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A subgroup of 17 carcinomas were microdissected and the tumour infiltration front with >75% tumour cell content, as assessed by visual examination of hematoxylin eosin stained preparations, was selected for gene expression analysis.
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A RF and two generic IVM preparations were selected to be tested in the work reported here.
With the advantages of zero order drug release, high correlation between in vitro– in vivo release and being less affected by factors other than related to the dosage form itself, osmotic pump preparations were selected to be used as the bio-mimetic DDS.
Since these preparations were selected on the basis of their insulin secretory pattern, this is likely to have introduced a bias, and thus the gene expression pattern described by us may not reflect that of islet preparations with a lower insulin secretory capacity.
The activated carbon (AC) used in the monolith preparation was selected from a series of ACs prepared from an anthracite and bituminous coals activated using KOH, NaOH and CO2, and having a variety of surface areas, micropore size distributions and packing densities.
Sunflower preparation was selected as the placebo agent as it is odorless and does not possess any known therapeutic effect.
Optimum formulation and processing parameter for herbal juice preparation was selected from the response surface methodology analysis.
The most suitable water matrix for the test material preparation was selected according to its similarity to natural waters while taking into account several practical aspects.
A plasma membrane preparation was selected that is considered free of intracellular organelles, although exhibiting 8% contamination of BLM with CM [ 38].
Satisfactory quality recordings (sharp image, sufficient bowel preparation) were selected.
The MS MS ion preparation mode was selected due to the high sensitivity and selectivity it provides.
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