ライフサイエンスコーパス: high-fat diet

1 protective immunity, which can be altered by high fat diet.

2 ting the adverse metabolic consequences of a high fat diet.

3 is development, and insulin resistance under high fat diet.

4 (PDH) within a single day of feeding mice a high fat diet.

5 function of these mice fed a control chow or high-fat diet.

6 and glucose intolerance in mice exposed to a high-fat diet.

7 , and hepatic steatosis when challenged with high-fat diet.

8 mber or size distribution on either a low or high-fat diet.

9 olic deficits caused by the consumption of a high-fat diet.

10 potently decreasing weight gain in mice on a high-fat diet.

11 is did not occur when Ad-FLD mice were fed a high-fat diet.

12 s of irisin were observed in mice fed with a high-fat diet.

13 ity to metabolic disease in the context of a high-fat diet.

14 hat were maintained on either a regular or a high-fat diet.

15 bolic deficits displayed by mice consuming a high-fat diet.

16 sing hZnT8 WT or hZnT8 R325W fed a normal or high-fat diet.

17 red with littermate controls) after eating a high-fat diet.

18 ke and greater diet-induced obesity when fed high-fat diet.

19 o the same extent as control mice when fed a high-fat diet.

20 db/db, streptozotocin-induced and mice fed a high-fat diet.

21 ion of adipose tissue when challenged with a high-fat diet.

22 I)) and wild-type mice (gsk3(WT)) were fed a high-fat diet.

23 fatty liver disease in mice maintained on a high-fat diet.

24 d decreases vascular inflammation induced by high-fat diet.

25 on of these mice fed chow or after 6 wk of a high-fat diet.

26 3 in mice fed either a normal chow diet or a high-fat diet.

27 imbalance, and reduced animal longevity on a high-fat diet.

28 e to reduce obesity even when mice are fed a high-fat diet.

29 ght gain and protected from hyperglycemia on high-fat diet.

30 and fibrosis prevented, on both low-fat and high-fat diets.

31 turbed in Gpr119(betacell-/-) mice on RC and high-fat diets.

32 Some mice were placed on an atherogenic high-fat diet (16% fat, 41% carbohydrate, and 1.25% chol

33 urthermore, in wild-type C57BL/6J mice fed a high fat diet, 2-weeks supplementation with Lab4 probiot

34 % fat, 15% protein, and 60-65% carbohydrate; high-fat diet: 40-45% fat, 15% protein, and 40-45% carbo

35 KEY POINTS: A high-fat diet (60% kcal from fat) is associated with mot

36 In a mouse model of high-fat diet, a new study teases apart these mechanisms

37 A high-fat diet accelerated stroke incidence.

38 eased Src kinase activity is associated with high-fat diet-accelerated progression of prostate tumors

39 e is essential to facilitate Src-induced and high-fat diet-accelerated tumor progression.

40 Adding a high-salt, high-fat diet accelerates endothelial senescence and ins

41 2+/-)Rosa(tdT+/-) mouse model subjected to a high-fat diet, adipocytes of atrial EAT derived from a s

42 Type 2 diabetes (T2D) was induced by high fat diet administration in M.sh.

43 Maintenance on a high-fat diet also did not affect the portion POMC neuro

44 High-fat diet also rapidly decreases adipose tissue ChRE

45 On a high-fat diet, although no differences in body weight an

46 reased body weight, which was exacerbated by high fat diet and driven by increased food intake.

47 n a mouse model of sporadic AAD induced by a high-fat diet and angiotensin II infusion, ADAMTS-4 defi

48 ice exhibit reduced effortful responding for high-fat diet and compulsive grooming, whereas group-hou

49 icient ovariectomized female mice were fed a high-fat diet and concomitantly administered with vehicl

50 to show an increase in RMR in response to a high-fat diet and deoxycorticosterone acetate-salt (DOCA

51 nant GDF15 induces weight loss in mice fed a high-fat diet and in nonhuman primates with spontaneous

52 bserved in hearts from rats fed a lard-based high-fat diet and in rodent and human cardiomyocytes upo

53 ture adipocytes in multiple tissues during a high-fat diet and in skin during hair follicle growth.

