ライフサイエンスコーパス: basal metabolic rate

1 d mouse hearts and explained by an increased basal metabolic rate.

2 which is equivalent to 4.0 +/- 0.1 times the basal metabolic rate.

3 thermogenesis and a paradoxical increase in basal metabolic rate.

4 ody mass and fat mass and had an increase in basal metabolic rate.

5 weight and that channel inhibition increases basal metabolic rate.

6 (p<0.02) and increased by a factor of 1.5 X basal metabolic rate.

7 Metabolic phenotyping demonstrated both basal metabolic rate and feeding were lower for the LERK

8 bies tend to have greater increases in their basal metabolic rate and lower rates of maternal energy

9 f beta based on a data set of 626 species of basal metabolic rate and mass in mammals.

10 B-deficient mice is accompanied by increased basal metabolic rate and total energy expenditure, witho

11 ted to resolve symptoms and to normalize the basal metabolic rate and/or serum protein-bound iodine l

12 gh-fat diet, MCK-DGAT1 mice displayed higher basal metabolic rates and 5-10% lower body weights compa

13 eing affected, including voluntary activity, basal metabolic rate, and diet-induced thermogenesis.

14 d libitum food intake at a test meal, normal basal metabolic rate, and evidence of autonomic dysfunct

15 ptors on melanocytes, modifies behaviour and basal metabolic rate, and mediates an interaction betwee

16 nergy expenditure (total energy expenditure, basal metabolic rate, and sleeping metabolic rate), and

17 Basal metabolic rates are significantly higher in obese

18 echniques as well as more modern measures of basal metabolic rate) are highlighted, as well as the ro

19 Basal metabolic rate (BMR) and daily ad libitum food int

20 A positive genetic correlation between basal metabolic rate (BMR) and maximal (VO(2)max) rate o

21 PMR(E) averaged 6.44 x basal metabolic rate (BMR) and PMR(C) averaged 4.52 x BM

22 nges in two key parameters of the S-I model: basal metabolic rate (BMR) and thermal conductance.

23 maternal life history investment traits and basal metabolic rate (BMR) correlate with relative brain

24 onutrient intakes, body composition, and the basal metabolic rate (BMR) in obese female patients duri

25 when nonpregnant and nonlactating (NPNL), 2) basal metabolic rate (BMR) increases in pregnancy and th

26 e previous studies have indicated that a low basal metabolic rate (BMR) is an independent predictor o

27 Basal metabolic rate (BMR) is the largest component of d

28 Basal metabolic rate (BMR) was measured by calorimetry,

29 diet + exercise (DE) or diet-only program on basal metabolic rate (BMR), bone mineral density (BMD),

30 Basal metabolic rate (BMR), sleeping metabolic rate (SMR

31 Total energy expenditure (TEE), basal metabolic rate (BMR), sleeping metabolic rate (SMR

32 vely as energy absorption <84% of calculated basal metabolic rate (BMR), wet weight (WW) absorption <

33 without direct selection on mass-independent basal metabolic rate (BMR).

34 s that tropical birds have evolved a reduced basal metabolic rate (BMR).

35 g a ratio of energy intake (EI) to estimated basal metabolic rate (BMRest).

36 Basal metabolic rates (BMRs) were calculated from weight

37 es, uncoupled from other parameters, such as basal metabolic rate, body size, or body temperature.

38 ical reactions and organism physiology (e.g. basal metabolic rates) but has not been examined at the

39 The mechanism underlying the regulation of basal metabolic rate by thyroid hormone remains unclear.

40 cal activity level (total energy expenditure/basal metabolic rate) by heart rate monitoring, a techni

41 ed lean body mass, fat mass, and had a lower basal metabolic rate compared to vehicle-treated and die

42 , and had greater immunocompetence and lower basal metabolic rates compared with chicks on both low L

43 REE/predicted basal metabolic rate correlated directly with burn size,

44 also allow for maintenance of a normal fetal basal metabolic rate despite low fetal insulin and gluco

45 FGFR4 ASO treatment increased basal metabolic rate during free-feeding conditions and,

46 ormone that exerts homeostatic regulation of basal metabolic rate, heart rate and contractility, fat

47 It was indexed to a calculated basal metabolic rate in normal volunteers and adult pati

48 mg/mg induced hyperphagia and an increase in basal metabolic rate in the C57BL/6J mouse in the absenc

49 arters of a century it has been assumed that basal metabolic rate increases as body mass raised to so

50 intake but do not become obese because their basal metabolic rate is also elevated.

51 Because basal metabolic rate is decreased in obesity, UCP2 expre

52 l energy reserves are low at conception, the basal metabolic rate is down-regulated to conserve energ

53 The unexpected increase in basal metabolic rate is not due to hyperthyroidism, comp

54 se in TEE is attributable to humans' greater basal metabolic rate (kcal day(-1)), indicating increase

55 gnificantly between Kv1.3(-/-) and controls, basal metabolic rate, measured at rest by indirect calor

56 The weight, basal metabolic rate, nutrient and electrolyte balance,

57 While the freezing process affects the basal metabolic rate of the cells, the optical metabolic

58 wer allometric scaling law characterizes the basal metabolic rates of isolated mammalian cells, mitoc

59 le evidence of energy-sparing adaptations in basal metabolic rate or dietary-induced thermogenesis du

60 Basal metabolic rate was increased in the sucrose group,

61 s on specific tissues, we found that hepatic basal metabolic rate was paradoxically decreased 1.7-fol

62 Basal metabolic rates were calculated with the Harris-Be

63 led increased ad libitum food intake, normal basal metabolic rate when adjusted for fat-free mass, pa

64 through the loss of fat mass and increase in basal metabolic rate with browning of white adipose tiss