ライフサイエンスコーパス: high-fat diet

1 uced weight gain and adiposity in mice fed a high fat diet.

2 yeloid or lymphoid cells were subjected to a high fat diet.

3 e the progression of NAFLD in the setting of high fat diet.

4 alters the metabolic phenotype in mice fed a high fat diet.

5 burden in miR-144 knockout mice receiving a high fat diet.

6 ation in an obesity mouse model induced by a high fat diet.

7 improves metabolic parameters in mice fed a high fat diet.

8 skeletal muscle adaptions to training during high-fat diet.

9 xercise, mediate adaptations to exercise and high-fat diet.

10 ts showed the environment in vivo tends to a high-fat diet.

11 ocephalic arteries of ApoE-deficient mice on high-fat diet.

12 d diabetes phenotypes in mice fed a constant high-fat diet.

13 r compartments in fat and are activated by a high-fat diet.

14 hibit some, but not all, of the effects of a high-fat diet.

15 ion and peripheral glucose clearance after a high-fat diet.

16 al glucose tolerance in mice made obese with high-fat diet.

17 lial hyperplasia, which is an indicator of a high-fat diet.

18 ody weight and adiposity in obese mice fed a high-fat diet.

19 ic health of maternal mice challenged with a high-fat diet.

20 metabolism at resting state, even when fed a high-fat diet.

21 abolished in mice overexpressing SIRT1 fed a high-fat diet.

22 e, and greater inflammation in AT when fed a high-fat diet.

23 rosclerosis was quantified after 12 weeks of high-fat diet.

24 ior were also normal, even after exposure to high-fat diet.

25 pose and liver inflammation in response to a high-fat diet.

26 R deletion and were further increased by the high-fat diet.

27 nsgenerational inheritance of responses to a high-fat diet(9), thus raising the exciting possibility

28 microvesicles are enhanced by exposure to a high fat diet, a known risk factor for atherosclerosis.

29 ithelial T lymphocytes occurs within 7 wk of high-fat diet administration and is not dependent on chr

30 id metabolism resulting from gene mutations, high-fat diets, alcohol, or circadian disruption can con

31 sympathetic nerve activity were obtained in high fat diet and normal chow fed male C57BL/6J mice.

32 osis was induced in miR-144 knockout mice by high fat diet and vascular lesions were quantified by Oi

33 by challenging mice with a combination of a high-fat diet and angiotensin II.

34 ient (Malat1(-/-)) mice that were fed with a high-fat diet and by studying the regulation of MALAT1 i

35 icient to improve liver damage in mice fed a high-fat diet and in mice fed a methionine-choline-defic

36 Cancer risk factors, such as high-sugar or high-fat diet and inflammation, impact cell competition-

37 stress in mice-elicited by a combination of high-fat diet and inhibition of constitutive nitric oxid

38 s immune homeostasis in Ldlr(-/-) mice under high-fat diet and limits atherogenesis.

39 Then we induced MetS by a combination of high-fat diet and olanzapine treatment.

40 e are concerns about the association between high-fat diets and cognitive decline, this study aimed t

41 umulate in adipose and muscle tissues during high-fat diets and contribute to a state of local inflam

42 how that the convergence of dietary factors (high-fat diet) and dysregulated WNT signaling (APC mutat

43 ontrast, mice with comorbid diabetes (aging, high-fat diet, and streptozotocin-induced diabetes) had

44 protection from weight gain on standard and high-fat diets, and an adiposity-dependent improvement i

45 found that when chimeric animals were fed a high-fat-diet, animals with low levels of chimerism show

46 emic blood from aged mice and upon feeding a high-fat diet (Apoe(-/-) mice).

