Weekly, mice were monitored for tumor size and evidence of morbidity related to the primary tumor or pulmonary metastases.
The mice were then awakened and their foot pad monitored for tumor size and signs of pain or ulceration twice a week.
All mice were monitored for tumor size and survival.
Our results do emphasize that stable but small populations (e.g., prairie chicken, Mauritius kestrel) that are often currently only monitored for population size should undergo genetic monitoring to evaluate the success of these programs.
Experiments were monitored for plant size and growth, and then at the end of the experiments, root and shoot mass, different measures of water-use efficiency (WUE) and shoot GS levels were recorded.
The four individual RNAseq libraries were monitored for insert size using the Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA) and validated regarding sequence content by cloning an aliquot of each library into a plasmid vector (Zero Blunt TOPO PCR cloning kit, Invitrogen, Darmstadt; Germany) followed by sequencing of 40 randomly selected clones from each sublibrary.
Animals fed with ±Doxycline (Dox) diet (200 mg/kg; Bio-Serv, Flemington, NJ) were monitored for tumor sizes using the Maestro™ In-Vivo Imaging System (CRi, Woburn, MA), as described in the approved Georgetown University IACUC protocol.
Moreover, using small juvenile C. concholepas of ca. 20 mm of peristomal length, collected in the field, we monitored for the body size and live weight traits in laboratory and field rearing conditions.
Cells were monitored for appropriate colony size and re-fed every three to four days.
The number of persistently infected (PI) animals imported and the probability of BVDV introduction were monitored for three herd sizes, four import profiles, and six testing strategies.
