Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Table 1.

HPLC gradient parameters used to separate tamoxifen and its metabolites using a ZORBAX Eclipse XDB-C18 column (150 mm x 2.1 mm I.D., 3.5 µm) at 30°C.

More »

Table 1 Expand

Table 2.

HPLC and MS parameters used to discriminate tamoxifen and its metabolites.

More »

Table 2 Expand

Table 3.

CYP2D6, CYP3A4, CYP3A5, SULT1A1, SULT1A2 and SULT1E1 genotype frequencies.

More »

Table 3 Expand

Table 4.

CYP2D6, CYP3A4, CYP3A5, SULT1A1, SULT1A2 and SULT1E1 allele frequencies. International codes for SNPs between parentheses.

More »

Table 4 Expand

Table 5.

Concentrations of tamoxifen and its metabolites (means (±SD), medians (in cursive) and ranges (in parentheses)) detected in patients with the CYP2D6, CYP3A4 and CYP3A5 genotypes.

More »

Table 5 Expand

Table 6.

Concentrations of tamoxifen and its metabolites (means (±SD), medians (in cursive) and ranges (in parentheses)) detected in patients with the SULT1A1, SULT1A2 and SULT1E1 genotypes.

More »

Table 6 Expand

Figure 1.

Concentrations of tamoxifen and its metabolites (means ± standard deviations, ng/mL) by CYP2D6 and SULT1A2 genotype subgroups established according to wt allele doses.

Sample sizes: CYP2D6: wt/wt = 80; wt/v = 30; v/v = 11//SULT1A2: wt/wt = 38; wt/v = 49; v/v = 34.

More »

Figure 1 Expand