David A. Cheresh
Affiliations: | Molecular Pathology | University of California, San Diego, La Jolla, CA |
Area:
Pathology, Molecular Biology, Oncology, Cell BiologyGoogle:
"David Cheresh"Children
Sign in to add trainee| Richard L. Klemke | grad student | 1996-2002 | UCSD School of Medicine (Neurotree) |
| Miller Huang | grad student | 2011 | UCSD |
| Steven K. Lau | grad student | 2011 | UCSD |
| Elizabeth L. Scheppke Smoot | grad student | 2011 | UCSD |
| Paul J. Bushway | grad student | 2012 | UCSD |
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Publications
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| Wu C, Weis SM, Cheresh DA. (2023) Tumor-initiating cells establish a niche to overcome isolation stress. Trends in Cell Biology |
| Zhu Z, Mesci P, Bernatchez JA, et al. (2019) Zika Virus Targets Glioblastoma Stem Cells through a SOX2-Integrin αβ Axis. Cell Stem Cell |
| Wettersten HI, Weis SM, Pathria P, et al. (2019) Arming tumor-associated macrophages to reverse epithelial cancer progression. Cancer Research |
| Carlson P, Dasgupta A, Grzelak CA, et al. (2019) Targeting the perivascular niche sensitizes disseminated tumour cells to chemotherapy. Nature Cell Biology |
| Pathria P, Takahashi H, Kaneda M, et al. (2019) Abstract 113: c-Kit-dependent tissue resident macrophage progenitors drive cancer progression Cancer Research. 78: 5006-5006 |
| Schmid MC, Khan SQ, Kaneda MM, et al. (2018) Integrin CD11b activation drives anti-tumor innate immunity. Nature Communications. 9: 5379 |
| Wang H, Lapek J, Fujimura K, et al. (2018) Pseudopodium-enriched atypical kinase 1 mediates angiogenesis by modulating GATA2-dependent VEGFR2 transcription. Cell Discovery. 4: 26 |
| Sun Q, Lesperance J, Wettersten H, et al. (2018) Proapoptotic PUMA targets stem-like breast cancer cells to suppress metastasis. The Journal of Clinical Investigation. 128: 531-544 |
| Rakhshandehroo T, Tan J, Grosshart B, et al. (2018) Abstract LB-049: Cancer stem cell-produced lysophosphatidic acid reprograms surrounding tumor cells to a stem-like state Cancer Research. 78 |
| Cosset É, Ilmjärv S, Dutoit V, et al. (2017) Glut3 Addiction Is a Druggable Vulnerability for a Molecularly Defined Subpopulation of Glioblastoma. Cancer Cell. 32: 856-868.e5 |