47 esoid X receptor null (Fxr(Delta/E)) mice on high-fat diet as well as wild-type C57BL/6 and glucagon-

48 Gestational high fat diet attenuated memory decline, synaptic dysfun

49 We show that high-fat diet attenuates the response of AgRP neurons to

50 Wild-type and PAI-1 knockout (KO) mice on a high-fat diet both became significantly heavier than lea

51 ced wheel running occurs when mice are fed a high-fat diet but is normalized when mice consume standa

52 al bacteria to offset the adverse effects of high fat diets, C57BL/6J mice were fed control/low fat (

53 tive of this study was to evaluate whether a high-fat diet can aggravate the liver disease caused by

54 demonstrate that both food restriction and a high-fat diet cause an endocannabinoid-dependent inhibit

55 nal inflammation when fed cholate-containing high fat diet (CCHF).

56 ved choline-deficient, l-amino acid-defined, high-fat diet (CDAHFD) for 6 weeks or (d) 9 weeks (n = 8

57 al to subcutaneous fat (VAT/SAT) ratio after high-fat diet challenge, in comparison to their wild-typ

58 cantly less body weight and fat mass when on high-fat diets compared with littermate controls and wer

59 ance and insulin resistance when raised on a high-fat diet, compared to wild-type (WT) mice.

60 nction in male and female offspring Maternal high-fat diet consumption prior to and throughout pregna

61 dults at moderate CVD risk, consumption of a high-fat diet containing SFA-reduced, MUFA-enriched dair

62 ism by feeding Sirt5 knockout mice (Sirt5KO) high-fat diets containing either C(8)/C(10) fatty acids

63 rteries of endothelial Fto-deficient mice on high-fat diet; conversely, direct addition of prostaglan

64 abolism in mice fed either regular chow or a high-fat diet, demonstrating that these metabolic effect

65 A high-fat diet did not alter arcuate NPY neuronal InsR ex

66 ionally, ablation of Pnoc(CeA) cells reduces high-fat-diet-driven increases in bodyweight and adiposi

67 e previously determined that male mice fed a high-fat diet exhibit macrophage infiltration into the h

68 B cell-specific Pdia1 deletion in young high-fat diet fed mice or aged mice exacerbated glucose

69 cise training protocol, in either low-fat or high-fat diet fed mice, did not require Bcl2-mediated au

70 ther increase insulin-positive islet area in high fat diet-fed mice and was unable to prevent or reve

71 sitivity in insulin-resistant aged chow- and high-fat diet-fed (HFD-fed) mice.

72 High-fat diet-fed ApoE(-/-) mice displayed an increased

73 lEVs from high-fat diet-fed ApoE(-/-) mice, but not those from mic

74 containing H2Ab1 siRNA were administered to high-fat diet-fed C57BL/6 mice.

75 prostaglandin D(2) rescued myogenic tone in high-fat diet-fed control mice.

76 VSG or sham surgery was performed in high-fat diet-fed male hepatocyte-specific p53 wild-type

77 Serum from high-fat diet-fed mice also enhanced the expression of t

78 used endothelium-specific knockout mice and high-fat diet-fed mice to assess the role of endothelial

79 n completely ameliorate disease phenotype in high-fat diet-fed mice.

80 nd in vivo in human islets transplanted into high-fat diet-fed mice.

81 of neuropathy and restores nerve function in high-fat diet-fed murine models of peripheral neuropathy

82 verexpressing mice and in serum and PGWAT of high-fat diet-fed RBP4-overexpressing mice vs. wild-type

83 atic vagal innervation, and are preserved in high-fat-diet-fed rats when the blood brain barrier is b

84 at CHRNA2 signaling is activated after acute high fat diet feeding and this effect is manifested thro

85 betic women and in a mouse model of maternal high fat diet feeding.

86 s in body weight or metabolic function after high fat diet feeding.

87 improved glucose tolerance when subjected to high-fat diet feeding.

88 r in vivo studies, ApoE(-/-) mice were fed a high-fat diet for 12 weeks.

89 Male C57BL/6J mice were fed with a high-fat diet for 16 weeks.

90 Aged ApoE knockout mice fed high-fat diet for 6 weeks developed hypertension, and my

91 Animals were fed a high-fat diet for 8 weeks and then sensitized and challe

92 rdiography in the Grb14-knockdown mice fed a high-fat diet for a period of four months.

