ライフサイエンスコーパス: lipid profile

1 iation between shorter height and an adverse lipid profile.

2 Raltegravir produced the most favorable lipid profile.

3 ffness, nitric oxide, endothelin 1, or blood lipid profile.

4 -C are routinely available from the standard lipid profile.

5 pressures, fasting blood glucose level, and lipid profile.

6 oral vitamin D3 or UVB does not improve the lipid profile.

7 scular inflammatory markers, such as CRP and lipid profile.

8 hough no changes were observed in the plasma lipid profile.

9 ism affect gene expression and the resulting lipid profile.

10 and are accompanied by improvements in serum lipid profile.

11 DKD(-)) and similar duration of diabetes and lipid profile.

12 LDLr(-/-) group despite the more atherogenic lipid profile.

13 Attributable change in fasting lipid profile.

14 risk, mainly attributed to an improvement in lipid profile.

15 ic syndrome, type 2 diabetes, and an adverse lipid profile.

16 ction with regard to a patient's atherogenic lipid profile.

17 ary outcome was the effect of REGN727 on the lipid profile.

18 andomized to the drug, despite improving the lipid profile.

19 to n-3 PUFA ratio and beneficially modulates lipid profile.

20 glucose homeostasis, fatty liver, and plasma lipid profile.

21 vement in insulin resistance, adipokine, and lipid profile.

22 ng/mL, is correlated with a more atherogenic lipid profile.

23 ing blood samples were collected to estimate lipid profile.

24 ctions and histology, insulin resistance and lipid profile.

25 is independently associated with an improved lipid profile.

26 r body weight and an unclear effect on blood lipid profile.

27 oorganisms based upon their species-specific lipid profile.

28 glucose tolerance test, a liver panel, and a lipid profile.

29 1, ABCG1 and CPT1A were also associated with lipid profile.

30 se and type 2 diabetes, as well as a healthy lipid profile.

31 ccompanied by specific changes in the fungal lipid profile.

32 ApoE loss in the context of a normal plasma lipid profile.

33 aortic roots, which correlated with altered lipid profiles.

34 and normoxia can be differentiated by their lipid profiles.

35 ht loss, and changes in body composition and lipid profiles.

36 rom cardiometabolic factors, including serum lipid profiles.

37 ttributed to oxidative stress and disordered lipid profiles.

38 grains have been reported to improve plasma lipid profiles.

39 d enabling a reliable evaluation of acquired lipid profiles.

40 k in part because of their effects on plasma lipid profiles.

41 ups and is associated with cardio-protective lipid profiles.

42 se-lowering actions and favorable effects on lipid profiles.

43 old children of mothers with ICP had altered lipid profiles.

44 r would not be expected to modify the plasma lipid profiles.

45 Three experiments compared pollen lipid profiles.

46 cerides are a commonly measured component of lipid profiles.

47 endence, especially in smokers with abnormal lipid profiles.

48 ED group experienced greater improvements in lipid profiles.

49 PN-cholestasis and has been shown to improve lipid profiles.

50 igh-fiber diets are associated with improved lipid profiles.

51 controlling for anthropometric variables and lipid profiles.

52 d its treatment are associated with abnormal lipid profiles.

53 rroborated by indirect measurements based on lipid profiles.

54 arriers in both cohorts had improved fasting lipid profiles.

55 il, and the United States endorse nonfasting lipid profiles.

56 ave been limited to measures of conventional lipid profiles.

57 R507, adversely altered kidney function and lipid profiles.

58 activity as shown by enzymatic analysis and lipid profiling.

59 dependent LC-MS(2) and LC-MS(3) analysis for lipid profiling.

60 uced a significant (P<0.001) increase in the lipid profile across the board and equally significantly

61 The plasma lipid profile, activity of liver enzymes, and oxidative

62 urthermore, soy significantly improved blood lipid profile, adipose tissue inflammation, and aortic s

63 HDL cholesterol versus those with an optimal lipid profile, adjusted hazard ratios for total CHD, CVD

64 n carbohydrate metabolism characteristics or lipid profile after the 24 wk of intervention.

