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    Multiple myeloma remains largely incurable. However, a few patients experience more than 10 years of relapse-free survival and can be considered as operationally cured. Interestingly, long-term disease control in multiple myeloma is not restricted to patients with a complete response, since some patients revert to having a profile of monoclonal gammopathy of undetermined significance. We compared…

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    • Analysis Of The Immune System Of Multiple Myeloma Patients Achieving Long-Term Disease Control By Multidimensional Flow Cytometry [Jan 2013] Pessoa deMagalhães @haematologica https://t.co/VnDFerZhvf #mmsm #ImmunoOnc #IDonc https://t.co/jErhgNL2bp

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    Protection from acute lymphoblastic leukemia relapse in the central nervous system (CNS) is crucial to survival and quality of life for leukemia patients. Current CNS-directed therapies cause significant toxicities and are only partially effective. Moreover, the impact of the CNS microenvironment on leukemia biology is poorly understood. In this study we showed that leukemia cells associated with…

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    • #Leukemia cells associated with the meninges of xenotransplanted mice, or co-cultured with meningeal cells, exhibit enhanced chemoresistance due to effects on both apoptosis balance and quiescence. https://t.co/v3grbKKC4w https://t.co/KmS15YORTt

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    There is prevailing evidence to suggest a decisive role for platelet-derived growth factors (PDGF) and their receptors in primary myelofibrosis. While PDGF receptor β (PDGFRβ) expression is increased in bone marrow stromal cells of patients correlating with the grade of myelofibrosis, knowledge on the precise role of PDGFRβ signaling in myelofibrosis is sparse. Using the Gata-1low mouse model for…

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    • Protein tyrosine phosphatases represent previously unrecognized contributors that control #PDGF signaling in #myelofibrosis. https://t.co/qcXNhTrhIN https://t.co/PgILJuCChE

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    Alterations of the tumor suppressor gene TP53 are found in different cancers, in particular in carcinomas of adults. In pediatric acute lymphoblastic leukemia (ALL), TP53 mutations are infrequent but enriched at relapse. As in most cancers, mainly DNA-binding domain missense mutations are found, resulting in accumulation of mutant p53, poor therapy response, and inferior outcome. Different…

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    • The strong and selective anti-leukemia activity of APR-246 in TP53-mutated ALL provides the basis to develop personalized therapy regimens for this high-risk subgroup of ALL. https://t.co/TvYTOPVIFu https://t.co/RyZwpfzIi4

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    Over the last 100 years the role of platelets in hemostatic events and their production by megakaryocytes have gradually been defined. Progressively, thrombocytopenia was recognized as a cause of bleeding, first through an acquired immune disorder; then, since 1948, when Bernard-Soulier syndrome was first described, inherited thrombocytopenia became a fascinating example of Mendelian disease. The…

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    • If you are looking for an outstanding, comprehensive and up to date review of Inherited Thrombocytopenia you will be hard pushed to find anything better than this one from the Nurdens. The PDF is free but I can not link to it directly. https://t.co/jKyPkulUeY https://t.co/mxLXc8B3wl