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A new pressure sequence for mercury porosimetry is introduced to generate further information on pore topology.
Animals were ventilated with a standard pressure sequence of 35/0 (peak-insufflation pressure [cmH2O]/PEEP [cmH2O]) for 1 min, 23/3 for 15 min, 18/3 for 5 min, 13/3 for 5 min and 23/3 for 5 min.
With the availability of a high pressure sample gas at the hydrogen refueling stations, the device uses only a pressure sequence to enrich the impurities without need of a temperature cycle.
The mini-hysteresis loops produced by this pressure sequence provide the information which distinguishes between the two possible values of connectivity for the network structure and allow a more accurate determination of the characteristics σ and μ for the pore size distribution.
If the calculations are followed for an increasing pressure sequence at the temperature T=180 K, the transition is found to be centered at p ↓ =84.3 MPa, whereas the transition pressure for decreasing pressure calculations is significantly lower, being centered at p ↑ =53.6 MPa.
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Since during the course of evolution GC dinucleotides are usually lost, this analysis suggests that there is a high evolutionary pressure for sequence conservation of OXPHOS promoter sequences, and these conserved stretches of DNA probably reflect important transcriptional regulatory elements, and possible nucleosome positioning that would contribute to transcriptional regulation [ 33].
Blood Pressure: 1 sequence.
The first root of Eq. (15), θ 1, was obtained for every pressure equilibration sequence.
After curing, the gels were directly dried for 24 h at room temperature in air, 24 h at 50 °C, and 3 h at 100 °C at ambient pressure in sequence.
In such models selection is modeled explicitly, allowing for variation of selection pressure across sequence sites and over time.
Numerous studies have observed the expected decreased selective pressure on sequence conservation after duplication through comparisons of synonymous and non-synonymous nucleotide substitutions [ 54].
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