461 results on '"Zhang, Xiang H.-F."'
Search Results
2. Leveraging preclinical models of metastatic breast cancer
3. BIGH3 mediates apoptosis and gap junction failure in osteocytes during renal cell carcinoma bone metastasis progression
4. Engineering small-molecule and protein drugs for targeting bone tumors
5. Osteoprogenitor-GMP crosstalk underpins solid tumor-induced systemic immunosuppression and persists after tumor removal
6. STAT5 confers lactogenic properties in breast tumorigenesis and restricts metastatic potential
7. Review old bone, new tricks
8. Elevated NRAS expression during DCIS is a potential driver for progression to basal-like properties and local invasiveness
9. Evolving cancer–niche interactions and therapeutic targets during bone metastasis
10. Unbiased metastatic niche-labeling identifies estrogen receptor-positive macrophages as a barrier of T cell infiltration during bone colonization
11. CBP/P300 BRD Inhibition Reduces Neutrophil Accumulation and Activates Antitumor Immunity in TNBC
12. Combining TIGIT Blockade with MDSC Inhibition Hinders Breast Cancer Bone Metastasis by Activating Antitumor Immunity
13. Integrative spatial omics reveals distinct tumor-promoting multicellular niches and immunosuppressive mechanisms in African American and European American patients with TNBC
14. Bone Endosteal Mimics Regulates Breast Cancer Development and Phenotype
15. Abstract IA05: Leveraging preclinical models of triple negative breast cancer for translational research
16. Abstract PR03: CSF-1R antibody targeting therapy with combined metronomic chemotherapy and immune checkpoint blockade enhance a B and T cell response to attenuate metastatic triple negative breast cancer
17. Nutrient Sensing in Macrophages Linked to Reorganized Tumor Vasculature
18. Hormonal modulation of ESR1 mutant metastasis
19. Lung mesenchymal cells elicit lipid storage in neutrophils that fuel breast cancer lung metastasis
20. Protein quality control through endoplasmic reticulum-associated degradation maintains haematopoietic stem cell identity and niche interactions
21. Resistance to natural killer cell immunosurveillance confers a selective advantage to polyclonal metastasis
22. UDP-glucose 6-dehydrogenase regulates hyaluronic acid production and promotes breast cancer progression
23. Bone Metastasis: Find Your Niche and Fit in
24. Supplementary Table 1 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
25. Supplementary Figure 7 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
26. Supplementary Figure 3 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
27. Supplementary Figure 2 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
28. Supplementary Figure 6 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
29. Supplementary Figure 5 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
30. Supplementary Figure 4 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
31. Data from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
32. Supplementary Figure 1 from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
33. Supplementary Figure Legend from Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
34. Associations amongst genes, molecules, cells, and organs in breast cancer metastasis
35. Bone as a New Milieu for Disseminated Tumor Cells: An Overview of Bone Metastasis
36. Correction: UDP-glucose 6-dehydrogenase regulates hyaluronic acid production and promotes breast cancer progression
37. Immuno-subtyping of breast cancer reveals distinct myeloid cell profiles and immunotherapy resistance mechanisms
38. RSPO2 and RANKL signal through LGR4 to regulate osteoclastic premetastatic niche formation and bone metastasis
39. Correction to: Hormonal modulation of ESR1 mutant metastasis
40. Targeted Inhibition of lncRNA Malat1 Alters the Tumor Immune Microenvironment in Preclinical Syngeneic Mouse Models of Triple-Negative Breast Cancer
41. Unique cellular protrusions mediate breast cancer cell migration by tethering to osteogenic cells
42. Metabolic enzyme PFKFB4 activates transcriptional coactivator SRC-3 to drive breast cancer
43. Supplementary Video 2 from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
44. Supplementary Figure S1-S7 from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
45. Supplementary Video 1 from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
46. Data from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
47. Supplementary Video 4 from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
48. Supplementary Raw Data from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
49. Supplementary Video 3 from Bone Metastasis Initiation Is Coupled with Bone Remodeling through Osteogenic Differentiation of NG2+ Cells
50. Supplementary Methods from Transcriptional Repression of SIRT3 Potentiates Mitochondrial Aconitase Activation to Drive Aggressive Prostate Cancer to the Bone
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