To strengthen these results additional cell lines were assessed.
Finally, the radiation response of two tumor lines were assessed in vivo.
To explore novel antitumor agents with high efficiency and low toxicity, a series of NO-donating scutellarin derivatives (14 17) were synthesized and the antiproliferative activities against MCF-7, HCT-116, PC-3 and HepG2 cancer cell lines were assessed.
Differences in total proportions of infected plants between the treatment and control groups, and between lines, were assessed using single and mixed effects generalized linear models and corresponding analyses of variance, assuming a binomial response and with the respective addition or subtraction of 0.5 for 0 or total infections.
METHODS: Levels of Sp1, Sp3, Sp4, and VEGF proteins in pancreatic cancer cell lines were assessed by immunoblot analysis.
Ventricular size and function of the two transgenic lines were assessed using echocardiography.
Four human AML cell lines were assessed for their sensitivity to daily treatment with AZA or DAC in 72 hour cell viability assays (Figure 1, Figure S1).
The cell lines were assessed for frameshift mutations in a selection of genes with cMS previously reported to develop mutations in MSI-High colon cancers.
Correlations between %HMGCR13 with %LDLR12 and %LDLR4 among statin or 25-hydroxycholesterol treated immortalized lymphoblast cell lines were assessed by linear regression.
The differentiation capacities of PRLR KO and WT cell lines were assessed in order to decipher the molecular events by which PRLR signaling contributes to the commitment to the brown adipose phenotype.
Supernatants of antigen specific T cell lines were assessed for cytokine concentrations with standard ELISA technique (R&D systems) or cytometric bead array (Bender systems) according to the manufacturers' recommendations.
