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Showing 1 to 12 of 12 for “"MEK5/ERK5"”.

  1. Dual Inhibition of the PI3K/Akt and MEK5/ERK5 Pathways for the Treatment of Breast Cancer

    … crosstalk mechanisms. New evidence suggests that MEK5/ERK5, a member of the MAPK family, is a crucial component in the proliferation and survival of several aggressive cancers. We hypothesize that inhibiting both PI3K/Akt and MEK5/ERK5 pathways will decrease cell viability while maintaining …

    duquesne Repository record for Dual Inhibition of the PI3K/Akt and MEK5/ERK5 Pathways for the Treatment of Breast Cancer (opens in a new tab)

  2. Investigation of a Novel Mitophagy Regulatory Pathway and Chemical Inducer

    … for autophagy regulators to identify the MEKK3-MEK5-ERK5 pathway as a potential regulator of mitophagy in the absence of exogenous damage. Here, I provide evidence that genetic or pharmacological inhibition of the MEKK3-MEK5-ERK5 pathway increases mitochondrial content by reducing …

    tenn-hsc Repository record for Investigation of a Novel Mitophagy Regulatory Pathway and Chemical Inducer (opens in a new tab)

  3. Analysis of the role of extracellular signal regulated kinase (ERK5) in the differentiation of muscle cells

    The MEK5/ ERK5 kinase module is a relatively new discovered mitogen-activated protein kinase (MAPK) signalling pathway with a poorly defined physiological function. Since ERK5 and its upstream activator MEK5 are abundant in skeletal muscle a function of the cascade during muscle differentiation was …

    wurz-thes Repository record for Analysis of the role of extracellular signal regulated kinase (ERK5) in the differentiation of muscle cells (opens in a new tab)

  4. Studies on signaling pathways induced by FLT3, an important oncogene in AML

    … to inhibit FLT3 and to determine the role of MEK5/ERK5 signaling in FLT3-ITD mediated transformation. Using phosphospecific antibodies, we have identified 3 novel phosphorylation sites in FLT3, Y726, Y793 and Y842, and studied their kinetics and specificity. The additional eight phosphorylated …

    lund Repository record for Studies on signaling pathways induced by FLT3, an important oncogene in AML (opens in a new tab)

  5. Design, Synthesis, & Biological Evaluation of Novel Het-Aromatic/Aromatic Analogs for the Treatment of HIV, Cancer, & Cognitive Dysfunctions

    … survival, metastasis, and chemo-resistance. The MEK5/ERK5 pathway, which is a member of MAPK signaling cascade, is involved in cell survival, anti-apoptotic signaling, angiogenesis, and cell motility. It is found to be significantly upregulated in breast cancers especially triple-negative breast …

    duquesne Repository record for Design, Synthesis, & Biological Evaluation of Novel Het-Aromatic/Aromatic Analogs for the Treatment of HIV, Cancer, & Cognitive Dysfunctions (opens in a new tab)

  6. Age-Related Effects on the Mitogen-Activated Protein Kinase and Phosphatidylinositol 3-Kinase Pathways in Breast Cancer and the Characterization of Novel MEK5 Inhibitors

    … signal-regulated kinases, ERK1/2 and ERK5, of the mitogen-activated protein kinase (MAPK) pathway, and in the phosphatidylinositol 3-kinase/Akt (PI3K/Akt) pathway. Further, the role of the MEK5-ERK5 cascade in breast cancer cell proliferation, migration, and invasion was analyzed. In …

    duquesne Repository record for Age-Related Effects on the Mitogen-Activated Protein Kinase and Phosphatidylinositol 3-Kinase Pathways in Breast Cancer and the Characterization of Novel MEK5 Inhibitors (opens in a new tab)

  7. Design, Synthesis and Evaluation of Diphenylamines as MEK5 Inhibitors

    … signal-Regulated Kinase) substrate. The MEK5/ERK5 pathway is involved in cell survival, anti-apoptotic signaling, angiogenesis, and cell motility. It is significantly up-regulated in specific tumor types including breast and prostate cancers. A novel series of compounds utilizing the …

    duquesne Repository record for Design, Synthesis and Evaluation of Diphenylamines as MEK5 Inhibitors (opens in a new tab)

  8. Serine 910 Phosphorylation of Focal Adhesion Kinase Is Critical for Costamere Assembly

    … and Src via parallel Raf-1→MEK1/2→ERK1/2 and MEK5ERK5 signaling pathways. Using co-immunoprecipitation, TIRF-microscopy and FRAP, ET-1 stimulation of NRVM expressing a nonphosphorylatable, S910A-FAK mutant decreased the interaction of paxillin and vinculin within costameres. This interaction …

    loyola-thes Repository record for Serine 910 Phosphorylation of Focal Adhesion Kinase Is Critical for Costamere Assembly (opens in a new tab)

  9. KLF4 IS A KEY DETERMINANT IN THE DEVELOPMENT AND PROGRESSION OF CEREBRAL CAVERNOUS MALFORMATIONS

    … Ccm1 deletion leads to activation of the MEKK3-MEK5-ERK5-MEF2 signaling cascade resulting in a marked upregulation of the transcription factor Krüppel-like factor 4 (KLF4) in ECs in vivo. KLF4 promotes an endogenous production of bone morphogenetic protein 6 (BMP6) in ECs that, in turn, …

    milano Repository record for KLF4 IS A KEY DETERMINANT IN THE DEVELOPMENT AND PROGRESSION OF CEREBRAL CAVERNOUS MALFORMATIONS (opens in a new tab)

  10. The effect of cAMP elevation on intracellular signalling pathways in prostate epithelial cells

    … Genetic or pharmacological inhibition of the MEK5/ERK5 signalling pathway significantly attenuated the rapid cAMP-mediated changes in LNCaP cell morphology, suggesting this pathway may be a possible target by which to inhibit the onset of neuroendocrine differentiation. To summarise, this …

    glasgow Repository record for The effect of cAMP elevation on intracellular signalling pathways in prostate epithelial cells (opens in a new tab)

  11. Rho GTPases in Neuronal Apoptosis and Neurodegeneration

    … CGNs evoked apoptosis via repression of unique MEK5/ERK5, p90Rsk, and Akt-dependent pro-survival pathways. Furthermore, selective inactivation of Rac induced the activation and translocation of the pro-apoptotic BH3-only protein Bad to the mitochondria, where it has been demonstrated to induce …

    denver Repository record for Rho GTPases in Neuronal Apoptosis and Neurodegeneration (opens in a new tab)