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Exact(6)
Seven d later rats were injected with 800 µg DNA at 2.0 mg/ml in PBS, divided into four 100 µl injections administered in the tibialii and gastrocnemii muscles, of either pCI, pMOG, pMOG-IFNbeta or pMOG-scr, respectively.
There was no evidence for DNA fragmentation into a nucleosomal ladder typical of apoptosis in the muscles of either group of mice.
Briefly, total genomic DNA was obtained from foot and mantle muscles of either fresh or frozen material stored since previous investigations.
The possibility of fibrosis being present in the grafted muscles of either genotype was investigated using Picrosirius Red staining of collagen in sections of grafted and sham-grafted muscles at 20 days post-surgery.
There was no evidence of centrally nucleated fibres in sham-operated muscles at any of the time points or in grafted muscles of either genotype at 3 days after grafting (Fig. 2C).
Electromyographic (EMG) traces were recorded from the first dorsal interosseous (FDI) and abductor digiti minimi (ADM) muscles of either the right or the left hand, by means of 9 mm diameter, Ag-AgCl surface cup electrodes.
Similar(54)
Most fish move by alternately contracting paired sets of muscles on either side of the backbone.
It begins on the sacrum (the large triangular bone at the base of the spinal column) and passes upward, forming a mass of muscle on either side of the spines of the lumbar vertebrae.
The direct administration of the pharmaceutical candidate WNT7a proteins to the tibialis anterior (TA) muscle of either wild-type or dystrophic (MDX) mice resulted in significant satellite stem cell expansion and fiber hypertrophy.
However, the injured muscle of either group had ~ 50% more collagen deposition compared to the respective uninjured muscles (p ≤ 0.005).
A single dose of PCV13 was administered by intramuscular injection into the deltoid muscle of either arm.
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