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The ISP1820 derivative χ9633 pYA4088) was present in both tissues on day 3, but was cleared by day 7. Groups of seven-week-old mice were intranasally immunized with 1±0.2×109 CFU each test strain.
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STUDY DESIGN: Mitochondrial respiration was measured polarographically with homogenates of fetal cerebral cortical tissues on day 16 (with saline solution, n = 8; with dexamethasone, n = 8), day 18 (with saline solution, n = 8; with dexamethasone, n = 8), and day 20 (with saline solution, n = 8; with dexamethasone,n = 8) of gestation.
We began topical Tat-Smad7 application 6 days after irradiation, (when mucosal damage was obvious) applying daily to day 9 and observed the treated tissues on day 10.
To test the efficacy of Tat-Smad7 in oral mucositis prevention, we exposed mice to fractionated cranial radiation and topically applied Tat-Smad7 to the oral cavity daily starting 24 h before irradiation through day 8 after initiation of irradiation and observed the treated tissues on day 9.
Viral loads tended to be highest from tissues taken on day 12 p.i.; however nasal cavity yielded the highest level of virus (7.7 × 10) compared to all other tissues on day 9, followed closely by liver (5.7 × 10) and spleen (4.9 × 10) tissues on day 12 (Table 3, Supplementary Material Figure S1). Figure 4 illustrates the tissues that were positive for virus on each sample day for both MPXV clades.
The clinical observation was further confirmed by histological analysis of the eye tissues on day 22 after immunization (Fig. 4C and D).
The pictures of injection sites) and adjacent tissues on day 7 after the seventh injection can be an illustration of that.
OBP gene expression in multiple tissues on day 3 of the fifth instar silkworm is consistent with EST representation in the database.
B. mori microarray database is composed of expression data for 22987 probes of 9 silkworm tissues on day 3 of the fifth instar in silkworm [ 25].
We then harvested the regenerating tissues on day 2, day 6, day 12, and day 20 post-injury, as well as non-injured radial nerve cord and used the samples for sequencing library preparation.
The pathological changes in the brain and spinal cord of mice were observed by light microscopic evaluation of H&E stained tissues on Day 18 and Day 40 PI.
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