65 Additionally, plasma lipid profiles also displayed an increase in palmitoleat

66 increased fat deposition was associated with lipid profile alterations characterized by an increase i

67 alteration effect of atherogenic diet on the lipid profile and antioxidant enzymes activities.

68 and kidney from each group were analyzed for lipid profile and antioxidant enzymes activities.

69 Only black African children had a blood lipid profile and associated dietary pattern likely to p

70 control mice on a high-fat diet reduced the lipid profile and atherosclerosis.

71 n the liver of A(2b)AR-null mice reduced the lipid profile and atherosclerosis.

72 ft common carotid artery (LCCA), and fasting lipid profile and C-reactive protein (CRP).

73 hanges, as its inhibition altered the fungal lipid profile and caused a shift in the host-bacterial i

74 emiological studies show that an unfavorable lipid profile and coronary artery disease (CAD) are risk

75 ave addressed the relationship between serum lipid profile and HOA.

76 Plasma lipid profile and homocysteine levels, blood pressure, o

77 or anthropometric variables, blood pressure, lipid profile and hormone levels.

78 feron alpha and RBV can significantly affect lipid profile and IR in HCV/HIV-coinfected persons.

79 mocysteine, ALT, alkaline phosphatase (ALP), lipid profile and liver ultrasonographic examination.

80 phenolic and fibre concentrations, on serum lipid profile and oxLDL of male Wistar rats fed a choles

81 nification phenotypes but still had the same lipid profile and reduced photosynthesis as dgd1 single

82 The association between serum lipid profile and RHOA was modeled using multivariable l

83 s to determine the association between serum lipid profile and the incidence of radiographic hand ost

84 ammation, reduced energy generation, altered lipid profiles and a pro-thrombotic state.

85 tics were employed to evaluate the generated lipid profiles and abundances.

86 ted the association of SFA intake with serum lipid profiles and ASVD mortality in a population-based

87 of a functional genetic variant of IL-32 on lipid profiles and CVD risk was therefore studied in who

88 Dyn1) has been shown to assemble on narrower lipid profiles and facilitate spontaneous membrane fissi

89 vention and were analyzed for carotenoid and lipid profiles and inflammatory markers.

90 of mutant animals, as well as altered plasma lipid profiles and inflammatory parameters.

91 mples were collected from offspring mice for lipid profiles and insulin resistance, indirect calorime

92 However, it may have positive effects on lipid profiles and insulin sensitivity during a weight-l

93 ost metabolism, we examined changes in serum lipid profiles and intrahepatic expression of lipid-rela

94 Baseline lipid profiles and metabolic syndrome rates (approximate

95 ations that are widely prescribed to improve lipid profiles and prevent cardiovascular disease, but t

96 Fibrates improve lipid profiles and prevent cardiovascular events in peop

97 inhibitors, a drug class designed to improve lipid profiles and prevent cardiovascular events.

98 overed and described as conferring favorable lipid profiles and reduced subclinical atherosclerotic d

99 rsely, there were insignificant decreases in lipid profiles and serum fasting glucose of patients wit

100 ing (MALDI-MSI) in order to characterize the lipid profiles and their spatial distribution.

101 HFD altered skeletal muscle lipid profiles and up-regulated genes involved in lipid

102 Integrated lipid profiling and metabolic flux analysis revealed tha

103 trongly associated outcomes included leptin, lipid profile, and blood pressure.

104 tant with respect to antibiotic sensitivity, lipid profile, and ethidium efflux.

105 sment of insulin resistance, serum ferritin, lipid profile, and liver function tests improved irrespe

106 high-sensitivity C-reactive protein (hsCRP), lipid profile, and white blood cell (WBC) count, at base

107 stroke, with a corresponding antiatherogenic lipid profile, and with increased longevity, without adv

108 by improving insulin sensitivity, improving lipid profiles, and maintaining islet morphology.

