NVHL lesions (or sham surgeries) were performed on post-natal day 7 (PND7) and animals were given brief exposure to alcohol during adolescent (PND 28 42).
Pregnancy diagnosis and blood collection were performed on post-insemination Days 40, 90, 120, 150, 180, 210, and at parturition or until the time of abortion detection.
Electron microscopy was performed on post-mortem lung tissue.
To confirm that the in vivo bioluminescence signals accurately represented the bacterial burden in vivo, traditional bacterial counts were performed on post-operative day 5 from bacteria adherent to the implant and present in the joint tissue (Figure 2C).
In vivo imaging was performed on post-operative days 0, 1, 3, 5, 7 and 10 as in Figure 3. Coatings B and C resulted in bioluminescence signals that were highest at the time of inoculation and were reduced to background levels by day 3 (Figure 6B).
However, the results of the ANOVAs performed on post-intervention values with pre-intervention values as covariates did not yield any significant effect for group (.349 ≥ P ≥.926) for all dependent variables.
The results of the univariate ANOVA performed on post-intervention fluency values with pre-intervention fluency values as covariates yield a significant effect only for the pre-intervention score entered as covariate (F 1,17) = 56.71, P < 0.001), with post-training being generally higher compared to pre-training in both intervention groups).
Treated animals were divided into five different groups according to the age at injection and subretinal injections of the viral vector were performed on post-natal day (P) 6, P15, P30, P90 and P180 in either the right or left eye (randomly selected) of Cngb3 −/− mice.
Plasma and effluent sampling was performed on post-injury day 18 (Patient 1, Table 1, antifungal treatment day 15) following a once-daily dose of L-AmB (5 mg/kg IV), with effluent recovered from two abdominal NPWT sites (midline and left lower quadrant, Figure 1).
To investigate whether DARC is also expressed in multiple sclerosis, immunohistochemistry was performed on post-mortem multiple sclerosis brain tissues of nine cases with multiple sclerosis analysing chronic active and chronic inactive lesions and compared to five control cases without any diagnosed neurological disease.
