<p><b>A–C,</b> YFP fluorescence intensities within the FP<sub>NLS</sub>FP-marked cell nuclei of each separately-cultured reporter line are shown in response to fifteen different steroids (10<sup>−8</sup> M each). Nuclear YFP measurements are shown as the mean +/− sd from 10 fields for each treatment condition. Gray bars, measurements for indicated assay plated independently into separated wells. Black bars, measurements from wells in which the three assays are co-cultured and separated by the bar-code. The dotted gray line represents the measurements obtained upon treatment of the independent assays with vehicle only. Steroids: 1: pregnenolone, 2: progesterone, 3: 11-deoxycorticosterone, 4: aldosterone, 5: 17-hydroxypregnenolone, 6: 17-hydr...
We have previously generated several transformed human mammary cell lines for the detection of stero...
A major focus in the current discovery of drugs targeting nuclear receptors (NRs) is identifying dru...
The aim of the work described in this report is to develop and characterize a cell-based androgen re...
<p>Representative images of <b>A,</b> the em1/em2 ratio and <b>B,</b> YFP-tagged AR showed the FP<su...
<p>FACS analysis of mCherry signals in (A) EP156T-AR-241B, (B) 957E/hTERT-AR-241B and (C) LNCaP-241B...
International audienceIn order to monitor the (anti)steroid activity of environmental samples, we es...
<p><b>A,</b> Fluorescence microscopy images of YFP-tagged AR and mCherry-NLS-mCherry nuclear marker ...
We have established highly sensitive and specific androgen and estrogen reporter cell lines which we...
<p>(A) FACS analysis of mCherry signals in EPT3-PT1-AR-241B cells. Cells were grown in androgen free...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids. Cells were lysed and ...
We have established highly sensitive and specific androgen and estrogen reporter cell lines which we...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids in the presence of tes...
To identify and prioritize chemicals that may alter steroidogenesis, an in vitro screening assay bas...
<p>(A–B) Cells were grown in Medium A with 10 nM testosterone (T) or 10 μM casodex (CDX). (A) Protei...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids in the presence of 5α-...
We have previously generated several transformed human mammary cell lines for the detection of stero...
A major focus in the current discovery of drugs targeting nuclear receptors (NRs) is identifying dru...
The aim of the work described in this report is to develop and characterize a cell-based androgen re...
<p>Representative images of <b>A,</b> the em1/em2 ratio and <b>B,</b> YFP-tagged AR showed the FP<su...
<p>FACS analysis of mCherry signals in (A) EP156T-AR-241B, (B) 957E/hTERT-AR-241B and (C) LNCaP-241B...
International audienceIn order to monitor the (anti)steroid activity of environmental samples, we es...
<p><b>A,</b> Fluorescence microscopy images of YFP-tagged AR and mCherry-NLS-mCherry nuclear marker ...
We have established highly sensitive and specific androgen and estrogen reporter cell lines which we...
<p>(A) FACS analysis of mCherry signals in EPT3-PT1-AR-241B cells. Cells were grown in androgen free...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids. Cells were lysed and ...
We have established highly sensitive and specific androgen and estrogen reporter cell lines which we...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids in the presence of tes...
To identify and prioritize chemicals that may alter steroidogenesis, an in vitro screening assay bas...
<p>(A–B) Cells were grown in Medium A with 10 nM testosterone (T) or 10 μM casodex (CDX). (A) Protei...
<p>Cells were treated for 24 h with various endogenous and synthetic steroids in the presence of 5α-...
We have previously generated several transformed human mammary cell lines for the detection of stero...
A major focus in the current discovery of drugs targeting nuclear receptors (NRs) is identifying dru...
The aim of the work described in this report is to develop and characterize a cell-based androgen re...