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This work describes the preparation of gold nanoparticles on flexible paper- and polymer-based substrates, and demonstrates their photothermally-induced heating property and surface-enhanced Raman spectroscopy (SERS) response.
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The presence of -COOH groups enhanced osteoblast proliferation, differentiation, and matrix mineralization on Ti substrates and demonstrate the potential for further investigations.
Our results show that A. niger undergoes significant morphological changes during growth on solid substrates and demonstrate that the intensity of contour sensing varies depending on the area of the hyphal tip which initiates contact with the substrate.
Finally, we reproduce the above-mentioned results with success on CFRP substrates, and demonstrate the applicability of the process on thermosensitive composite parts with results comparable to the state-of-the-art in the visible range.
Substrate specificity of GALT2-GALT6 was investigated using various potential acceptor substrates and demonstrated that GALT2-GALT6 ispecificic for model AGP sequences (Fig. 2).
They used a PDMS film for the substrate and demonstrated flexible 3D metamaterials with a negative index of refraction in the near infrared regime [20].
Using direct DPN, it was possible to pattern a two-component DNA array on the oxidised silicon substrate and demonstrate its sequence-specific activity by hybridisation with complementary fluorophore-labeled probes (Fig. 3c). Figure 3 a Atomic force microscopy tapping mode image of thiol-modified oligonucleotides DPN patterned on a gold surface [86].
We have identified heparin binding domains that mediate the interaction of heparanase with its HS substrate and demonstrated that a peptide corresponding to Lys158-Asn171 (KKDC), inhibits heparanase enzymatic activity [29].
We then identified ErbB4 as a novel p35/Cdk5 kinase substrate, and demonstrated that Cdk5 is an upstream regulator of ErbB4/PI3-kinase signaling by positively controlling tyrosine phosphorylation of the PI3-kinase docking site Y1056.
To this end, we employed enzymatic assays with a fluorogenic substrate and demonstrated that the immunoprecipitates of APPL1 exhibit deacetylase activity sensitive to the class I/II HDAC inhibitor TSA.
Docking of substrates and PyrBPs demonstrates that differences at the −3 and −4 positions relative to the first aspartate rich motif (FARM) are important factors in the ability of the lepidopteran enzyme to produce homologous isoprenoid structure and to be selectively inhibited by larger PyrBPs.
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