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After cooling the solutions were transferred to test-tubes and brought to volume using dilute HCl while sample splits of 0.25 g were analyzed.
Fatty acids composition of milk (10 mL), diets (1 g), and diced muscle (2 g) were analyzed by gas chromatography.
Twenty samples (from 4.2 g to 13.8 g, with an average wet weight of 8.9 g) were analyzed.
Probe sets enriched by 1.5-fold or greater in Pde1C-driven EGFP-positive cells compared with whole cortex (Supplemental Fig. 3 g ) were analyzed further.
Data in A, B, E and G were analyzed by ANOVA with Bonferroni post-tests, *p<0.05, ***p<0.001, ns = not significant.
During the study period, 343 neonates with a gestational age of more than 37 weeks and a birth BW above 2500 g were analyzed.
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Fat acidity (KOH mg/100 g) was analyzed in three replicates by the AOAC ([1970]) method.
Consequently, the effect of the network coupling topology on the H2 norm of the transfer function G is analyzed.
The polymorphism 3199A > G was analyzed specifically in patients with febrile convulsions [30] or with migrainous vertigo [31] excluding a positive correlation.
Furthermore, the specificity of CTMS-MNPs@SiO2 nanoparticles binding with His-tagged multimeric protein G was analyzed by SDS-PAGE (Figure 5D).
As the reproductive mode of N. cervinus makes this recommendation meaningless, the sign of g was analyzed without taking into account its absolute value.
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