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Although the cause for bone marrow fibrosis in patients with myelofibrosis remains controversial, it has been hypothesized that it is caused by extensive fibroblast proliferation under the influence of cytokines generated by the malignant megakaryocytes. Moreover, there is no known drug therapy which could reverse the process. We studied the fibroblasts in a novel system using the hanging drop method, evaluated whether the fibroblasts obtain from patients are part of the malignant clone of not and, using this system, we screen a large library of FDA‐approved drugs to identify potential drugs candidates that might be useful in the treatment of this disease, specifically which would inhibit fibroblast proliferation and the development of bone marrow fibrosis. We have found that the BM fibroblasts are not part of the malignant clone, as previously suspected and two immunosuppressive medications—cyclosporine and mycophenolate mophetil, as most potent suppressors of the fibroblast collagen production thus potentially inhibitors of bone marrow fibrosis production in myelofibrosis.  相似文献   
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Cuphea luteola is described from cerrado vegetation in Noel Kempff Mercado National Park, eastern Bolivia. It is assigned to sectionEuandra subsectionOidemation and is distinguished by yellow flowers, linear uninerved leaves, and the inner surface of the floral tube pilose and without vesicles. Several species of the subsection share one or more characters withC. luteola, but none are closely similar.  相似文献   
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Sla2p, also known as End4p and Mop2p, is the founding member of a widely conserved family of actin-binding proteins, a distinguishing feature of which is a C-terminal region homologous to the C terminus of talin. These proteins may function in actin cytoskeleton-mediated plasma membrane remodeling. A human homologue of Sla2p binds to huntingtin, the protein whose mutation results in Huntington's disease. Here we establish by immunolocalization that Sla2p is a component of the yeast cortical actin cytoskeleton. Deletion analysis showed that Sla2p contains two separable regions, which can mediate association with the cortical actin cytoskeleton, and which can provide Sla2p function. One localization signal is actin based, whereas the other signal is independent of filamentous actin. Biochemical analysis showed that Sla2p exists as a dimer in vivo. Two-hybrid analysis revealed two intramolecular interactions mediated by coiled-coil domains. One of these interactions appears to underlie dimer formation. The other appears to contribute to the regulation of Sla2p distribution between the cytoplasm and plasma membrane. The data presented are used to develop a model for Sla2p regulation and interactions.  相似文献   
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Benefits and costs of group living may be differentially influenced by kinship or familiarity and depend on context. For example, aggregation with kin may be costly in a mating context due to the risk of inbreeding, but beneficial in social interactions because it may reduce within‐group competition. Research investigating aggregation behaviour in different contexts is scarce, especially in gregarious invertebrates. In the present study, we investigated the aggregation among adult European earwigs (Forficula auricularia) by comparing the aggregation behaviour of groups composed of individuals from two different families with the aggregation dynamics of groups composed of individuals from the same family (siblings). Aggregation behaviour was measured both during the night (active phase) and during the day (inactive phase). Our results showed enhanced aggregation among individuals from the same family at night, but lack of such preferences during the day. These findings demonstrate that earwigs are able to recognize familiar relatives and that this information is used for aggregation decisions at night, while they are most active, but not during the day when they rest.  相似文献   
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