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Loss of Androgen Receptor-Dependent Growth Suppression by Prostate Cancer Cells Can Occur Independently from Acquiring Oncogenic Addiction to Androgen Receptor Signaling.
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- PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011475
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- Article
Detection and Quantification of the Evolution Dynamics of Apoptosis Using the PET Voltage Sensor <sup>18</sup>F-Fluorobenzyl Triphenyl Phosphonium.
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- Journal of Nuclear Medicine, 2009, v. 50, n. 5, p. 774, doi. 10.2967/jnumed.108.061283
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- Article
A hemi‐spleen injection model of liver metastasis for prostate cancer.
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- Prostate, 2020, v. 80, n. 14, p. 1263, doi. 10.1002/pros.24055
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- Article
Androgen receptor (AR) suppresses normal human prostate epithelial cell proliferation via AR/β-catenin/TCF-4 complex inhibition of c-MYC transcription.
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- Prostate, 2014, v. 74, n. 11, p. 1118, doi. 10.1002/pros.22828
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- Article
Androgen withdrawal fails to induce detectable tissue hypoxia in the rat prostate.
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- Prostate, 2014, v. 74, n. 8, p. 805, doi. 10.1002/pros.22803
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- Article
Of mice and men-warning: Intact versus castrated adult male mice as xenograft hosts are equivalent to hypogonadal versus abiraterone treated aging human males, respectively.
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- Prostate, 2013, v. 73, n. 12, p. 1316, doi. 10.1002/pros.22677
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- Article
Adaptive auto-regulation of androgen receptor provides a paradigm shifting rationale for bipolar androgen therapy (BAT) for castrate resistant human prostate cancer.
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- Prostate, 2012, v. 72, n. 14, p. 1491, doi. 10.1002/pros.22504
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- Article
Tasquinimod prevents the angiogenic rebound induced by fractionated radiation resulting in an enhanced therapeutic response of prostate cancer xenografts.
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- Prostate, 2012, v. 72, n. 6, p. 638, doi. 10.1002/pros.21467
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- Article
The quinoline-3-carboxamide anti-angiogenic agent, tasquinimod, enhances the anti-prostate cancer efficacy of androgen ablation and taxotere without effecting serum PSA directly in human xenografts.
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- Prostate, 2007, v. 67, n. 7, p. 790, doi. 10.1002/pros.20573
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- Article
PC3, but not DU145, human prostate cancer cells retain the coregulators required for tumor suppressor ability of androgen receptor.
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- Prostate, 2006, v. 66, n. 12, p. 1329, doi. 10.1002/pros.20483
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- Article
Identification of ABR‐215050 as lead second generation quinoline‐3‐carboxamide anti‐angiogenic agent for the treatment of prostate cancer.
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- Prostate, 2006, v. 66, n. 16, p. 1768, doi. 10.1002/pros.20509
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- Article
Dissociation between androgen responsiveness for malignant growth vs. expression of prostate specific differentiation markers PSA, hK2, and PSMA in human prostate cancer models.
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- Prostate, 2003, v. 54, n. 4, p. 249, doi. 10.1002/pros.10199
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- Article
Engineering a Prostate-Specific Membrane Antigen-Activated Tumor Endothelial Cell Prodrug for Cancer Therapy.
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- Science Translational Medicine, 2012, v. 4, n. 140, p. 1, doi. 10.1126/scitranslmed.3003886
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- Article
Characterization of structural, biochemical, pharmacokinetic, and pharmacodynamic properties of the LSD1 inhibitor bomedemstat in preclinical models.
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- Prostate, 2024, v. 84, n. 10, p. 909, doi. 10.1002/pros.24707
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- Article
Targeting the fibroblast growth factor pathway in molecular subtypes of castration‐resistant prostate cancer.
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- Prostate, 2024, v. 84, n. 1, p. 100, doi. 10.1002/pros.24630
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- Article
Third generation quinoline‐3‐carboxamide transcriptional disrupter of HDAC4, HIF‐1α, and MEF‐2 signaling for metastatic castration‐resistant prostate cancer.
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- Prostate, 2023, v. 83, n. 15, p. 1470, doi. 10.1002/pros.24606
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- Article