ライフサイエンスコーパス: BMR

1 BMR cells proliferated actively for 7-20 population doub

2 BMR in the no pulses arm was noninferior (+1.7% increase

3 BMR increased gradually throughout pregnancy at a mean (

4 BMR is distinguished by its adaptations to life undergro

5 BMR proved sufficient to treat esotropia <50 PD and BMR+

6 BMR recession was an appropriate surgical option for tre

7 BMR was associated with 190/270 phenotypes in univariabl

8 BMR, SMR, 24-h EE, respiratory quotient, heart rate, and

9 BMRs reside underground, in self-excavated tunnels that

10 nditure falls in a semi-log manner from ~10x BMR for events lasting 1 day and reaches an asymptote of

11 The flavoprotein domain of P450BM-3 (BMR), which is functionally analogous to eukaryotic NADP

12 Four athletes exceeded 2.5x BMR at 30 and 52 weeks (maximum: 2.74), but mean MS for

13 ting 1 day and reaches an asymptote of ~2.5x BMR at approximately 28 weeks.

14 t evidence exists to support higher absolute BMR/RMR and TDEE in pubertal than in prepubertal adolesc

15 dies supported significantly higher absolute BMR/RMR during puberty (SMD: 1.10-5.93), and all of the

16 difference and an 18% difference in absolute BMR/RMR and TDEE, respectively.

17 alignment comparing treatment by adjustable BMR vs adjustable BMR+SRT.

18 Five had undergone adjustable BMR ranging from 4.5 to 6.5 mm.

19 Three had undergone adjustable BMR+SRT, all with 4-mm medial rectus muscle recessions.

20 ng treatment by adjustable BMR vs adjustable BMR+SRT.

21 and 3 favoring significantly lower adjusted BMR/RMR during puberty.

22 nd ease of digestion for animal agriculture, BMR is a recessive plant gene usually found in annual gr

23 his study, hordatines extracted from BSG and BMR using a deep eutectic solvent were structurally inte

24 ereas slopes for the equations of PMR(C) and BMR vs. M(b) did not differ.

25 etween circulating leptin concentrations and BMR occurred only because of inadequate control for the

26 .3%) in antagonistically selected lines, and BMR was slightly, but not significantly, lower (4.2%).

27 tive genetic covariance between VO(2)max and BMR was positive and statistically different from zero.

28 tic correlation was detected between MMR and BMR.

29 2%) in lines selected for increased MMR, and BMR was slightly, but not significantly, higher (2.5%).

30 ved sufficient to treat esotropia <50 PD and BMR+SRT for greater esotropia in patients with MBS-assoc

31 brain size to maternal investment times and BMR, we provide a direct quantitative comparison of brai

32 late pregnancy had higher energy intakes and BMRs.

33 between phenotypes warrant further study, as BMR is modifiable.

34 Avian BMRs evolved predominantly at a constant rate and withou

35 the following: (a) complex formation between BMR and NADPH; (b) reduction of FAD with formation of th

36 pecies to determine the relationship between BMR and burrow use in mammals.

37 Owing to this interplay between BMRs and T(b), many ecologists and evolutionary physiolo

38 BMD, BMR, muscle strength, VO2max, and energy expended during

39 f weight gain were not greater in the bottom BMR group (0.3 +/- 1.0 kg/y) than in the top BMR group (

40 n preoperative esotropia before treatment by BMR was 39.5 PD ( 15 PD) with mean postoperative esotrop

41 n preoperative esotropia before treatment by BMR was 39.5 PD (+/- 15 PD) with mean postoperative esot

42 n preoperative esotropia before treatment by BMR+SRT was 70.8 PD ( 5.9 PD) with mean postoperative es

43 n preoperative esotropia before treatment by BMR+SRT was 70.8 PD (+/- 5.9 PD) with mean postoperative

44 defined as energy intake <130% of calculated BMR or WW intake <40 g . d(-1) was seen in 71% and 82% o

45 In conclusion, BMR might affect a wide range of health-related outcomes

46 hrough increases in BMR could have decoupled BMR from T(b) and caused different evolutionary routes t

47 The flavoprotein domain (BMR) of P450BM-3 is soluble and contains an equimolar ra

48 ealed no positive genetic trend for elevated BMR in high-MMR lines.

