ライフサイエンスコーパス: lean

1 ed to bridge a trace interval in associative leaning.

2 Bronchoalveolar lavage fluid from 23 lean, 12 overweight, and 20 obese subjects were examined

3 n overweight-to-obese sedentary (Ob/Sed) and lean active (L/Ac) individuals through dynamic, static,

4 Conversely, in response to drinking glucose, lean adolescents demonstrated increased PFC brain perfus

5 charides, glucose and fructose, in obese and lean adolescents.

6 hippocampal blood flow in obese relative to lean adolescents.

7 t glucose clearance and exercise capacity in lean adult mice.

8 owing loss of reward ('disappointment'), and Lean Amount birds failed to show a normal positive contr

9 One hundred lean and 100 overweight participants were recruited for

10 fusion-based orthorhombic structures, alpha''lean and alpha''iso.

11 ograde, trans-synaptic, viral tracer in male lean and db/db mice and whole-cell patch-clamp recording

12 inhibitory control was not different between lean and db/db mice.

13 Serum metabolite profiles of adult lean and juvenile mice were comparable, while that of ad

14 contrast, there were no differences between lean and nonlean individuals in the clock hour of food c

15 respectively) (all P < 0.01) but not between lean and obese (SUVmax, 7.9 [range, 4.2-17.3] vs. 4.0 [r

16 were unaffected by FAST versus BFAST in both lean and obese cohorts (all P > 0.1).

17 Five week old lean and obese female C57BL6/J mice were mated with chow

18 esized to reflect variable toxicokinetics in lean and obese individuals during times of increasing an

19 sducin), in oral and extra-oral tissues from lean and obese mice, remains poorly characterized.

20 rotein expression in response to exercise in lean and obese mice.

21 fibroblast growth factor 21 (FGF21) in both lean and obese mice.

22 obestatin levels were not different between lean and obese participants (P = 0.41).

23 In both lean and obese participants, infusion of escalating dose

24 ts of exogenous obestatin on forearm flow in lean and obese subjects and assessed its influence on ET

25 xidase protein ratio in previously sedentary lean and obese young men.

26 serum metabolomics profiling in a cohort of lean and obese, young, Chinese individuals.

27 ls have less metabolic BAT activity than the lean and young, but the role of the SNS in this decline

28 l tissues were endoscopically collected from lean, and morbidly obese subjects before and 3 months af

29 ced in the stomach and duodenum, compared to lean, and returned to normality post-LSG.

30 5g per 100g, comparing favourably with other lean animal products.

31 or men, each SD-increment increase in muscle lean area, muscle quality, and strength was associated w

32 women, each SD-increment increase in muscle lean area, muscle quality, and strength was associated w

33 ndensate from obese asthmatic (OA) patients, lean asthmatic (LA) patients, and obese nonasthmatic (ON

34 ndensate from obese asthmatic (OA) patients, lean asthmatic (LA) patients, and obese nonasthmatic (ON

35 edible portion on fresh weight basis in raw lean beef (A-age), lamb, pork and chicken average 1.58,

36 a on the total and haem iron contents in raw lean beef, chicken, lamb and pork meat samples.

37 Four age-matched (48.5 +/- 4.7 years) lean (BMI <25 kg/m(2)) females served as control subject

38 ype of Dab2 knockout mice was their striking lean body composition under a high fat and high caloric

39 white postmenopausal women, with a tall and lean body habitus and higher rates of scoliosis, pectus

40 Prior to and after bed rest, lean body mass (dual-energy X-ray absorptiometry) and qu

41 ation remained substantial when adjusted for lean body mass (highest HR: 1.05 [95% CI: 1.01 to 1.10]

42 rolled RCT was powered on a 5% difference in lean body mass (LBM) at 1 month.

43 rther aim was to estimate a patient-specific lean body mass (LBM) from these MR-AC data.

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

45 ptake lean body mass (SUL), calculated using lean body mass (LBM), is essential for the semiquantific

46 e during an energy deficit helps to preserve lean body mass (LBM), particularly when combined with ex

47 Lean body mass (LBM), skeletal muscle index (SMI), and f

48 n = 38,292) and appendicular (arms and legs) lean body mass (n = 28,330) measured using dual energy X

49 SUV corrected for lean body mass (SUL and SULpeak) were obtained.

50 The standardized uptake lean body mass (SUL), calculated using lean body mass (L

51 nome-wide association studies for whole body lean body mass and find five novel genetic loci to be si

52 B11, VCAN, ADAMTSL3, IRS1, and FTO for total lean body mass and for three single-nucleotide polymorph

53 efficacy endpoints were the median change in lean body mass and handgrip strength over 12 weeks and w

54 ) individuals from 33 cohorts for whole body lean body mass and in 45,090 (42,360 of European ancestr

55 ines was found to have beneficial effects on lean body mass and leg power in elderly men.

