ライフサイエンスコーパス: LBM

1 LBM can be obtained automatically from limited-whole-bod

2 LBM derived from limited-whole-body data using the propo

3 LBM of the whole body could be automatically estimated f

4 LBM was also calculated using predictive equations that

5 LBM was assessed by anthropometry.

6 LBM was measured by total-body dual-energy x-ray absorpt

7 +/- 2, 11 +/- 2, and 15 +/- 2 pmol x kg(-1) LBM x min(-1), respectively (P < 0.001, baseline vs. day

8 8 environmental samples were collected at 10 LBM.

9 In men receiving ADT, LBM decreased significantly after 12, 24, and 36 months.

10 of early nutrition supplementation on adult LBM and muscle strength.

11 level had a positive association with adult LBM and muscle strength.

12 changes in body fat (r = 0.39, P = 0.01) and LBM (r = -0.34, P = 0.03).

13 inear regression model adjusting for age and LBM, an increase in DES excretion of 1 microg/g creatini

14 luate the effects of population ancestry and LBM on measures of excess adiposity (BMI, %BF, and FMI).

15 were associated with changes in body fat and LBM, but did not explain much variance in either measure

16 e examined the hypothesis that higher FM and LBM are associated with greater survival in MHD patents

17 es that account for variation in both FM and LBM are recommended for normalization of EE in mice.

18 ory markers, the highest quartiles of FM and LBM were associated with greater survival in women: HRs

19 ing for the independent assessment of FM and LBM.

20 e studied to define the link between IMF and LBM.

21 C-reactive protein and LBM were inversely related (r = -0.71, p < 0.01).

22 This new methodology which couples SPT and LBM is validated using a kinetic Monte Carlo (kMC) algor

23 ce interval (CI): 1.16, 1.82), while TBF and LBM were not.

24 close phylogenetic proximity of some WS and LBM loNDV suggests that viral transmission may occur amo

25 Based on the movements of traders between LBMs, weighted and directed networks were constructed an

26 mononucleated (SMMs) and large binucleated (LBMs) myocytes.

27 t failed to detect class I viruses from both LBM and WS.

28 Larch budmoth (LBM) population dynamics across the European Alps, a cla

29 Thirty Vietnamese and 8 Cambodian LBMs were visited, and structured interviews were conduc

30 Consequently, LBMs with the largest combination of risk factors for be

31 e-scarce settings with extensively developed LBM systems, commonly found in South-East Asia.

32 x-specific quantitative effects of different LBM formulations on liver SUV have not been well studied

33 in the right hepatic lobe and corrected for LBM using the sex-specific James and Janmahasatian formu

34 diated shifting of the optimal elevation for LBM population growth is the mechanism for elevational e

35 H9N2-infected SPF chickens and chickens from LBM showed that pan-IAV FRET-PCR had a higher detection

36 The profiles of sellers operating at a given LBM could be reliably predicted using basic information

37 derestimated by %BF in individuals with high LBM.

38 percentiles" in both sexes, whereas a higher LBM was protective in women.

39 patients, higher FM in both sexes and higher LBM in women appear to be protective.

40 (HR = 2.44, 95% CI: 1.38, 4.34) and higher %LBM decreased risk of death (HR = 0.41, 95% CI: 0.23, 0.

41 quickly and easily, may be used to identify LBMs suitable for implementing interventions.

42 was significantly greater than the change in LBM in the placebo group (mean change [SD], +1.9 [1.6] k

43 The threshold-like change in LBM outbreak pattern highlights how interacting species

44 Change in LBM was a significant predictor of serum ferritin (P < 0

45 Changes in LBM and regional lean mass were associated with changes

46 = 127) had significantly greater changes in LBM at all measured time points than younger men.

47 P =.002) were directly related to changes in LBM.

48 y (n = 36) had a greater rate of decrease in LBM compared with men who had received more than 6 month

49 erone therapy has been reported for gains in LBM and muscle strength.

50 months resulted in a significant increase in LBM associated with functional improvement in patients u

51 did not result in a significant increase in LBM.