49 The gene encoding BMR has been divided into the coding regions for the FAD

50 We extracted BMR, body-composition, demographic, and laboratory data

51 M(b) exceeded the slope for the equation for BMR vs. M(b), whereas slopes for the equations of PMR(C)

52 els, narrow-sense heritability (h(2)(N)) for BMR was <0.1, but estimates of h(2)(N) for VO(2)max were

53 Omission of pulses is noninferior for BMR.

54 greater reduction in esotropia resulted from BMR+SRT than from BMR (P = .036).

55 in esotropia resulted from BMR+SRT than from BMR (P = .036).

56 suggests that some fossil crown mammals had BMRs approaching the lowest rates of extant mammals.

57 gain more weight than do adults with a high BMR who are living in a typical Western environment.

58 t gain more weight than did adults with high BMRs, implying that habitual differences in food intake

59 efinition, the BMR was different in the high-BMR group (2001 +/- 317 kcal/d; n = 86) than in the low-

60 In conclusion, higher BMR might reduce lifespan.

61 ugh some ageing theories suggest that higher BMR should reduce lifespan.

62 of relatively larger brains requires higher BMRs.

63 However, BMR, SMR, and TEE were lower in African American girls t

64 6 mo without experiencing a large decline in BMR, BMD, or select components of energy expenditure.

65 Although the declines in BMR were significant, they were small and may not have b

66 A significant decrease in BMR and energy expended during sitting and walking occur

67 There were no significant differences in BMR of terrestrial, semi-fossorial and fossorial mammals

68 and thermodynamic control of the flavins in BMR is significantly different from that in microsomal P

69 ld ambient temperatures through increases in BMR could have decoupled BMR from T(b) and caused differ

70 ate gestational weight gain and increases in BMR, which are not totally offset by reductions in AEE.

71 MMR and correlated responses to selection in BMR.

72 lyses support our predictions that shifts in BMR and thermal conductance confer important adaptations

73 Only 2% of the observed variability in BMR was attributable to within-subject effects, of which

74 We partitioned the variance in BMR into within- and between-subject effects and explore

75 ake or activity counterbalance variations in BMR as a risk factor for weight gain in a typical Wester

76 that lead to both increases and decreases in BMRs were linked to abrupt changes towards colder ambien

77 ass-independent MMR and low mass-independent BMR.

78 nt positive feedback loop as T(b) influences BMR(1-3).

79 We assessed whether adults with a low BMR gain more weight than do adults with a high BMR who

80 Adults with low BMRs did not gain more weight than did adults with high

81 2001 +/- 317 kcal/d; n = 86) than in the low-BMR group (1510 +/- 222 kcal/d; n = 77), but they were c

82 s breeding in temperate habitats had a lower BMR than did temperate residents, suggesting that these

83 We included pre-existing data for mammalian BMR and 16 life history traits.

84 Overall, mammalian BMR is dictated primarily by environmental ambient tempe

85 Mammalian BMRs evolved with rapid bursts but without a long-term d

86 ctively exploited the diversity in mammalian BMRs under diverse, often-adverse historical thermal env

87 We measured BMR of 69 species of tropical birds, the largest data se

88 aily energy need was determined by measuring BMR and assessing physical activity with 8-d self-report

89 of these traits of interest is Brown midrib (BMR).

90 outcomes of bilateral medial rectus muscle (BMR) recession in patients diagnosed with AACE at our st

91 ming that this is the formation of the NADPH-BMR complex.

92 antly reduced pupal mass relative to its non-BMR counterpart, alongside a significant reduction in ad

93 irements were energy absorption of >/=81% of BMR and WW absorption of >/=21 g . d(-1), which were equ

94 The cytochrome c reductase activity of BMR could be fully reconstituted with the individual dom

95 c independent contrasts, and a comparison of BMR of 13 phylogenetically matched pairs, one species fr

96 hat marsupials lack a partial correlation of BMR with brain size.

