ORCID as entered in ROS

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2024, 'The Novel Anticancer Aryl-Ureido Fatty Acid CTU Increases Reactive Oxygen Species Production That Impairs Mitochondrial Fusion Mechanisms and Promotes MDA-MB-231 Cell Death', International Journal of Molecular Sciences, 25, http://dx.doi.org/10.3390/ijms251910577
,2024, 'The inositol-requiring enzyme 1 (IRE1) endoplasmic reticulum stress pathway promotes MDA-MB-231 cell survival and renewal in response to the aryl-ureido fatty acid CTU', International Journal of Biochemistry and Cell Biology, 171, http://dx.doi.org/10.1016/j.biocel.2024.106571
,2023, 'Inclusion of the in-chain sulfur in 3-thiaCTU increases the efficiency of mitochondrial targeting and cell killing by anticancer aryl-urea fatty acids', European Journal of Pharmacology, 939, http://dx.doi.org/10.1016/j.ejphar.2022.175470
,2022, 'The aryl-ureido fatty acid CTU activates endoplasmic reticulum stress and PERK/NOXA-mediated apoptosis in tumor cells by a dual mitochondrial-targeting mechanism', Cancer Letters, 526, pp. 131 - 141, http://dx.doi.org/10.1016/j.canlet.2021.11.022
,2021, 'PTU, a novel ureido-fatty acid, inhibits MDA-MB-231 cell invasion and dissemination by modulating Wnt5a secretion and cytoskeletal signaling', Biochemical Pharmacology, 192, http://dx.doi.org/10.1016/j.bcp.2021.114726
,2019, 'Aryl-urea fatty acids that activate the p38 MAP kinase and down-regulate multiple cyclins decrease the viability of MDA-MB-231 breast cancer cells', European Journal of Pharmaceutical Sciences, 129, pp. 87 - 98, http://dx.doi.org/10.1016/j.ejps.2018.12.015
,2017, 'A Novel Arylurea Fatty Acid That Targets the Mitochondrion and Depletes Cardiolipin to Promote Killing of Breast Cancer Cells', Journal of Medicinal Chemistry, 60, pp. 8661 - 8666, http://dx.doi.org/10.1021/acs.jmedchem.7b00701
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