54 al proteins in human skeletal muscle after a high-fat diet and resistance exercise.

55 retinal disease, we weaned mice to chow or a high-fat diet and tested the hypothesis that diet-induce

56 eration tissues were fed a low-fat diet or a high-fat diet and treated with vehicle or dasatinib.

57 vulnerable to the anxiogenic effects of the high fat diet, and obese male mice showed decreased loco

58 sorders, obesity was induced in mice using a high fat diet, and the mice were subsequently stressed u

59 ue size at the aortic root and the aorta for high-fat diet animals as compared with Ldlr(-/-) control

60 ts against hepatic steatosis in mice fed the high-fat diet, as a novel agonist of these receptors.

61 scle cells, and in SIRT3 knockout mice fed a high-fat diet, as well.

62 olipoprotein E (ApoE) knockout mice fed with high-fat diet, BM nestin(+) cells regulate the egress of

63 id lesions were induced in FVB mice fed on a high-fat diet by streptozotocin injection followed by li

64 Both stress and high fat diet can alter the gut microbiota and contribut

65 Vsig4 (-/-) mice are susceptible to high-fat diet-caused obesity and murine hepatitis virus

66 Here the authors show that high fat diet causes calpain-1-dependent degradation of

67 When hyperlipidemic mice are given a high fat diet, CC appear in aortic sinus within 1 week.

68 brogates their abnormal phenotype, even upon high-fat diet challenge.

69 ion, and were more insulin resistant after a high-fat diet challenge.

70 Under a high-fat diet, deletion of PKD1 in beta-cells worsened h

71 d peripheral macrophages and is required for high fat diet-dependent weight gain in mice.

72 Mice fed with a high-fat diet developed steatohepatitis reminiscent of h

73 High-fat diet equally worsened glucose tolerance in AgRP

74 e (IKK) occurs rapidly upon consumption of a high-fat diet, even prior to significant weight gain.

75 In murine obesity induced by a high fat diet, ex vivo IgM and IgG were elevated with un

76 ecent studies demonstrate that rodents fed a high fat diet exhibit retinal dysfunction concomitant wi

77 In high-fat diet fed and genetically obese ob/ob mice, P300

78 EDL fibre bundles obtained from chronic high-fat diet fed mice had enhanced mitochondrial oxidat

79 us (EDL) fibre bundles obtained from chronic high-fat diet fed mice had lower basal oxygen consumptio

80 nalysis of intestinal and renal tissues from high-fat diet fed mice, critical for maintaining metabol

81 Transplantation of AT-LSK sorted from high fat diet-fed (HFD) mice is sufficient to induce ATM

82 c clamps and ex vivo in isolated islets from high-fat diet-fed betaPKD1KO mice without changes in isl

83 ance and motivation in female offspring from high-fat diet-fed dams.

84 In high-fat diet-fed mice with skeletal muscle-specific kno

85 nhibition in a mouse model of T2DM (i.e., in high-fat-diet-fed animals).

86 re assessed during cold stress and following high fat diet feeding.

87 While aging impairs the osteogenic lineage, high-fat diet feeding activates expansion of the adipoge

88 privation and excessive storage of energy by high-fat diet feeding dampen the suppressive effect of l

89 dy site-specific myeloid cell behavior after high-fat diet feeding or tumor necrosis factor stimulati

90 le to the negative metabolic consequences of high-fat diet feeding than male mice, for reasons that a

91 ood intake and weight gain in lean mice upon high-fat diet feeding, and this injection paradigm reduc

92 proved insulin sensitivity despite prolonged high-fat diet feeding.

93 e) mice, but this effect was attenuated with high-fat diet feeding.

94 ased RNA-seq analysis in liver from mice fed high-fat diet +/- Fenretinide.

