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Additionally, supplementation of PEG 6000 to the crude enzyme mixture increased the cellulase activity linearly with the concentration of PEG.
Additionally, supplementation of enzymes produced the highest total ABE production yield of 0.311 g/g and volumetric productivity of 0.102 g/L h.
Additionally, supplementation of diabetic mice with CWP improvement in the architecture of lymphoid tissues and rescued from apoptosis through direct effects on the Bax and Bcl-XL proteins.
Additionally, supplementation with certain cobalamin compounds protected the cells from neurotoxicity and increased cell growth [ 170, 171].
Additionally, supplementation with omega-3 fatty acids has been found to decrease triglyceride levels and increase HDL cholesterol levels [ 17, 22], while another study found that supplementation did not alter triglyceride or total cholesterol levels [ 21].
Additionally, supplementation with infant formula at one month had a clear dose-response effect on breastfeeding with the aORs of weaning increasing as the proportion of breastfeeding decreased from high-partial breastfeeding (aOR = 2.00; 95% CI 1.31 to 3.05) to low-partial breastfeeding (aOR = 13.8; 95% CI 5.70 to 33.63).
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Additionally, dietary supplementation with the Nrf2 inducer tertbutylhydroquinone attenuated 3-NP toxicity in Nrf2 competent mice, but not in Nrf2 deficient mice [20].
Additionally, oral supplementation of silibinin prevents colon carcinogenesis [ 16].
41– 43 Additionally, methyl supplementation has been show to improve theta rhythm power in humans.
Additionally, DHA supplementation is associated with elevated markers of trophoblast proliferation, measured in placentas obtained at term of pregnancy [ 102].
11, 35– 38 Additionally, methyl supplementation with Met has been shown to reverse lead-induced memory deficits and to reduce seizures in a transgenic mouse model.
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