152 results on '"Cato, Laura"'
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2. Supplementary Figure 7 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
3. Supplementary Figure 12 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
4. Data from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
5. Supplementary Figure 3 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
6. Supplementary Figure 2 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
7. Supplementary Table 5 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
8. Supplementary Figure 9 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
9. Supplementary Table 6 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
10. Supplementary Table 1 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
11. Supplementary Table 3 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
12. Supplementary Figure 8 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
13. Supplementary Materials and Methods from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
14. Supplementary Figure 5 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
15. Supplementary Figure 6 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
16. Supplementary Table 7 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
17. Supplementary Table 4 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
18. Supplementary Table 2 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
19. Supplementary Figure 4 from Thio-2 Inhibits Key Signaling Pathways Required for the Development and Progression of Castration-resistant Prostate Cancer
20. A chemical probe for BAG1 targets androgen receptor-positive prostate cancer through oxidative stress signaling pathway
21. Role of Androgen Receptor Variants in Prostate Cancer: Report from the 2017 Mission Androgen Receptor Variants Meeting.
22. Predictions of Colloidal Molecular Aggregation Using AI/ML Models.
23. Thio-2 inhibits key signaling pathways required for the development and progression of castration resistant prostate cancer.
24. Highly disordered histone H1−DNA model complexes and their condensates
25. Investigation of the interactions between linker histones H1/H5 and HMGB1
26. Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
27. Vitamin D receptor regulates autophagy in the normal mammary gland and in luminal breast cancer cells
28. Supplementary Data from Identification of an Imidazopyridine-based Compound as an Oral Selective Estrogen Receptor Degrader for Breast Cancer Therapy
29. Supplementary Table S2 from Identification of an Imidazopyridine-based Compound as an Oral Selective Estrogen Receptor Degrader for Breast Cancer Therapy
30. Data from Identification of an Imidazopyridine-based Compound as an Oral Selective Estrogen Receptor Degrader for Breast Cancer Therapy
31. Figure S1 from Identification of an Imidazopyridine-based Compound as an Oral Selective Estrogen Receptor Degrader for Breast Cancer Therapy
32. Identification of an Imidazopyridine-based Compound as an Oral Selective Estrogen Receptor Degrader for Breast Cancer Therapy
33. Hormone-Responsive Cancers
34. Contributors
35. Targeting the BAG-1 family of co-chaperones in lethal prostate cancer
36. EZH2 Oncogenic Activity in Castration-Resistant Prostate Cancer Cells Is Polycomb-Independent
37. Androgen receptor splice variant 7 functions independently of the full length receptor in prostate cancer cells
38. Characterization of the interaction between HMGB1 and H3—a possible means of positioning HMGB1 in chromatin
39. Identification of the Role of Linker Histone H1 in Estrogen Receptor Binding and Activity
40. EZH2 Oncogenic Activity in Castration-Resistant Prostate Cancer Cells Is Polycomb-lndependent
41. Chapter 29 - Hormone-Responsive Cancers
42. ARv7 Represses Tumor-Suppressor Genes in Castration-Resistant Prostate Cancer
43. Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
44. Author response: Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer
45. Abstract 1806: TRIM24 is an oncogenic transcriptional activator in prostate cancer
46. Abstract 864: Androgen receptor stability in prostate cancer is regulated by the cochaperone Bag-1L
47. TRIM24 Is an Oncogenic Transcriptional Activator in Prostate Cancer
48. Highly disordered histone H1--DNA model complexes and their condensates.
49. Abstract 4677: Control of androgen receptor function by the genomic action of the cochaperone Bag-1L
50. Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing.
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