain, <i>kpsF</i>...
<p>(A) HCT 116 cells were treated with FKC at the indicated concentrations for 48 hours, and subsequ...
<p>Apoptosis assay was used to analyze (A) N87 or (C) Calu-3 cells after DVD-Ig proteins, mAbs, or c...
Contains fulltext : 135974.pdf (publisher's version ) (Open Access)Functional morp...
<p>(<b>A</b>) Time-course of cell viability of mock-treated or <i>C. neoformans</i>-infected (KN99α)...
<p>PMA stimulated THP1 cells were stimulated with 20 μg/ml Rv3416 or 15 μg/ml Nef or both for 24h or...