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For evaluation, samples were divided in four groups (Fig. 1): CTRL: healthy non-operated knees of the placebo-treated animals (n = 8); OA: operated knees of the placebo group (n = 8); CTRL + DC: non-operated healthy knees of the diacerein-treated animals (n = 8); OA + DC: osteoarthritic knees of the diacerein-treated animals (n = 8).
The quantitative results in Fig. 3 (Ctrl) and Additional file 1 (Ctrl) support this observation.
All persons were examined by the same trained ultrasonographer (CW = US1) and examination was repeated in 8 persons (6 PsA, 1 RA, and 1 CTRL) by another trained ultrasonographer (MS = US2), and both US1 and US2 have a rheumatological background.
Single chloroplasts were wrapped in discrete bundles finer than those present in the dark (Fig. 2c; for quantitative evaluation see Additional file 1, Ctrl: Energy of actin distribution pattern in F-actin baskets surrounding chloroplasts).
Similar(56)
In SPG4 neurons, the motility of mitochondria (amount of actively transported mitochondria) was unchanged (SPG4: 23.5 ± 0.58%, Ctrl: 19.1 ± 0.52%, P = 0.487).
In total, 299 (CTRL), 157 (Trak1 WT), and 173 (Trak1 hyrt) mitochondria were analyzed.
N = 15 (ctrl), 65 66 (auxin added) cells from three pooled replicates.
The size (volume) of individual GFP clones located in the junctional zone (n = 85 in control [ctrl] epidermis; n = 161 in ATRA-treated epidermis), IFE (n = 1184 ctrl, 1525 ATRA), infundibulum (n = 81 ctrl, 152 ATRA), SG (n = 53 ctrl, 80 ATRA), and HF (n = 65 ctrl, 293 ATRA) was determined, and the cumulative frequency distribution of clone sizes was plotted.
These data were confirmed by western blotting (P<0.01, Ctrl versus HCb24h; Figure 2e).
INOC pigs that did not demonstrate MHD were euthanized on D13; CTRL pigs on D14.
We analysed 864 specimens (207 STEC, 449 STEC-HUS and 208 CTRL).
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