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The body weight decline in the R-fed groups after day 9 reflected the body weight decline in the UR-fed groups due to increased tumour burden.
Daily weight was monitored and animals were euthanized when the mice became moribund and severe weight-loss was observed (>20% body weight decline).
This is in contrast to the Honolulu-Asia Aging study, a study of Japanese-American men, in which baseline body weight was not related with dementia onset, but rate and degree of body weight decline were [ 14].
Mice that received sera from LAH-HBc VLP plus CTB* group displayed a slower body weight decline than the PBS and blank control groups and the final protection rate was 60% (6/10).
Similarly, TLR ligand exposure induced a rapid decrease in body temperature and body weight in Casp8ΔIEC mice, whereas no such temperature or body weight decline was observed in wild-type (Casp8fl) animals (figures 2A and 3A, see online supplementary figure S2A).
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Average adult body weight declined from 2001 to 2002, but less so in M than in units that remained C in both years.
As individuals get older, body weight declines primarily because of loss of lean tissue [ 45], while IMCL and liver steatosis tend to increase [ 46].
A line by parity interaction was also observed for body weight, since body weight declined going from the third to the fourth parity in the LP line but not the V line.
This inverse relationship is a natural consequence of the observation that UFR is relatively independent of BMI, at least in adolescents and adults: In a given stratum, as body weight and therefore BMI increase, the rate of urinary flow per kilogram body weight declines.
At the 5-mg dose, mean body weight declined slightly from baseline in 3 trials, was essentially unchanged in 2 trials, and increased slightly in the trial of add-on to TZD (which may reflect, at least in part, the weight effects of the TZD).
The body weights declined from an average of 35.0 ± 1.1 kg pre-kaolin to 32.9 ± 0.7 kg at time of sacrifice.
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