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Amino-acids. --- Mice. --- Tyrosine.
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Blockade. --- Endogenous. --- Norepinephrine. --- Tyrosine.
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Dissertations --- Tyrosine --- Medical sciences
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This dissertation by Amanda Nordigården focuses on the FLT3 tyrosine kinase receptor's role in acute myeloid leukemia (AML). It explores the mutations of FLT3, particularly internal tandem duplications (FLT3-ITD), which are frequently observed in AML and are associated with poor prognosis and relapse. The research investigates the signaling pathways and drug resistance mechanisms in FLT3-ITD mutations, aiming to improve therapeutic strategies. Key findings include the identification of apoptotic mechanisms and the potential of canertinib, a pan-ERBB inhibitor, as a treatment option. The work contributes to the understanding of FLT3 mutations and their impact on AML treatment, offering insights into potential therapeutic advancements.
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Swine --- Farmyard manure --- Tyrosine
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PROTEIN-TYROSINE KINASE --- TYRPHOSTINS --- PROTEIN-TYROSINE KINASE --- TYRPHOSTINS
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[Development of the new treatments for systemic sclerosis: tyrosine kinase inhibitors versus immunotherapy] Systemic sclerosis is an autoimmune disease involving progressive skin fibrosis, inflammation and microvascular disorders. The spread of the sclerosis to various internal organs causes their dysfunction. The involvement of cellular and humoral immunity justified the use of immunosuppressive therapy. However, the results obtained with them are insufficient to allow healing. Recently, the identification of tyrosine kinases as new targets involved in the pathophysiological process has motivated the use of specific inhibitors. Despite clearly demonstrated benefits in vivo, first efficacy and safety clinical trials obtained with imatinib are mixed. The development and testing of more targeted inhibitors will be followed with interest La sclérose systémique est une maladie évolutive auto-immunitaire impliquant une fibrose cutanée, des phénomènes inflammatoires et des anomalies microvasculaires. La propagation de la sclérose à divers organes internes provoque leur dysfonction. L’implication de l’immunité cellulaire et humorale a justifié l’usage de traitements immunosuppresseurs. Les résultats obtenus avec ceux-ci sont toutefois insuffisants pour permettre une guérison. Plus récemment, l’identification des tyrosines kinases comme nouvelles cibles impliquées dans le processus physio-pathologique, a motivé l’emploi d’inhibiteurs spécifiques. Malgré des avantages démontrés in vivo, les résultats en essais cliniques concernant l’efficacité et la sécurité obtenus avec l’imatinib sont mitigés. Le développement et l’essai d’inhibiteurs plus ciblés devront être suivis avec intérêt
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