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It is suggested that the major evolutionary changes that have occurred in the transition from ancestral haemoglobins to non-symbiotic haemoglobins and leghaemoglobins are a hexacoordinate to pentacoordinate haem transition, decrease in the CD-loop and N- and C-termini, and protein compaction into a globular structure.
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The temperature/magnitude of the melting transition decreased upon inorganic modification.
Thus, the external energy required for this transition decreases (i.e., W C1 becomes less negative) in order to maintain all three transitions at the same rate.
The most abundant DLF1 expression is found in the SAM, and it peaks during vegetative-to-reproductive phase transition, decreasing gradually during inflorescence development.
In compatible phase status, the presence of KGM prolonged the gelation to occur for disordering the gelatin coil-helix transition, decreased the gel strength.
The temperature of the ferroelectric phase transition decreases at a reduction of average pore diameters and the temperature interval of stability of ferroelectric phase essentially enlarges.
Increasing activation energy was obtained for diamond powders of increasing sizes, and the critical pressure of the diamond to graphite phase transition decreased.
When the amount of Zr4 + increased up to 2 wt%, the critical temperature of phase transition decreased to 50 °C while the visible optical transmissivity almost remained the same.
According to structural phase diagram of the related LaAlO3 SrTiO3 system [15], the temperature of rhombohedra-to-cubic transition decreases almost linearly from 850 K in "pure" LaAlO3 to 350 K in the sample with nominal composition La0.2Sr0.8Al0.2Ti0.8O3.
Significantly, though the thermal hysteresis of the first-order transition decreases with the measurement field, collapse of such a behavior to a critical point is not observed in LTC, unlike earlier observations in some other manganites.
As x values increased from 0.0 to 0.125, a dielectric temperature-dependent anomaly consistent with a phase transition decreased linearly from 528 K for the pure BiVO4 end member to 264 K for the solid-solution composition at x = 0.125.
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