93 Compared with Foxp3cre mice, after 13 wk of high-fat diet, Foxp3creInsrfl/fl mice exhibited improved

94 usly, we found that PLA2G2A protects mice on high-fat diets from weight gain and insulin resistance.

95 DHEA in male iWAT and eWAT in response to a high-fat diet further strengthen the inference regarding

96 ler increases in FGF21 after the low-protein high-fat diet gained more weight after 6 months in free-

97 Mice were divided into control and high fat diet groups with or without exercise training.

98 On a high-fat diet, HDAC6-deficient mice were depleted in rep

99 ht, a second objective was to determine if a high fat diet (HF) would alter GWI outcomes.

100 r low-fat counterparts (LF mice), mice fed a high-fat diet (HF mice) had impairments in inflammatory

101 OB enhances healthy aging in mice fed with a high-fat diet (HF).

102 een obesity and AD by feeding APP/PS1 mice a high fat diet (Hfd) and evaluating behavioral, physiolog

103 ve been implicated in the mechanism by which high fat diet (HFD) and saturated fatty acids (SFA) modu

104 Here, we show that high fat diet (HFD) feeding alters intestinal IgA(+) imm

105 In response to high fat diet (HFD) feeding for 6 or 18 weeks, WT and AI

106 We have previously shown that high fat diet (HFD) for 2 weeks increases airway hyperre

107 female mice were fed a normal chow (NC) or a high fat diet (HFD) for 5 weeks before mating, then also

108 ested the hypothesis that Nod2 protects from high fat diet (HFD)-dependent hepatic cancer.

109 sly reported that GDNF is protective against high fat diet (HFD)-induced hepatic steatosis in mice th

110 a growing body of evidence illustrating that high fat diet (HFD)-induced maternal obesity can regulat

111 xperimental diabetic neuropathy induced by a high fat diet (HFD).

112 et responsive QTLs in F2 mice fed control or high fat diet (HFD).

113 y changes occurring in response to a chronic high fat diet (HFD).

114 hondrial metabolic proteins in response to a high fat diet (HFD).

115 n adult Hhip mice (Hhip +/- vs. Hhip+/+) fed high fat diets (HFD).

116 In Experiment 2, rats received a high-fat diet (HFD) after 3-week abstinence.

117 s demonstrate that in comparison with males, high-fat diet (HFD) allergic female mice exhibit a reduc

118 Rats fed with a high-fat diet (HFD) and 10 muL of daily oral CAGE exhibi

119 developed mild insulin resistance when fed a high-fat diet (HFD) and had reduced food intake during r

120 ed into two groups fed either a control or a high-fat diet (HFD) and then the mice on each diet were

121 red these with the effects of a prototypical high-fat diet (HFD) as well as cessation of exposure on

122 Mice fed a high-fat diet (HFD) become obese and develop osteoarthri

123 PTOA was induced in C57Bl/6 mice fed with high-fat diet (HFD) by surgically destabilising the meni

124 Previous studies showed that 12 weeks of high-fat diet (HFD) consumption caused not only prediabe

125 fatty liver progress to NASH, and mice fed a high-fat diet (HFD) develop fatty liver but are resistan

126 t et al. showed that feeding maternal mice a high-fat diet (HFD) during lactation attenuated the acti

127 ulin resistance in offspring of mothers on a high-fat diet (HFD) during pregnancy.

128 rate in a murine prostate cancer model, that high-fat diet (HFD) enhances the MYC transcriptional pro

129 In mice, we previously found that maternal high-fat diet (HFD) exposure results in reduced fetal gr

130 s of a non-pharmacological intervention in a high-fat diet (HFD) fed mouse model, capable of recapitu

131 Here, we showed that maternal high-fat diet (HFD) feeding during lactation in mice eli

132 Control and ACC2 iKO mice were subjected to high-fat diet (HFD) feeding for 24 weeks to induce obesi

133 High-fat diet (HFD) feeding further exacerbates the K2KO

134 ngs exist regarding the impact of short-term high-fat diet (HFD) feeding on the development of allerg

135 emia and glucose intolerance after long-term high-fat diet (HFD) feeding.

