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The resulting pie graph indicated strain differences in the distribution of syllable categories (Fig. 1c).
Both gene content and codon usage indicated strain evolution in the infant gut from an early colonizer to late colonizer phenotype.
Statistical analysis of the 11 genes (without multiple test correction) indicated strain differences with a p-value of 0.00022 or less.
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Cadmium measurements in lung tissue indicated strain-dependent differences in disposition of QDs in the lung.
b The indicated strains were grown in liquid THY (sucrose+) flasks for 24 h, and the cell density was determined by measuring the OD660.
This result indicated strain-specific effects of genetic ablation of GSK-3α on glucose metabolism and led us to generate tissue-specific deletions of GSK-3α on the ICR background.
Unless otherwise indicated strains were grown to exponential phase in yeast extract peptone dextrose (YEPD) or synthetic complete media.
The indicated strains were also 10-fold serial diluted and spotted on SC plates or SC-R plates containing the indicated concentration of canavanine.
Unless otherwise indicated, strains were grown using LB agar plates, LB agar brothor Tryptic Soy agar containing 5% sheep's blood (SBA, HealthLink) at 37°C.
The comparison of P. acnes strains indicated strain-specific uptake efficiencies.
These data already indicated strain-specific differences in the gene repertoires of both C. ulcerans isolates.
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