52 n . kg(-1) . d(-1) in promoting increases in LBM and losses of fat mass when combined with a high vol

53 nificant nitrogen retention and increases in LBM, weight, and strength.

54 Pressure-permeability relationships in LBM transport were governed primarily by changes in diff

55 iation records reveals elevational shifts in LBM outbreak epicenters that coincide with temperature f

56 ons favorable for perpetuating HPAIV H5N1 in LBMs.

57 More than 80% of these traders operated in LBMs located in the most densely populated areas, Ha Noi

58 rcentage lean body mass (%LBM) or change in %LBM in older subjects.

59 rogen excretion) but not with 3-y change in %LBM.

60 ids in healthy, aged women and men increased LBM and decreased fat mass.

61 yses of variance revealed that PRT increased LBM and ALM (P < 0.01); reduced trunk fat mass by 2.5 kg

62 As a result of the intervention, LBM increased (P < 0.05) in the PRO group (1.2 +/- 1.0 k

63 quirements) diets providing 33 +/- 1 kcal/kg LBM to young men who were randomly assigned (n = 20/grou

64 ols (29.9 +/- 0.26 and 29.6 +/- 0.27 kcal/kg LBM, respectively; P < 0.01).

65 oups (33.2 +/- 0.27 vs 34.7 +/- 0.27 kcal/kg LBM; P < 0.01).

66 t also serves an unexpected role in limiting LBM cell number in this early phase.

67 nd HG (p < 0.01) were all reduced in the low LBM group, but not when related to total LBM.

68 onfounders, the intervention group had lower LBM (beta = -0.75; P = 0.03), appendicular skeletal musc

69 (-7.4 +/- 6.6 kg), BMI (-2.6 +/- 2.2 kg/m), LBM (-2.5 +/- 8.7 kg), and fat mass (-3.4 +/- 5.8 kg) wa

70 ed length of acute hospital stay, maintained LBM, improved body composition and hepatic protein synth

71 igate the structure of the live bird market (LBM) contact network and the implications for virus spre

72 tional virologic study in live bird markets (LBM) in Hanoi, Vietnam, in October 2001.

73 which is associated with live-bird markets (LBM) in the Northeast United States, was first detected

74 etween 1994 and 2002 from live-bird markets (LBMs) in the northeastern United States and from three o

75 Vietnamese and Cambodian live bird markets (LBMs) to sustain circulation of highly pathogenic avian

76 loNDV isolates from U.S. live bird markets (LBMs) were analyzed and found to be genetically distinct

77 s isolated from Hong Kong live bird markets (LBMs) were not detected by a USDA-validated matrix gene

78 /100 mL leg/min) and loss of lean body mass (LBM) (-4.1% +/- 1.9%); P < 0.05.

79 of total body fat (TBF) and lean body mass (LBM) (n = 10,525) were followed for 13.6 (standard devia

80 rly individuals can increase lean body mass (LBM) and decrease fat, but interactive effects of growth

81 It is not clear how lean body mass (LBM) and fat mass (FM) compare in their associations wit

82 f early nutrition with adult lean body mass (LBM) and muscle strength in a birth cohort that was esta

83 y hyperinsulinemic clamp and lean body mass (LBM) and total body fat were assessed by (18)O-water adm

84 owered on a 5% difference in lean body mass (LBM) at 1 month.

85 me that evaluates whole-body lean body mass (LBM) based on CT data from limited-whole-body coverage w

86 of body mass index (BMI) and lean body mass (LBM) depletion on handgrip (HG) force and inspiratory mu

87 estimate a patient-specific lean body mass (LBM) from these MR-AC data.

88 Lean body mass (LBM) is a complex trait for human health.

89 outcomes included change in lean body mass (LBM) measured by dual-energy x-ray absorptiometry, quadr

90 A profound loss of lean body mass (LBM) occurred in both groups during the intervention per

91 ine excretion as an index of lean body mass (LBM) or muscle mass in healthy men and women.