136 DIO mice were fed high-fat diet (HFD) for 12 weeks and then treated daily

137 Mice were fed a high-fat diet (HFD) for 12 weeks before food allergen se

138 AA formation in an established model of AAA, high-fat diet (HFD) in Ldlr (-/-) mice.

139 s-induced insulin resistance with short-term high-fat diet (HFD) in young mice.

140 Feeding C57BL/6J mice a high-fat diet (HFD) inhibited hepatic Sirt1/mTORC2/Akt s

141 As high-fat diet (HFD) is a potent inducer of gut dysbiosis

142 Consuming a high-fat diet (HFD) is a risk factor for obesity and dia

143 gene expression, we analyzed the impact of a high-fat diet (HFD) on Abcc8 knockout mice.

144 Here, we explored the effects of a high-fat diet (HFD) on energy balance, gut microbiota, a

145 The influence of maternal high-fat diet (HFD) on metabolic response to ozone was e

146 However, mice fed a high-fat diet (HFD) only develop fatty liver without sig

147 They were fed a high-fat diet (HFD) or regular chow for 4 weeks.

148 d L2-IL1B mice) were fed a chow (control) or high-fat diet (HFD) or were crossbred with mice that exp

149 lobule membrane (MFGM-PL) supplementation to high-fat diet (HFD) rats during pregnancy and lactation

150 We demonstrate that a high-fat diet (HFD) reproducibly changes gut microbial c

151 Chronic high-fat diet (HFD) results in the accumulation of a mon

152 fed a control diet, plasmas from mice fed a high-fat diet (HFD) showed delayed PG and reduced PG vel

153 aluation paradigm, we found that exposure to high-fat diet (HFD) suppresses the intake of nutritional

154 b/ob (obese) or heterozygote (lean) mice fed high-fat diet (HFD) that received either 17beta-Estradio

155 -/-) .Leiden mice received 16 weeks either a high-fat diet (HFD) to induce obesity, or chow as refere

156 ntial metal distribution in adult mice fed a high-fat diet (HFD) were examined.

157 icantly increased in NT(+/+) mice fed with a high-fat diet (HFD) which were improved in NT-deficient

158 en diet), or a diet enriched in lipid alone (high-fat diet (HFD)).

159 A previous study demonstrated that a high-fat diet (HFD), administered for one-three-days, in

160 Obesity was induced by high-fat diet (HFD), and blood pressure (BP) was measure

161 When challenged with high-fat diet (HFD), IRMOE mice are protected from diet-

162 Under an obesogenic high-fat diet (HFD), male offspring of exercised C57BL/6

163 ed mice fed a standard chow diet, short-term high-fat diet (HFD), or long-term HFD.

164 When mice were fed a high-fat diet (HFD), we found that fatty liver and dysli

165 ance to obesity and fatty liver induced by a high-fat diet (HFD), whereas liver-specific IMP2 overexp

166 High-fat diet (HFD)-fed Ad-GcR(-/-) mice were protected

167 r and cellular aspects of atherosclerosis in high-fat diet (HFD)-fed L13a KO and intact (control) mic

168 Furthermore, high-fat diet (HFD)-fed mice exhibit the downregulation

169 t in fatty livers in obese individuals or in high-fat diet (HFD)-fed mice.

170 and to prevent hepatic lipid accumulation in high-fat diet (HFD)-fed rodents.

171 ney (uninephrectomy [UniNx]) in mice reduced high-fat diet (HFD)-induced adipose tissue inflammation,

172 ate the role of neurovascular dysfunction in high-fat diet (HFD)-induced cognitive impairment.

