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A description that appears to refer to a similar effect of the gap phase can be found in Tanemura & Lang (1973 ▸).
At this stage of the discussion on the plane-wave image, the gap phase in the second term in the cosine function in equation (39) does not significantly affect the moiré-fringe pattern under discussion.
It was found that, when the front crystal of a bicrystal is strained, significant modification to the moiré fringe pattern can occur owing to the local variation of the gap phase caused by the strain.
The activation of these two cellular processes (transcription and protein biosynthesis) revealed a global increasing in the cell metabolism in response to the L. intracellularis infection and it has also been described to occur during the gap phase 1 (G1) of the host cell cycle [ 22].
The fringes are inclined as if the intrinsic moiré pattern has a parallel component (Δ d/ d), but that is in reality due to the contribution from the gap phase, which varies with x, being caused by the variation of u in equation (47).
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The syncytial nuclear cleavage cycles are non-canonical mitotic cycles lacking the gap phases as well as cytokinesis.
Cyclin D1 is an important regulator in the early stages of the cell cycle, controlling the transition from the first gap phase to the synthesis phase.
Furthermore, the above gap phase does not agree with their gap phase ' '.
Cell cycle lengthening occurs via the introduction of a gap phase for the first time to the cell cycle, G1 in Xenopus and G2 in Drosophila [reviewed in [2]].
The small scale gap phase cycles would operate as nested dynamics within larger scale infrequent non-stand-replacing disturbance cycles that occur at landscape scale.
The resting (contractile) myocyte is maintained in a non-proliferative gap phase (G0); the activated myocyte enters the G1 phase where the necessary elements are assembled to permit entry into the synthetic phase (S phase) of DNA replication.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com