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Even though peritectic coupled growth (PCG) has been often discussed in the literature, it remains poorly understood in comparison to eutectic coupled growth (ECG).
The early stages of growth revealed the onset of coupled growth and phase competition.
They are observed either as transients that seed the formation of coupled growth structures, or as the final microstructure.
Based on the eutectic growth and undercooling theories, the possibility of the R/α peritectic coupled growth in the rapidly solidified peritectic Fe-Mo alloy was discussed.
The measured data show sudden acceleration of crystal growth kinetics at a medium undercooling, giving evidence for a transition from coupled growth to uncoupled growth.
In agreement with previous studies, it was found that these oscillations lead to stable coupled growth only for a limited range of the control parameters.
Similar(45)
mTOR functions as a key metabolic hub, coupling growth signals to nutrient availability.
The CEBPs are important in a number of terminal differentiating systems [39]; E2Fs in promoting cell-cycle progression [40], [41]; NOTCH1 is coupling growth and differentiation [42]; SMand and LEF1 connect to TGFβ and WNT signaling [43].
Signalling mechanisms coupling growth factor receptor activation to Nox activity remain largely unknown.
The constituents of the pre-RC can be regarded as relay stations coupling growth regulatory pathways with DNA replication (Williams and Stoeber, 1999).
RLFs, which form the core of the initiation machinery, act as relay stations coupling growth regulatory and DNA damage response pathways to chromosomal replication.
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