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Cooperativity and Equilibrium with FOXA1 Define Androgen Receptor Transcriptional Program
PubMed Full text in PMC Similar studies Analyze with GEO2R
Cooperativity and Equilibrium with FOXA1 Define Androgen Receptor Transcriptional Program [array]
FoxA1 inhibits androgen receptor expression and suppresses prostate cancer metastasis [DU145, ChIP-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
FoxA1 inhibits androgen receptor expression and suppresses prostate cancer metastasis [LNCaP, ChIP-seq]
Effect of FOXA1 overexpression in prostate cancer
FOXA1 overexpression effect on prostate cancer cell line
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Dual Role of FoxA1 in Androgen Receptor Binding to Chromatin, Androgen Signaling and Prostate Cancer
Dual Role of FoxA1 in Androgen Receptor Binding to Chromatin, Androgen Signaling and Prostate Cancer [ChIP_seq, DHS_seq]
Dual Role of FoxA1 in Androgen Receptor Binding to Chromatin, Androgen Signaling and Prostate Cancer [Expression Array]
Pioneer factor FOXA1 defines GATA2- and AR-mediated transcriptional program in prostate cancer
Pioneer factor FOXA1 defines GATA2- and AR-mediated transcriptional program in prostate cancer [gene expression]
Pioneer factor FOXA1 defines GATA2- and AR-mediated transcriptional program in prostate cancer [ChIP-Seq]
Darolutamide antagonizes androgen signaling by blocking enhancer and super-enhancer activation
PubMed Full text in PMC Similar studies
Darolutamide antagonizes androgen signaling by blocking enhancer and super-enhancer activation [RNA-seq]
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Darolutamide antagonizes androgen signaling by blocking enhancer and super-enhancer activation [ChIP-seq]
Crosstalk between androgen and proinflammatory signaling activates a distinct transcription program in prostate cancer cells
Next Generation Sequencing Facilitates Quantitative Analysis of effect of knockdown of GATA2 on AR binding sites
Selective Targeting of PARP2 Inhibits Androgen Receptor Signaling and Prostate Cancer Growth Through Disruption of FOXA1 Function
Genome-wide occupation of AR, FOXA1, and H3K27AC in LNCaP cells treated with selective PARP2 inhibitor UPF-1069
Gene expression profilings for prostate cancer cells after inhibition of PARP1 or PARP2 using pharmaceutical or siRNA-based approaches
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