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A Novel Androgen Receptor Splice Variant Is Upregulated during Prostate Cancer Progression
PubMed Full text in PMC Similar studies Analyze with GEO2R
Expression data from AR3 transgenic and wild-type mouse prostates
Genome-wide impact of ART-27 loss on androgen-regulated transcription in prostate cancer cells
Hormone-Independence of Prostate Cancer Cells is Supported by the Androgen Receptor without Binding to Classical Response Elements
Late passage LNCaP prostate tumor cells treated with androgen receptor shRNA or androgen R1881
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Androgen receptor splice variants mediate enzalutamide resistance in castration-resistant prostate cancer cell lines
Modulation of Androgen Receptor Signaling in Hormonal Therapy-Resistant Prostate Cancer Cell Lines
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression VI
PubMed Full text in PMC Similar studies SRA Run Selector
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression V
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression IV
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression III
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression II
The miR-96 and RARG signaling axis governs androgen signaling and prostate cancer progression I
Molecular Features of Hormone-Refractory Prostate Cancer Cells by Genome-wide Gene-expression Profiles
Stable overexpression of MED19 in androgen-dependent LNCaP cells promotes growth under conditions of androgen deprivation
PubMed Full text in PMC Similar studies
Transcriptome profiles of alternative MED19 LNCaP and control LNCaP cells cultured under androgen deprivation with vehicle or R1881
Genome-wide maps of the androgen receptor and H3K27 upon MED19 overexpression in LNCaP cells
Transcriptional profiles induced by either androgen depletion or androgen receptor knockdown
Effect of individual HDAC knockdown on expression of androgen induced genes
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