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EDN1 is one of three 21-amino acid peptide family members (EDN1, EDN2, and EDN3) [ 28], and it is known to be a proangiogenic modulator that promotes endothelial cell proliferation and migration through two G protein coupled receptors (ETAR and ETBR) [ 16].
These authors suggest that NOSIP is a novel type of modulator that promotes translocation of eNOS from the plasma membrane to intracellular sites, thereby uncoupling eNOS from plasma membrane caveolae and inhibiting NO synthesis.
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Taken together, RASSF1A and NF2 appear to be positive modulators that promote mammalian Hippo signaling in multiple tissue types.
PD-L1 silencing accelerates anti-tumour immune responses and strongly potentiates DC anti-tumour capacities, when combined with mitogen-activated kinase (MAPK) modulators that promote DC activation.
Some, though, were hopeful of a new combined HRT drug that contains equine oestrogen and bazedoxifene, a selective oestrogen receptor modulator, that can modulate any damaging effects of oestrogen on uterus and breast tissue.
One of these genes, DRAM1 (damage-regulated-autophagy modulator), encodes a phylogenetically conserved lysosomal protein that promotes autophagy (Refs 77, 80, 81).
The Myocyte enhancer factor 2 (MEF2) is a Ca2+-regulated transcription factor that promotes neuronal survival [42] and is also a key modulator of activity-dependent synaptic development [43].
That promotes re-watching.
Raloxifene is a selective estrogen receptor modulator that may produce toxic oxidative species in metabolism.
Thus, in the rest of this paper, we present an OFDM/OQAM modulator that delivers a signal denoted, but keeping in mind that this modulator corresponds to an FBMC modulator as shown in Figure 1.
Raloxifene is a selective estrogen receptor modulator that inhibits bone resorption.
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