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PCR products of 305 and 446 bp were derived from wild-type and mutant alleles, respectively.
Arterial SBP (systolic BP) and DBP (diastolic BP) were derived from the BP waveform and are given in mmHg.
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3B-399 (6058–6456 bp) was derived from 3B-531 by removing the 5'-region 5'-regionnd SmaI digestion, and 3by206 waSacInerandd by exonucleaSmaIII digestion of 3B-226 followed by recirculandzation.
The 37-gene aligned matrix contained 15,495 bp, of which 11,340 bp was derived from the 13 PCGs, 2,528 bp from the two rRNA genes, and 1,627 bp from the 22 tRNA genes.
There are numerous TE-derived HS sites in the human genome: 3,229 HS sites (~23%) include TE sequence and 11% of all positions covered by HS sites (454,564 bp) are derived from TEs.
BP cells were derived from L, by benzo[a]pyrene treatment.
This central cassette was flanked by homology arms (HA) of approximately 600 800 bp that were derived from sequences in the vicinity of exon-7.
Under the optimized PCR conditions (annealing temperature of 55 °C) the product targets approximately 550 and 400 bp in length, were derived from inverse PCR and 5′-RACE, respectively.
Means and standard deviations of GHb (6.9 ± 1.2%) and systolic BP (140.6 ± 18.3 mmHg) were derived from the German DETECT study [ 13].
After this filtration, 6896 cofunctional associations among 1474 genes were derived from GO-BP annotations.
Systolic blood pressure was measured by the tail-cuff system (Softron BP-98A; Softron, Tokyo, Japan), and values were derived from an average of 6 8 measurements per animal at each time point.
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