173 Normal diet (ND) and high-fat diet (HFD)-induced DM mice were randomized into

174 ial transcription factor A (TFAM) attenuates high-fat diet (HFD)-induced fat gain and IR in mice in c

175 High-fat diet (HFD)-induced inflammation and steatosis o

176 High-fat diet (HFD)-induced inflammation is associated w

177 transport and ATP synthesis, and aggravating high-fat diet (HFD)-induced NAFLD.

178 Here, we demonstrate that high-fat diet (HFD)-induced obesity impairs CD8(+) T cel

179 High-fat diet (HFD)-induced obesity is associated with a

180 uromuscular dysfunctions in a mouse model of high-fat diet (HFD)-induced obesity.

181 ial vanilloid subfamily 1 (TRPV1) to counter high-fat diet (HFD)-induced obesity.

182 ipose tissue thermogenesis in the context of high-fat diet (HFD)-induced obesity.

183 esity, hyperglycemia, and liver steatosis in high-fat diet (HFD)-treated male mice.

184 ly in AT and AT MDCs of wild-type mice fed a high-fat diet (HFD).

185 liver and further increases with fasting or high-fat diet (HFD).

186 ionship has been also found in rodents fed a high-fat diet (HFD).

187 hondrial activity in both strains exposed to high-fat diet (HFD).

188 ) basally and following a short-term (7-day) high-fat diet (HFD).

189 tly increased in KCs of wild-type mice fed a high-fat diet (HFD).

190 ance and insulin sensitivity when exposed to high-fat diet (HFD).

191 Male Wistar rats were fed either a high-fat diet (HFD; 35% fat) or a standard diet (3.5% fa

192 normal diet, n=4; PCSK9-normal diet, n=6) or high-fat diet (HFD; WT-HFD, n=3; PCSK9-HFD, n=6).

193 We find that short-term high-fat-diet (HFD) feeding of mice activates prepronoci

194 otein E knockout mice (ApoE(-/-)) were fed a high-fat-diet (HFD) for up to four-months prior to MRI o

195 e report that cardiac dysfunction induced by high-fat-diet (HFD) persists for two subsequent generati

196 Our previous reports showed that high-fat-diet (HFD)-fed mice with liver-specific knockou

197 KO mice), we showed that AKT1 is involved in high-fat-diet (HFD)-induced growth and survival of beta

198 (tMCAO) in T2D/obese mice (after 7 months of high-fat diet [HFD]) and age-matched controls.

199 use gut microbiota in a manner distinct from high-fat diets (HFDs).

200 sexes consuming more sucrose, sucralose and high fat diet if from obese mothers.

201 ption factor A (TFAM) and inhibited maternal high fat diet-impaired placental efficiency and glucose

202 Modulating nutrient supply through high-fat diet improved survival, whereas high-glucose di

203 nating feeding mice with a low-fat diet or a high-fat diet in a 1-week switch protocol caused further

204 This rhythmic pattern is altered by high-fat diet in a ligand-independent manner.

205 insulin resistance induced by a hypercaloric high-fat diet in humans.

206 echocardiograms to investigate the role of a high-fat diet in IAV-associated cardiac damage.

207 ed in obese patients and after 24 weeks of a high-fat diet in mice, accompanying signs of AT inflamma

208 ormin prevented weight gain in response to a high-fat diet in wild-type mice but not in mice lacking

209 spheres as well as tumorigenesis induced by high-fat diets in an in vivo mouse model.

210 aloric control diet and a 3-day hypercaloric high-fat diet (increase of 75% in energy, 81-83% energy

211 ed that germ-free zebrafish are resistant to high fat diet induced EEC silencing.

212 Unexpectedly, high fat diet induced extensive atherosclerosis in miR-1

213 g Rebaudioside A and sucralose on NASH using high fat diet induced obesity mouse model by substitutin

214 impact on weight gain and energy balance in high fat diet induced obesity.

