Sentence examples for vitro were used from inspiring English sources

Microarrays of pre-treated cell lines either sensitive or resistant to glucocorticoid in vitro were used to define a sensitive/resistant gene signature.

Approximately one week old midbrain cells (6 8 days in vitro) were used for all experiments.

Untreated neuronal cultures at 14 days in vitro were used for this purpose, and neurons could be easily distinguished as containing either high- or low- levels of Aβ.

Synthetic DNA fragments which display high affinity for the histone octamer in vitro were used to study the relationships between the consensus tetranucleotide sequences in Figures 1 and 2 and nucleosome stability and positioning activity.

In a recent study by Bild et al. [3], gene signatures of Myc, Ras, E2F3, Src, and beta-catenin defined in vitro were used to predict Ras mutation status in human lung tumors and to predict the response of a panel of breast cancer cell lines to Src or Ras inhibitors.

ssRNA transcripts synthesized in vitro were used as template.

Chemical polysialylation in vitro was used to create a long-acting form of OXM, the polysialic acid oxyntomodulin (PSA OXM) conjugate.

Incorporation of [14C]-glucose into everted jejunal rings in vitro was used to evaluate the effect of GIP on sodium-glucose co-transporter (SGLT).

A medullary slice preparation from neonatal rat that produces inspiratory-related output in vitro was used.

The intact and mature rat sympathetic neuron in vitro is used to analyze the basic effects of the naturally released ACh.

DNA extracted from blood and methylated in vitro was used as a positive control.