56 , and was a composite of stable or increased lean body mass and stability or improvement in two of th

57 d increased serum levels of WISP2, increased lean body mass and whole body energy expenditure, hyperp

58 morphisms were significantly associated with lean body mass either genome wide (p < 5 x 10(-8)) or su

59 ry taxa in recipient animals correlated with lean body mass gain; liver, muscle, and brain metabolism

60 Over 12 weeks, lean body mass increased in patients assigned to anamore

61 insight into the genetics of lean body mass.Lean body mass is a highly heritable trait and is associ

62 ificantly increased skeletal muscle mass and lean body mass over time.

63 t of the 9 measures left the association for lean body mass virtually unchanged (lowest HR: 1.33 [95%

64 stic was associated with BMD loss, but lower lean body mass was associated with greater BMD loss at b

65 However, after developing HF, loss of total lean body mass was disproportionate; men with HF lost 65

66 y) subjects from 25 cohorts for appendicular lean body mass was successful for five single-nucleotide

67 Lean body mass was the predominant anthropometric risk f

68 hip ratio to 1.37 [95% CI: 1.33 to 1.42] for lean body mass).

69 ical impedance-derived measures of fat mass, lean body mass, and fat percentage.

70 Anamorelin significantly increased lean body mass, but not handgrip, strength in patients w

71 Lean body mass, consisting mostly of skeletal muscle, is

72 Juvenile lean body mass, estimated using urinary creatinine excre

73 ood and skeletal muscle ammonia, increase in lean body mass, improved grip strength, higher skeletal

74 ssed by the change in SUVpeak, normalized to lean body mass, of the most (18)F-FDG-avid lesion (PERCI

75 methods including percentage change in SUVs, lean body mass-corrected (SUL) SULpeak, SULmax, and tota

76 se experience weight loss, including loss of lean body mass.

77 anthropometric measures after adjustment for lean body mass.

78 ar VCAN, ADAMTSL3, and IRS1 for appendicular lean body mass.

79 difference in both skeletal muscle mass and lean body mass.

80 ngs provide new insight into the genetics of lean body mass.Lean body mass is a highly heritable trai

81 than after placebo to maintain euglycemia in lean but not in overweight people.

82 n and quantification of BAT mass not only in lean, but also in obese, mouse phenotypes, in which this

83 For single-pulse laser ignition at lean conditions, the flame kernel separates through thir

84 mixed meal did not differ between obese and lean control subjects.

85 before and after bariatric surgery and in 10 lean control subjects.

86 The prevalence of polyneuropathy was 3.8% in lean controls (n = 2), 11.1% in the obese participants w

87 dition) from a weight management program and lean controls from a research website.

88 se blunted acetylcholine responses in KK and lean controls, but had no impact in KW, attributing reco

89 monocyte gene expression profile compared to lean controls.

90 bese (DIO) mice as compared with age-matched lean controls.

91 ompared to alcohol-addicted and non-addicted lean controls.

92 sorted monocytes of 35 obese children and 16 lean controls.

93 igh-fat diet for 12-14 weeks, or age-matched lean controls.

94 adian rhythms of Vo2 were conserved in young lean CT-1(-/-) mice (2 mo), CT-1 deficiency caused a pha

95 t-term and long-term outcomes as organs from lean donors.

96 -1beta, IL-6, and IL-17 in VAT explants from lean donors.

97 parison with metabolically healthy obese and lean donors.

98 n (EGP) rate was higher in OB+DM than OB and Lean during hyperinsulinemia.

99 for all three tested fish species, including lean fish containing 1% lipid.

100 By subtype, in addition to lean fish, consumption of large fatty fish showed a posi

101 M on highly uniform SERS substrates based on leaning gold-capped nanopillars, which showed an in-wafe

102 lipolysis, both models of AMPK-ASKO mice are lean, having smaller adipocytes with lower TAG and highe

103 breeding Nox1 knockout mice with db/db mice: lean (HdbWnox1), lean Nox1 knockout (HdbKnox1), obese (K

104 esponses during an oral glucose challenge in lean healthy participants.

