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Nor does the synthesis stop there.
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If a plant is placed in a dark environment, chlorophyll synthesis stops because the gene is no longer expressed.
The accumulation of reserves in the cotyledons or elsewhere ceases, respiratory rate declines rapidly, and cell division, with associated protein and nucleic-acid synthesis, stops.
When cells are irradiated with UV, most DNA synthesis stops for at least 15 20 minutes before it continues again when the replication forks have been repaired [45].
A reasonable explanation for these observations is that the 10 µM IPTG-dependent expression of mutant RNR proteins provides a dNTP pool that is too small for the cells to be able to finish replication after rifampicin-treatment when all mRNA synthesis stops, whereas 30 µM IPTG is sufficient to provide nucleotides also for replication run-out.
In fact, CRP levels often drop rapidly when synthesis stops [ 4].
However, its synthesis stops with the induction of neutrophil maturation [ 17].
Fatty acid synthesis stops when a certain chain length is reached, and the acyl-ACP is used for membrane synthesis.
Initially starch was produced at a much higher rate than TAG, but when nitrogen starvation progressed starch synthesis stopped.
Crossing the two strains, enzyme synthesis began within a few minutes after the z + gene entered the recipient, but after an hour or so, enzyme synthesis stopped.
This implies that short sequences are not short because the strand synthesis stops prematurely, but due to a rapid decrease in the quality of the flowgram (raw sequence) resulting from early out-of-phase synthesis.
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