109 nd an exciting coalescence of genome mining, lipid profiling, and tracer studies collectively has led

110 n, or hyperlipidemia; body mass index (BMI); lipid profile; and levels of glucose or glycosylated hem

111 ted in non-immune-related diseases including lipid profiles, anthropomorphic measurements, cancer and

112 We defined an "optimal" lipid profile as HDL cholesterol >/=40 mg/dL (men) or >/

113 1,954, 55% male, 45 +/- 6 years) had fasting lipid profiles assessed, 2002 to 2005.

114 Cardiovascular risk factor distribution and lipid profile at baseline were less beneficial in men th

115 By comparing whole-tissue lipid profiles between our lines, we show that each line

116 ed fat, achieved greater improvements in the lipid profile, blood glucose stability, and reductions i

117 .45) but no improvement in the overall serum lipid profile, blood pressure, and glycemic control comp

118 can help individuals to achieve their target lipid profile, body composition, and fitness and glycaem

119 Diet reversal could improve lipid profile but could not prevent renal complications

120 d EPF volume reduction paralleled changes in lipid profile but not with improved glycemic profile var

121 f CHD and CVD than participants with optimal lipid profiles but no difference in survival after a med

122 ion of phosphatidic acid (PA) and changes in lipid profiles, but the enzymatic basis and the function

123 Molecular lipid profiling by mass spectrometry may improve cardiov

124 Lipid profiling by mass spectrometry of mitochondria iso

125 examined 1,340,614 U.S. adults who underwent lipid profiling by vertical spin density gradient ultrac

126 We therefore investigated whether lipid profiling can inform diabetes prediction by perfor

127 We investigated how polar lipid profiles change during leaf development and in res

128 Changes in TBR did not correlate with lipid profile changes.

129 ion display improved glucose sensitivity and lipid profiles combined with increased oxygen consumptio

130 ow-up, 21% of patients who received diet had lipid profile compatible with dyslipidemia compared with

131 The polar lipid profile consisted of phosphatidylethanolamine, dip

132 or knockdown of Tm6sf2 in mice alters serum lipid profiles, consistent with the association observed

133 e tissue and cultured myotubes, and temporal lipid profiles correlated with transcript profiles of ge

134 Dissection of the PSR1-induced lipid profiles corroborates its role in coordinating mul

135 ontent and diabetes risk and demonstrate how lipid profiling could aid in clinical risk assessment.

136 Transcriptome and cuticular lipids profiling coupled with comprehensive microscopy r

137 TLR3 deficiency also modified the plasma lipid profile, decreasing VLDL levels due to decreased t

138 and depression; but it may adversely affect lipid profiles depending on how the beverage is prepared

139 This survey revealed substantial lipid profile differences between neurons and whole brai

140 Such changes masked the modifications in the lipid profile due to the injury and only after summing t

141 s possible to unveil the real changes in the lipid profile due to the lesion.

142 distribution of plasma lipids, we performed lipid profiling during oral glucose tolerance testing, p

143 directly measured components of the standard lipid profile explained >86% of the variance in percenti

144 is revealed significant perturbations in the lipid profile following CA-diet feeding, with increased

145 karyotic pathway, resulting in the switch of lipid profile from 16:3 to 18:3.

146 The analysis of lipid profiles from cells grown on cholesterol revealed

147 Our data showed better improvement in lipid profiles from long-term low-fat diet intake in the

148 nitoring with proper spatial distribution of lipid profiles from tumor tissues after plate imprinting

149 ases and controls in terms of lung function, lipid profile, glucose tolerance, glycated haemoglobin A

150 e demonstrated improvement in blood glucose, lipid profile, glycated haemoglobin and other parameters

151 Collectively, these data show that lipid profiling greatly benefits from an isopropanol pre

152 ants, including 30 individuals with a normal lipid profile (group H), 30 patients with hypertriglycer

153 sease, and particularly those with favorable lipid profiles, have reduced incidence of coronary heart

154 Rabbits serum lipid profile, hematology and histology were investigate

155 d other segment/wall-specific CIMT measures, lipid profile, high-sensitivity C-reactive protein (hsCR

156 mice exhibited similar body weight and serum lipid profiles; however, both MKP-1(+/-) and MKP-1(-/-)

157 A 60 min lipid profiling HPLC-QTOF method for the lipophilic phas

158 nhibitor, exhibited favorable changes in the lipid profile in a phase II study.