105 Fourteen lean, healthy individuals randomly received either palm

106 or general intelligence (g) in nonhumans but lean heavily toward mammalian data.

107 gene profile in steatotic hepatocytes versus lean hepatocytes.

108 enhance the presence and activity of BAT in lean humans but also to improve the metabolic profile of

109 ain-imaging studies reveal that obese versus lean humans show greater responsivity of reward and atte

110 the seasonal beiging response in SC WAT from lean humans.

111 el formation process in ways that extend the lean ignition limit.

112 beginning of the biological night, than did lean individuals (low body fat) (log-rank P = 0.009).

113 do not show excess liver fat, whilst 16% of lean individuals develop NAFLD.

114 mulated glucose uptake rates in obese versus lean individuals were eradicated when normalised to whol

115 KEY POINTS: In lean individuals, 6 weeks of extended morning fasting in

116 ucose uptake rates are lower in obese versus lean individuals, but this difference is abolished when

117 up-regulates lipid turnover genes in SCAT of lean individuals.

118 y rich interpretations as far as cognitively lean interpretations are conceivable, and apply this rat

119 We have previously reported that lean juvenile offspring born to diet-induced obese rats

120 d flame speeds (at early times), an extended lean limit, increased combustion efficiency, and decreas

121 f Omega3 fatty acids (Omega3FA) on fatty and lean liver in hepatic surgery.

122 Fatty liver outcomes were compared with lean liver to assess steatosis-independent effects.

123 ese beneficial effects were also observed in lean liver, albeit at a smaller scale.

124 led multiple beneficial effects in fatty and lean livers in mice.

125 otably, mice with metastases in fatty versus lean livers were associated with improved survival.

126 We conclude that in healthy lean males, stimulation of EE and HGP is sustained durin

127 three separate infusion protocols in healthy lean males: A) 10-h overnight GCG infusion (6 ng/[kg x m

128 ody fat mass (-6.9 +/- 0.5 kg), appendicular lean mass (-0.7 +/- 0.1 kg), and appendicular fat mass (

129 es mean +/- SE: -7.9 +/- 0.6 kg), whole-body lean mass (-1.0 +/- 0.2 kg), whole-body fat mass (-6.9 +

130 abdominal fat (25.8%), trunk fat (18%), and lean mass (1.8%) were apparent (P < .001 for changes wit

131 evaluated the relation between appendicular lean mass (ALM) and relative leukocyte telomere length (

132 ietary pattern techniques) with appendicular lean mass (ALM), quadriceps strength (QS), and bone mine

133 Formula-fed infants gained more lean mass (difference: 303 g; 95% CI: 137, 469 g) than b

134 ual X-ray absorptiometry and examined as leg lean mass (LLM), ALM, and the ratio of ALM to body mass

135 lt translates into long-term preservation of lean mass (LM) in older adults remains unknown.

136 body (4.8% and 4.1%) and total appendicular lean mass (LM; 3.0% and 2.1%) compared to AA genotype, w

137 an BMI >/=30 exhibited substantially greater lean mass (SMD: 0.53; 95% CI: 0.19, 0.87) and leg streng

138 a bivariate GWAS meta-analysis of total-body lean mass (TB-LM) and total-body less head bone mineral

139 Appendicular lean mass also decreased in RDA compared with 2RDA (P =

140 erform bivariate GWAS analyses of total body lean mass and bone mass density in children, and show ge

141 m litters exposed to 0.8 ppm ozone had lower lean mass and fat mass than pooled control offspring.

142 GTx-026 significantly increased body weight, lean mass and grip strength by 60-80% over vehicle-treat

143 The participants had substantially greater lean mass and leg strength gains when PS and RET were us

144 In mdx mice SR8278 increased lean mass and muscle function, and decreased muscle fibr

145 itiating ART with TDF/FTC, no differences in lean mass and regional fat were found with RAL when comp

146 tput, whole body weight and composition, leg lean mass and skeletal muscle fibre area all remained un

147 de increased facial and body hair, increased lean mass and strength, decreased fat mass, deepening of

148 THg increased 0.4 ppm for each gram of lean mass catabolized in the higher dose birds.

149 Lean mass decreased less in the combination and resistan

150 Birds lost 6-16% of their lean mass during the fast, and THg increased an average

151 mostly accounted for by an increase in trunk lean mass found in 2RDA (+1.39 +/- 1.09 kg, P < 0.001).