95 s were rendered insulin-resistant by feeding high fat diet for 16 weeks.

96 ignal transducer protein of IL-6, were fed a high-fat diet for 12 weeks.

97 actor receptor 2 knockout mice, either fed a high-fat diet for 12-14 weeks, or age-matched lean contr

98 rendered obese and pre-diabetic by feeding a high-fat diet for 15 weeks and then treated with LH-21 o

99 m-graecum), C57BL/6J mice were fed a low- or high-fat diet for 16 weeks with or without 2% (w/w) fenu

100 rofiling of aortas from Apoe(-/-) mice fed a high-fat diet for 4 weeks, 8 weeks, or 4 months revealed

101 e 32 weeks and after 20 weeks of standard or high-fat diet, Gucy1a3(-/-)/Ldlr(-/-) mice exhibited a s

102 ic syndrome-accompanying features induced by high-fat diet (HF), such as dyslipidaemia, glucose intol

103 mine the effects of two different diets-very high fat diet (HFD) and moderately high fat plus cholest

104 Male C57BL/6J mice raised on high fat diet (HFD) become prediabetic and develop insul

105 search demonstrated that a brief (two weeks) high fat diet (HFD) caused insulin resistance in rat ske

106 Under conditions of high fat diet (HFD) consumption, glucose dyshomeostasis

107 reverse some of the negative consequences of high fat diet (HFD) consumption.

108 In this study we fed mice a high fat diet (HFD) for seven weeks followed by addition

109 To examine if a parental high fat diet (HFD) influences metabolic health in two g

110 We examined the effect of chronic high fat diet (HFD) on amyloid deposition and cognition

111 s of age, and to HF diabetic mice induced by high fat diet (HFD) plus streptozotocin (STZ) in C57BL/6

112 lysis of the effects after placing mice on a high fat diet (HFD) regimen demonstrated that running di

113 Atherosclerosis was induced by feeding high fat diet (HFD) to mice for 10 weeks, followed by fi

114 ows: (i) Control, (ii) Control + L/Zi, (iii) High Fat Diet (HFD), and (iv) HFD+ L/Z.

115 ceptible to the harmful cognitive effects of high fat diet (HFD)-induced IR due to apoE isoform-speci

116 0mvarphiKD) which resists the development of high fat diet (HFD)-induced metabolic diseases due to en

117 BALB/c mice are known to be resistant to high fat diet (HFD)-induced obesity, however the genetic

118 herapeutic effects of NRG4 overexpression on high fat diet (HFD)-induced obesity.

119 We established a standardized mouse model of high fat diet (HFD)-induced steatosis followed by Omega3

120 ensitive, glucose-tolerant, and resistant to high fat diet (HFD)-induced toxicity.

121 sed fuel oxidation and oxidative damage upon high fat diet (HFD).

122 lar brown adipose tissue (BAT) in mice fed a high fat diet (HFD).

123 at mass, and liver steatosis when fed with a high fat diet (HFD).

124 mitic acid (PA)- or oleic acid (OA)-enriched high-fat diet (HFD) (20% of calories from FA) or a norma

125 High-fat diet (HFD) accelerates these effects in apoE4-T

126 ential exposure to postnatal over nutrition, high-fat diet (HFD) after weaning, followed later by ova

127 onse of human skeletal muscle to 9 days of a high-fat diet (HFD) alone (Sed-HFD) or in combination wi

128 Maternal high-fat diet (HFD) alters hypothalamic developmental pr

129 A maternal high-fat diet (HFD) alters the offspring's feeding regul

130 of vitamin D-enriched mushrooms extracts on high-fat diet (HFD) animal model of non-alcoholic steato

131 and liver as distinct features of mice fed a high-fat diet (HFD) as well as obese patients.

132 atosis formation in transgenic CCDC3 mice on high-fat diet (HFD) by reducing the expression of hepati

133 event metabolic disorders induced by a later high-fat diet (HFD) challenge.

