ライフサイエンスコーパス: high-cholesterol

1 on at low cholesterol and the beta-region at high cholesterol.

2 ex, and history of angina, hypertension, and high cholesterol.

3 ial extended benefit to CHD patients without high cholesterol.

4 tor that favors rapid fusion pore opening at high cholesterol.

5 LDL receptor knockout (Ldlr(+/-)) mice on a high-cholesterol (0.15%) diet, induced diabetes with str

6 treatment for 10,000 55-year-old women with high cholesterol (10-year CHD risk, 7.5%) was projected

7 ints [CI, 2.4 to 8.1 percentage points]) and high cholesterol (5.7 percentage points [CI, 2.0 to 9.4

8 evated blood pressure, more than 1 in 10 had high cholesterol, 58% consumed more fat than recommended

9 ly to respond have been identified as having high cholesterol absorption and low cholesterol biosynth

10 High cholesterol absorption is associated with risk alle

11 ow cholesterol absorption than in those with high cholesterol absorption.

12 in the NPC2 (HE1) gene that cause abnormally high cholesterol accumulation in cells.

13 ors (smoking, diabetes, high blood pressure, high cholesterol and angina) were quantified with logist

14 r adult women was positively associated with high cholesterol and blood pressure (both adult gender e

15 ercise and lower prevalence of hypertension, high cholesterol and diabetes cannot be inferred from th

16 iding adults (aOR = 1.24; 95% CI 1.02-1.52), high cholesterol and diabetes in the adult-parent sample

17 remedies for metabolic conditions including high cholesterol and diabetes.

18 ers fed a normal diet, a high fat diet, or a high cholesterol and high fat diet (HCHFD).

19 plasma membrane invaginations enriched with high cholesterol and sphingolipid content; they also con

20 Using isocaloric high-fat/high-cholesterol and low-fat/no-cholesterol diets in a 4

21 ertension, diet-controlled diabetes type II, high cholesterol, and a past history of numerous cutaneo

22 loric intake), medications for hypertension, high cholesterol, and diabetes during follow-up and addi

23 elating running and walking to hypertensive, high cholesterol, and diabetes medication use (condition

24 albumin, elevated C-reactive protein levels, high cholesterol, and higher levels of glucose.

25 usual source of care; diagnoses of diabetes, high cholesterol, and hypertension; self-reported health

26 sk factors, including smoking, hypertension, high cholesterol, and obesity, versus 36% of women and 3

27 f medical attention, including hypertension, high cholesterol, and osteoarthritis, were positively as

28 risk factors such as smoking, hypertension, high cholesterol, and type 2 diabetes mellitus, but that

29 sociated with diabetes, high blood pressure, high cholesterol, asthma, arthritis, and poor health sta

30 stones, Glaucoma, Gout, Atrial Fibrillation, High Cholesterol, Asthma, Basal Cell Carcinoma, Malignan

31 ported history of diabetes, hypertension, or high cholesterol at baseline, the multivariate-adjusted

32 Consistently, high cholesterol atherogenic diet-challenged Sort1 knock

33 epatic ceramide and fatty acid metabolism in high cholesterol atherogenic diet-fed mice.

34 ld male C57BL/6J mice were fed with either a high-cholesterol atherogenic diet (HCD) or matching norm

35 When challenged with a high fat/high cholesterol/bile salt diet, T39(-/-) mice or mice w

36 HaSCP-2 showed high cholesterol binding activity and SCP-2 inhibitors (

37 Synaptic vesicles contain unusually high cholesterol, but the exact role of cholesterol in f

38 at is widely prescribed for the treatment of high cholesterol, can correct excess hippocampal protein

39 here is 2-fold substrate specificity for the high cholesterol chemical activity l(d) phase over the l

40 ificity for cholesterol in the l(d) phase of high cholesterol chemical activity over cholesterol in t

41 Mice fed high fat, high cholesterol, cholate (HFHCC) diet for three weeks c

42 phosphatidylcholine (DOPC) lipid bilayers at high cholesterol concentration (>45 mol%) was investigat

43 In addition, the favorable effect of a high cholesterol concentration, and of POPC versus DOPC,

44 ue to the spontaneous curvature induced at a high cholesterol concentration.

