Lucio Miele
Affiliations: | Molecular and Cellular Biochemistry Program | Loyola University Chicago, Chicago, IL, United States |
Area:
Molecular Biology, OncologyWebsite:
https://www.medschool.lsuhsc.edu/genetics/faculty_detail.aspx?name=Miele_LucioGoogle:
"Lucio Miele"Mean distance: (not calculated yet)
Parents
Sign in to add mentorErich Lanka | grad student | 1983-1987 | Max-Planck-Institut für molekulare Genetik |
Children
Sign in to add traineeNicole S. Darack | grad student | 2004 | Loyola University Chicago |
Joaquina Mascarenhas | grad student | 2006 | University of Illinois, Chicago (BME Tree) |
Lu Hao | grad student | 2009 | Loyola University Chicago |
Yin Peng | grad student | 2010 | Loyola University Chicago |
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Publications
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Monticone G, Huang Z, Csibi F, et al. (2022) Targeting the Cbl-b-Notch1 axis as a novel immunotherapeutic strategy to boost CD8+ T-cell responses. Frontiers in Immunology. 13: 987298 |
Perrone C, Pomella S, Cassandri M, et al. (2022) MET Inhibition Sensitizes Rhabdomyosarcoma Cells to NOTCH Signaling Suppression. Frontiers in Oncology. 12: 835642 |
Hoang VT, Matossian MD, La J, et al. (2021) Dual inhibition of MEK1/2 and MEK5 suppresses the EMT/migration axis in triple-negative breast cancer through FRA-1 regulation. Journal of Cellular Biochemistry |
Bhatt AB, Wright TD, Barnes V, et al. (2021) Diverse and converging roles of ERK1/2 and ERK5 pathways on mesenchymal to epithelial transition in breast cancer. Translational Oncology. 14: 101046 |
Bhatt AB, Patel S, Matossian MD, et al. (2021) Molecular Mechanisms of Epithelial to Mesenchymal Transition Regulated by ERK5 Signaling. Biomolecules. 11 |
Monticone G, Miele L. (2021) Notch Pathway: A Journey from Notching Phenotypes to Cancer Immunotherapy. Advances in Experimental Medicine and Biology. 1287: 201-222 |
Majumder S, Crabtree JS, Golde TE, et al. (2020) Targeting Notch in oncology: the path forward. Nature Reviews. Drug Discovery |
Chang TC, Matossian MD, Elliott S, et al. (2020) Evaluation of deacetylase inhibition in metaplastic breast carcinoma using multiple derivations of preclinical models of a new patient-derived tumor. Plos One. 15: e0226464 |
Hoang VT, Matossian MD, Ucar DA, et al. (2020) ERK5 Is Required for Tumor Growth and Maintenance Through Regulation of the Extracellular Matrix in Triple Negative Breast Cancer. Frontiers in Oncology. 10: 1164 |
Matossian MD, Burks HE, Elliott S, et al. (2020) A novel screening approach comparing kinase activity of small molecule inhibitors with similar molecular structures and distinct biologic effects in triple-negative breast cancer to identify targetable signaling pathways. Anti-Cancer Drugs. 31: 759-775 |