159 owning of white adipose tissue, and improved lipid profile in an AdipoR1-expressing but not an AdipoR

160 Nevertheless, biochemical analysis of the lipid profile in blood in vitro remains the most common

161 weeks, which produced only minor changes in lipid profile in C57/BL6 mice, markedly augmented the le

162 deficiency is associated with an unfavorable lipid profile in cross-sectional analyses, correcting fo

163 onal appetite regulation but can improve the lipid profile in healthy young males.

164 well as a more beneficial blood glucose and lipid profile in homozygous transgenic mice, in both sex

165 urthermore, IAP supplementation improves the lipid profile in mice fed a standard, low-fat chow diet.

166 F-1 improved overall insulin sensitivity and lipid profile in serum and reduced body adiposity, but w

167 To better describe the frequency and lipid profile in the general population, we as part of t

168 ative stress and improved (p<0.05) the serum lipid profile in the high-fat dietary groups; meanwhile,

169 body metabolism, we aimed at studying muscle lipid profiles in a temporal manner.

170 udies in humans have related birth weight to lipid profiles in adulthood.

171 otic plaque size without altering the plasma lipid profiles in apolipoprotein E-deficient mice.

172 c studies measure and discover metabolic and lipid profiles in biological samples, enabling a better

173 ators produced, whereas similarities between lipid profiles in blister fluid and epidermis indicated

174 ight) for an additional 4 wk improved plasma lipid profiles in both APOE3 and APOE4 mice.

175 nfounders is thus necessary to compare serum lipid profiles in clinical studies.

176 enhanced ethanol clearance, altered hepatic lipid profiles in favor of increased levels of polyunsat

177 Distinct lipid profiles in lymphomas with high and low MYC expres

178 s and cell samples to investigate changes in lipid profiles in MYC-induced lymphoma.

179 en performed at doses insufficient to affect lipid profiles in populations with inadequate control of

180 gle-nucleotide polymorphism (SNP) in IL32 on lipid profiles in RA patients and individuals, suggestin

181 Studies of children's blood lipid profiles in relation to asthma are few, and the re

182 he Genotype-Tissue Expression project and of lipid profiles in the Ludwigshafen Risk and Cardiovascul

183 e diel cycle, we observed temporally dynamic lipid profiles in three cellular compartments: host cora

184 iquid chromatography/mass spectrometry-based lipid profiling in 189 individuals who developed type 2

185 w-egg diet (<2 eggs/wk) affected circulating lipid profiles, in particular high-density lipoprotein (

186 lipid extraction and measurement by UPLC-MS lipid profiling, including four protein precipitation me

187 tent as assessed by noninvasive (1)H-MRS and lipid profiling independent of changes in hepatic de nov

188 Quantitative lipid profiles indicated increased polyunsaturation of f

189 pe and fish-oil supplementation on the blood lipid profile, inflammatory markers, vascular function (

190 Secondary outcomes included lipid profiles, inflammatory markers, 24-h ambulatory bl

191 diometabolic health markers, namely obesity, lipid profile, insulin resistance, and blood pressure.

192 abdominal fat mass distribution, along with lipid profile, insulin sensitivity, and high-sensitivity

193 The blood lipid profile is associated with asthma, airway obstruct

194 We sought to examine whether the lipid profile is associated with concurrent asthma, alte

195 Intriguingly, this lipid profile is reminiscent of detergent-insoluble memb

196 ption promotes development of an unfavorable lipid profile is strong and suggests that the upper adde

197 ved nutritional profile considering the full lipid profile, key vitamins, minerals, and micronutrient

198 es have been associated with dyslipidemia, a lipid profile known to increase cardiovascular disease r

199 Lipid profile levels were statistically significant on c

200 t was independently associated with improved lipid profile, losing deep subcutaneous adipose tissue w

201 ] </=60 ml/min/1.73 m(2)), fibrates improved lipid profiles (lowered total cholesterol [-0.32 mmol/l,