45 lesterol-phospholipid mixtures consisting of high cholesterol concentrations has proved elusive in li

46 liquid-ordered-state domains (which form at high cholesterol concentrations).

47 coronary heart disease, high blood pressure, high cholesterol concentrations, and abnormal glucose-in

48 small rafts formed without photooxidation at high cholesterol concentrations.

49 malnutrition, not to a protective effect of high cholesterol concentrations.

50 ole of CYP2E1 in promoting liver fibrosis by high cholesterol-containing fast-food (FF).

51 3), In high-cholesterol-containing lipid bilayers, where gp41 F

52 He had exceptionally high cholesterol content (760 mg/dL; to convert to milli

53 SEP mutants p.E297G and p.R432T increased at high cholesterol content but did not reach the capacity

54 GUVs of high cholesterol content containing the breakdown produc

55 However, the high cholesterol content of the envelope (ca. 40 to 50 m

56 d domains, two properties that depend on the high cholesterol content of the viral membrane.

57 High cholesterol content shifted E17betaG to Michaelis-M

58 However, at high cholesterol content, a switch toward the C-terminus

59 llular membranes, in particular those with a high cholesterol content.

60 The proportion with high cholesterol decreased from 72% to 55%.

61 ase, high blood pressure, stroke, emphysema, high cholesterol, diabetes, arthritis, and asthma) and m

62 Upon feeding a 2% high cholesterol diet (HCD), Ldlr-/-xLcat-/- mice accumu

63 ptically transparent zebrafish larvae, fed a high cholesterol diet (HCD), to monitor processes of vas

64 laque signal correlated with the duration of high cholesterol diet (r(2)=0.33, P<0.05).

65 n LDLR wildtype (WT) mice fed a high fat and high cholesterol diet and it only lowered TG in LDLR WT

66 When challenged with a high fat, high cholesterol diet for 15 weeks, serum levels of high

67 d SRB1- antisense oligonucleotides and fed a high cholesterol diet for 16 weeks to induce severe hype

68 c lesions were produced in 38 rabbits with a high cholesterol diet for 4 months; 5 groups of rabbits,

69 ect was abrogated upon feeding the mice a 2% high cholesterol diet in association with accumulation o

70 riately regulated in the liver of mice fed a high cholesterol diet or chow diet supplemented with the

71 At the end of low and high cholesterol diet periods, liver biopsies were taken

72 overexpression of ABCA1 in C57BL/6 mice on a high cholesterol diet results in an atheroprotective lip

73 o Ldlr(-/-) mice and then fed a high fat and high cholesterol diet, significant increase in atheroscl

74 sorption of fewer calories from the high fat/high cholesterol diet, thereby resulting in less fat mas

75 After 15 weeks of feeding, the high fat/high cholesterol diet, wild type, and CEL(-/-) mice gain

76 pigs were fed either a normal (NORM, n=6) or high cholesterol diet, with (HICHOL-ARG, n=6) or without

77 ice markedly increased the susceptibility to high cholesterol diet-induced liver injury and abolished

78 D68) in the aortas of LDLR knockout mice fed high cholesterol diet.

79 E-null (ApoE(-/-)) and wild-type mice fed a high cholesterol diet.

80 mption of comparable amounts of the high fat/high cholesterol diet.

81 mice, and these effects were exacerbated by high cholesterol diet.

82 asal low fat diet or a western-type high fat/high cholesterol diet.

83 lesterol content induced by consumption of a high cholesterol diet.

84 Similar results were obtained on a high fat, high cholesterol diet.

85 d their plasma cholesterol level following a high cholesterol diet.

86 All animals were fed a high-cholesterol diet (1.25%) for 6 or 12 weeks.

87 -) mice on either chow (314 +/- 41 cells) or high-cholesterol diet (395 +/- 53 cells).

