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Due to the D area, the area of FM slightly decreased during the model runs, but this area decrease was compensated by an increase in AR area.
This decrease was compensated by an increased intake in carbohydrates and sugar, respectively, 42.5 and 16.7 energy-percent to 46.5 and 22.6 energy-percent.
This decrease was compensated by the reintroduction of PUP1 in the mutant (SFY160).
It seems that this decrease was compensated for a strong development of the medial layer of the masseter muscle [30] that is inserted in a deep fossa on the dorsomedial side of the enlarged lateral crest (i.e., upper masseteric crest) in rodents of the cavioid type.
This decrease was compensated for, in part, by increased hepatic arterial blood flow.
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This decrease is compensated for by an increase in the maternal hematocrit and hemoglobin concentration, which is equivalent in both indigenous and migrant populations (8, 9).
Since decreased CBF was compensated for increased cerebral blood volume due to recruitment of collateral pathway from extracerebral artery in patients with cerebrovascular disease [ 19], in patients with CAS as well as those without CAS, the influence of changes in cardiac output on cerebral oxygenation is likely to be large.
In short, as the annealing temperature was increased, the average density gradually decreased and the decrease in density was compensated by expansion of dimension, i.e., AH and LD.
In their exclusion, both θG and θRCG decreased substantially and the decrease of θRCG was compensated by an increase in τRCG.
The decrease in PGC1α was compensated for by an increase in the PGC1α-related coactivator (PRC; 187%).
We further found that mice deficient of the TLR-4 receptor were not protected from saturated fat-induced hepatic steatosis, hepatic DAG accumulation, PKCε activation or insulin resistance as assessed by hyperinsulinemic-euglycemic clamp studies, when the decreased caloric intake was compensated for.
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