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In continuation of our previous efforts in the analysis of organic compounds of pharmaceutical importance through azo dye chemical derivatization with 4-carboxyl-2,6-dinitrobenzene diazonium (CDNBD) ion [36, 37, 38, 39, 40, 41, 42, 43, 44], we report in this paper a new simple, accurate and precise colorimetric method for the assay of nifedipine in bulk samples and tablet dosage forms.
The newly identified AICE may also improve previous efforts in the analysis of heterologous promoters for the overexpression of the lipopeptide antibiotic friulimicin in Actinoplanes friuliensis [ 76].
Much of the recent efforts in the analysis of protein-protein interaction networks has focused on finding functional dependencies between the so-called hubs and their topological roles in the network [ 4, 5].
Much of the recent efforts in the analysis of protein-protein interaction (PPI) networks has therefore focused on finding functional dependencies between so-called hubs, defined as proteins involved in many interactions, and their topological roles in the network [ 22- 24].
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To reduce the computational effort required in the analysis of tall building structures, various simplifications by means of simplifying assumptions have been attempted.
However, efforts were made in the analysis of the findings of this trial to overcome these limitations.
While the main point of this study was to evaluate the wisdom of focusing solely on repeat hits in postscreening efforts, the analysis of the determinants of binding of the repeat hits to the anti-ADP3 antibodies was also carried out and provided interesting data.
Knoblach et al. (2003) have concentrated their efforts on the analysis of luminal proteins in purified rough microsomes from mouse liver and have detected BiP, GRP94, lectin-like chaperones (calnexin, calreticulin), peptidylprolyl isomerases, thiol disulphide oxidoreductases (PDI, P5 (CaBP1), ERp72, ERp57, ERp44, ERp29, and ERp46).
A great effort is typically invested in the analysis of the obtained spectra; whereas, little time is usually spent optimizing the measurement parameters used to obtain these spectra.
In spite of these progressive compensatory efforts, the analysis of striatal transcription suggests that the postsynaptic DA response is diminishing over time.
There was also an effort towards the analysis of inter-strand variations in amino acid and codon usage in three DnaE-based groups of bacteria [ 2], but it focused only on the overall compositional features of those three groups.
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