88 ion was highest in hypertensive animals on a high-cholesterol diet (43.9+/-0.7%, versus 12.0+/-2.0% f

89 aorta after both chow (503 +/- 67 cells) or high-cholesterol diet (648 +/- 81 cells).

90 d on either regular mouse chow (ApoE-R) or a high-cholesterol diet (ApoE-C) for 25 weeks.

91 randomized to three groups: normal diet (N), high-cholesterol diet (HC) and HC diet plus simvastatin

92 ivate a homeostatic program in response to a high-cholesterol diet (HCD) and regulate both the differ

93 )H oxidase placed on either a normal diet or high-cholesterol diet (HCD) for 2 weeks.

94 , and Abca1(-/-)Abcg1(-/-) mice fed either a high-cholesterol diet (HCD) or a Western diet (WTD).

95 that feeding adult zebrafish (Danio rerio) a high-cholesterol diet (HCD) resulted in hypercholesterol

96 Feeding a high-cholesterol diet (HCD) supplemented with a red fluo

97 nd premature deaths in response to high-fat, high-cholesterol diet (HFC).

98 mice (Apoe(-/-) ) challenged with a high-fat high-cholesterol diet affirmed the use of NR in other in

99 5 kg) were made atherosclerotic by feeding a high-cholesterol diet after endothelial aortic injury.

100 ractions in apoE(-/-) mice fed a normal or a high-cholesterol diet after short-term (ie, 18 hours) si

101 ate that psychosocial stress and a high-fat, high-cholesterol diet aggravate cardiovascular disease,

102 us 12.0+/-2.0% for normotensive animals on a high-cholesterol diet and 4.7+/-4.7% for animals on stan

103 Mice were fed a high-cholesterol diet and killed 24 weeks after transpla

104 ection in vivo, we analyzed the effects of a high-cholesterol diet and reduced apolipoprotein E (apoE

105 lesions in pigs that have been induced by a high-cholesterol diet and stenosis, and the effect of th

106 andomized to receive a normal (control) or a high-cholesterol diet and treated with vehicle or rosigl

107 wild-type (WT) females consuming a high-fat/high-cholesterol diet and tumor growth was evaluated.

108 hepatic cholesterol in wild-type mice fed a high-cholesterol diet but is not effective in FXR-null m

109 hown that C57BL/6J mice exposed to CIH and a high-cholesterol diet develop dyslipidemia, atherosclero

110 oE-deficient background or challenged with a high-cholesterol diet developed autoantibodies.

111 ring the second half of a 26-week regimen of high-cholesterol diet did not regress, but did significa

112 The mice received a high-fat, high-cholesterol diet during the last 3 weeks to induce

113 ApoE(-/-) mice fed a high-cholesterol diet exhibited higher blood cholesterol

114 Breast tumors from animals fed the high-fat/high-cholesterol diet exhibited the fastest progression.

115 r atherosclerotic lesions after high-fat and high-cholesterol diet feeding.

116 is induced in response to LXR activation and high-cholesterol diet feeding.

117 ApoE(-/-) BL/6 and BALB/c mice consumed a high-cholesterol diet for 10, 16, and 24 weeks with equi

118 n E-deficient (apoE-/-) mice that consumed a high-cholesterol diet for 12 weeks and age-matched apoE+

119 ld-type cells, and provided them a high-fat, high-cholesterol diet for 14 weeks.

120 +; or BL:TG:Ealpha, IA(b)+IE(k)+, were fed a high-cholesterol diet for 16 weeks and evaluated histomo

121 The mice were maintained on a high-fat/high-cholesterol diet for 16 weeks.

122 poprotein E-deficient (Apoe(-/-)) mice fed a high-cholesterol diet for 16 wk developed more severe at

123 Experimental animals placed on a high-cholesterol diet for 2 or more weeks exhibit an inf

124 arteries of normal pigs that had been fed a high-cholesterol diet for 4 weeks.

125 tor-deficient (LDLR-/-) mice maintained on a high-cholesterol diet for 6 weeks with either a HD-Ad co

126 cient mice, and the chimeric mice were fed a high-cholesterol diet for 8 weeks.