134 rozygous mice (S2HET) were challenged with a high-fat diet (HFD) containing 45% of kilocalories from

135 Feeding a high-fat diet (HFD) coupled with sugar, mimicking a West

136 In addition, high-fat diet (HFD) feeding induced vascular miR-204 and

137 effects of hyperinsulinaemia associated with high-fat diet (HFD) feeding on the cardiac beta2 -adrene

138 During high-fat diet (HFD) feeding, macrophage-specific JAK2 kn

139 ecies and their changes induced by long-term high-fat diet (HFD) feeding.

140 rodents and causes excess weight gain during high-fat diet (HFD) feeding.

141 Mice fed a high-fat diet (HFD) for 10 weeks were divided into group

142 of C57BL/6J mice fed a low-fat diet (LFD) or high-fat diet (HFD) for 12 weeks.

143 and p35IL-12(-/-) (p35(-/-)) mice were fed a high-fat diet (HFD) for 12 weeks.

144 rats of both sexes that were maintained on a high-fat diet (HFD) for 6 weeks prior to DRG inflammatio

145 Here, we report that mice fed a high-fat diet (HFD) for as little as 1-3 days show incre

146 In C57BL/6 (B6) mice, obesity induced by a high-fat diet (HFD) has major effects on visceral epidid

147 mmation pathways in the obesity induced by a high-fat diet (HFD) in rodents.

148 range with significant weight reduction in a high-fat diet (HFD) induced diabetic mouse model and a g

149 ss (CC) mouse genetic resource population to high-fat diet (HFD) induced T2D-like disease to evaluate

150 ABSTRACT: The consumption of a high-fat diet (HFD) is associated with myenteric neurode

151 this study was to understand the impacts of high-fat diet (HFD) on the insulin-adrenergic receptor s

152 (ACE2KO) and wild-type (WT) mice were fed a high-fat diet (HFD) or a control diet and studied at 6 m

153 d replacement mice were fed either a control high-fat diet (HFD) or an HFD supplemented with 3% n-3 P

154 ene expression in C57BL/6NTac mice fed a 60% high-fat diet (HFD) or control diet for up to 16 weeks.

155 f multi-tissues from outbred mice fed with a high-fat diet (HFD) or regular chow at weeks 1, 9, and 1

156 Maternal obesity and high-fat diet (HFD) predisposes offspring to obesity and

157 Consumption of a high-fat diet (HFD) results in suppression of ATP citrat

158 Experiments using parabiotic mice fed a high-fat diet (HFD) showed differential trafficking of A

159 /6 J mice were fed a control diet (CON) or a high-fat diet (HFD) with or without 0.2% (w/w) RES durin

160 High-fat diet (HFD), body weight (BW) gain, and impaired

161 When challenged with a high-fat diet (HFD), CD36Tg mice showed unexpected atten

162 modification accumulation in mice exposed to high-fat diet (HFD), injected with streptozotocin, or bo

163 After 16 weeks of a high-fat diet (HFD), M(IL10) mice became markedly obese

164 Despite becoming obese on a high-fat diet (HFD), mice lacking FcgammaRIIB globally o

165 fed mice either a chow diet (CD), a 16 week high-fat diet (HFD), or a CR diet to compare and contras

166 When fed a high-fat diet (HFD), the transgenic mice displayed a sig

167 In C57BL/6J mice fed a high-fat diet (HFD), treatment with BBR decreased inflam

168 d in NASH patients, diabetic db/db mice, and high-fat diet (HFD)-fed mice.

169 s after ischemia reperfusion injury (IRI) in high-fat diet (HFD)-fed mice.

170 High-fat diet (HFD)-fed MNK2-KO show less weight gain th

171 In a mouse model, high-fat diet (HFD)-fed offspring have cognitive and exe

172 in Ern1(f/f); Lyz2-Cre mice largely reversed high-fat diet (HFD)-induced M1-M2 imbalance in white adi

173 lose), fiber markedly protected mice against high-fat diet (HFD)-induced metabolic syndrome, the effe

174 ry immune responses and markedly exacerbated high-fat diet (HFD)-induced NAFLD pathogenesis.

