ライフサイエンスコーパス: lipid profile

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

2 ism affect gene expression and the resulting lipid profile.

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

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

5 ing blood samples were collected to estimate lipid profile.

6 ctions and histology, insulin resistance and lipid profile.

7 is independently associated with an improved lipid profile.

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

9 oorganisms based upon their species-specific lipid profile.

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

11 1, ABCG1 and CPT1A were also associated with lipid profile.

12 sition, and blood pressure, and improved the lipid profile.

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

14 ccompanied by specific changes in the fungal lipid profile.

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

16 iation between shorter height and an adverse lipid profile.

17 Raltegravir produced the most favorable lipid profile.

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

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

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

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

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

23 and are accompanied by improvements in serum lipid profile.

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

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

26 Attributable change in fasting lipid profile.

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

28 rovements in clinical markers, primarily the lipid profile.

29 ildren in objective terms through changes in lipid profile.

30 dolutegravir (DTG)-based regimen may improve lipid profile.

31 cacious and well tolerated, and improved the lipid profile.

32 estigating the association of NPs with serum lipid profile.

33 ct this toxic metalloid species has on their lipid profile.

34 ion between higher NP levels and a favorable lipid profile.

35 and normoxia can be differentiated by their lipid profiles.

36 controlling for anthropometric variables and lipid profiles.

37 rroborated by indirect measurements based on lipid profiles.

38 arriers in both cohorts had improved fasting lipid profiles.

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

40 ave been limited to measures of conventional lipid profiles.

41 R507, adversely altered kidney function and lipid profiles.

42 demonstrating molecular changes in glycerol lipid profiles.

43 aortic roots, which correlated with altered lipid profiles.

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

45 rom cardiometabolic factors, including serum lipid profiles.

46 ttributed to oxidative stress and disordered lipid profiles.

47 grains have been reported to improve plasma lipid profiles.

48 d enabling a reliable evaluation of acquired lipid profiles.

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

50 olites; however, this was easily seen in the lipid profiles.

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

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

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

54 ing testosterone was associated with altered lipid profiles.

55 ent mice also had altered hepatic and plasma lipid profiles.

56 hanisms involved in sleep-associated adverse lipid profiles.

57 activity as shown by enzymatic analysis and lipid profiling.

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

59 Haematological tests (blood sugar, HbA1c and lipid profile, 31.8%), OCT (27.4%), refraction (9.9%), B

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

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

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

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

64 ere were no significant differences in blood lipid profiles among six treatment groups.

65 Using lipid profiling analyses, we here identify dietary fatty

66 Lipid profile analysis revealed that total cholesterol (

67 ssociations between third trimester maternal lipid profile and birthweight outcomes are driven by pre

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

69 our findings demonstrate that cell-intrinsic lipid profile and changes in the fatty acid metabolism c

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

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

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

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

74 that bempedoic acid has favorable effects on lipid profile and hsCRP levels and an acceptable safety

75 -/-) mice, largely independent of effects on lipid profile and inflammation, but rather by decreasing

76 n ALK(+) ALCLs, squalene alters the cellular lipid profile and protects cancer cells from ferroptotic

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

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

79 This study determined the baseline lipid profile and searched for major adverse cardiovascu

80 to explore the associations between maternal lipid profile and small-for-gestational-age neonates.

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

82 tration), fasting glucose concentration, and lipid profile and to explore whether downregulation of a

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

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

85 r ATGL inhibitory factors altered neutrophil lipid profiles and breast tumor lung metastasis in mice.

86 ucted to assess the effects of time-updating lipid profiles and cumulative exposure to statins on sur

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

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

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

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

93 Helminth infections improve lipid profiles and may lower blood pressure.

94 Baseline lipid profiles and metabolic syndrome rates (approximate

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

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

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

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

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

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

101 p with lower blood pressure levels, improved lipid profile, and diminished sympathetic responses to s

102 e, metabolic risks, an increased atherogenic lipid profile, and elevated ALT overtime.

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

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

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

106 e, mean blood pressure, unhealthy behaviors, lipid profiles, and exercise frequency.

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

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

109 Interestingly, specific lipid profiles are associated with longevity, and increa

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

111 those that did not (n = 213) on the basis of lipid profile at baseline using a model with an area und

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

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

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

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

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

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

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

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

120 tion or stiffness, systemic inflammation, or lipid profile, but resulted in reductions in BP and fast

121 Molecular lipid profiling by mass spectrometry may improve cardiov

122 Lipid profiling by mass spectrometry of mitochondria iso

123 We demonstrate that bioactive lipid profiles can be readily detected from three-dimens

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

125 drial dysfunction, hormone level elevations, lipid profile changes, and altered levels of phenolic mi

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

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

128 triple-negative subtypes showed more complex lipid profiles compared with luminal A and HER2 subtypes

129 The polar lipid profile consisted of phosphatidylethanolamine, dip

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

131 ely enrolled patients (N = 130) had detailed lipid profile consisting of traditional lipid parameters

132 ation in the liver and displayed an improved lipid profile, contributing to their overall healthier p

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 Transcriptome and cuticular lipids profiling coupled with comprehensive microscopy r

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

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

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

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

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

141 as a significant desirable health effects on lipid profiles, fasting blood sugar and body composition

142 imal source foods and breakfast skipping) on lipid profiles, fasting blood sugar and body composition

143 itative aspects of the mycoloop by analysing lipid profiles (fatty acids, sterols) of two chytrids in

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

145 ]), lower maternal serum thyroid hormone and lipid profiles ([Formula: see text]), and up-regulated g

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

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

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

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

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

151 Rabbits serum lipid profile, hematology and histology were investigate

152 ity, despite human-like CVD-risk-prone blood lipid profiles, hypertension, and mild atherosclerosis.

