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In this study the development of the reactive nanocomposite from choice of materials through processing steps, handling and application methods are described.
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The key step in this process was the development of the novel reactive intermediate 9-aminomethylminocycline 4, which can be readily prepared from commercially available minocycline in two synthetic steps.
However, this does not exclude the potential role of epitope spreading in the development of the cross-reactive response.
Current available evidence points to the direct involvement of genes that synthesize and transfer sialic acid to the LOS in the development of the cross-reactive anti-ganglioside antibodies thought to be the effectors in a large majority of GBS and MFS cases [ 25, 26].
The HI test developed by the HPA had high specificity [5] and as no other influenza viruses were circulating during the second wave in England the issue of the development of cross reactive antibodies,which may occur with exposure to antigenically-related influenza viruses, did not arise.
Regardless of the development of reactive gliosis within the striatum, loss of the grey matter is extensive and results in the compensatory enlargement of lateral brain ventricles.
A key cell type involved in the development of the tumor-promoting reactive stroma appears to be the myofibroblast [ 9, 10].
I will briefly discuss the possibility that imprinted genes affect the development of crying, reactive crying and the development of collaborative action.
First physical, chemical and even biologically based processes for building functional adherents and surfaces are addressed, second the development of novel reactive polymers incorporating atmospheric carbon dioxide, and third the investigation of interactions between solid surfaces and polymers or ambient factors.
It is evident that the development of reactive gliosis and the alterations in astrocyte morphology are conditioned by the intensity and rate of neuronal degeneration in the context of the neuron-glia relationship [ 64].
Furthermore, we show that the early, acute downregulation of Dp71 in normal animals may be an important, decisive step in the development of reactive gliosis, upstream of the physiological alterations.
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