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Nanocrystallites act as building blocks for more complex aggregates at asphaltene concentrations exceeding 90 100 mg/l.
When an emulsion is the precursor of the dried copolymer aggregates, either onion-like structures (case ii) or vesicles mixed with more complex aggregates are formed (case iii).
All crystallins have in common the fact that they are globular, water-soluble proteins capable of refracting light either alone (monomers) or in combinations of various numbers of molecules (dimers, tetramers, or more complex aggregates), can be densely packed, and remain stable for the lifetime of the organism (Piatigorsky 2007).
Specifically, the detailed investigation of the silver MIF absorption spectra for different concentrations of deposited R6G performed by Zhao et al. [11] has shown that the thickness of the deposited R6G layer and its composition (fraction of monomers, dimers, and more complex aggregates) influences the shift, width, and amplitude of the SPR peak.
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With increasing asphaltene content, more and more complex molecular aggregates are formed.
Crystal structures of these complexes show individual complexes, dimers, supramolecular columnar packing or more complex supramolecular aggregates.
In the 1990s, the supramolecular chemistry field began to use its fundamental knowledge of noncovalent interactions (e.g., H-bonds, metal ligand interactions, electrostatic interactions, and the solvophobic effect) to enable the preparation of more complex multicomponent aggregates formed in self-assembly processes.
Our recent studies in cultured cell provide strong evidence that amyloidogenic conformational templating of αS can readily occur under certain conditions [ 42], but the situation in vivo is likely more complex and aggregate formation can involve several mechanisms.
This fractal image analysis provides quantitative evidence to support the observation that condition medial aggregates are more complex in nature and also implicates that protein composition of the corona phase, instead of concentration, dictates aggregate structure.
The impedance of the aggregates shows more complex behavior.
We also provide a suite of more complex analysis techniques, such as aggregate functionality scores, phenotype-specific gene prioritization, and statistical methods for disease-gene finding in case/control studies without any need for data reformatting or computational expertise.
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