175 eas AEG-1(DeltaHEP) mice were protected from high-fat diet (HFD)-induced NASH.

176 We used a mouse model of high-fat diet (HFD)-induced obesity and assessed immune

177 transcripts and metabolites in response to a high-fat diet (HFD)-induced obesity and/or exercise.

178 y polypeptide (GIP) receptor (GIPR) prevents high-fat diet (HFD)-induced obesity in mice due to speci

179 Rats with high-fat diet (HFD)-induced obesity increase daytime eat

180 High-fat diet (HFD)-induced obesity is accompanied by in

181 e relevance of adipose tissue ERalpha during high-fat diet (HFD)-induced obesity using female aP2-Cre

182 it is protected against a cold challenge and high-fat diet (HFD)-induced obesity with associated insu

183 kout (GPRKO) female mice were protected from high-fat diet (HFD)-induced obesity, blood glucose intol

184 lergic airway disease exacerbation caused by high-fat diet (HFD)-induced obesity.

185 izes insulin resistance and hyperglycemia in high-fat diet (HFD)-induced obesity.

186 mine the contributions of macrophage Nrp1 in high-fat diet (HFD)-instigated insulin resistance in viv

187 downregulated during weight gain induced by high-fat diet (HFD).

188 ed diabetic phenotype when challenged with a high-fat diet (HFD).

189 d enhanced insulin sensitivity in mice fed a high-fat diet (HFD).

190 stance and glucose intolerance in rats fed a high-fat diet (HFD).

191 ive pancreatic islet dysfunction with age or high-fat diet (HFD).

192 The role of A2AARs in regulating high-fat-diet (HFD)-induced metabolic derangements is un

193 Overconsumption of high-fat diets (HFDs) can critically affect synaptic and

194 following 24 weeks on SFA- or MUFA-enriched high-fat diets (HFDs) or low-fat diet.

195 KEY POINTS: Maternal high-fat diet impairs brown adipocyte function and corre

196 to obesity despite chronic consumption of a high fat diet in macaque dams.

197 with control littermates after 10 weeks of a high-fat diet in male mice.

198 High-fat diet in sedentary mice led to endoplasmic retic

199 rnal transcriptome is not recapitulated by a high-fat diet in young adult mice, it is significantly p

200 nduced reduction of plasma TGs in mice fed a high-fat diet, in postprandial clearance studies, and wh

201 A high-fat diet increased cardiac PPARalpha expression, fa

202 A high-fat diet increases bacterial lipopolysaccharide (LP

203 In high-fat diet induced fatty-liver mice, AM580 reduced Ap

204 CAST overexpression did not influence high fat diet-induced body weight and fat mass gain thro

205 RNA activator (SRA) (SRAKO) are resistant to high fat diet-induced obesity with a phenotype that incl

206 ity runner; LCR) displayed susceptibility to high fat diet-induced steatosis in association with redu

207 on of ER stress in mice completely abolishes high fat diet-induced upregulation of TRIP-Br2 in BAT.

208 in obese adipose tissue and have shown that high-fat diet-induced (HFD-induced) insulin resistance i

209 terozygous for p32 are resistant to age- and high-fat diet-induced ailments, including obesity, hyper

210 ssed highly in the liver, protects mice from high-fat diet-induced and aging-induced obesity and hepa

211 -/- mice with Arhgef1-deficient BM prevented high-fat diet-induced atherosclerosis, while reconstitut

212 eptor (LDLR) and Arhgef1 were protected from high-fat diet-induced atherosclerosis.