92 Repletion of lean body mass (LBM) that patients lose in human immunodeficiency virus

93 butions of fat mass (FM) and lean body mass (LBM) to body weight, which vary according to age, sex, p

94 um ferritin, after change in lean body mass (LBM) was controlled for, were evaluated in subjects in t

95 of 18 AL (P < 0.001), while lean body mass (LBM) was unchanged.

96 , and 22 +/- 2 pmol x kg(-1) lean body mass (LBM) x min(-1) (P < 0.05, days 5 and 10 vs. baseline).

97 her total body mass (TBM) or lean body mass (LBM), 2) compared the independent contributions of LBM a

98 after adjustment for age and lean body mass (LBM), DES excretion in rapid decliners was 30% greater t

99 mass (SUL), calculated using lean body mass (LBM), is essential for the semiquantification of (18)F-F

100 gy deficit helps to preserve lean body mass (LBM), particularly when combined with exercise.

101 Lean body mass (LBM), skeletal muscle index (SMI), and fat mass (FM) wer

102 ients lost 8 +/- 1% of their lean body mass (LBM), whereas oxandrolone-treated patients had preserved

103 rophy [33.2 +/- 0.27 kcal/kg lean body mass (LBM)] than for both HIV-infected and healthy controls (2

104 The low bone mass (LBM) phenotype is the result of both the osteoblasts and

105 he diet with the percentage lean body mass (%LBM) or change in %LBM in older subjects.

106 e value (SUV) normalized by lean body mass ([LBM] SUL) is becoming a popular metric for quantitative

107 body composition (including lean body mass [LBM], appendicular lean mass [ALM], and fat mass); objec

108 Mean LBM decreased significantly from baseline, by 1.0% at mo

109 The older group had a mean LBM smaller than that of the younger group, which was ac

110 rt properties of the lens basement membrane (LBM) from the bovine eye.

111 In men, LBM increased by 0.1 kg with placebo, 1.4 kg with testos

112 fr1 inactivation in all limb bud mesenchyme (LBM) cells during limb initiation.

113 The lattice Boltzmann method (LBM) is adopted to simulate fluid flow and Knudsen diffu

114 he other hand, the Lattice Boltzmann Method (LBM) tracks the movement of collections of molecules, wh

115 urvival with higher FM% and higher "FM minus LBM percentiles" in both sexes, whereas a higher LBM was

116 At 36 months, LBM decreased by 2.8% in men age >/= 70 years and by 0.9

117 The hemagglutinin gene of most LBM isolates examined appeared to have been the result o

118 Most LBMs were connected to one another, suggesting that the

119 The average maximal accumulation of LBM (386 g/mo; 95% CI: 372, 399) occurred 0.5 y before t

120 2) compared the independent contributions of LBM and fat mass (FM) to EE, and 3) investigated whether

121 to estimate the independent contributions of LBM and FM to EE.

122 the Janmahasatian formula for estimation of LBM in modern PET scanners and display workstations is r

123 er day [P=.05]; 6.9 [1.7] vs 3.8 [2.9] kg of LBM [P=.005]; greater strength gains for various upper a

124 o 31% post-neoadjuvant therapy, with loss of LBM (-3.0 +/- 5.4 kg, P < 0.0001), but not FM (-0.3 +/-

125 The mean (+/-SD) loss of LBM (kg) at 1 month was -3.7 +/- 8.7 in the EN-S group,

126 esults were compared with the measurement of LBM from whole-body CT (reference standard) and the resu

127 les of FM and percentage FM (FM%) but not of LBM were associated with greater survival: HRs of 0.51 (

128 The results of LBM measurement evaluated with this technique were much

129 rage) to 0.998 (longer coverage) and SEMs of LBM ranging from 0.14 to 0.33 kg.

130 ibution of FM to EE is comparable to that of LBM in normal mice (expressed per gram of tissue) but is

131 tage of FM appears to be superior to that of LBM.

132 e to the current policy of a complete ban of LBMs in some areas.