127 d one carotid artery, and animals were fed a high-cholesterol diet for two months to create various s

128 poE(-/-), wild-type (Agtr2+) mice consumed a high-cholesterol diet from 4 weeks of age.

129 Diabetic mice on the high-cholesterol diet had accelerated development of dia

130 TTR-Abcb11 mice fed a high-cholesterol diet had greater increases in plasma an

131 ein composition resulting from the high-fat, high-cholesterol diet in this model.

132 We noted that a high-fat, high-cholesterol diet increased expression of the Notch

133 A high-cholesterol diet leads to significant increases in

134 The effects of high-fat/high-cholesterol diet on body composition, plasma lipids

135 This was exacerbated by feeding mice a high-cholesterol diet or, more dramatically, by inactiva

136 Moreover, a high-cholesterol diet resulted in up to 3-fold increase

137 A high-cholesterol diet significantly facilitated A. phago

138 sgenic Yucatan minipigs were fed a high-fat, high-cholesterol diet to induce atherosclerosis and subj

139 ty lipoprotein receptor(-/-) mice were fed a high-cholesterol diet to investigate the functional role

140 Yorkshire swine fed a high-cholesterol diet underwent left circumflex ameroid

141 osclerotic lesion development in response to high-cholesterol diet was enhanced in Panx1 (del) Apoe (

142 The induction of Cyp7A1 expression by a high-cholesterol diet was impaired in NCoA6(L2m/L2m) mic

143 ate lesion development in mice if a high-fat/high-cholesterol diet was started after infection, indic

144 orally treated for 1 week with HSP-65, and a high-cholesterol diet was started after the last treatme

145 gh-fat diet and C57BL/6 mice fed a high-fat, high-cholesterol diet were injected with recombinant Nef

146 standard chow, a high-cholesterol diet, or a high-cholesterol diet with hypertension induced by angio

147 on of rat-IgG or saline; 13 weeks, continued high-cholesterol diet).

148 rd diet/periodontally healthy); 2) group Hc (high-cholesterol diet); 3) group HcP (high-cholesterol d

149 suppressed by cholesterol enrichment and by high-cholesterol diet, and facilitated following cholest

150 diet, followed by LDLR(-/-) that were fed a high-cholesterol diet, ApoE(-/-) that were fed normal ch

151 Here we show that in rats on a high-cholesterol diet, cholesterol levels in hippocampal

152 CXCR2, in the spleen in apoE(-/-) mice fed a high-cholesterol diet, compared with the other 3 groups.

153 rta was highest in ApoE(-/-) that were fed a high-cholesterol diet, followed by LDLR(-/-) that were f

154 red to 2 groups of Sprague-Dawley rats fed a high-cholesterol diet, ie, one group received MCT concom

155 In response to a high-cholesterol diet, IRA B cell numbers increase prefe

156 andomly assigned to receive standard chow, a high-cholesterol diet, or a high-cholesterol diet with h

157 After 16 weeks of a high-cholesterol diet, P2X7-deficient mice showed smalle

158 In Abcg1(-/-) mice fed a high-cholesterol diet, plasma levels of 7-ketocholestero

159 In LDLR-deficient mice fed a high-cholesterol diet, T cell-specific ABCG1 deficiency

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

161 cholesterol after maintenance on a high-fat, high-cholesterol diet, the MPO-Tg animals developed a 2-

162 At the end of 8 weeks of a high-cholesterol diet, the rabbits were killed, and the

163 lpha/beta-deficient bone marrow and fed on a high-cholesterol diet, they had markedly decreased early

164 ere fed either a normal (NORM group; n=7) or high-cholesterol diet, with (CHOL-ATR group; n=7) or wit

165 be (cholesterol-lowering drug), and high-fat/high-cholesterol diet, with or without ezetimibe.

166 A high-cholesterol diet, with or without periodontitis, re

167 arginase II gene (Arg II(-/-) mice) prevents high-cholesterol diet-dependent decreases in vascular NO

168 on area and cholesterol content of high-fat, high-cholesterol diet-induced atherosclerotic lesions.