215 etabolic stress induced in mice by feeding a high-fat diet induced greater DNA damage in osteoblast o

216 in alveolar and interstitial macrophages in high-fat diet induced obese mice were lower than regular

217 on, we treated regular chow diet-fed mice or high-fat diet induced obese mice with lipopolysaccharide

218 increases paralleled profiles from long-term high-fat diet induced obesity in males.

219 ammation in both models, disturbed flow- and high fat diet-induced atherosclerosis, whereas Nck2 dele

220 Furthermore, established high fat diet-induced hepatic steatosis was effectively

221 e conclude that LCN2 is dispensable for both high fat diet-induced obesity and its therapeutic reduct

222 mic overexpression of SH2B1 protects against high fat diet-induced obesity and metabolic syndromes.

223 n wild-type mice, NaHS treatment ameliorates high fat diet-induced obesity and metabolism disorders,

224 lerated fat mass loss on a normal diet after high fat diet-induced obesity.

225 of streptozocin-induced type 1 diabetes and high fat diet-induced type 2 diabetes mouse models and l

226 iated pMos and protected Ldlr(-/-) mice from high-fat diet-induced atherosclerosis.

227 ity and dyslipidemia, it protected mice from high-fat diet-induced glucose intolerance and insulin re

228 ptozotocin-induced beta-cell destruction and high-fat diet-induced glucose intolerance.

229 IRAK2 kinase inactivation also reduced high-fat diet-induced metabolic diseases.

230 Here we show that CSE knockout exacerbated high-fat diet-induced mouse obesity as well as its relat

231 with choline-deficient l-amino acid-defined high-fat diet-induced NASH.

232 hionyl-leucyl-phenylalanine, are elevated in high-fat diet-induced obese mice.

233 contrast, pADORA(1) signaling facilitates a high-fat diet-induced obesity (DIO).

234 mogenic genes in BAT, and are protected from high-fat diet-induced obesity and development of insulin

235 ic transfer of the EAT gene to mice prevents high-fat diet-induced obesity, insulin resistance and fa

236 ue-specific lymphangiogenesis during 16-week high-fat diet-induced obesity.

237 ression and increases food intake leading to high-fat diet-induced obesity.

238 Of note, the MARC2 KO mice were resistant to high-fat diet-induced obesity.

239 esulted in better glucose tolerance during a high-fat diet-induced regain phase (all, P < .05).

240 pecific and whole-body insulin resistance in high-fat-diet-induced obese mice.

241 eased energy expenditure and amelioration of high-fat-diet-induced obesity and markedly improved gluc

242 l6 enhances lipid catabolism and ameliorates high-fat-diet-induced steatosis.

243 e-specific MyD88 or IRAK2 deficiency reduced high-fat-diet-induced weight gain, increased energy expe

244 Herein we investigated whether gestational high fat diet influences the offspring susceptibility to

245 diac-specific deletion of PKBalpha/beta or a high fat diet inhibits insulin-induced phosphorylation o

246 and 530 significant changes were due to the high-fat diet intervention.

247 ta-analysis of microbiome sequence data from high-fat-diet intervention studies.

248 High-fat diet is associated with elevated plasma homocys

249 When mice with CrAT deletion were fed a high-fat diet, kidney disease was more severe and develo

250 chromosome complement in combination with a high-fat diet led to enhanced weight gain in the presenc

251 these data provide the first evidence that a high-fat diet may be a risk factor for the development o

252 Here, we investigate the effects of maternal high-fat diet (MHFD) at different stages of pre- or post

253 After a high fat diet, mice lacking CD69 on lymphoid cells devel

254 Using a high-fat diet model of obesity in mice and breast tissue

255 om the SFA-rich high-fat diet to a MUFA-rich high-fat diet; nerve conduction velocities and intraepid

256 The low-fiber, high-fat diet of AN people and exposure to carcinogens d

257 fection negated the deleterious effects of a high-fat diet on cardiac function and remodeling, and ac