152 ials (RCTs) reporting the efficacy of PS for lean mass gain, strength gain, and physical mobility imp

153 in lower body weight and fat mass and higher lean mass in animals and adult humans.

154 The 96-week percentage changes in fat and lean mass in the 2 PI arms were not different, thus the

155 gene-based genome-wide association study of lean mass index (LMI) in 1000 unrelated Caucasian subjec

156 The fat mass index (FMI) and lean mass index (LMI) were surrogates of adiposity and s

157 teraction, P < 0.05), and reduced whole-body lean mass loss after 7 d (CON compared with LEU: -1.5 +/

158 e (grams per day) and BMD, ALM, appendicular lean mass normalized for height (ALM/ht(2)), and QS (200

159 emale Tsc1 (tg) mice exhibit a higher fat to lean mass ratio at advanced ages than age-matched wild t

160 m age to 6-mo corrected age (CA) gained more lean mass than did those fed term formula (TF).

161 ait whereas genetic variants contributing to lean mass variation remain largely unknown.

162 and MBD3 genes was a novel locus underlying lean mass variation.

163 on BMI, but was confounded by differences in lean mass versus fat mass when modeled on weight.

164 Loss of appendicular lean mass was also greater with HF (-419.9 versus -318.2

165 Lean mass was estimated by dual X-ray absorptiometry and

166 sulted in abnormal substrate utilization and lean mass wasting.

167 omen with HF, loss of total and appendicular lean mass were also greater than in non-HF participants

168 of intervention, whole-body and appendicular lean mass were measured by using dual-energy X-ray absor

169 Fat mass and lean mass were measured using dual-energy-x-ray absorpti

170 Peripheral and central fat depots and lean mass were measured using standardized and centrally

171 aintained muscle quality (peak torque/kg leg lean mass) after 14 d of bed-rest inactivity (CON compar

172 to the previously observed association with lean mass, an even distribution of daily protein intake

173 th age, namely, to produce less fat and more lean mass, and enhances insulin sensitivity and energy e

174 r implantation prevents anorexia and loss of lean mass, and their inhibition after symptom onset reve

175 n in adipose tissue weight with no change in lean mass, assessed by magnetic resonance imaging.

176 (in kg/m(2))]) and body composition (fat and lean mass, body fat percentage) between predominantly br

177 Body composition, including fat mass, lean mass, bone mineral content, and bone mineral densit

178 ipose tissue inflammation and have increased lean mass, femoral length, and bone volume.

179 tion recipients, exercise is able to improve lean mass, muscle strength, and, as a consequence, aerob

180 was associated with disproportionate loss of lean mass, particularly among men.

181 es were attributable to greater accretion of lean mass, rather than fat mass.

182 d that activin A primarily triggered loss of lean mass, whereas IL6 was a major mediator of fat loss.

183 T3 or AAT3 decreases adiposity and increases lean mass.

184 ts revealed increased fat mass and decreased lean mass.

185 F%, suggesting association with both fat and lean mass.

186 ntrations (THg) in relation to reductions in lean mass.

187 iotropic effects on bone mineral density and lean mass.Bone mineral density and lean skeletal mass ar

188 man plot showed that the differences in mean lean masses between the studied technique and the refere

189 and leaner carcasses, as well as demand for lean meat from progressively health conscious consumers,

190 Concentration values in the edible (lean) meat fraction were significantly lower compared to

191 leucine decreases energy intake in healthy, lean men.

192 brite/beige) adipocytes is correlated with a lean, metabolically healthy phenotype, but whether a cau

193 deletion has no effect on insulin action in lean mice but sensitizes the liver to insulin during the

194 cts of ozone were also assessed in obese and lean mice deficient in gammadelta T cells and their wild

195 but not Spp1-deficient, mice into the VAT of lean mice fed a normal diet recapitulated the essential

196 aintained euglycemia comparable with that of lean mice for >6 weeks after cessation of CDN1163 admini

197 Conversely, ATM Exos obtained from lean mice improve glucose tolerance and insulin sensitiv

198 HDL from healthy humans and lean mice inhibits palmitate-induced adipocyte inflammat

199 PVN neurons fired spontaneously; whereas, in lean mice the majority of liver-related PVN neurons were

200 females, stress caused the gut microbiota of lean mice to more closely resemble that of obese mice.