169 In a high-fat, high-cholesterol diet-induced rodent model of NAFLD, we

170 but not in Senp2(+/+)/Ldlr(-/-), mice fed a high-cholesterol diet.

171 when maintained on a Western-type, high-fat, high-cholesterol diet.

172 the liver in response to both fasting and a high-cholesterol diet.

173 in L-TGH KO mice challenged with a high-fat, high-cholesterol diet.

174 d atherosclerosis was induced with a 16-week high-cholesterol diet.

175 nal biglycan content in diabetic mice on the high-cholesterol diet.

176 late excess cholesterol when maintained on a high-cholesterol diet.

177 Seven ApoE(-/-) and 7 LDLR(-/-) received a high-cholesterol diet.

178 ndotheliazation of the abdominal aorta and a high-cholesterol diet.

179 L receptor-deficient mice and administered a high-cholesterol diet.

180 eptor-deficient C57BL/6J mice fed a high-fat/high-cholesterol diet.

181 (-1) for 5 weeks beginning 3 weeks after the high-cholesterol diet.

182 -/-)) mice that develop atherosclerosis on a high-cholesterol diet.

183 e receptor for LDL that were maintained on a high-cholesterol diet.

184 ifestyle that includes a uniformly high-fat, high-cholesterol diet.

185 more than 2-fold in the livers of mice fed a high-cholesterol diet.

186 apolipoprotein E (apoE)-deficient mice fed a high-cholesterol diet.

187 ury in apoE-deficient (apoE(-/-)) mice fed a high-cholesterol diet.

188 land White rabbits were fed normal chow or a high-cholesterol diet.

189 bbits (n=31) using aortic balloon injury and high-cholesterol diet.

190 tion in plaque burden in Ldlr(-/-) mice on a high-cholesterol diet.

191 oliferating cells from mice fed the high-fat/high-cholesterol diet.

192 up Hc (high-cholesterol diet); 3) group HcP (high-cholesterol diet/periodontitis); and 4) group P (st

193 nduction through de-endothelialization and a high-cholesterol diet; 14 were then thrombus triggered.

194 compared with wild type mice under high fat/high cholesterol dietary conditions (80.1 +/- 3.7 versus

195 ant reduction (54%, P<0.01) of the high-fat, high-cholesterol dieteninduced atherosclerotic plaques w

196 High fat/high cholesterol diets exacerbate beta-amyloidosis in mo

197 On both regular chow and high fat, high cholesterol diets, expression of CETP in LCAT-Tg mi

198 profiles between regular basal and high fat/high cholesterol diets.

199 On both the low- and the high-cholesterol diets, whole liver and isolated hepatoc

200 s of Mexico and Americans consuming low- and high-cholesterol diets.

201 and variations in the environment due to the high-cholesterol disease state.

202 racteristics similar to wild type CCK1R in a high cholesterol environment.

203 from atherosclerotic lesions because of the high-cholesterol environment.

204 D was induced by 5/6 nephrectomy in high-fat high-cholesterol fed apolipoprotein E-deficient mice.

205 High cholesterol-fed, 26-week-old apoE-deficient mice re

206 approach to prepare supported membranes with high cholesterol fractions close to the cholesterol solu

207 The odds ratios for high cholesterol (>/=240 mg/dL), by increasing quartile

208 ociated with decreased serum cholesterol and high cholesterol has been associated with increased like

209 coronary heart disease and with and without high cholesterol have demonstrated consistently that sta

210 were studied after a 3-mo normal (n = 7) or high cholesterol (HC) (n = 7) diet, HC diet supplemented

211 ere randomized to 3 groups fed a normal (N), high cholesterol (HC), or HC+simvastatin (HC+S) diet for

212 weeks: control (4% fat and 0% cholesterol); high cholesterol (HC; 4% fat and 1% cholesterol); high f

213 s of age, were randomized to a normal (N) or high-cholesterol (HC) diet (2% cholesterol, 15% lard) wi

214 Mice were fed a normal (ND) or high-cholesterol (HC) diet beginning at 5 weeks postinfe

215 mice were placed on either a normal (ND) or high-cholesterol (HC) diet for 2 weeks.

