ライフサイエンスコーパス: on a @2 diet

1 emented with nuts, or a control diet (advice on a low-fat diet).

2 overall survival (35 versus 63 days for mice on a folate-restricted diet).

3 els increased dramatically following 28 days on a LP diet.

4 a polysaccharide-rich standard diet but not on a PD diet.

5 own periodicity that was longer than animals on a chow diet.

6 ion of weight gain in mice on an HFD but not on a chow diet.

7 not reduced by the inflammation in the mice on a chow diet.

8 protein tolerance and lethal hyperammonemia on a chow diet.

9 es of glucose synthesis compared to athletes on a mixed diet.

10 ture, likely enables giant pandas to survive on a bamboo diet.

11 ts on HFD than in controls and diabetics fed on a normal diet.

12 umor-derived angiogenesis in mice maintained on a normal diet.

13 iver-specific PPARgamma null mice maintained on a normal diet.

14 low cytometry than did those of apoE-/- mice on a normal diet.

15 as comparable to that of wild-type (WT) mice on a normal diet.

16 D diet were also observed in Lrh-1(-/-) mice on a normal diet.

17 ciated with normal aging compared with those on a normal diet.

18 ckground, become obese on a high fat but not on a low fat diet.

19 significant larger decreases for TT carriers on a low-fat diet.

20 iption omega-3-acid ethyl esters in patients on a low-fat diet.

21 ffer cells is evident in eNos(-/-) mice even on a low-fat diet.

22 Mice lacking MGAT2 have a normal phenotype on a low-fat diet.

23 imals fed a high-salt diet compared to those on a regular diet.

24 assium ATPase (H,K-ATPase) compared to those on a regular diet.

25 dy weight, food intake or energy expenditure on a regular diet.

26 luconeogenic genes and hyperglycemia in mice on a regular diet.

27 PON3Tg/LDLR null mice than in LDLR null mice on a western diet.

28 ted in CD11d(-/-)/ApoE(-/-) mice after 16 wk on a Western diet.

29 severe hepatic steatosis following placement on a high fat diet.

30 reduced autophagy had worn off after 7 weeks on a high fat diet.

31 d body weight compared to the wild-type mice on a high fat diet.

32 s Bim and Puma had been ablated were studied on a high-fat diet.

33 produces significantly enhanced weight gain on a high-fat diet.

34 sensitivity and are resistant to weight gain on a high-fat diet.

35 d insulin resistance when animals are placed on a high-fat diet.

36 ultimately corresponding to less weight gain on a high-fat diet.

37 ate phenotype seen in heterozygous null mice on a high-fat diet.

38 ocytes, fatty livers, and insulin resistance on a high-fat diet.

39 TS-c potently decreasing weight gain in mice on a high-fat diet.

40 their susceptibility to obesity when placed on a high-fat diet.

41 on and control of body weight in mice placed on a high-fat diet.

42 bited absence of Pparg circadian rhythmicity on a high-fat diet.

43 atherosclerosis development in apoE-/- mice on a high-fat diet.

44 in our samples that increased in proportion on a high-fat diet.

45 therosclerosis development in ApoE(-/-) mice on a high-fat diet.

46 k for fatty liver disease in mice maintained on a high-fat diet.

47 weight gain in recipient wild-type mice fed on a high-fat diet.

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

49 ration was blunted in mice lacking PER1/2 or on a high-fat diet.

50 s in the aortic sinus following 10 and 16 wk on a high-fat diet.

51 tics of rats on a high-fat diet toward those on a standard diet.

52 taining 25% palm oil and compared with those on a standard diet.

53 eta expression in the macula densa increases on a high-salt diet.

54 mined after C75 injection in rats maintained on a ketogenic diet.

55 terns, hyperphagia, or excessive weight gain on a palatable diet.

56 activity that restricts insect reproduction on a synthetic diet.

57 , gain weight and accumulate excess body fat on a chronic HF diet.

58 ice to development of cholesterol gallstones on a lithogenic diet.

59 given to restore these bacteria to patients on a low FODMAP diet.

60 18-70 years who had coeliac disease and were on a gluten-free diet.

61 lities or their presenting clinical features on a gluten-free diet.

62 the vaccine in patients with coeliac disease on a gluten-free diet.

63 ogy at diagnosis and after at least one year on a gluten-free diet.

