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Furthermore, we compared BSSL size variations with DC-SIGN binding capacity of breast milks.
Our results reveal that the DC-SIGN binding capacity of breast milk is highly variable among mothers as well as among groups of mothers from differing geographical regions.
After identifying variation in DC-SIGN binding capacity of breast milk derived from a group of mothers from the Netherlands, we investigated the level of variation within and between different cohorts.
The activity of such enzymes may add an additional level of complexity to the observed link between BSSL genotypes and DC-SIGN binding capacity of breast milk and enzyme expression levels may vary over time during lactation as can the post-translational glycosylation profiling which may also influence strength of binding [30].
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We investigated the association and γ-carboxylation status of GRP with microcalcifications occurring in skin and breast cancers and tested the mineral binding capacity of both protein forms, which may help understanding the mechanism behind the previously reported association of GRP with pathological mineralization.
The rs9383935 risk allele A showed decreased activity of reporter gene in both the MCF-7 and BT-474 breast cancer cell lines, which might be due to an altered binding capacity of miR-27a to the 3′ untranslated region (3′ UTR) sequence of CCDC170.
The binding capacity of tumor cells to blood vessel-lining endothelium through E-selectin was closely correlated to the metastatic capability of breast cancer cells.
Flow cytometry examination in U87-MG (human glioblastoma) and MDA-MB-231(human breast cancer) cell lines, which have moderate level and low level expression of c-MET, respectively, confirmed the specific binding capacity of rh-HGF to c-MET.
The chloride binding capacity of RAC was also analyzed.
Chloride binding isotherms reflect the chloride binding capacity of a specific cementitious material in concrete (Luping and Nilsson 1993).
Increasing the dose of biomass increased the binding capacity of the biomass.
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