216 ApoE(-/-) mice fed a low-cholesterol (LC) or high-cholesterol (HC) diet were infected with approximat

217 lar brain damage in old ApoE(-/-) mice fed a high-cholesterol (HC) diet with dietary controlled intak

218 on of double-balloon injury and a nine-month high-cholesterol (HC) diet.

219 and zebrafish exposed to high-fat (HFDs) or high-cholesterol (HCDs) diets develop acute innate infla

220 is of asthma, high blood pressure, diabetes, high cholesterol, heart problems, or any other physical

221 w that in 9-month-old APP23 mice, a high-fat/high-cholesterol (HF) diet provided for 4 months exacerb

222 ce dietary atherosclerosis in mice, high-fat/high-cholesterol (HF) diets are frequently supplemented

223 following four diets: control (C), high-fat/high-cholesterol (HF), control and 1% cholate (CA) and H

224 were fed either regular chow or a high-fat, high-cholesterol (HFC) diet for 3 months.

225 ; 15% fat and 0% cholesterol); and high fat, high cholesterol (HFHC; 15% fat and 1% cholesterol).

226 We explored the effects of a high-fat, high-cholesterol (HFHC) diet on vascular responses in ba

227 explores effects of prolonged exposure to a high cholesterol high fat (HCHF) diet on LTL in a baboon

228 18 men, 20 to 90 years of age, without known high cholesterol, high triglycerides, cardiovascular dis

229 Adjustment for self-reported high cholesterol, high triglycerides, high blood pressur

230 We examined the hypothesis that a high-cholesterol, high-fat (HCHF) diet can directly caus

231 e on the LDLR knockout background were fed a high-cholesterol/high-fat diet containing cholate, howev

232 se, depression, diabetes, self-rated health, high cholesterol, hypertension, peripheral vascular dise

233 high cholesterol typically progress to full high cholesterol in 2-3 years, and pre-diabetic patients

234 ely associated with diagnosed depression and high cholesterol in adulthood, and masculine gender expr

235 mental disorder, hypertension, obesity, and high cholesterol in parents and those same conditions in

236 e Y140A construct also behaved like CCK1R in high cholesterol in regard to its internalization, sensi

237 ve effects on cardiac apoptosis in rats with high cholesterol intake.

238 e metastatic effects of hypercholesterolemia.High cholesterol is a risk factor for breast cancer recu

239 than 90%, except for high blood pressure and high cholesterol level (negative predictive values, 33%

240 sence of diagnosed hypertension or diagnosed high cholesterol level, and menopausal status.

241 cular disease, fasting plasma glucose level, high cholesterol level, overweight, current smoking, hig

242 ry risk factors, eg, high blood pressure and high cholesterol level.

243 st common (grade 1 or 2) adverse events were high cholesterol levels (14 of 30 patients), nausea (11

244 High cholesterol levels also lead to overproduction of A

245 ompared with normal HSFs, EEs in NPFs showed high cholesterol levels and an altered organization of r

246 r risk factors for CHD (high blood pressure, high cholesterol levels and evidence on the electrocardi

247 High cholesterol levels greatly increase the risk of car

248 death, and only one quarter of persons with high cholesterol levels have attained recommended levels

249 High cholesterol levels in circulating immune complexes

250 eports of high blood pressure, diabetes, and high cholesterol levels in fathers were accurate: Positi

251 High cholesterol levels in the blood increase the risk o

252 High cholesterol levels increase APP and apoE expression

253 Therefore, high cholesterol levels may decrease the efficacy of dar

254 In mice, high cholesterol levels mobilize HSPCs into the bloodstr

255 rmal C57BL6 mice and failed to normalize the high cholesterol levels of apoE-deficient mice due to in

256 ameliorate the negative effects of high fat/high cholesterol levels on cognition and amyloid patholo

257 e prevalence or diagnosis of hypertension or high cholesterol levels or on the use of medication for

258 er, after adjustment for age, race, smoking, high cholesterol levels requiring medication, body mass

259 vascular disease, diabetes, hypertension, or high cholesterol levels were followed through 2009.

