Mostrando 119,541 - 119,560 Resultados de 120,423 Para Buscar '"apoptosis"', tiempo de consulta: 0.81s Limitar resultados
  1. 119541
    “…Results support a mechanistic basis for the importance of SOD2 in proliferation and apoptosis of mesothelial cells and its potential use as a biomarker of early responses to mesotheliomagenic minerals.…”
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  2. 119542
    “…Monoclonals that we were able to develop from tumor specific proteins derived from colon and pancreas cancer were found capable of targeting those tumors to induce apoptosis. We were also able to define immunogenic membrane proteins from lung (squamous and adenoCa) as well as prostate neoplasms. …”
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  3. 119543
    “…Studies have shown that miRNAs play a critical role in human cancer and they can influence the level of cell proliferation and apoptosis by modulating gene expression. Currently, methods for the detection and measurement of miRNA expression include small and moderate-throughput technologies, such as standard quantitative PCR and microarray based analysis. …”
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  4. 119544
    “…BACKGROUND: The tumor suppressor gene p53 is involved in multiple cellular pathways including apoptosis, transcriptional control, and cell cycle regulation. …”
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  5. 119545
    “…The loss of cell viability induced by SHP2 silencing could not be explained by a significant increase in apoptosis alone as demonstrated by terminal deoxyribonucleotidyl transferase-mediated nick-end labelling and propidium iodide staining. …”
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  6. 119546
    “…Galectin-3 is multifunctional protein, which is involved in regulation of cell growth, cell adhesion, cell proliferation, angiogenesis and apoptosis. Cyclin D1 together with other cyclin plays an important role in cell cycle control. …”
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  7. 119547
    “…Moreover, 1,25(OH)D has anti-proliferative and pro-differentiation effects in human melanoma cells. 1,25(OH)D has been shown to induce apoptosis in human melanoma cell lines and has an inhibitory effect on the spreading of melanoma cells in vitro. …”
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  8. 119548
  9. 119549
    “…The A431 parental cells acutely treated with Ctx rapidly activated FGFR3 and their concomitant exposure to Ctx and PD173074 resulted in synergistic apoptosis. CONCLUSION: Cross-suppression of AREG/EREG expression may explain the tight co-expression of AREG and EREG, as well as their tendency to be more highly expressed than other EGFR ligands to determine Ctx efficacy. …”
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  10. 119550
    por Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F.J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A., de Bruijn, Renée F.A.G., Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J., Chibnik, Lori B., Gislason, Gauti K., Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B., Phan, Thanh G., Oostra, Ben A., Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Wright, Margaret J., Franke, Barbara, Martin, Nicholas G., Thompson, Paul M., Nalls, Michael A., Uitterlinden, Andre G., Au, Rhoda, Elbaz, Alexis, Beare, Richard J., van Swieten, John C., Lopez, Oscar, Harris, Tamara B., Chouraki, Vincent, Breteler, Monique M.B., De Jager, Philip L., Becker, James T., Vernooij, Meike W., Knopman, David, Fazekas, Franz, Wolf, Philip A., van der Lugt, Aad, Gudnason, Vilmundur, Longstreth, W.T., Brown, Mathew A., Bennett, David A., van Duijn, Cornelia M., Mosley, Thomas H., Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J., Ikram, M. Arfan, Seshadri, Sudha
    Publicado 2012
    “…These associations implicate genes related to apoptosis (HRK), development (WIF1), oxidative stress (MSR3B), ubiquitination (FBXW8), enzymes targeted by new diabetes medications (DPP4), and neuronal migration (ASTN2), indicating novel genetic influences that influence hippocampal size and possibly the risk of cognitive decline and dementia.…”
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  11. 119551
    “…These systems provide insights regarding the emergence of key systems at different points in eukaryotic evolution, such as ADP ribosylation, interaction of myosin VI with cargo proteins, mediation of apoptosis, hyphal heteroincompatibility, hedgehog signaling, arthropod toxins, cell-cell interaction molecules like teneurins and different signaling messengers. …”
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  12. 119552
    “…Peripheral blood mononuclear cells (PBMC) were stimulated by rIL-21 (100 ng/ml) in the presence or absence of anti-CD40 and/or anti-IgM, and changes of IL-21R, activation-associated surface markers (CD25, CD69 and CD40), the proliferation, apoptosis and differentiation of B cells were analyzed by flow cytometry. …”
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  13. 119553
    “…The mRNA expression level of tumor protein T53 and transforming growth factor beta receptor 1 were found significantly reduced in critically ill patients, whereas the expression of Janus kinase 2, caspase 3 apoptosis-related cysteine peptidase, interleukin 10, and myxovirus resistance 1 were extremely increased in critically ill patients. …”
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  14. 119554
  15. 119555
  16. 119556
  17. 119557
    “…Inversely, PEDF–DTX-5 mg/kg and PEDF–CTX-10 mg/kg delayed the most CL1 tumor growth (15, 11 and 5 days for PEDF–DTX-5 mg/kg, PEDF–CTX-10 mg/kg and single treatments, respectively) with elevated apoptosis and serum thrombospondin-1 as possible mechanism and marker, respectively. …”
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  18. 119558
    “…ADORA3 is instead involved in the induction of p53-mediated apoptosis in lung cancer cell lines. Since in our model p53 is inactivated, ADORA3 does not negatively affect tumor growth but remains expressed on tumor cells. …”
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  19. 119559
    “…The treatment of HNSCC with a specific inhibitor of c-Src, initially resulted in reduced Stat3 and Stat5 activation and subsequently an arrest of cell proliferation and increased apoptosis. However, the inhibition of c-Src only caused a persistent inhibition of Stat5, whereas the inhibition of Stat3 was only transient. …”
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  20. 119560
    “…Moreover, this mitotic delay enhanced chromosomal abnormalities and apoptosis. CONCLUSIONS: We have identified NUP214, a member of the massive nuclear pore complex, as a novel miR-133b target. …”
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