64 nes in the liver and serum, compared to mice on a normal chow diet.

65 ed with batf3(-/-) or wt bone marrow and put on a western type diet.

66 -density lipoprotein receptor-deficient mice on a Western-type diet.

67 iated enhanced inhibition of ENaC in animals on a high-potassium diet.

68 ccumulate excess cholesterol when maintained on a high-cholesterol diet.

69 reduction in plaque burden in Ldlr(-/-) mice on a high-cholesterol diet.

70 and effects on NAFLD, with special emphasis on a low-carbohydrate diet.

71 y ganglionic blockade or by weaning the mice on a carbohydrate-free diet.

72 gree to which subjects developed fatty liver on a choline-deficient diet.

73 or samples from subjects with celiac disease on a gluten-containing diet.

74 m and at 50% in liver TR1 of mice maintained on a selenium deficient diet.

75 effectors produced only females when raised on a limited tetracycline diet.

76 bserved an increase in survival time in mice on a glutamine restriction diet.

77 On a normal diet (10% fat), MacGHR KO and littermate con

78 Animals on a CR diet (30% CR; N = 23) were compared to ad libitu

79 After 1 week on a high fat diet, 4-week-old Pdx1(+/-) Becn1(+/-) mice

80 ly 3-fold up-regulation in the liver of mice on a high-fat diet (42% calories from fat).

81 In contrast, in DIO-R mice, maintenance on a HF diet (45% or 60%) had no effect on lipid-induced

82 Ts65Dn dams were maintained on a choline-supplemented diet (5.1 g/kg choline chlorid

83 nonsignificant tendency to higher urinary pH on a random diet (6.31 versus 6.09; P=0.09).

84 On a high-salt diet, all mice with D(5)(-/-) kidneys exc

85 As a result, after twelve weeks on a lithogenic diet, all of the LIRKO mice develop gall

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

87 AntimiR treatment of mice on a high-fat diet also resulted in increased lean and m

88 EPCs from mice on a LCHP diet also manifest lower levels of activated (

89 Ad-GsKO mice maintained at thermoneutrality on a standard diet also had normal energy balance.

90 LDLR(-/-) pregnant dams on a Western diet also had litters with significant IUGR

91 On a high-fat diet, although no differences in body weig

92 = 10) and healthy (n = 9) controls after 3 d on a eucaloric diet and again after 3 d on a diet of sim

93 Harmine-treated mice gained less weight on a high fat diet and displayed increased energy expend

94 mice also fail to develop hepatic steatosis on a high fat diet and manifest half-normal serum choles

95 Hig2 expression increased in livers of mice on a high-fat diet and during fasting, two states associ

96 ted Na(+) retention, elevated blood pressure on a high-Na(+) diet and increased surface expression of

97 the observed lifespan extension is prevented on a high-protein diet and in FoxO-null flies.

98 /-), and CGD-sensitive C57L mice were placed on a lithogenic diet and then analyzed for CGD at the bi

99 DNA microarray at baseline after weight loss on a low-calorie diet and after weight maintenance.

100 antly poorer disease resistance than females on a low-quality diet and in poor condition.

101 0b) have less adipose tissue when maintained on a normal chow diet and are resistant to diet-induced

102 Also, we found that OP rats were hyperphagic on a regular chow diet and gained more weight compared t

103 - mice deficient in macrophage p38alpha MAPK on a Western diet and found that they had a marked incre

104 ensitivity], 10 subjects with celiac disease on a gluten-containing diet, and 52 presumed healthy ind

105 d substantially improved glucose homeostasis on a high-fat diet, and hyperinsulinemic-euglycemic clam

106 hat compared with wild-type and apoE-/- mice on a normal diet, apoE-/- mice on a Western high-fat die

107 and littermate LDLR(-/-) mice were initiated on a high-fat diet at 6 months of age, followed 1 week l

108 e-deficient (Apoe(-/-)) strains, was started on a Western diet at 6 weeks of age and maintained on th

109 ldosterone was measured in diabetic patients on a high-sodium diet, before and after angiotensin II s

110 With mice on a standard chow diet, body weight and glucose homeost

111 After 16 to 18 weeks on a high-fat diet, both groups of mice had similar fast

112 While on a high-fat diet, both male and female betaIGF2KO mice

113 Within 10 days on a high-salt diet, BP increased similarly in ES and SS

114 undetectable in biopsy samples from patients on a gluten-free diet but expanded rapidly and specifica

115 sed coeliac patients that initially improved on a gluten-free diet but then relapsed despite a strict

116 ngth of jejunal villi and have normal growth on a normal diet but were less susceptible (P<0.01) to H

117 nockin mice had normal levels of hepatic fat on a chow diet, but when challenged with a high-sucrose

118 ats on a high-potassium diet than from those on a control diet, but this was not a result of altered

119 e8 is increased in human obesity and in mice on a high-fat diet, but its role in obesity is unknown.