201 increases in food intake and weight gain in lean mice upon high-fat diet feeding, and this injection

202 Furthermore, injection of lean mice with doxorubicin, a DNA damage-inducing drug,

203 e mice compared with those in HDM-challenged lean mice, and this was accompanied by high IL-33 and IL

204 In lean mice, DPD promoted metabolic inefficiency by increa

205 In lean mice, intraperitoneal (i.p.) or intracerebroventric

206 In lean mice, the divalent GLP-1 analogues were superior to

207 ils, and airway responsiveness in obese than lean mice.

208 lammation in obese mice but had no effect in lean mice.

209 and insulin resistance when administered to lean mice.

210 ian variations inversely with food intake in lean mice.

211 ils, and airway responsiveness in obese than lean mice.

212 e, and memory formation in obese, but not in lean mice.

213 e and increases VEGF serum concentrations in lean mice.

214 mitochondrial biogenesis and angiogenesis in lean mice.

215 insulin sensitivity and glucose tolerance in lean mice.

216 sphorylation site in SIRT1 in obese, but not lean, mice, and this phosphorylation was catalyzed by ca

217 of administration in overweight, rather than lean, mice.

218 different in obese-stimulated compared with lean mini-pigs.

219 tures' reluctance, entomophagy practices are leaning more towards incorporating insects into food pro

220 LPS stimulation compared with those born to lean mothers, at the level of secreted immune mediators

221 d 4 ligands compared to those collected from lean mothers.

222 nknown and may contribute to the recovery of lean muscle.

223 Forty-nine healthy lean (n = 29) and obese (n = 20) adults provided SCAT bi

224 n three groups: lean women without diabetes (Lean, n = 25), obese women without diabetes (OB, n = 26)

225 esel engines, the poor thermal durability of lean nitrogen oxides (NOx ) aftertreatment systems remai

226 based on stimulation and body weight (i.e., lean nonstimulated, obese nonstimulated, and obese stimu

227 Methods: Twenty adult lean normal subjects (10 women and 10 men; mean age +/-

228 Twenty adult lean normal subjects (10 women and 10 men; mean age +/-

229 ted selective catalytic reduction filter and lean-NOx trap after-treatment technologies can reduce th

230 ckout mice with db/db mice: lean (HdbWnox1), lean Nox1 knockout (HdbKnox1), obese (KdbWnox1), and obe

231 In this study, we report that in lean offspring of non-HFD-fed dams, essential promoter r

232 MCL) were determined in young lean (YL), old lean (OL), and old overweight (OO) males.

233 Leaning on a wealth of findings on the role of reward in

234 ning (35 % as calories) diet (AFLD model) or lean or high-fat (12 or 60 % derived from fat, respectiv

235 id not differ among cohorts of normoglycemic lean or obese and type 2 diabetes mellitus patients unde

236 AT atrophy or alter metabolic phenotypes in lean or obese animals.

237 h2 is associated with enlarged adipocytes in lean or obese mice.

238 e tissues is associated with overexposure of lean organs to circulating triglycerides (TGs) and nones

239 Changes for all fat and lean outcomes were not different between the PI arms or

240 n the nucleus of the solitary tract (NTS) of lean ovariectomized (OVX) rodents.

241 oss a 24-h day in 3 age-matched, male groups-lean, overweight/obese (OW/OB), and OW/OB with T2DM-in c

242 ldine-based LOHC system composed of hydrogen-lean, partially hydrogenated, and fully hydrogenated for

243 cemic status in well-characterized obese and lean participants and investigate the association of spe

244 oad in healthy lean participants.Ten healthy lean participants with a body mass index (in kg/m(2)) of

245 response to an oral glucose load in healthy lean participants.Ten healthy lean participants with a b

246 This study investigated whether lean patients (Ln) with T2D exhibit increased ectopic an

247 ing altered growth and body-composition (fat/lean percentage) and impaired glucose/insulin-metabolism

248 explaining increased energy expenditure and lean phenotype in these mice.

249 Finally, the lean phenotype of Ati-CB1-KO mice and the increase in al

250 l models, overexpression of GDF15 leads to a lean phenotype, hypophagia and other improvements in met

251 m and Coriobacteriaceae taxa associated with lean phenotype, increased in WD + PDX mice.

