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The in vitro plasma protein and brain tissue binding of GSK1034702 were determined in mouse, rat, dog, marmoset, monkey and human tissue by equilibrium dialysis.
The relative levels of each SHMT2 isoform was determined in mouse liver and kidney by western blot analyses (Figure 7).
Presence of the transgene was determined in mouse tail genomic DNA by PCR, using primer1 (5-CCTACGGCGTGCAGTGCTTCAGC-3) and primer2 (5-CGGCGAGCTGCACGCTGCCGTCCTC-3).
Regional expression of the GI appetite hormones CCK, PYY and GCG was also determined in mouse.
STAT1 binding profiles have been determined in mouse macrophages [ 65] and T cells [ 66].
Concentrations of RAs were determined in mouse plasma by our LC-MS method [ 24].
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Pharmacokinetics and dosimetry of 213Bi-DOTATATE was determined in mice, in combination with renal protection.
ET-1 and NOx were determined in mice to evaluate vascular endothelial function after TiO2 NP exposure.
The injurious roles of TNF-α, TLR4, and NF-κB in O3-induced lung pathogenesis have been determined in mice.
The pharmacokinetics (PK) and therapeutic effect of 2P-EPI (Mw ~ 100 kDa) were determined in mice bearing human ovarian carcinoma A2780 xenografts.
The median lethal dose (LD50) of Te NRs and potassium tellurite (K2TeO3) were determined in mice and the subacute toxicity was also evaluated.
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