97 y, we aimed to estimate the casual effect of BMR on parental attained age, a proxy for lifespan, usin

98 ne to investigate the independent effects of BMR on phenotypes with significant univariable associati

99 consider plant age, and that the effects of BMR on plant defenses should also be studied.

100 ared these measurements with 59 estimates of BMR for temperate birds.

101 ry physiologists posit that the evolution of BMR and T(b) must have been coupled during the radiation

102 r this resistance, we examined the growth of BMR fibroblasts in vitro of the species Spalax judaei an

103 dition of 2 electron equivalents per mole of BMR results in the reduction of the high potential flavi

104 tion of the second mole of NADPH per mole of BMR.

105 The top and bottom 15th percentiles of BMR, adjusted for fat-free mass (FFM), fat mass, age, an

106 However, presence of BMR significantly reduced pupal mass relative to its non

107 The kinetics of reduction of BMR with NADPH were studied by stopped-flow spectrophoto

108 ur results suggest that cancer resistance of BMR is conferred by massive necrotic response to overpro

109 ion of several additional reduced species of BMR.

110 ironments and will enable the utilization of BMR models for biomedical research in the fight against

111 Cells and tissues of BMRs express very low levels of DNA methyltransferase 1.

112 When the effect of FM on BMR is removed, any association with leptin concentratio

113 t have imposed strong selective pressures on BMR to compensate for increased rates of heat loss and t

114 We suggest that a positive BMR-brain size correlation is a placental trait related

115 the health effects of genetically predicted BMR across the phenome sex-specifically.

116 Genetically predicted BMR was inversely associated with father's and mother's

117 ease in effect size of genetically predicted BMR, 0.46 and 1.36; 95% confidence interval 0.07-0.85 an

118 and independently (r(2) < 0.001) predicting BMR from the UK Biobank and applied them to a genome-wid

119 and independently (r(2) < 0.001) predicting BMR from the UK Biobank and applied them to over 1,000 p

120 obtained 217/219 genetic variants predicting BMR and applied them to 1,150/1,242 phenotypes in men/wo

121 l of 178 and 180 genetic variants predicting BMR in men and women were available for father's and mot

122 The blind mole rat (BMR), Spalax galili, is an excellent model for studying

123 On the social scale, the blind mole rat (BMR; Spalax ehrenbergi) is an extreme.

124 Resting O2 consumption rate (BMR) or minimal O2 consumption rate (MOC) declines with

125 Basal metabolic rate (BMR) and daily ad libitum food intake both increased wit

126 ic correlation between basal metabolic rate (BMR) and maximal (VO(2)max) rate of oxygen consumption i

127 PMR(E) averaged 6.44 x basal metabolic rate (BMR) and PMR(C) averaged 4.52 x BMR.

128 ters of the S-I model: basal metabolic rate (BMR) and thermal conductance.

129 investment traits and basal metabolic rate (BMR) correlate with relative brain size, but current hyp

130 y composition, and the basal metabolic rate (BMR) in obese female patients during the initial 3 y aft

131 onlactating (NPNL), 2) basal metabolic rate (BMR) increases in pregnancy and the increase is positive

132 e indicated that a low basal metabolic rate (BMR) is an independent predictor of future weight gain,

133 bservationally, higher basal metabolic rate (BMR) is associated with metabolism-related disorders, ca

134 Basal metabolic rate (BMR) is the largest component of daily energy demand in

135 exhibit adaptations in basal metabolic rate (BMR) to exploit such unique niches.

136 Basal metabolic rate (BMR) was measured by calorimetry, total energy expenditu

137 ly, the association of basal metabolic rate (BMR) with mortality is mixed, although some ageing theor

138 inuously by their high basal metabolic rate (BMR)(1).

139 r diet-only program on basal metabolic rate (BMR), bone mineral density (BMD), energy expended during

140 Basal metabolic rate (BMR), sleeping metabolic rate (SMR), 24-h EE, respirator

141 rgy expenditure (TEE), basal metabolic rate (BMR), sleeping metabolic rate (SMR), and minimal SMR (MS

142 ion <84% of calculated basal metabolic rate (BMR), wet weight (WW) absorption <23 g .