213 weeks of VWR exercise in obese mice rescued high-fat diet-induced decreased muscle GLUT4 protein and

214 To determine if high-fat diet-induced diabetes in mice can model retinal

215 ansporter ZIP14 during pharmacologically and high-fat diet-induced ER stress using Zip14(-/-) (KO) mi

216 e, Nox2-deficient mice are protected against high-fat diet-induced hepatic steatosis and insulin resi

217 led that SLC13A5 deletion protects mice from high-fat diet-induced hepatic steatosis and that mutatio

218 ific gp130 knockout mice were protected from high-fat diet-induced hepatic steatosis as well as from

219 he counteractive effect of PM2.5 exposure on high-fat diet-induced hepatic steatosis was mediated thr

220 ntrols adipose tissue lipolysis and prevents high-fat diet-induced hepatic steatosis.

221 is in the mouse liver but protects mice from high-fat diet-induced hyperglycemia.

222 , without affecting mechanisms implicated in high-fat diet-induced insulin resistance.

223 A-L exacerbates or alleviates, respectively, high-fat diet-induced mitochondrial dysfunction, hepatos

224 PLD1 expression was decreased in high-fat diet-induced NAFLD.

225 Here we report that in the NTS of high-fat diet-induced obese (DIO) rats, the apoA-IV mRNA

226 normalised elevated levels of FGF21 in both high-fat diet-induced obese mice and in genetically obes

227 primary bone marrow-derived macrophages and high-fat diet-induced obese mice.

228 rove hepatic glucose and lipid metabolism in high-fat diet-induced obese mice.

229 PM2.5 exposure relieved hepatic steatosis in high-fat diet-induced obese mice.

230 cells, zebrafish and in live tissues from a high-fat diet-induced obese mouse model.

231 adipose tissues were resistant to developing high-fat diet-induced obesity and had significantly redu

232 Finally, moderate alcohol prevented high-fat diet-induced obesity and metabolic dysfunction.

233 rexpression of Id1 causes age-associated and high-fat diet-induced obesity in mice.

234 High-fat diet-induced obesity is a major risk factor for

235 acute fasting) and excessive energy storage (high-fat diet-induced obesity) blunt the effect of lepti

236 trol intervention protects offspring against high-fat diet-induced obesity.

237 with type 2 diabetes, and C57BL/6J mice with high-fat diet-induced obesity.

238 Mice with high-fat diet-induced simple hepatic steatosis and lipid

239 virus-mediated depletion of COP1 ameliorates high-fat diet-induced steatosis in mouse liver and impro

240 ed thermogenic EE, which protected mice from high-fat diet-induced weight gain at ambient temperature

241 ponse, which requires domains that influence high-fat-diet-induced chronic inflammation and alter cel

242 mption of stevioside prevents development of high-fat-diet-induced diabetic hyperglycaemia in wild-ty

243 stine-specific disruption of Hif2a, in which high-fat-diet-induced hepatic steatosis and obesity were

244 roves mitochondrial function and ameliorates high-fat-diet-induced hepatic steatosis, glucose toleran

245 rgeted activation of Hh signaling suppresses high-fat-diet-induced obesity and improves whole-body gl

246 e used mouse models of a regular diet and of high-fat-diet-induced obesity to investigate the role of

247 receptors control pancreatic dysfunction in high-fat-diet-induced obesity.

248 ned with increased oxygen consumption during high-fat-diet-induced obesity.

249 sts increased insulin secretion and reversed high-fat-diet-induced weight gain and insulin resistance

250 DNA microbiome sequencing, which showed that high-fat diet induces reduction of Parasutterella sp. in

251 othesis, behavioral tests including chow and high-fat diet intake, meal patterns, conditioned place p

252 On high-fat diet, JAK2L mice had hepatic steatosis and insu

253 ation to a ketogenic low carbohydrate (CHO), high fat diet (LCHF) during 3 weeks of intensified train

254 We previously demonstrated that a high fat diet leads to changes in chromatin accessibilit

255 We verified that high fat diet lipid accumulation is also capable of indu

256 Furthermore, the high fat diet lowered bone marrow B cell frequency accom

257 Female mice fed a high-fat diet maintain CX3CL1-CX3CR1 levels while male m

258 more susceptible to the adverse effects of a high-fat diet, manifested in increased body weight and a

259 w the metabolism of myristic acid stimulates high-fat diet-mediated prostate tumor progression.

