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These stages were selected based on the selective changes that take place during the elaboration of the mesocorticolimbic DA circuitry [21][22][23][24][25].
Fifteen ten-week-old female SD rats (200 250 g, Vitalriver Inc., Beijing, China), in similar development stages, were selected as the animal model.
A pair of images, one each from pre- and postcontrast stages, were selected such that they had very little motion between them as confirmed by observers and manual registration parameters.
HIV-seropositive patients from all disease stages were selected, including those with acute disease, chronic antiretroviral untreated disease and long-term antiretroviral treated disease.
These stages were selected since the TUNEL assay indicated that there was no increase in apoptotic cell death in the bud stage, with apoptosis starting to increase at the mid-somite stage.
Parasites in mid-trophozoite (25 hpi) stages were selected for polyamine extraction.
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In addition, two small East African goats in the mid lactation stage were selected in each herd for milk yield measurements.
Several predictive models based on preoperative prostate specific antigen level, biopsy Gleason score, and clinical stage were selected to predict those men having a > or =20% probability of lymph node involvement.
An additional 18 SNPs with Pper-allele<0.05 in the discovery stage were selected for replication in a subset of five OCAC studies (n = 1,233 serous invasive cases; n = 3,364 controls).
Statistically-determined differentially expressed genes (Benjamini p-value of <0.05) at each transitional stage were selected for further analysis.
The 11 most significant SNPs p-values<0.001 p-values<0.001covery stage were selected fromreplicathen in indiscovery stagees.
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CEO of Professional Science Editing for Scientists @ prosciediting.com