120 tin degradation occurred also in uremic mice on a normal-phosphate diet, but they did not develop AMC

121 e show that SMRT(+/-) mice are normal weight on a regular diet, but develop increased adiposity on a

122 oth wild-type and RELMbeta KO mice were lean on a standard chow diet, but, upon switching to a high-f

123 carotid lesions were induced in FVB mice fed on a high-fat diet by streptozotocin injection followed

124 NMR profiling demonstrates that maintenance on a ketogenic diet causes a 25% reduction of myocardial

125 ormed on retinas of cbs(+/-) mice maintained on a high-methionine diet (cbs(+/-) HM).

126 Here we show that in rats on a high-cholesterol diet, cholesterol levels in hippoc

127 On a chow or on a high-fat diet, Cnr1(flox/flox); Phox2b-Cre mice hav

128 osis and no evidence of hepatic inflammation on a high-fat diet compared to a low-fat diet.

129 nd this occurred to a greater extent in rats on a high-K diet compared with a normal-K diet.

130 In hGCGR mice on a high fat diet, compound 9m at 3, and 10 mpk po in f

131 We showed that iNKT cell-deficient mice on a low-fat diet, considered a normal diet for mice, di

132 sponse to cocaine in rats that gained weight on a 'junk-food' diet, consistent with greater responsiv

133 The aortas of apoE-/- mice on a Western diet demonstrated greater numbers of FR-pos

134 which develop significant insulin resistance on a high-fat diet, despite no difference in adiposity.

135 Ksp-Cre mice rapidly developed hyperkalemia on a high-K+ diet, despite a 10-fold increase in serum a

136 Mice with increased Fto expression on a high-fat diet develop glucose intolerance.

137 We report that apoE-/- mice on a high-fat diet develop PAH as judged by elevated rig

138 asm(-/-)/ldlr(-/-) mice on a modified diet did not accumulate body fat and were

139 demonstrated that Fyn knockout (FynKO) mice on a standard chow diet display increased glucose cleara

140 On a normal salt diet, dKO and single-knockout mice exhi

141 We conclude that athletes on a LCHF diet do not compensate for reduced glucose ava

142 ation became obese (with increased fat mass) on a chow diet due to increased food intake and reduced

143 mt1(+/+) and Shmt1(-/-) dams were maintained on a standard AIN93G diet (Dyets), an AIN93G diet lackin

144 As predicted, crickets on a high-quality diet eclosed more quickly, and at a la

145 pancreatic insulin content, MIP-CreERT mice on a chow diet exhibited normal ambient glycemia, glucos

146 miR-223(-/-) mice on a high-fat diet exhibited an increased severity of sy

147 FGFR4-deficient mice on a normal diet exhibited features of metabolic syndrom

148 Spiders reared on a restricted diet exhibited consistent variation in a

149 during short-term treatment, wild-type mice on a calorie-restricted diet experienced significant dec

150 mpaired glucose tolerance if their dams were on a high-fat diet, experienced prenatal stress, or both

151 In celiac patients on a gluten-free diet, exposure to gluten induces the ap

152 s) were divided into groups that were placed on a normal chow diet, fasted for 24 hours, or fasted fo

153 Compared with dams on a control diet, female C57BL/6J mice fed an obesogeni

154 Thus, on a high NaCl diet fenoldopam causes natriuresis by inh

155 salt homeostasis in male Wistar rats placed on a cholate-rich diet for 5 days and in cultured primar

156 ononuclear cells, healthy humans were placed on a controlled diet for 1 week, then given fish oil and

157 General Clinical Research Center and placed on a controlled diet for 7 days.

158 racil DNA glycosylase (Ung(-/-)) were placed on a folate-deficient diet for 8 months.

