Exact(1)
We identified differentially expressing miRNAs and mRNA at a various time schedules (0, SCI 24 h, 48 h, 72 h, 1 week) via DNA microarray and real-time reverse transcription (RT -PCR confiRT -PCR.
Similar(59)
Cell counts and viability were determined by trypan blue exclusion counting on a hemocytometer at various time intervals.
Cell counting and viability assay were performed using trypan blue dye and a hemocytometer at various time points including 0, 0.5, 1, 2, 4, 6, and 8 h.
(A) shows responses at various time points after i.v. administration of 1.7 kBq 211At.
All-cause mortality was coded as a binary variable at various time points: 30, 90, 180 and 365 days.
The width of the wound area was monitored with an inverted microscope at various time points.
Cell counts were performed using a Z1 particle counter at various time points.
At various time points, a sample was removed from the reaction mixture and analyzed as described above (Glycosylase Activity Assays).
At various time points, a P with H decoupling NMR spectrum was collected using Bruker AV-400 MHz NMR.
The turbidity value was measured at various time intervals using a HACH turbidimeter model 2,100 N.
After treatment, the tumor volume was monitored by measuring the tumor dimensions at various time points using a caplier.
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