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We hypothesized that the combination of a proliferating factor (fibroblast growth factor 2) and a differentiating hormone (dexamethasone) would allow us to induce spleen-derived stromal cells to proliferate and at the same time to express osteoblast-specific genes.
Macrophages isolated from ascites stimulate angiogenesis in vitro in chorioallantoic membrane of chicken embryos and release proliferating factor for human umbilical vein endothelial cells (HUVEC) [ 4].
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For neuronal differentiation, neurospheres were plated on laminin-coated glass coverslips in NBN media without proliferating factors.
IL4 and IL13 have a key role in the induction of IgE switching by stimulating transcription from the germline promoter site of IgE, via STAT6 sites, 23 and are also B cell proliferating factors.
The fact that miRNAs could act as cell proliferating factors in certain cancers and apoptotic factors in another has evoked the necessity of studying their cooperative functions in order to provide a holistic picture of miRNA regulations in cancer biology and pathogenesis.
This is achieved through a series of stepwise acquisitions of key abilities, such as disrupting signaling pathways, inactivating control mechanisms like apoptosis and the immune response, gaining access to unlimited proliferating factors as well as acquiring mobility and the potential to colonize new tissues [ 32].
Serum, inflammatory cytokines IL-1α and IL-1β and the neural progenitor cell (NPC) proliferating growth factors bFGF and PDGF all increased the number of reactive cells on the gel, in agreement with their reported roles in cell activation, migration and proliferation at the site of injury.
One InDel marker (CID_C_477164) in the CDS of a TCP [Teosinte branched 1 (tb1) Cycloidea, Proliferating cell factor (PCF)] transcription factor (TF) gene localized at CaqDF1.1 and CaqDM1.1 QTL region was associated strongly (R: 25.8 28.6% at 9.8 10.7 LOD) with DF and DM traits (Table 2, Fig. 4B).
Lamin B has been shown to be involved in replication, as it localizes with the replication factor proliferating cell nuclear antigen (PCNA) in the replication machinery during late S phase [ 29].
Among the genes being downregulated, the cell-cycle regulating kinases ERK1, CDC-like kinase 3, cyclin-dependent kinase 10 and the DNA-replication factor proliferating cell nuclear antigen (PCNA) were found.
Binding between the processivity factor proliferating cell nuclear antigen (PCNA) in complex with an inhibitory protein called TIP identified regions involved in binding between TIP and PCNA, and the authors concluded that TIP binding disrupts the PCNA trimer formation and decreases its activity.
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