202 h oral glucose tolerance tests (OGTT), serum lipid profiles, magnetic resonance imaging (MRI) for ass

203 to statin monotherapy to further modify the lipid profile may include combination therapy to either

204 The developed lipid profiling method was applied to mitochondrial samp

205 designed to clarify the relationship between lipid profile, morbidity as assessed by Killip classific

206 Our results demonstrate that serum lipid profiles need to be interpreted with caution since

207 tory cytokines were significantly decreased, lipid profiles normalized, and liver function and histol

208 Fasting for >8 h, as previously required for lipid profiles, normally only occurs a few hours before

209 a convenience sample of consecutive clinical lipid profiles obtained from 2009 through 2011 from 1,35

210 Moreover, the reproducibility of lipid profiles obtained in both polarity modes was evalu

211 , was associated with adverse changes in the lipid profile of children with hypercholesterolemia, alt

212 The aim of this work was to analyse the lipid profile of different bakery products currently com

213 ed its suitability for the evaluation of the lipid profile of human blood plasma samples.

214 rylation and thus activity, we monitored the lipid profile of nocodazole-synchronized mouse NIH 3T3 f

215 CVD focuses on controlling or improving the lipid profile of patients at risk.

216 The initial lipid profile of patients with acute myocardial infarcti

217 mption did not have an adverse effect on the lipid profile of people with T2D in the context of incre

218 The lipid profile of the livers of DR mice is correspondingl

219 ques were employed to fully characterise the lipid profile of these Mediterranean seaweeds, such as G

220 We sought to further analyze the hepatic lipid profile of these mice by electrospray ionization m

221 The lipid profiles of cell body- and synapse-enriched region

222 Lipid profiles of cells grown with excess phosphate cons

223 as to describe changes in the fatty acid and lipid profiles of children with PN-cholestasis who were

224 Lipid profiles of fatm and ram2 suggested that FatM incr

225 Lipid profiles of fish oil extracted from trout heads, s

226 ted diseases, better cognitive function, and lipid profiles of healthy aging.

227 ss spectrometry (ME-SIMS) to investigate the lipid profiles of neuronal cells.

228 transcript abundance and changes in cuticle lipid profiles of resistant and susceptible plants.

229 Lipid profiles of serum, liver and adipose tissues, bile

230 These results demonstrated that the lipid profiles of the studied species are of nutritional

231 onounsaturated fatty acids distinguished the lipid profiles of the three crab species.

232 (DESI-MS) imaging was applied to analyze the lipid profiles of thin tissue sections of 68 samples of

233 s used in an imaging mode to interrogate the lipid profiles of thin tissue sections of canine spontan

234 We performed a comparative pollen lipid profiling of 22 commonly allergenic plant species

235 he detection of 36 lipid species but allowed lipid profiling of individual organs.

236 Here, an in-depth lipid profiling of induced lung sputum using high-resolu

237 To determine whether lipid profiling of liver tissue can identify metabolic s

238 e a method for direct, quantitative, in vivo lipid profiling of oil-producing microalgae using single

239 A quantitative lipid profiling of patient plasma was also conducted by

240 Lipid profiling of the C. reinhardtii cells revealed tha

241 s no statistically significant difference in lipid profiles or atherosclerotic lesion development bet

242 o have different effects on hunger, satiety, lipid profiles, or other inflammatory and metabolic risk

243 To address this, we investigated lipid profiles over 24 h in human skeletal muscle in viv

244 and better glycemic control (p = 0.001) and lipid profiles (p = 0.01).

