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In conclusion, our data has identified a previously unrecognized role for TAMs in contributing to the increased production of CCL20 that recruits CCR6+ Treg-cells and promotes CRC development in mice.
Our data has identified a low uptake of these MBS-funded items by eligible patients in the practice, despite a recent focus on preventive health care, as evidenced by significant government investment in the establishment of an Australian National Preventive Health Agency [ 32].
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But, of critical import, our data have identified a surprising level of within-species divergence and lays bare these differences to further study.
Our data have identified a promoter region derived from PB103464.00.0 that is able to direct exclusively liver-stage expression of genes of interest.
Our data have identified important Mφ cell surface CD4-interacting proteins, as well as regulatory proteins involved in internalization and degradation.
Our data have identified one important cellular deficit that potentially constitutes a major pathogenesis process, namely a reduction in GJ-mediated glucose transfer in the cochlea of Cx30 mutant mice.
Our data have identified an important role for BX647187 in human PCa development and progression.
Our data have identified a novel role for E-cadherin in differentiation of LCs.
Thus, our data have identified a new region involved in the prognosis of osteosarcomas.
Our data have identified Npnt as a crucial regulator of AV canal differentiation and ECM composition by controlling Bmp4-Has2 signaling.
While our data have identified significant transport barriers of adiponectin across endothelium in vitro, our in vivo studies have demonstrated minimal changes in adiponectin uptake into skeletal muscle.
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CEO of Professional Science Editing for Scientists @ prosciediting.com