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Gradients of group I and II metals across membranes represent a classical way to store potential energy, and these ions play roles in osmotic regulation, generation of action potentials, and signaling.
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These were turned over to artificial monopolies and rate regulation generations ago.
Pseudogene transcripts can provide a novel tier of gene regulation through generation of endogenous siRNAs or miRNA-binding sites.
In protonemata, transcript accumulation was increased in genes involved in cell wall synthesis, photosynthetic processes, carbohydrate biosynthesis, cellular morphogenesis, cell size regulation, cell generation, cell cycle processes, and cytokinesis (Supplementary Figure S1; Supplementary Table S1).
Regulation and generation of ROS is controlled by the oxidoreductase enzymes.
This result indicates that 3'UTR regulation in generation of iPS cells from somatic cells is largely reversal of that in embryonic development.
This result indicates that the direction and extent of 3'UTR regulation in generation of iPS cells reflect the difference between source cells and iPS cells.
These ΨEs may function in gene regulation through generation of transcribed pseudogenes, or regulatory alternate transcripts.
The mechanism(s) of actions appears to be via cell cycle regulation, ROS generation, NF-kB inhibition and ATX inhibition.
Synonymous codons may also play a role in gene regulation and generation of the correct protein conformation [ 6- 8].
These transcriptional regulatory elements are capable of achieving tissue specific transgene expression, improved transcriptional regulation, and generation of multimeric pri-miR activators of RNAi [ 11, 12].
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