252 ease in RBM28 mRNA expression in breeds with lean phenotypes.

253 nt-sensing mechanisms after the ingestion of lean pork between obese, overweight, and healthy-weight

254 em efficiency measures and the employment of lean practices and process improvements can have positiv

255 matography-mass spectroscopy in nondiabetic, lean, predominantly nonischemic, advanced heart failure

256 To identify whether lean processes can be used to improve wait times for sur

257 before, during, and after implementation of lean processes over 3 fiscal years (FYs) at a tertiary c

258 systems redesign and standardization (SOP), Lean quality improvement, SOP + TT combination, or Lean

259 mation and enhances tissue insulin action in lean rats and 2) prevents muscle metabolic alterations a

260 In 12-week-old lean rats, UnAG (4-day, twice-daily subcutaneous 200-mic

261 er grafts from Zucker rats transplanted into lean recipients.

262 ients is reduced compared with allografts in lean recipients.

263 Lean red meat and low-fat dairy produced a similar glyce

264 scle biopsies were taken from eight Trained, Lean sedentary, Obese and T2DM subjects.

265 nsity and lean mass.Bone mineral density and lean skeletal mass are heritable traits.

266 or height, WB lean soft tissue, appendicular lean soft tissue, and WB and skeletal site-specific BMC

267 define the mean trajectories for height, WB lean soft tissue, appendicular lean soft tissue, and WB

268 the field and assess the viability of water-lean solvents for postcombustion CO2 capture.

269 ility of postcombustion CO2 capture by water-lean solvents, by separating fact from fiction for both

270 nd thermodynamic properties of notable water-lean solvents, with a discussion of how such properties

271 echnical performance; systems interventions (Lean & SOP, 2 & 3) improved nontechnical skills and tech

272 as key mediators of this injury in a normal (lean) state, but data about their role in a steatotic li

273 d between our unique polygenic mouse Fat and Lean strains that were generated by divergent selection

274 Eight lean subjects were studied by measuring arteriovenous co

275 ld in obese subjects with NGT and IGT versus lean subjects with NGT (8.0 +/- 1.1 and 9.2 +/- 0.7 vs.

276 ed that pregnant, obese women, compared with lean subjects, have decreased plasma volume expansion al

277 ntolerant humans compared with biopsies from lean subjects.

278 llite cells probably impacts the recovery of lean tissue following a severe burn, contributing to pro

279 Bed rest resulted in 1.4 +/- 0.2 kg lean tissue loss and a 3.2 +/- 0.9% decline in quadricep

280 role for satellite cells in the aetiology of lean tissue recovery following a severe burn injury.

281 osure methods to extend EPS applicability to lean tissue.

282 a weight-loss intervention on the masses of lean tissues and organs in humans is not well known.

283 ndicate that methylmercury is mobilized from lean tissues during protein catabolism and results in ac

284 e pollutant methylmercury accumulates within lean tissues of birds and other animals.

285 lipolysis, and better fatty acid handling by lean tissues.

286 apparently healthy, demonstrate an increased lean-to-fat ratio, and show dramatically improved insuli

287 uality improvement, SOP + TT combination, or Lean + TT combination.

288 Using a "lean" version of the model-free approach S(2) order para

289 whereas the adipocyte-conditioned media from lean volunteers had no effect on IL32 mRNA levels.

290 lipids showed maximal difference at 5:00 AM (lean vs. OW/OB) and at 5:00 PM (OW/OB vs. T2DM).

291 an obese typical Chinese piglet breed and a lean Western breed was used to identify genetic and mate

292 Lean wildtype and obese db/db mice were pretreated with

293 sal condition were compared in three groups: lean women without diabetes (Lean, n = 25), obese women

294 microscopy of IMCL) were determined in young lean (YL), old lean (OL), and old overweight (OO) males.

295 In lean young adults, 24-h SER transiently elevated subject

296 nd cold-induced activation of BAT and WAT in lean young adults.

297 Zucker diabetic fatty (ZDF) and Male Zucker lean (ZL) control rats were studied at 13 weeks.

298 ns were conducted in 3 groups (Wistar-Kyoto, lean ZSF1, and obese ZSF1) at 20 and 25 weeks of age.

299 aster muscle of obese Zucker rats (OZR; with lean Zucker rats (LZR) as controls), we determined indic

300 Male lean Zucker rats received water (control, n = 8) or meld