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The CREB family contains activators and repressors that may interact through positive and negative feedback loops.
Presumably this relates to a combination of: (a) insufficient time available for initial instabilities to evolve into a steady state; (b) primary α-branches may interact through solute diffusion in the confined sample volume; (c) the inevitable presence of thermo-solutal flow; and (d) a long-term sample position dependent drift in the furnace to sample heat transfers.
Therefore, MDSCs and Treg cells may interact through indirect ways in tumor microenvironment.
Importantly, such proline-rich regions act as ligands for SH3 domains, raising the possibility that Dvl and Grb2 may interact through their respective proline-rich and SH3 domains.
These cell types may interact through direct contact, but soluble mediators are also likely to be critical.
Together, these findings indicate that brain evolution and trophic adaptations may interact through phenotypic integration of brain size and head shape.
Similar(52)
Since the 9E10 and A14 antibodies both recognized the C-terminal domain of the Myc protein while the N262 and the 3C7 are directed versus the N-terminus of the protein, the most feasible explanation is that Myc may interacts through its N-terminus with an unknown protein of the centrosome.
Other virtual particles may contribute to the summation as well; for example, two photons may interact indirectly through virtual electron positron pairs.
There is no evidence to show that TrkA and p75NTR interact directly, so they may interact indirectly through the convergence of downstream signaling pathways and/or share adaptor molecules, rather than through direct receptor-receptor interactions [ 59].
Genes and regulatory sequences that are narrowly or widely spaced on a chromosome may interact productively through higher order chromatin structures such as solenoids, small and giant loops, and minibands [ 128- 130].
Wnt5a may interact with Ror2 through this domain [ 48].
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