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Since FTIR analysis indicated that in the post-implant material alkane oxidation was the prevalent modification of the alkane groups we further characterize the interaction between the oxidized alkane polymers and TLR1/2 receptors.
In the subsequent sections we further characterize the receptor systems using the transfer functions for the linearized versions of these models (see Methods sections for details).
In the present study, using the same animal model we further characterize the effects of MSC administration on renal function and structure, along with the possible mechanisms associated with the therapeutic effects.
We further characterize hilar and CA3 OXTR distribution regarding to overlap with GABA immunoreactivity.
We further characterize four classes of InhA inhibitors that show novel binding modes, and provide evidence of their successful target engagement as well as their in vivo activity.
We further characterize the conformational transitions with a new measure ΦFunc, and demonstrate that local unfolding may be due, in part, to competing intra-protein interactions.
We further characterize the PDUG architecture by studying the properties of the hub nodes that are responsible for the scale-free connectivity of the PDUG.
Here, we further characterize this eNK1 dimer and show it elicits significantly greater c-MET activation, cell migration, and proliferation than the eNK1 monomer.
We further characterize the equilibrium payoffs that can be achieved in the bargaining game in which the seller makes all the offers, as the discount factor goes to one.
We further characterize the exfoliated Te by Raman spectroscopy.
In this section we further characterize the different groups of customers discovered in the UniCoop dataset.
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