Matches in Nanopublications for { ?s ?p "Long term incubation with IL-6 has been shown to increase basal glucose transport in 3T3-L1 adipocytes, whereas acute stimulation had no effect IL-6 transiently (30-90 min) increased SOCS-3 expression in HepG2 cells and rat liver cells and that this was associated with an impaired effect of insulin to increase IRS-1 tyrosine phosphorylation, p85 binding, and downstream PKB/Akt phosphorylation." ?g. }
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- _5 value "Long term incubation with IL-6 has been shown to increase basal glucose transport in 3T3-L1 adipocytes, whereas acute stimulation had no effect IL-6 transiently (30-90 min) increased SOCS-3 expression in HepG2 cells and rat liver cells and that this was associated with an impaired effect of insulin to increase IRS-1 tyrosine phosphorylation, p85 binding, and downstream PKB/Akt phosphorylation." provenance.
- _7 value "Long term incubation with IL-6 has been shown to increase basal glucose transport in 3T3-L1 adipocytes, whereas acute stimulation had no effect IL-6 transiently (30-90 min) increased SOCS-3 expression in HepG2 cells and rat liver cells and that this was associated with an impaired effect of insulin to increase IRS-1 tyrosine phosphorylation, p85 binding, and downstream PKB/Akt phosphorylation." provenance.
- _7 value "Long term incubation with IL-6 has been shown to increase basal glucose transport in 3T3-L1 adipocytes, whereas acute stimulation had no effect IL-6 transiently (30-90 min) increased SOCS-3 expression in HepG2 cells and rat liver cells and that this was associated with an impaired effect of insulin to increase IRS-1 tyrosine phosphorylation, p85 binding, and downstream PKB/Akt phosphorylation." provenance.
- _5 value "Long term incubation with IL-6 has been shown to increase basal glucose transport in 3T3-L1 adipocytes, whereas acute stimulation had no effect IL-6 transiently (30-90 min) increased SOCS-3 expression in HepG2 cells and rat liver cells and that this was associated with an impaired effect of insulin to increase IRS-1 tyrosine phosphorylation, p85 binding, and downstream PKB/Akt phosphorylation." provenance.