<p>Crystal violet dye exclusion showing the effect of TGFβ1 treatment and co-treatment with AqE, AlE, CA or CI on cell proliferation (A). Linear relationship between cell number and absorbance is shown (B). Data represents mean ± SD of three independent experiments done in quadruplicates. p value: <sup>###</sup>p<0.001 is a comparison between control vs. TGFβ1 treatment. p value: ***p<0.001 is a comparison between TGFβ1 and corresponding treatment.</p
<p>Bars correspond to means of three independent experiments. Data are expressed as percentage of co...
<p>ARPE-19 cells were seeded in chamber slides, treated with TGFβ1 or co-treated with TGFβ1 and vari...
<p><b>Copyright information:</b></p><p>Taken from "Troglitazone suppresses transforming growth facto...
<p>Scratch assay showing migratory capacity of ARPE-19 cells upon TGFβ1 induction and on treatment w...
<p>The effects of dyes on cell viability were combined for each concentration and compared between 3...
<p>(A) MTT assay of proliferation of cells treated with different concentrations of TQ and DG for 48...
<p>MTT assay showing the effect of AqE, AlE, CA, CI and GA on viability of ARPE-19 cells. Data repre...
<p>Treatment of ARPE-19 cells with TGFβ1 alone or co-treated with various concentrations of AqE, AlE...
<p>Subconfluent VSMCs were stimulated for 48(20 ng/mL, every 24 h) or TGFβ (1 ng/mL), alone or in co...
<p>(<b>A, B</b>) HT-29 cells were grown in 6-well plates until confluent. Next, cell monolayers were...
<p>(A) Cellular growth was determined by measuring the percent confluence (by microscopic quantifica...
<p>Panels (A–D): MTT assay determined cell viability of AML cells. 8,000 cells per well were seeded ...
<p>(A) The absorbance value of MTS assay with different treatments; the mannitol group was set as hy...
<p>HMEC-1 cells were seeded to a density of 1,500 cells/well. After 24 h of incubation, a zero point...
FPTEC, HREC and HK-2 were seeded onto 96-well plates at sub-confluent density and proliferation asse...
<p>Bars correspond to means of three independent experiments. Data are expressed as percentage of co...
<p>ARPE-19 cells were seeded in chamber slides, treated with TGFβ1 or co-treated with TGFβ1 and vari...
<p><b>Copyright information:</b></p><p>Taken from "Troglitazone suppresses transforming growth facto...
<p>Scratch assay showing migratory capacity of ARPE-19 cells upon TGFβ1 induction and on treatment w...
<p>The effects of dyes on cell viability were combined for each concentration and compared between 3...
<p>(A) MTT assay of proliferation of cells treated with different concentrations of TQ and DG for 48...
<p>MTT assay showing the effect of AqE, AlE, CA, CI and GA on viability of ARPE-19 cells. Data repre...
<p>Treatment of ARPE-19 cells with TGFβ1 alone or co-treated with various concentrations of AqE, AlE...
<p>Subconfluent VSMCs were stimulated for 48(20 ng/mL, every 24 h) or TGFβ (1 ng/mL), alone or in co...
<p>(<b>A, B</b>) HT-29 cells were grown in 6-well plates until confluent. Next, cell monolayers were...
<p>(A) Cellular growth was determined by measuring the percent confluence (by microscopic quantifica...
<p>Panels (A–D): MTT assay determined cell viability of AML cells. 8,000 cells per well were seeded ...
<p>(A) The absorbance value of MTS assay with different treatments; the mannitol group was set as hy...
<p>HMEC-1 cells were seeded to a density of 1,500 cells/well. After 24 h of incubation, a zero point...
FPTEC, HREC and HK-2 were seeded onto 96-well plates at sub-confluent density and proliferation asse...
<p>Bars correspond to means of three independent experiments. Data are expressed as percentage of co...
<p>ARPE-19 cells were seeded in chamber slides, treated with TGFβ1 or co-treated with TGFβ1 and vari...
<p><b>Copyright information:</b></p><p>Taken from "Troglitazone suppresses transforming growth facto...