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

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

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

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

157 The platelet lipidome revealed an altered lipid profile in mildly hyperlipidemic mice.

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

159 n the impacts of saturated fat intake on the lipid profile in the context of whole-food-based low-car

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

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

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

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

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

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

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

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

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

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

170 tein convertase subtilisin/kexin type 9, and lipid profiles in patients.

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

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

173 iendly protocol for quantitative analysis of lipid profiles in subcellular structures.

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

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

176 depends on the capability of high-resolution lipid profiling in live cells and, potentially, in singl

177 ritonavir-boosted darunavir, with a superior lipid profile, in adults with HIV who were treatment nai

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

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

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

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

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

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

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

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

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

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

188 Single cell lipid profiling is a powerful tool to connect membrane c

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

190 Serum liver enzymes and lipid profile levels in WD fed mice were significantly h

191 Lipid profile levels were statistically significant on c

192 nd long sleep are associated with an adverse lipid profile, likely through different biological pathw

193 izome powder (TRP) supplementation on tissue lipid profile, lipid metabolism, health indices, oxidati

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

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

196 Lipid profiling may capture preclinical molecular altera

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

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

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

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

201 We studied the relationship between lipid profile obtained within 72 hours of presentation,

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

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

204 he increase in GML concentrations alters the lipid profile of broiler meat.

205 We observed that MDM2 and MDMX alter the lipid profile of cells to favor ferroptosis.

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

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

208 We therefore analyzed the lipid profile of fetal serum from untreated ICP, UDCA-tr

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

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

211 The initial lipid profile of patients with acute myocardial infarcti

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

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

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

215 The method was used to investigate the lipid profiles of 77 samples of bread wheat, spelt, eink

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

217 Lipid profiles of cells grown with excess phosphate cons

218 Lipid profiles of fatm and ram2 suggested that FatM incr

219 conclusive, this study demonstrates that the lipid profiles of HD tissues was more similar to DD tiss

220 Hepatic lipid profiles of L lactis subsp cremoris-supplemented m

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

222 nstrate that MRM-Profiling distinguishes the lipid profiles of resistant and nonresistant E. coli str

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

224 Finally, we observe altered lipid profiles of the DeltalpqN mutant during biofilm ma

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

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

227 aging was applied to study the metabolic and lipid profiles of various types of renal tissues, includ

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

229 n untargeted metabolite and targeted complex lipid profiling of BM plasma to identify significant dif

230 Metabolomics and complex lipid profiling of cells and tumors with reduced Aqp7 re

231 Lipid profiling of E3hom TPs was conducted using chromat

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

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

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

235 Thus, metabolite and complex lipid profiling of the BM plasma identifies differences

236 sferrin and transferrin saturation and serum lipid profile on a routine follow-up examination.

237 ly affected the circulating levels of NPs or lipid profile) or low-quality studies were taken into ac

238 ect on HbA1c, body weight, body composition, lipid profile, or BP.

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

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

241 els of adiponectin, and an unfavorable blood lipid profile (p < 0.001).

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

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

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

245 tary saturated fat may improve their overall lipid profile provided they focus on a high-quality diet

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

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

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

249 tients, resulting in dramatic improvement in lipid profile results.

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

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

252 Analysis of bacterial membrane lipid profiles revealed that the esxC mutant was less ab

253 Lipid profiling revealed a significant reduction in fatt

254 Lipid profiling revealed ala4/5 rosettes had perturbatio

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

256 Lipid profiling revealed that sEH deletion decreased ret

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

258 Lipid profiling shows decreased total galactolipid and p

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

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

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

262 mild and severe CFTR gene mutation types and lipid profiles, suggesting a possible way to realize per

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

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

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

266 Machine learning was used to identify lipid profiles that discriminated between CHR and contro

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

268 Within the lipid profile, the principal target is lowering LDL chol

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

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

271 Here, we first utilized global lipid profiling to fully characterize the lipid synthesi

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 he association between NPs and components of lipid profile [total cholesterol (TC), low-density lipop

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 population, the effect of Adv36 infection on lipid profile varied between healthy individuals and ind

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

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

284 date the biology of sleep-associated adverse lipid profile, we conduct multi-ancestry genome-wide sle

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

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

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

288 These lipid profiles were indicative of oxidative stress and d

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

290 tory traits, waste valorization, protein and lipid profiles were measured for each diet treatment.

291 l parameters, transcription, metabolite, and lipid profiles were measured.

292 The lipid profiles were remarkably similar in whole C. neofo

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

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

295 , such as glucose, BMI, insulin, HOMA-IR and lipid profile, were also investigated.

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 Changes in the lipid profile with ascent included a decrease in triglyc

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

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