260 blood pressure, 1.88 (95% CI,1.67-2.13) for high cholesterol levels, 2.72 (95% CI, 2.38-3.12) for as

261 ns between perfluorooctanoic acid (PFOA) and high cholesterol levels, but studies of hypertension and

262 s were reliable, except for hypertension and high cholesterol levels.

263 than the RRs for obese men who smoked or had high cholesterol levels.

264 r =10 years, hypertension, macroalbuminuria, high cholesterol, low high-density lipoprotein, high C-r

265 Diets containing high cholesterol markedly increased the expression of AB

266 ood and cerebrovasculature and combined with high cholesterol may be a key component to the accumulat

267 P=0.03 for males and P<10(-4) for females), high cholesterol medication use in runners (P<10(-4) for

268 reductions in the odds for hypertension and high cholesterol medication use per METhr/d run or per M

269 stive CHRNA3-CHRNA5 findings with respect to high-cholesterol-medication use and distrustful attitude

270 Tumors from high-fat/high-cholesterol mice had significantly higher microvess

271 Canalicular BSEP, mostly present in raft (high cholesterol) microdomains in control rats, was larg

272 Thus, at high cholesterol mole fraction, this unfavorable free en

273 At similar high cholesterol mole fractions, the in-plane elasticity

274 higher proportion of hypertension, diabetes, high cholesterol, obesity, and lower education, income,

275 g, still one of two people with diabetes has high cholesterol, one of three has high blood pressure,

276 Mice fed diets containing high cholesterol or an LXR-selective agonist exhibited a

277 igher odds of hip replacement, lower odds of high cholesterol or cholesterol medication use and highe

278 stment for covariates including a history of high cholesterol or coronary artery disease.

279 y, smoking, and physical inactivity, but not high cholesterol or diabetes mellitus.

280 utants can be partially rescued on a diet of high cholesterol or one that includes the insect steroid

281 er, associations with lipid disorders (e.g., high cholesterol or triglycerides), which are major risk

282 y lipoprotein receptor(-/-) mice consuming a high-cholesterol or chow diet.

283 bcb11) and FVB/NJ mice (controls) were fed a high-cholesterol or high-fat diet for 12 weeks.

284 R [odds ratio] 1.43; heart disease: OR 1.68; high cholesterol: OR 1.26; stroke: OR 1.99; arthritis; O

285 More than 90% of borderline high cholesterol patients are retested within the 3 year

286 cal bilayered membrane with an exceptionally high cholesterol/phospholipid ratio.

287 tion; history of hypertension, diabetes, and high cholesterol; postmenopausal hormone use; alcohol in

288 y, low high-density lipoprotein cholesterol, high cholesterol ratio, high C-reactive protein, hyperte

289 cardiac threat posed by high blood pressure, high cholesterol, smoking, obesity, physical inactivity,

290 We examined hypertension, heart disease, high cholesterol, stroke, arthritis, asthma, chronic obs

291 sion on 2 visits, prediabetes, diabetes, and high cholesterol than eczema alone.

292 limoles per liter, multiply by 0.0259) and a high cholesterol to triglycerides ratio (1.52) in very l

293 obesity (body mass index >/= 30 kg/m2), and high cholesterol (total blood cholesterol >/= 240 mg/dL

294 Patients with borderline high cholesterol typically progress to full high cholest

295 infected patients who required treatment for high cholesterol were given 20 mg atorvastatin per day.

296 , alcohol, tobacco, high blood pressure, and high cholesterol were major causes of disease burden.

297 A total of 7594 patients with high cholesterol were studied, along with 2764 patients

298 -, and gld.apoE-/- mice were maintained on a high cholesterol Western diet and received daily simvast

299 Purely dietary models, such as high-fat/high-cholesterol, Western diet, and choline-deficient, a

300 High cholesterol, which induced beta-sheets, promoted fu