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Our data showed significantly higher concentrations of IL-1 β in the subretinal fluid of RRD patients compared with the vitreous fluid of control patients.
Factor indicates mean intensity of spots in apoplastic washing fluid of VL43-infected plants/mean intensity of spot in apoplastic washing fluid of control plants.
The median of IL-1 β concentration in the subretinal fluid of RRD patients (0.25 pg/ml, range: 0.10 1.97 pg/ml) was significantly higher than the vitreous fluid of control patients (0.02 pg/ml, range: 0.01 0.03 pg/ml).
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The bacterial density in the tissue-cage fluid of untreated controls approximately remained at 10 CFU/ml during the whole course of treatment.
False-positive BAL galactomannan tests have been reported for patients with airways colonized by either Aspergillus spp. or Penicillium spp. [ 8, 9], but neither was cultured from the BAL fluid of our controls with high OD indices.
Whereas alveolar epithelial lining fluid of normal controls contained high levels of GSH [ 272], patients with IPF had substantially decreased levels of GSH in epithelial lining fluid, BAL fluid, and BAL cells, and had a decreased ratio of reduced to oxidized glutathione (GSH/GSSG) [ 273- 276].
If dysnatremia was identified, it was treated using CRRT with diluted or concentrated substitution fluid to control the speed of correction [ 12, 13].
In comparison, much lower levels were detected in the amniotic fluids of a control group of 217 boys who did not develop autism.
The results indicated highly skewed BV14 and BV16 in the synovial lesion tissue and BV16 in synovial fluid of RA, while control synovial material had diverse BV distribution.
We quantified levels of antioxidant enzymes in the BAL fluid of exposed and control subjects, which had been previously concentrated 10-fold by ultra-filtration using the Ultrafree-CL, NMWL 5,000, centrifugal filter unit (Millipore, Billerica, MA, USA).
The cutoff value was determined based on the CEA/GAPDH mRNA ratio and CK20/GAPDH mRNA ratio levels in the peritoneal lavage fluid of the negative control and T1 samples.
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