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Pollen mixtures from each sampling date and site were analyzed for weight, total protein, total fatty acids (FAs), and FA composition.
Feces were collected during 12 h of fasting and analyzed for weight and fat content.
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The grafted homopolymer and block copolymer brushes were analyzed for molecular weight, molecular weight distribution, chain grafting density, composition and hydrodynamic thickness (HT) using gel permeation chromatography multi-angle laser light schromatography multi-anglee size analaser and atomic force microscopy (AFM) techniques.
When E14.5, 16.5, and 18.5 wild-type and transgenic embryos were analyzed for body weight, body lengths, lung weights, and breathing scores of premature pups (Additional file 1: Figure S2A-D), no statistically significant differences were obtained between the two genotypes for all parameters examined.
Individual patients were analyzed for categorical weight loss ≥ 2 kg and weight gain ≥ 1 kg.
All plant samples were analyzed for the weight, length of the longest roots, and number of leaves.
Initially, the proteins were analyzed for molecular weight and amino acid content, as well as their ability to facilitate cell adhesion and proliferation.
The records for all patients were analyzed for age, weight, parity, primary diagnosis, uterine size, operative time, blood loss, analgesia, hospital stay, resumption of diet, incidence of morcellation, and surgical complications.
In addition to the clinical score, the mice were analyzed for body weight loss.
It was then analyzed for molecular weight changes by gel permeation chromatography.
Excised hearts from 4 groups of mice were analyzed for heart weight index changes using H&E staining, TUNEL-positive assays and Western Blotting protein.
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