159 ockout mice and wild-type animals were place on a high-carbohydrate diet for 16 weeks, and mitochondr

160 studied at baseline and every 4 to 6 months on a high-fat diet for 2 years.

161 L-SACC1 and wild-type mice were placed on a high-fat diet for 3 months, then several biochemica

162 r-deficient (Ldlr(-/-)) mice were maintained on a high-fat diet for 3 weeks followed by 6 weeks of or

163 Furthermore, FAT-D2KO animals that were kept on a high-fat diet for 8 weeks gained more body weight a

164 e carbohydrates/d) for 3 wk and, thereafter, on a hypocaloric diet for 6 mo.

165 -) and MKP-1(-/-)/ApoE(-/-)) were maintained on a normal chow diet for 16 weeks.

166 Female LDLRKO mice were maintained on a Western diet for 8 wk and then divided into 2 group

167 Placing 8 healthy subjects on a Western-style diet for 1 month induced a 71% increa

168 Furthermore, in the context of mice on a Western diet, genetically induced deficiency of mas

169 , they are commonly used to monitor patients on a gluten-free diet (GFD).

170 either active celiac disease (ACD) or those on a gluten-free diet (GFD).

171 methionine- and choline-deficient diet, mice on a high-fat diet given streptozotocin, and mice with d

172 we previously reported that during refeeding on a low-fat diet, glucose tolerance is normal but insul

173 sterol levels in serum compared to group fed on a control diet (groundnut oil).

174 ts [BMI (kg/m(2)): 30.6 +/- 1.2] were placed on a hypercaloric diet (>1000 kcal simple carbohydrates/

175 KO mice on a cholic acid diet had higher hepatic and serum bile

176 ype mice, interleukin (IL) 10-deficient mice on a normal diet had decreased levels of colonic H2S syn

177 Gpihbp1 knockout mice on a chow diet have milky plasma and plasma triglyceride

178 Mice on a high-fat diet have increased oxLDLs and systemic an

179 tant and consistent influence, larvae raised on a good-quality diet having substantially higher PO ac

180 Analysis of the effects after placing mice on a high fat diet (HFD) regimen demonstrated that runni

181 mpared with wild-type littermates (controls) on a high fat diet (HFD), Tg mice exhibited increased ad

182 -) mice gain more weight than wild-type mice on a high-fat diet (HFD) and that key liver and white ad

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

184 a group fed on the same diet or a group fed on a high-fat diet (HFD) rich in saturated fats for 3 we

185 The offspring of dams on a high-fat diet (HFD) versus balanced diet (BD), from

186 Whole-body IKKepsilon knockout mice on a high-fat diet (HFD) were protected from insulin res

187 ance, and insulin resistance when maintained on a high-fat diet (HFD), and were unable to maintain mu

188 We found that on a high-fat diet (HFD), Chga-KO mice (KO-DIO) remain m

189 Despite becoming obese on a high-fat diet (HFD), mice lacking FcgammaRIIB globa

190 On a high-fat diet (HFD), PFKFB3(+/-) mice gained much l

191 is, KO mice gain significantly more fat mass on a high-fat diet (HFD), yet are surprisingly resistant

192 egular diet, but develop increased adiposity on a high-fat diet (HFD).

193 in obesity- and diabetes-prone C57BL/6J mice on a high-fat diet (HFD).

194 et-induced obesity when POLG mice are placed on a high-fat diet (HFD).

195 However, female rats maintained on a "Westernized" diet high in fat and sugar (HE diet)

196 ent of TICs and tumorigenesis in mice placed on a Western diet high in cholesterol and saturated fat

197 ic hypertension relative to wild types (WTs) on a high-salt diet (HSD); this was attenuated by a PGI(

198 sulin sensitivity in these mice was improved on a standard chow diet in the absence of any weight dif

199 4 d postweaning in mice that were maintained on a normal diet (including increases in Proteobacteria

200 t's general condition improved substantially on a lactose-free diet, including hypercalcaemia, hyperc

201 When placed on a high-sugar diet, Irf6 cKO mice show a 35-fold incre

202 tory receptor neurons, and long-term feeding on a camphor diet led to reversible downregulation of TR

203 d reduced adiposity, protection from obesity on a high-fat diet, low plasma lipid levels, and a neuro

