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Differences in the metabolic responses of rodents fed a HFD vs. "cafeteria" Western diet have been previously noted, although both dietary challenges can induce obesity and hepatosteatosis, cafeteria-fed rats display increased inflammation in fat and liver tissue (32).
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A "branched" alae defect in nhr-23 (RNAi) animals was previously noted, although a defect in seam cell number was not seen (Kostrouchova et al. 1998, 2001).
The ability of PMA to cause RCAN1.4 upregulation has been previously noted in the literature [17], [38], although to date the exact role of PKC in the regulation of RCAN1.4 expression has not been investigated.
The low responsiveness of P. tarapacana's foliar traits to elevation gradients has been previously noted (González et al. 2002), although its biochemical composition has shown to be more responsive to these gradients (González et al. 2007).
This has been previously noted (Burgess-Herbert et al. 2009), although the mechanism responsible for the high false-positive rate was unknown.
Although some changes in the pattern of WGA labelling have been previously noted [21] these changes have not been quantified.
Both increases and decreases in dietary intake have been previously noted in response to stress.
As has been previously noted, the difference from Sect.
However, several exceptions have been previously noted in the literature.
Although rhod2-AM is typically used as a probe of mitochondrial Ca2+, it also accumulates in lysosomes as has been previously noted.
Gene duplication has been previously noted in ruminants.
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