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Showing 1 to 4 of 4 for “"IACS-010759"”.

  1. Oxidative Phosphorylation: A Critical Feature and Novel Therapeutic Target In Melanoma Brain Metastases

    … of OXPHOS in MBM pathogenesis was tested using IACS-010759, a potent OXPHOS inhibitor currently in phase I clinical trials. IACS-010759 treatment of an RCAS-TVA mouse model of spontaneous MBM and lung metastasis significantly decreased the incidence of detectable MBMs but did not affect primary …

    uthsc Repository record for Oxidative Phosphorylation: A Critical Feature and Novel Therapeutic Target In Melanoma Brain Metastases (opens in a new tab)

  2. Mitochondrial Stress Signals Induce a Drug Tolerant Persister Phenotype in Triple Negative Breast Cancer Cell Models

    … including inhibition of ETC complex-1 using IACS-010759. Through transcriptomic analyses, following ETC inhibition, we observed high expression of interferon signalling, which was accompanied by downregulation of 13 genes encoded within mitochondrial DNA (mtDNA). We also directly detected a …

    queens Repository record for Mitochondrial Stress Signals Induce a Drug Tolerant Persister Phenotype in Triple Negative Breast Cancer Cell Models (opens in a new tab)

  3. Increased Oxidative Phosphorylation In An Ipsc- Derived Model of Rothmund-Thomson Syndrome Associated Osteosarcomagenesis

    … We utilized the specific inhibitor of complex I, IACS-010759, and examined the nature of oxidative phosphorylation after treatment. We found significantly decreased maximal respiration and cell proliferation after treatment at physiological doses. Transcriptional changes that occurred after …

    uthsc Repository record for Increased Oxidative Phosphorylation In An Ipsc- Derived Model of Rothmund-Thomson Syndrome Associated Osteosarcomagenesis (opens in a new tab)

  4. Cryo-EM studies of substrate and inhibitor binding to mammalian respiratory complex I

    … cancers reliant on oxidative phosphorylation (IACS-010759), the structure of mouse complex I inhibited by IACS-2858 – a tighter binding derivative – was resolved to a global resolution of 3.0 Å. The inhibitor, which bears little resemblance to ubiquinone-10 (Q₁₀), occupies the entrance to the …

    cambridge Repository record for Cryo-EM studies of substrate and inhibitor binding to mammalian respiratory complex I (opens in a new tab)