204 WT mice on a low-iron diet maintained normal serum intact Fgf23

205 Although TG mice on a normal diet maintained normal cardiac energetics an

206 On a high-fat diet, male G alpha(i2)(G184S) mice are res

207 After 8 to 16 weeks on a Western diet, male and female mice were assessed fo

208 d a large number of brain neurons affordable on a cooked diet may thus have been a major positive dri

209 lack of support for protein leverage effects on a low-protein diet may stem from the fact that protei

210 On a high-fat diet, MCK-DGAT1 mice displayed higher basa

211 However, on a high-fat diet, MGAT2-deficient mice are protected a

212 When placed on a high-fat diet, mice lacking BAI1 had increased numb

213 On a standard diet, mice overexpressing ChREBP remained

214 gh-fat diet (with or without fructose), mice on a Western-type diet, mice on a methionine- and cholin

215 nted by co-housing with offspring of mothers on a regular diet (MRD) and transferable to germ-free mi

216 On a high protein diet, mutant mice display disease exac

217 d the development of hypertension in SS rats on a high-salt diet (n = 7-8, p < 0.05).

218 he increased weight gain of SMRT(mRID1) mice on a high-fat diet occurs predominantly in fat with adip

219 ral administration of NPY in the Acb in rats on a free-choice diet of saturated fat, 30% sucrose solu

220 Wild-type FVB and ALDH2 mice were placed on a 4% alcohol diet or a control diet for 14 weeks.

221 nse of females feeding for two and five days on a control diet or a diet containing either a low or a

222 ness over 5 wk, rising to twice that of mice on a normal diet or CD11c(-/-) mice fed a WD.

223 agA mutant strain and maintained the animals on a regular diet or a high-salt diet.

224 type littermate control mice were maintained on a standard chow diet or subjected to 4 weeks of high-

225 EF, CON, and SUP rats were either maintained on a control diet, or the choline-supplemented diet.

226 lia of diabetic individuals, mice maintained on a high-fat diet, or cultured corneal epithelial cells

227 osis, col(V) sensitization of ApoE(-/-) mice on a regular chow diet overcame IL-10-mediated inhibitio

228 hed significantly more compared with animals on a normal caloric diet (P < 0.05).

229 d mean plasma levels of CySS in participants on a regulated diet (P = .034).

230 On a chow diet, plasma levels of leptin are decreased, a

231 After 12 weeks on a high-fat diet, postprandial tyrosine phosphorylatio

232 In adult mice maintained on a high-fat diet, Ppif ablation normalized fasting glu

233 All participants were placed on a low-calorie diet, prescribed increases in physical

234 Interventions: Participants were placed on a low-calorie diet, prescribed increases in physical

235 double knockouts) or placing Abcb4(-/-) mice on a high-fat diet protected against liver injury, with

236 For mice placed on a warfarin-containing diet, quantitative chemical and

237 e A(2b)AR ligand BAY 60-6853 in control mice on a high-fat diet reduced the lipid profile and atheros

238 dequate calcium intake is not achieved while on a nondairy diet, requiring investigation into optimal

239 When these animals were subsequently placed on a normal diet, resonance ratios reverted to those see

240 However, maintenance on a high-fat diet revealed a gene by environment intera

241 onstrate that mice lacking Irf5, when placed on a high-fat diet, show no difference in the growth of

242 In contrast, CAR null mice maintained on a chow diet showed spontaneous insulin insensitivity,

243 in vitro and ex vivo results, Efnb1 KO mice on a high salt diet showed a statistically significant h

244 However, female Pyy(-/-) mice on a high-fat diet showed a greater propensity to gain b

245 y been found to be altered in Npc1(-/-) mice on a high fat diet, showed related, but small, changes i

246 METHODS AND On a high-fat diet, smooth muscle 22alpha (SM22alpha)-TF

247 More importantly, after 3 months on a western-type diet, SMS2(-/-)-->LDLr(-/-) mice showe

248 During the first week on a high-salt diet, SS rats and SS rats with only one f

249 "clamped" to match the FM of mice maintained on a low-fat diet (standard diet [SD] mice).