133 ion of metabolic activity of tumors based on LBM-normalized standardized uptake value.

134 protein turnover for creatinine excretion or LBM eliminated the age effects.

135 after adjustment for creatinine excretion or LBM.

136 t was not due to reduced subcutaneous fat or LBM, but rather preferential loss of abdominal fat (P <

137 Division of EE by either TBM or LBM is confounded by body mass variation.

138 Participants' LBM and appendicular skeletal muscle mass were measured

139 old mice revealed a low bone mass phenotype (LBM) in both the distal femur and the vertebra of Krox20

140 llele led to Fgfr1 inactivation in posterior LBM cells.

141 or standard PN regimens during HSCT preserve LBM.

142 Alternative approaches to preserve LBM are needed.

143 s oxandrolone-treated patients had preserved LBM (+9 +/- 4%), P < 0.05.

144 ercepts of the regression equations relating LBM to average daily creatinine excretion were the same

145 ard LBM measurements and thus offers routine LBM-based SUV quantification in PET/MR.

146 to lentogenic class I viruses found in U.S. LBMs and wild waterfowl.

147 sed to calculate a reference LBMADP A second LBM estimate was derived from available MR-AC data using

148 Some LBMs that have been banned still are very active, and th

149 wded systems, while the proposed coupled SPT-LBM predicts the same behaviour as the kinetic Monte Car

150 -AC is shown to correlate well with standard LBM measurements and thus offers routine LBM-based SUV q

151 o) with a baseline and at least one on-study LBM assessment.

152 Over the 3-y study, %LBM increased by 2.6 +/- 3.6%.

153 The results indicate that LBM over-predicts the diffusion in 2D crowded systems, w

154 The LBM so obtained was compared with results from conventio

155 ote an automated program that determined the LBM from a CT with limited fields of acquisition and app

156 nes from representative H7 isolates from the LBM and elsewhere were sequenced, and the sequences were

157 he observed transport characteristics of the LBM are discussed in the context of established membrane

158 t strategic positions; and estimation of the LBM of the whole body on the basis of a predetermined re

159 bility of a method for the estimation of the LBM using the data of the low-dose CT from PET/CT acquir

160 Krox20(+/-) splenocytes, suggesting that the LBM is attributable to Krox20 haploinsufficiency in the

161 onnected to one another, suggesting that the LBM network may support large-scale disease spread.

162 icant effect on solute transport through the LBM that was opposite of the expected electrokinetic beh

163 ay to incorporate the crowding effect to the LBM.

164 is the predominant mechanism underlying the LBM phenotype of Krox20-deficient mice.

165 ly related to the viruses circulating in the LBMs.

166 The %LBM, defined as total body nonfat, nonbone tissue weight

167 eceived nandrolone decanoate increased their LBM by 3.1 +/- 2.2 kg (P < 0.0001).

168 A third LBM estimate was obtained from a sex-specific formula (L

169 A crowding-adaptation to LBM has been developed using SPT, allowing fast simulati

170 played a closer phylogenetic relationship to LBM-origin NDV.

171 Total LBM was determined by 40K counting in all subjects, and

172 low LBM group, but not when related to total LBM.

173 Unadjusted LBM and grip strength were similar in 2 groups.

174 To identify genomic loci underlying LBM, we performed a gene-based genome-wide association s

175 2+) transients were prolonged in SMMs versus LBMs and Ca(2+) release was disorganized in SMMs with re

176 was bromodeoxyuridine positive (SMMs versus LBMs: 3.1% versus 0.8%; P<0.05), and p16(INK4a) negative

177 d older groups, and the precision with which LBM could be determined from creatinine excretion was no

178 ation dynamics and reconstructed Alpine-wide LBM defoliation records reveals elevational shifts in LB

179 the proposed method correlated strongly with LBM derived from whole-body CT data, with correlation co

180 as significantly positively associated with %LBM at baseline (beta = 0.033, P = 0.006; adjusted for s

181 In women, LBM increased by 0.4 kg with placebo, 1.2 kg with HRT (P