<p>Data is presented from genital skin fibroblasts cell lines obtained from AIS patients with AR mutations AR-F764L (GSF571), AR-R840C (GSF840) and AR-P766S (GSF851). Cells were maintained in 5% SD-FBS media for 12 hr and treated with the indicated compound for 18 hr in 5%SD-FBS. Tested compounds given at logarithmic concentrations (10<sup>−14</sup> to 10<sup>−5</sup> M) include the following AR agonist: DHT (-○-), Mibolerone (-▵-), and R1881(-□-).</p
<p>A. LAPC4 cells were androgen deprived for 72 hours and then treated with a synthetic androgen (R1...
This review focuses on the role played by protein partners of ligand-activated extra-nuclear AR in t...
<p>(A) FACS analysis of mCherry signals in EPT3-PT1-AR-241B cells. Cells were grown in androgen free...
<p>Data of fold-increase are presented from 6 genital skin fibroblasts cell lines obtained form norm...
<p><b>A.</b> AR transactivation in breast cancer cells. MDA-MB-231 cells plated in DME+5%csFBS were ...
<p><i>Values calculated by applying the 4-parameter curve fit algorithm available in SigmaPlot to mu...
<p>Values calculated by applying the 4-parameter curve fit algorithm available in SigmaPlot to multi...
<p>(A) Western blot analysis of nuclear and cytoplasmic AR expression in LNCaP C4-2B, PC-3, and E006...
Copyright © 2006 by The Endocrine SocietyThere is increasing evidence that sensitization of the andr...
<p>AR was overexpressed in DPCs by transfected with pcDNA3-hAR and cultured in the presence of DHT o...
<p>(A) Luciferase reporter assay. The luciferase reporter construct containing the PSA-enhancer regi...
<p>(A) Luciferase activity measured in 22RV1 cells transfected with ARE-luc reporter and treated +/-...
Koh, JohnAndrogen Receptor (AR) antagonists, such as bicalutamide and flutamide have been used widel...
<p>(A) Cytogenetic analysis of AR status in normal male control and E006AA cells as determined by Fl...
textabstractThe aim of the studies described in the next chapters was, first, to prove that the AR i...
<p>A. LAPC4 cells were androgen deprived for 72 hours and then treated with a synthetic androgen (R1...
This review focuses on the role played by protein partners of ligand-activated extra-nuclear AR in t...
<p>(A) FACS analysis of mCherry signals in EPT3-PT1-AR-241B cells. Cells were grown in androgen free...
<p>Data of fold-increase are presented from 6 genital skin fibroblasts cell lines obtained form norm...
<p><b>A.</b> AR transactivation in breast cancer cells. MDA-MB-231 cells plated in DME+5%csFBS were ...
<p><i>Values calculated by applying the 4-parameter curve fit algorithm available in SigmaPlot to mu...
<p>Values calculated by applying the 4-parameter curve fit algorithm available in SigmaPlot to multi...
<p>(A) Western blot analysis of nuclear and cytoplasmic AR expression in LNCaP C4-2B, PC-3, and E006...
Copyright © 2006 by The Endocrine SocietyThere is increasing evidence that sensitization of the andr...
<p>AR was overexpressed in DPCs by transfected with pcDNA3-hAR and cultured in the presence of DHT o...
<p>(A) Luciferase reporter assay. The luciferase reporter construct containing the PSA-enhancer regi...
<p>(A) Luciferase activity measured in 22RV1 cells transfected with ARE-luc reporter and treated +/-...
Koh, JohnAndrogen Receptor (AR) antagonists, such as bicalutamide and flutamide have been used widel...
<p>(A) Cytogenetic analysis of AR status in normal male control and E006AA cells as determined by Fl...
textabstractThe aim of the studies described in the next chapters was, first, to prove that the AR i...
<p>A. LAPC4 cells were androgen deprived for 72 hours and then treated with a synthetic androgen (R1...
This review focuses on the role played by protein partners of ligand-activated extra-nuclear AR in t...
<p>(A) FACS analysis of mCherry signals in EPT3-PT1-AR-241B cells. Cells were grown in androgen free...