250 We demonstrated that mice maintained on a VLP diet succumb to lethal challenge at greater rat

251 ShK-186 did not alter weight gain in mice on a chow diet, suggesting that the obesity-inducing die

252 POMC neurons became defective in obese mice on a high-fat diet, suggesting that loss of glucose sens

253 teatosis, insulin resistance, or dysglycemia on a sucrose-enriched diet, suggesting that elevated ins

254 Finally, on a high-cholesterol diet, Tcad/ApoE-DKO mice increased

255 On a Western diet, Tg(Prkcb)apoE-/- and apoE-/- mice did

256 he CaV1.1 pore gain more body weight and fat on a chow diet than control mice, without changes in foo

257 was lower in renal tissue obtained from rats on a high-potassium diet than from those on a control di

258 ediate maple syrup urine disease mice placed on a high protein diet that mimics the catabolic stress

259 al proximal and distal tubule transport, but on a low NaCl diet the increased RAAS activity prevents

260 After 3 weeks on a high fat diet, the decreased fasting plasma glucose

261 On a high fat diet, the mice were protected from insulin

262 ent of adipose tissue (AT) mass accumulation on a high-fat diet, the FynKO mice remained fully glucos

263 On a high-fat diet, the Hfe(/) mice exhibit increased fa

264 In liver FXR-knockout mice on a high-protein diet, the plasma concentration of newl

265 itive rats became hypertensive after 4 weeks on a high-NaCl diet, their plasma marinobufagenin levels

266 dult obese mice, 2 months after being placed on a high-fat diet, there was a striking increase of lep

267 On a 4% diet, these mice have no phenotype, but on a 60%

268 When placed on a high-fat diet, these double-knockout mice developed

269 a 4% diet, these mice have no phenotype, but on a 60% fat diet, they resist diet-induced obesity beca

270 IL-1alpha/beta-deficient bone marrow and fed on a high-cholesterol diet, they had markedly decreased

271 aner and shorter than the wild-type controls on a regular chow diet; they were also resistant to high

272 hyperkalemia and body weight loss when kept on a regular-salt diet, thus mimicking PHA-1.

273 Additional studies showed that, on a high-salt diet, Tmem27(Y/-) mice had lower renal bl

274 E (ApoE)-null mice that had been maintained on a high-fat diet to induce atherosclerosis.

275 shifts the metabolic characteristics of rats on a high-fat diet toward those on a standard diet.

276 Larvae were then raised on a clean diet until sexual maturity ( approximately 18

277 -density lipoprotein receptor-deficient mice on a Western-type diet using RNA sequencing and in silic

278 On a gluten-free diet, visits to primary care decreased

279 On a HF diet, vitamin D-deficient mice had ~2-fold great

280 VitD3-replete diet (VitD(HI) mice) and mice on a VitD3-deficient diet (VitD(LO) mice), the inflammat

281 rculosis burdens did not differ between mice on a VitD3-replete diet (VitD(HI) mice) and mice on a Vi

282 say detected individuals with celiac disease on a gluten-containing diet vs controls with an area und

283 The RPF response on a high-sodium diet was also higher than expected (47+

284 eatosis and insulin resistance in CBA/J mice on a sucrose-enriched diet was paralleled by increased h

285 that experienced prenatal stress and/or were on a high-fat diet weighed more beginning on postnatal d

286 LRP6(+/-) mice on a high fat diet were protected against diet-induced o

287 y lipoprotein receptor-null (Ldlr(-/-)) mice on a high-fat diet were orally administered with vehicle

288 MMP14 haploinsufficient mice, animals placed on a high-fat diet were unable to remodel fat pad collag

289 Crickets on a high-quality diet were not in better condition at t

290 nonobese, adult male C57BL/6 mice maintained on a normal chow diet were subjected to a microbiome dep

291 Spiders reared on a restricted diet were more aggressive towards prey a

292 ive pediatric patients (18 years or younger) on a gluten-containing diet who tested positive for TGA-

293 nium into proteins and had the same lifespan on a chemically defined diet with or without selenium su

294 lues identified subjects with celiac disease on a gluten-containing diet with 100% sensitivity (95% C

295 ose levels in imprinting control region mice on a high fat diet with diet-induced obesity following s

296 ed cholesterol efflux, and injection of mice on a western-type diet with locked nucleic acid-antisens

297 (controls) and 9 mouse models of NAFLD: mice on a high-fat diet (with or without fructose), mice on a

298 These animals developed obesity on a high-fat diet, with severe insulin resistance and h

299 atherosclerotic lesions in ApoE-p50-DKO mice on a normal chow diet without preexisting atherosclerosi

300 On a high-salt diet, WT mice with Tmem27(Y/-) kidneys ha