245 story, Fasting Blood Glucose, dyslipidaemia, lipid profile, parity and use of oral contraceptive pill

246 ion to improved adipokine, inflammatory, and lipid profiles, PPARgamma activation in mature adipocyte

247 Conventional lipid profiling procedures involve the analysis of tissu

248 e possible effects of L/Zi administration on lipid profile, protein genes associated with oxidative s

249 Here we use the lipid profiles, radiocarbon, and stable carbon isotopic

250 ons, inducing weight loss, and improving the lipid profile reduces cardiovascular risk in people with

251 boratories, and clinicians alike, nonfasting lipid profiles represent a simplification without negati

252 physical activity, systolic blood pressure, lipid profile, retinopathy, estimated glomerular filtrat

253 Although the lipid profile returns to near pretreatment levels after

254 A comparison of anemone lipid profiles revealed a subset of lipids that show dra

255 Lipid profiling revealed a significant reduction in fatt

256 Fat body lipid profiling revealed changes in both carbon chain le

257 Lipid profiling revealed lower monogalactosyl but higher

258 Lipid profiling revealed that 34C species of phosphatidy

259 Lipid profiling revealed that sEH deletion decreased ret

260 density profiles with a newly invented basic lipid profile scaling method that minimizes the number o

261 Lipid profiling shows decreased total galactolipid and p

262 LC-MS-based lipid profiling shows that 11 lipids with specific chemi

263 es mellitus, smoking, body mass index (BMI), lipid profile, social deprivation, SMI diagnosis, prescr

264 trometry (IMS), we determined alterations of lipid profiles specifically localized to the retinal pig

265 ial function; but (ii) there is no effect on lipid profiles--supporting specificity.

266 e 1 diabetes have a less atherogenic fasting lipid profile than those without diabetes but paradoxica

267 heightened oxidative stress, and atherogenic lipid profile that may increase women's risk for coronar

268 In conclusion MALDI-MSI described specific lipid profiles that could be used as sensors of oxygen l

269 ion, current smoking, diabetes mellitus, and lipid profile, the former NFL athletes still had signifi

270 that the strains had significantly different lipid profiles: the BL-04 membrane contained higher perc

271 protein hepatic-specific (CREBH), modulates lipid profiles to protect the liver from injuries upon t

272 We have applied mass spectrometry-based lipid profiling to study the levels of arachidonate-cont

273 We applied mass spectrometry-based lipid profiling to study the substrate specificities of

274 sample was drawn from each to determine the lipid profile (total cholesterol, triglycerides, low-den

275 Serum biomarkers included lipid profile [total cholesterol, high-density lipoprote

276 g biomarker discovery approach that compares lipid profiles under pathological and physiologically no

277 ion procedure for high-throughput untargeted lipid profiling using UPLC-MS.

278 In early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels

279 Serum lipid profile variables were analysed as continuous vari

280 relapses were not associated with any of the lipid profile variables.

281 ion were characterized by colony morphology, lipid profile via thin-layer chromatography and matrix-a

282 In addition lipid profile was done in all the patients with normal s

283 A lipid profile was obtained after an overnight fast.

284 le-nucleotide polymorphisms (SNPs), of serum lipid profiles, we identified a major linkage signal for

285 Using mass-spectrometry-based global lipid profiling, we identify individual lipids that are

286 ptive thermogenesis, and serum metabolic and lipid profile were assessed in LCN2-deficient mice fed a

287 Body weight, adipocyte size, and plasma lipid profile were not affected by isoflavone supplement

288 nd after intervention, 24-h food records and lipid profile were obtained.

289 sessment for insulin resistance, hormone and lipid profiles were also assessed.

290 C-reactive protein (CRP), interleukin-6, and lipid profiles were determined with high-sensitivity ass

291 ypercholestrolemic rats for 28days and serum lipid profiles were estimated.

292 Centesimal composition and lipid profiles were evaluated in muscle tissue of four s

293 Lipid profiles were matched to the specific IL-32 genoty

294 esicle-like structures, and altered cellular lipid profiles were seen in conidia grown on a variety o

295 mission electron microscopy and quantitative lipid profiling were used to examine the effects of diph

296 lysis of variance was used for comparison of lipid profile, whereas Kruskal-Wallis test was used for

297 s spectral data reveal tissue type-dependent lipid profiles which are consistent across the n = 110 s

298 t differences for fasting plasma glucose and lipid profiles within both groups after 12 wk.

299 t circumference, fasting plasma glucose, and lipid profiles within both groups over 24 wk.

300 yceride form improve glucose sensitivity and lipid profiles without weight gain in diabetic mice.