<p>Parasites were incubated with 100 µM iron chelator and resuspended in Schneider's fresh medium after 24 h or 48 h of treatment. Cell density was determined daily for eight days by counting with a hemocytometer. Proliferation of parasites cultivated in the control medium as well as the growth of parasites continually cultured in the presence of 100 µM 2,2-dipyridyl were also monitored. Bars represent means and standard errors obtained from three independent experiments.</p
<p>Parasites were cultured for 72 h in the presence of the compounds (0–50 μg/mL). Growth inhibition...
Background: Iron is an essential element for the survival of microorganisms in vitro and in vivo, ac...
<p>Trophozoite stage parasites (26–30 h) of the 3D7 and Dd2 strains of <i>P. falciparum</i> expressi...
<p>Parasites were cultivated at 25°C in Schneider's medium supplemented with 20% of fetal bovine ser...
<p>Parasites were incubated at 25°C in Schneider's medium in the absence (control) or presence of 25...
. was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected paras...
. was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected paras...
Two types of iron chelators, desferrioxamine (DFO) and 2,2-bipyridyl (BIP), selected for their diffe...
Two types of iron chelators, desferrioxamine (DFO) and 2,2-bipyridyl (BIP), selected for their diffe...
<p>Parasites were incubated at 25°C in Schneider's medium in the absence (control) or presence of 25...
<p>Ring stage parasites were cultured in the presence of DMSO (control) or chloroquine or indicated ...
<p>Parasites were treated with 15 μM TPEN for 24 and 48 hr and then re-inoculated into fresh medium....
<div><p>Background</p><p>Iron is an essential element for the survival of microorganisms <i>in vitro...
<p><i>L. (V.) braziliensis-</i>infected macrophages were treated with 17-AAG or with amphotericin B ...
<p>A) Epimastigotes were incubated with different concentrations of CsA (10, 20 and 40 µM). Untreate...
<p>Parasites were cultured for 72 h in the presence of the compounds (0–50 μg/mL). Growth inhibition...
Background: Iron is an essential element for the survival of microorganisms in vitro and in vivo, ac...
<p>Trophozoite stage parasites (26–30 h) of the 3D7 and Dd2 strains of <i>P. falciparum</i> expressi...
<p>Parasites were cultivated at 25°C in Schneider's medium supplemented with 20% of fetal bovine ser...
<p>Parasites were incubated at 25°C in Schneider's medium in the absence (control) or presence of 25...
. was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected paras...
. was analyzed by the use of the chelator 2,2-dipyridyl. Treatment with 2,2-dipyridyl affected paras...
Two types of iron chelators, desferrioxamine (DFO) and 2,2-bipyridyl (BIP), selected for their diffe...
Two types of iron chelators, desferrioxamine (DFO) and 2,2-bipyridyl (BIP), selected for their diffe...
<p>Parasites were incubated at 25°C in Schneider's medium in the absence (control) or presence of 25...
<p>Ring stage parasites were cultured in the presence of DMSO (control) or chloroquine or indicated ...
<p>Parasites were treated with 15 μM TPEN for 24 and 48 hr and then re-inoculated into fresh medium....
<div><p>Background</p><p>Iron is an essential element for the survival of microorganisms <i>in vitro...
<p><i>L. (V.) braziliensis-</i>infected macrophages were treated with 17-AAG or with amphotericin B ...
<p>A) Epimastigotes were incubated with different concentrations of CsA (10, 20 and 40 µM). Untreate...
<p>Parasites were cultured for 72 h in the presence of the compounds (0–50 μg/mL). Growth inhibition...
Background: Iron is an essential element for the survival of microorganisms in vitro and in vivo, ac...
<p>Trophozoite stage parasites (26–30 h) of the 3D7 and Dd2 strains of <i>P. falciparum</i> expressi...