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Hoffman, B.G. et al. Locus co-occupancy, nucleosome positioning, and H3K4me1 regulate the functionality of FOXA2-, HNF4and and PDX1-bound loci in islets and liver.
GRKs are able to regulate the functionality of both G protein-coupled receptors (GPCR) and growth factor receptors and to directly control cytosolic, cytoskeletal or nuclear signaling components of pathways relevant for these processes.
In practice, standards seek to regulate the functionality of the market by facilitating transactions of carbon credits and reducing the required efforts in order to obtain information on the potential trading partners and the quality of carbon credits.
One study demonstrated that cardiac stem cells and early committed cells expressing c-kit, MDR1, and Sca-1 express c-Met and IGF-1 receptors and synthesize and secrete corresponding ligands, HGF and IGF-1, suggesting that these factors may act in an autocrine manner to regulate the functionality of these cells [ 71].
Furthermore, since these cells express receptors for HGF and IGF-1, it is possible that paracrine factors secreted from transplanted BMSCs into the myocardium or transplanted circulating blood-derived progenitor cells may regulate the functionality of these cardiac resident stem cells, thereby leading to cardiac repair and protection.
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However, the role of Gadd45a in regulating the functionality of ATM−/− HSCs is unknown.
The G protein βγ subunit regulates the functionality of the α-subunit in addition to mediating downstream signaling pathways.
One advantage for the cell of using factors that function in all stages of the mRNA lifecycle is the ability to regulate the synthesis and functionality of mRNAs by regulating these factors.
Here we address the hypothesis that Aldh1b1 may regulate the timing of the appearance and eventual functionality of beta cells.
Application of GrowMatch to eliminate and/or properly regulate these functionalities led to the identification of 30 growth medium-specific regulatory constraints.
Regulate the soil temperature.
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