<p>3T3-L1 preadipocytes were induced to differentiate with induction medium containing MDI (M, IBMX (0.5 mM); D, dexamethasone (0.5 µM); I, insulin (5 µg/ml)), insulin (5 µg/ml), and FBS (10%) in the presence or absence of 10 µM of the test compounds for 8 days. On day 8, the cellular TG contents were quantified by AdipoRed assay. Values are mean ± SE of data from three independent experiments with three replicates. *P or <sup>#</sup>P<0.05 and **P or <sup>##</sup>P<0.01 vs. control (no chemical).</p
<p>(A) 2-deoxy glucose uptake in L6 myotubes. Cells were incubated for 16 h with different extracts ...
<p>3T3-L1 preadipocytes were treated with or without each of the test compounds at a final concentra...
<p>A. Synchronous reentry of the cell cycle by growth arrested 2 days post-confluent 3T3-L1 preadipo...
<p>The compounds that bind PPARγ were added to 3T3-L1 pre-adipocytes to test their adipogenic capaci...
<p>A, Adipogenesis in 3T3-L1 fibroblasts was induced by standard adipogenesis-inducing mix. Intracel...
<p>Fluorimetric quantification of lipid accumulation was performed using Nile red staining. The degr...
<p>(A) 3T3-L1 preadipocytes were induced to differentiate with induction medium containing MDI, insu...
<p>3T3-L1 adipocytes were pretreated with 10 mM Nac, 200 μM Mito-TEMPO, or 50 μM Mdivi-1 for 30 min ...
<p>(A) The whole cell culture dish view of the oil red O stain of NIH/3T3 cells induced with (R7) or...
<p>(A) hASCs were grown to confluency (Day 0) and induced to differentiate with an optimised adipocy...
<p>(A) 3T3-L1 adipocytes were pretreated with 10 mM Nac, 200 μM Mito-TEMPO, or 50 μM Mdivi-1 for 30 ...
<p>A. Oil Red O staining of PGE<sub>2</sub>-treated 3T3-L1 cells. Cells (undifferentiated cells: U) ...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>hUCB-MSCs were grown in conditioned media at the absence or presence of Pam<sub>3</sub>CSK<sub>4<...
<p>The 3T3-L1 murine preadipocytes were incubated for one day with growth medium containing Emdogain...
<p>(A) 2-deoxy glucose uptake in L6 myotubes. Cells were incubated for 16 h with different extracts ...
<p>3T3-L1 preadipocytes were treated with or without each of the test compounds at a final concentra...
<p>A. Synchronous reentry of the cell cycle by growth arrested 2 days post-confluent 3T3-L1 preadipo...
<p>The compounds that bind PPARγ were added to 3T3-L1 pre-adipocytes to test their adipogenic capaci...
<p>A, Adipogenesis in 3T3-L1 fibroblasts was induced by standard adipogenesis-inducing mix. Intracel...
<p>Fluorimetric quantification of lipid accumulation was performed using Nile red staining. The degr...
<p>(A) 3T3-L1 preadipocytes were induced to differentiate with induction medium containing MDI, insu...
<p>3T3-L1 adipocytes were pretreated with 10 mM Nac, 200 μM Mito-TEMPO, or 50 μM Mdivi-1 for 30 min ...
<p>(A) The whole cell culture dish view of the oil red O stain of NIH/3T3 cells induced with (R7) or...
<p>(A) hASCs were grown to confluency (Day 0) and induced to differentiate with an optimised adipocy...
<p>(A) 3T3-L1 adipocytes were pretreated with 10 mM Nac, 200 μM Mito-TEMPO, or 50 μM Mdivi-1 for 30 ...
<p>A. Oil Red O staining of PGE<sub>2</sub>-treated 3T3-L1 cells. Cells (undifferentiated cells: U) ...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>hUCB-MSCs were grown in conditioned media at the absence or presence of Pam<sub>3</sub>CSK<sub>4<...
<p>The 3T3-L1 murine preadipocytes were incubated for one day with growth medium containing Emdogain...
<p>(A) 2-deoxy glucose uptake in L6 myotubes. Cells were incubated for 16 h with different extracts ...
<p>3T3-L1 preadipocytes were treated with or without each of the test compounds at a final concentra...
<p>A. Synchronous reentry of the cell cycle by growth arrested 2 days post-confluent 3T3-L1 preadipo...