260 ice, consistent with the hypothesis that the high-fat diet-mediated reduction of hippocampal SIRT1 co

261 Here, we report that maternal high-fat diet (MHFD) induces a shift in microbial ecolog

262 When challenged with a high-fat diet, mice carrying one copy of KD-mTOR mutant

263 The high-fat diet not only accelerated Src-induced prostate

264 nt-associated osteomyelitis in normal versus high-fat-diet obese/T2D mice and found that S. aureus in

265 When challenged with a high-fat diet, Ocy-PPARgamma(-/-) mice retain glycemic c

266 and attenuates the inflammatory impact of a high fat diet on glucose tolerance and insulin resistanc

267 egates the detrimental effects of a maternal high-fat diet on glucose tolerance and hepatocyte glucos

268 ed at two different doses to C57BL/6 mice on high fat diet or standard diet for a period of 17weeks.

269 ophagy was induced in beta cells by either a high-fat diet or a combined high-fat and high-glucose di

270 tively by caloric deficit and not altered by high-fat diet or stress.

271 Our data showed that rats fed a high-fat diet or that were centrally administered thapsi

272 nning to obtain mechanistic insight into how high-fat diets perturb stem cell function and cause canc

273 atherosclerotic plaque in rats feeding with high fat diet plus balloon injury.

274 We found that a high-fat diet promotes myofibroblast differentiation by

275 Consumption of a high-fat diet protects mice from ventilator-induced lung

276 female mice display increased weight gain on high-fat diet, reduced behavioral despair, and increased

277 High fat diet reduces the expression of CEACAM1 (carcino

278 re elevated in adipose depots in response to high-fat diet regimens and during the aging process; how

279 ght the potential of probiotics to attenuate high-fat diet-related metabolic disorder.

280 It is currently not fully understood how a high-fat diet reprograms adipose-derived stem cells into

281 ith a smaller increases in body weight under high-fat diet, smaller fat deposits, increased beta-oxid

282 th Il6 gene (controls), were fed a chow or a high-fat diet; some mice were given injections of recomb

283 Furthermore, dusp6-deficient mice have a high-fat-diet-specific transcriptomic response to revers

284 llular carcinogenesis using a streptozotocin-high fat diet (STZ-HFD) induced nonalcoholic steatohepat

285 tively) were fed regular chow (control) or a high-fat diet supplemented with 30% d-fructose in drinki

286 very 4-6 months for 2 years after starting a high-fat diet supplemented with fructose.

287 s, insulin secretion and autoimmunity with a high-fat diet supports a shared mechanism for type 1 (T1

288 When placed on the atherogenic high-fat diet, the KO mice developed features of nonalco

289 In response to the high-fat diet, the T allele was associated with a higher

290 When fed a high-fat diet, these mice exhibited normal food intake b

291 lation exposure of mice fed normal chow or a high-fat diet to airborne fine particulate matters (PM2.

292 In high-fat diet-treated mice, knockout of the endothelial

293 meliorated hepatic steatosis induced by both high-fat diet treatment and leptin deficiency.

294 In response to a high-fat diet, TRIB3 MOE mice exhibited greater weight g

295 esterol mediates the metastatic effects of a high-fat diet via its oxysterol metabolite, 27-hydroxych

296 Steatotic liver induced by high-fat diet was more vulnerable to IRI.

297 Induction of Cyp2e1 protein by high-fat diet was suppressed in Gsta4(-/-) and dKO group

298 oprotein receptor-null (Ldlr(-/-)) mice on a high-fat diet were orally administered with vehicle cont

299 ced weight gain in mice that had access to a high-fat diet, while not altering general locomotor acti

300 With this aim, rats were fed a high fat diet with 5% sucrose in the drinking water (HFS