<p>Mitochondrial potential was assayed by measuring the absorbance of safranin O. 10 nM FCCP was added at 4, 5, 6, 7, 8, and 9 min (curves 2–4). 0.2% ethanol or ethanol solutions leading to 2 µM C<sub>12</sub>TPP (curves 1 and 4) or 2 µM SkQ1 (curve 3) were added at 2 min. Oligomycin (1 µg/ml) was added at 1 min. For other conditions, see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0061902#s2" target="_blank">Materials and methods</a>.</p
<p>Panel <b>A</b>. Shown are traces of fluorescence in the medium described in “Materials and Method...
AbstractThe ability of low concentrations (5–15 μM) of long-chain fatty acids to open the permeabili...
The mutual effects of NaNO(2) + CdCl(2) and NaNO(2) + ZnCl(2) on the oxidative phosphorylation of ra...
<p><b>A.</b> HL-1 cardiomyocytes were treated with the mitochondrial uncoupler FCCP (10 µM) or vehic...
Uncouplers of mitochondrial oxidative phosphorylation, including carbonilcyanide p-triflouromethoxyp...
The synthesis of a mitochondria-targeted derivative of the classical mitochondrial uncoupler carbony...
<p>Effects of 2 µM SkQ1, 2 µM C<sub>12</sub>TPP or 200 µM TPP on the dependence of mitochondrial mem...
The mechanism of uncoupling of oxidative phosphorylation by carbonyl cyanide p-(trifluoromethoxy)phe...
Uncouplers of oxidative phosphorylation have relevance to bioenergetics and obesity. The mechanisms ...
<p><b>A</b>. TMRM fluorescence was monitored as an indicator of <i>Δψ</i><sub><i>m</i></sub>. FCCP (...
AbstractThe stimulation of respiration by long-chain fatty adds and FCCP was studied with oligomycin...
The ability of low concentrations (5-15 microM) of long-chain fatty acids to open the permeability t...
The mechanism of uncoupling of oxidative phosphorylation by carbonyl cyanide p-trifluoromethoxy)phen...
Rhodamine 123 (RH-123) was used to monitor the membrane potential of mitochondria isolated from rat ...
The ability of low concentrations (5-15 mu M) of long-chain fatty acids to open the permeability tra...
<p>Panel <b>A</b>. Shown are traces of fluorescence in the medium described in “Materials and Method...
AbstractThe ability of low concentrations (5–15 μM) of long-chain fatty acids to open the permeabili...
The mutual effects of NaNO(2) + CdCl(2) and NaNO(2) + ZnCl(2) on the oxidative phosphorylation of ra...
<p><b>A.</b> HL-1 cardiomyocytes were treated with the mitochondrial uncoupler FCCP (10 µM) or vehic...
Uncouplers of mitochondrial oxidative phosphorylation, including carbonilcyanide p-triflouromethoxyp...
The synthesis of a mitochondria-targeted derivative of the classical mitochondrial uncoupler carbony...
<p>Effects of 2 µM SkQ1, 2 µM C<sub>12</sub>TPP or 200 µM TPP on the dependence of mitochondrial mem...
The mechanism of uncoupling of oxidative phosphorylation by carbonyl cyanide p-(trifluoromethoxy)phe...
Uncouplers of oxidative phosphorylation have relevance to bioenergetics and obesity. The mechanisms ...
<p><b>A</b>. TMRM fluorescence was monitored as an indicator of <i>Δψ</i><sub><i>m</i></sub>. FCCP (...
AbstractThe stimulation of respiration by long-chain fatty adds and FCCP was studied with oligomycin...
The ability of low concentrations (5-15 microM) of long-chain fatty acids to open the permeability t...
The mechanism of uncoupling of oxidative phosphorylation by carbonyl cyanide p-trifluoromethoxy)phen...
Rhodamine 123 (RH-123) was used to monitor the membrane potential of mitochondria isolated from rat ...
The ability of low concentrations (5-15 mu M) of long-chain fatty acids to open the permeability tra...
<p>Panel <b>A</b>. Shown are traces of fluorescence in the medium described in “Materials and Method...
AbstractThe ability of low concentrations (5–15 μM) of long-chain fatty acids to open the permeabili...
The mutual effects of NaNO(2) + CdCl(2) and NaNO(2) + ZnCl(2) on the oxidative phosphorylation of ra...