Showing results (31-40 of 55) with videos related to
Sort By:
Pageof 6
Molecular Cancer Therapeutics|July 28, 2021
SLC7A11 Is a Superior Determinant of APR-246 (Eprenetapopt) Response than TP53 Mutation StatusKenji M Fujihara, Mariana Corrales Benitez, Carlos S Cabalag, et al.Oncotarget|November 19, 2016
Novel metastatic models of esophageal adenocarcinoma derived from FLO-1 cells highlight the importance of E-cadherin in cancer metastasisDavid S Liu, Sanne J M Hoefnagel, Oliver M Fisher, et al.Molecular Biology of the Cell|January 21, 2021
The TIM22 complex mediates the import of sideroflexins and is required for efficient mitochondrial one-carbon metabolismThomas D Jackson, Daniella H Hock, Kenji M Fujihara, et al.Cell Death & Disease|March 1, 2024
Caspase-2 protects against ferroptotic cell deathSwati Dawar, Mariana C Benitez, Yoon Lim, et al.ACS Chemical Biology|June 13, 2022
Multiparametric High-Content Cell Painting Identifies Copper Ionophores as Selective Modulators of Esophageal Cancer PhenotypesRebecca E Hughes, Richard J R Elliott, Xiaodun Li, et al.Annals of Surgery|June 23, 2022
Potential Clinical Utility of a Targeted Circulating Tumor DNA Assay in Esophageal AdenocarcinomaCarlos S Cabalag, Michael Yates, Mariana Benitez Corrales, et al.Cell Death & Disease|July 16, 2021
Mutant p53-reactivating compound APR-246 synergizes with asparaginase in inducing growth suppression in acute lymphoblastic leukemia cellsSophia Ceder, Sofi E Eriksson, Ying Yu Liang, et al.The Journal of Clinical Investigation|August 2, 2014
Hedgehog signaling regulates FOXA2 in esophageal embryogenesis and Barrett's metaplasiaDavid H Wang, Anjana Tiwari, Monica E Kim, et al.EMBO Molecular Medicine|December 14, 2020
A thiol-bound drug reservoir enhances APR-246-induced mutant p53 tumor cell deathSophia Ceder, Sofi E Eriksson, Emarndeena H Cheteh, et al.International Journal of Molecular Sciences|June 2, 2021
Mutant p53 Mediates Sensitivity to Cancer Treatment Agents in Oesophageal Adenocarcinoma Associated with MicroRNA and SLC7A11 ExpressionAnn-Kathrin Eichelmann, George C Mayne, Karen Chiam, et al.Pageof 6