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1. CDK9 inhibition inhibits multiple oncogenic transcriptional and epigenetic pathways in prostate cancer

2. Library size confounds biology in spatial transcriptomics data

4. Author Correction: CDK9 inhibition constrains multiple oncogenic transcriptional and epigenetic pathways in prostate cancer

5. The molecular consequences of androgen activity in the human breast

8. Activity and safety of enobosarm, a novel, oral, selective androgen receptor modulator, in androgen receptor-positive, oestrogen receptor-positive, and HER2-negative advanced breast cancer (Study G200802): a randomised, open-label, multicentre, multinational, parallel design, phase 2 trial

9. An androgen receptor switch underlies lineage infidelity in treatment-resistant prostate cancer

10. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

11. Role of Androgen Receptor Variants in Prostate Cancer: Report from the 2017 Mission Androgen Receptor Variants Meeting.

12. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

16. The androgen receptor is a tumor suppressor in estrogen receptor–positive breast cancer

17. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

18. Opposing transcriptional programs of KLF5 and AR emerge during therapy for advanced prostate cancer

19. Selective inhibition of CDK9 in triple negative breast cancer

21. Luminal breast cancer identity is determined by loss of glucocorticoid receptor activity

24. A reciprocal feedback between the PDZ binding kinase and androgen receptor drives prostate cancer

30. Supplementary Figures 1-9 from Dual Roles of PARP-1 Promote Cancer Growth and Progression

31. Data from Dual Roles of PARP-1 Promote Cancer Growth and Progression

32. Supplementary Methods , Table 1 from Dual Roles of PARP-1 Promote Cancer Growth and Progression

33. Data from Novel Selective Agents for the Degradation of Androgen Receptor Variants to Treat Castration-Resistant Prostate Cancer

34. Data from Lipidomic Profiling of Clinical Prostate Cancer Reveals Targetable Alterations in Membrane Lipid Composition

35. Figure S4: Evaluation of AR variant binding to known AREs and Snail promoters from Disrupting Androgen Receptor Signaling Induces Snail-Mediated Epithelial–Mesenchymal Plasticity in Prostate Cancer

36. Figure S2: Effect of treatment protocol on migration in PC3 and PC-3(AR)2 cells from Disrupting Androgen Receptor Signaling Induces Snail-Mediated Epithelial–Mesenchymal Plasticity in Prostate Cancer

37. Data from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

38. Data from The Magnitude of Androgen Receptor Positivity in Breast Cancer Is Critical for Reliable Prediction of Disease Outcome

39. Supplementary Figure Legends from Androgen and Estrogen Receptors in Breast Cancer Coregulate Human UDP-Glucuronosyltransferases 2B15 and 2B17

40. Supplementary Figure 1 from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

41. Supplementary Materials and Methods from Androgen and Estrogen Receptors in Breast Cancer Coregulate Human UDP-Glucuronosyltransferases 2B15 and 2B17

42. Supplementary Figure 3 from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

44. Supplementary data from MicroRNA-194 Promotes Prostate Cancer Metastasis by Inhibiting SOCS2

45. Supplementary Figure 2 from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

46. Supplementary Figure 3 from Evidence for Efficacy of New Hsp90 Inhibitors Revealed by Ex Vivo Culture of Human Prostate Tumors

47. Supplementary Figure 5 from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

48. Supplementary Figure 2 from Evidence for Efficacy of New Hsp90 Inhibitors Revealed by Ex Vivo Culture of Human Prostate Tumors

49. Supplementary Table 2 from Comparative Biomarker Expression and RNA Integrity in Biospecimens Derived from Radical Retropubic and Robot-Assisted Laparoscopic Prostatectomies

50. Supplementary Table 2 from Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development

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