258 Triple transgenic dams were administered high fat diet or regular chow throughout 3 weeks gestati

259 Mice were fed a standard diet, a high fat diet, or these diets supplemented isocaloricall

260 bunit up-regulation, and in the setting of a high-fat diet, p110gamma ablation failed to protect agai

261 With consumption of a high-fat diet, Plin5(LKO) mice accumulated intrahepatic

262 he injection of P5 peptide into WT mice on a high-fat diet prevents macrophage accumulation in adipos

263 Gestational high fat diet protects offspring against the development

264 Male DIO B6 mice maintained on a high-fat diet received five intraperitoneal injections o

265 ght and body fat than did control mice fed a high-fat diet, resulting in ameliorated glucose toleranc

266 We have previously described that mice fed a high-fat diet rich in polyunsaturated fatty acids (HFD-P

267 f neutrophils in bone marrow than mice fed a high-fat diet rich in saturated fatty acids (HFD-S).

268 Male mice Mus musculus fed a high-fat diet rich in SFAs developed robust peripheral n

269 ROCK2(+/-) mice on a high-fat diet showed increased energy expenditure accomp

270 Apoe null mice challenged with high-fat diet showed similar metabolic changes in circul

271 2(S587A) mice that were fed either a chow or high-fat diet showed similar weight gain as the wild-typ

272 rnal metformin treatment along with maternal high fat diet significantly increased mouse placental ab

273 High-fat diet stimulated lipid-specific mitochondrial ad

274 d and showed similarity to those observed in high-fat diet studies.

275 n Tgr5(-/-), but not Fxr(Delta/E) mice fed a high-fat diet, suggesting a role for intestinal Fxr.

276 or 16-wks) on either a low-fat, high-fat, or high-fat diet supplemented with 1.5X branched chain amin

277 testinal serotonin of mice fed for 9 wk on a high-fat diet supplemented with different sources of fib

278 In obese mice on a high-fat diet, the effects of metformin to reduce body w

279 oma, and metabolic derangements induced by a high-fat diet; therefore, elucidating the intracellular

280 t when female Ppp1r15a mutant mice are fed a high fat diet they gain less weight than wild type litte

281 rsed by switching the mice from the SFA-rich high-fat diet to a MUFA-rich high-fat diet; nerve conduc

282 Mice were fed a high-fat diet to induce obesity and to study immunomodul

283 Using a high-fat diet to induce obesity, we examined preneoplast

284 ale C57BL/6J mice were fed either low-fat or high-fat diet to induce obesity.

285 I, Tan and Hang et al. report that feeding a high-fat diet to mice compromised the function of the or

286 n of calsyntenin 3beta predisposes mice on a high-fat diet to obesity.

287 hepatic transcriptional response in mice on high-fat diet treated with metformin was largely ablated

288 from mice who have undergone normal diet vs high-fat diet treatments.

289 The addition of cholesterol to a high-fat diet triggered hepatic pathology reminiscent of

290 Young mice administered a high-fat diet upon weaning exhibit the most dramatic phe

291 eding the hep-LAL-ko mice a vitamin A excess/high-fat diet (VitA/HFD) further increased hepatic chole

292 ry of antibiotics in individuals consuming a high-fat diet was associated with the greatest risk for

293 For one group (n = 8), the high-fat diet was enriched with saturated long-chain FAs

294 tro from male and female mice fed control or high-fat diet, we demonstrated that macrophages derived

295 ce (C57BL/6J mice, 33 weeks old), fed with a high fat diet which increases adipose tissue favouring o

296 s collected from mice on a choline-deficient high-fat diet, which developed chronic liver inflammatio

297 were randomly assigned to receive chow diet, high fat diet with sugar in drinking water (Western diet

298 late the effect of dietary fat, we generated high-fat diets with varying fatty acid balance and type.

299 Mice were fed a well-defined high fat diet, with (HFD/ATI) or without (HFD) nutrition

300 liver steatosis that developed in mice fed a high-fat diet, with or without combination with an inhib