143 on on mass-independent basal metabolic rate (BMR).

144 have evolved a reduced basal metabolic rate (BMR).

145 ed data for basal or resting metabolic rate (BMR/RMR), total daily energy expenditure (TDEE), and/or

146 essed as a multiple of basal metabolic rate (BMR; kcal/day)(1)(,)(2)(,)(3)(,)(4) and known as "metabo

147 (CNSR, R2IM), and bone marrow relapse rate (BMR, R2pulses; ALL only, noninferiority margin 5%).

148 Estimation of basal metabolic rates (BMRs) suggests that some fossil crown mammals had BMRs a

149 Basal metabolic rates (BMRs) were calculated from weight by using the equations

150 Blind mole rats (BMRs) are small rodents, characterized by an exceptional

151 ych showed that tropical birds had a reduced BMR, compelling evidence for a connection between the li

152 to 2020 in the Bangkok Metropolitan Region (BMR), which includes Bangkok Metropolis and its five adj

153 al BMR, whereas residual PMR(C) and residual BMR were not correlated.

154 (E) were positively correlated with residual BMR, whereas residual PMR(C) and residual BMR were not c

155 spent grain (BSG) and barley malt rootlets (BMR), common waste products of beer processing that have

156 Blind mole rats Spalax (BMR) are small subterranean rodents common in the Middle

157 In sorghum-sudangrass, BMR expressed plants have lower amounts of lignin, which

158 cal activity levels were calculated as TEE - BMR and TEE/BMR, respectively.

159 d activity energy expenditure (AEE) as TEE - BMR.

160 TEE, BMR, SMR, and MSMR were 15-26% higher during pregnancy t

161 and dopamine correlated positively with TEE, BMR, SMR, and MSMR.

162 levels were calculated as TEE - BMR and TEE/BMR, respectively.

163 measured MS (total energy expenditure [TEE]/BMR) using doubly labeled water during ultra-endurance c

164 e data presented support the hypothesis that BMR has a discrete multidomain structure.

165 Previous studies indicated that BMR is highly variable, but the cause of this variation

166 Here we show that BMR and T(b) were decoupled in approximately 90% of mamm

167 The BMR decreased from 1.12 +/- 0.04 kcal/min at baseline to

168 The BMR spends its entire life underground, protecting itsel

169 Here we sequence and analyse the BMR genome and transcriptome, highlighting the possible

170 By definition, the BMR was different in the high-BMR group (2001 +/- 317 kc

171 We discuss the BMR's unique behavioral phenotype, particularly in the c

172 Following cell hyperplasia, the BMR genome DNA loses methylation, resulting in the activ

173 Here we report that cancer resistance in the BMR is mediated by retrotransposable elements (RTEs).

174 Although this mechanism is enhanced in the BMR, we show that it functions in mice and humans.

175 Unraveling the neural basis of the BMR's behavior, in comparison to that of social rodents,

176 The remarkable traits of the BMR, together with its genomic and transcriptomic inform

177 he initial 1-3 mo after an RYGB, whereas the BMR moderately decreased.

178 xhibit adaptive long-term responses in their BMR.

179 Compared to BMR, the electron-accepting properties of the recombinan

180 h FFM and FM are significant contributors to BMR.

181 With a 1:1 ratio of NADPH to BMR, the absorbance changes can be fit to five consecuti

182 BMR group (0.3 +/- 1.0 kg/y) than in the top BMR group (0.5 +/- 1.5 kg/y) (P = 0.17).

183 FAW, we tested the effect of seed treatment, BMR, and plant age on FAW growth, development, and plant

184 cal profiles of all AACE cases who underwent BMR recession from 2015 to 2024 were recruited.

185 In pregnant women, body weight, BMR, and energy intake increased but total daily energy

186 When BMR is titrated with NADPH or sodium dithionite under an

187 e capacity also increased with NPP (and with BMR and food intake), because species of high-NPP enviro

188 abolic rate (BMR) and PMR(C) averaged 4.52 x BMR.