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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 ercise and lower prevalence of hypertension, high cholesterol and diabetes cannot be inferred from th
14 iding adults (aOR = 1.24; 95% CI 1.02-1.52), high cholesterol and diabetes in the adult-parent sample
15 ers fed a normal diet, a high fat diet, or a high cholesterol and high fat diet (HCHFD).
16                    Using isocaloric high-fat/high-cholesterol and low-fat/no-cholesterol diets in a 4
17 loric intake), medications for hypertension, high cholesterol, and diabetes during follow-up and addi
18 elating running and walking to hypertensive, high cholesterol, and diabetes medication use (condition
19 albumin, elevated C-reactive protein levels, high cholesterol, and higher levels of glucose.
20 usual source of care; diagnoses of diabetes, high cholesterol, and hypertension; self-reported health
21 sk factors, including smoking, hypertension, high cholesterol, and obesity, versus 36% of women and 3
22 f medical attention, including hypertension, high cholesterol, and osteoarthritis, were positively as
23  risk factors such as smoking, hypertension, high cholesterol, and type 2 diabetes mellitus, but that
24 sociated with diabetes, high blood pressure, high cholesterol, asthma, arthritis, and poor health sta
25 ported history of diabetes, hypertension, or high cholesterol at baseline, the multivariate-adjusted
26                                Consistently, high cholesterol atherogenic diet-challenged Sort1 knock
27 epatic ceramide and fatty acid metabolism in high cholesterol atherogenic diet-fed mice.
28 ld male C57BL/6J mice were fed with either a high-cholesterol atherogenic diet (HCD) or matching norm
29              When challenged with a high fat/high cholesterol/bile salt diet, T39(-/-) mice or mice w
30                               HaSCP-2 showed high cholesterol binding activity and SCP-2 inhibitors (
31          Synaptic vesicles contain unusually high cholesterol, but the exact role of cholesterol in f
32 at is widely prescribed for the treatment of high cholesterol, can correct excess hippocampal protein
33 here is 2-fold substrate specificity for the high cholesterol chemical activity l(d) phase over the l
34 ificity for cholesterol in the l(d) phase of high cholesterol chemical activity over cholesterol in t
35                           Mice fed high fat, high cholesterol, cholate (HFHCC) diet for three weeks c
36 phosphatidylcholine (DOPC) lipid bilayers at high cholesterol concentration (>45 mol%) was investigat
37       In addition, the favorable effect of a high cholesterol concentration, and of POPC versus DOPC,
38 ue to the spontaneous curvature induced at a high cholesterol concentration.
39 lesterol-phospholipid mixtures consisting of high cholesterol concentrations has proved elusive in li
40  liquid-ordered-state domains (which form at high cholesterol concentrations).
41 coronary heart disease, high blood pressure, high cholesterol concentrations, and abnormal glucose-in
42 small rafts formed without photooxidation at high cholesterol concentrations.
43  malnutrition, not to a protective effect of high cholesterol concentrations.
44 ole of CYP2E1 in promoting liver fibrosis by high cholesterol-containing fast-food (FF).
45                                       3), In high-cholesterol-containing lipid bilayers, where gp41 F
46                         He had exceptionally high cholesterol content (760 mg/dL; to convert to milli
47 SEP mutants p.E297G and p.R432T increased at high cholesterol content but did not reach the capacity
48                                      GUVs of high cholesterol content containing the breakdown produc
49                                 However, the high cholesterol content of the envelope (ca. 40 to 50 m
50 d domains, two properties that depend on the high cholesterol content of the viral membrane.
51                                              High cholesterol content shifted E17betaG to Michaelis-M
52                                  However, at high cholesterol content, a switch toward the C-terminus
53 llular membranes, in particular those with a high cholesterol content.
54 hase, to approximately 2 x 10(-9) cm(2)/s in high-cholesterol-content phases, to approximately 2 x 10
55                          The proportion with high cholesterol decreased from 72% to 55%.
56 ase, high blood pressure, stroke, emphysema, high cholesterol, diabetes, arthritis, and asthma) and m
57                            Upon feeding a 2% high cholesterol diet (HCD), Ldlr-/-xLcat-/- mice accumu
58 ptically transparent zebrafish larvae, fed a high cholesterol diet (HCD), to monitor processes of vas
59 Animals were killed after being fed either a high cholesterol diet (n = 4) or a control diet (n = 4)
60 laque signal correlated with the duration of high cholesterol diet (r(2)=0.33, P<0.05).
61             When challenged with a high fat, high cholesterol diet for 15 weeks, serum levels of high
62 c lesions were produced in 38 rabbits with a high cholesterol diet for 4 months; 5 groups of rabbits,
63 ect was abrogated upon feeding the mice a 2% high cholesterol diet in association with accumulation o
64 duced either by feeding the mice a high fat, high cholesterol diet or by crossing op mice with apolip
65 riately regulated in the liver of mice fed a high cholesterol diet or chow diet supplemented with the
66                        At the end of low and high cholesterol diet periods, liver biopsies were taken
67 overexpression of ABCA1 in C57BL/6 mice on a high cholesterol diet results in an atheroprotective lip
68                      In mice fed a high fat, high cholesterol diet to increase endogenous apoB-contai
69         When the mice were challenged with a high cholesterol diet, cleavage of SREBP-1 and -2 was re
70 o Ldlr(-/-) mice and then fed a high fat and high cholesterol diet, significant increase in atheroscl
71 sorption of fewer calories from the high fat/high cholesterol diet, thereby resulting in less fat mas
72      After 15 weeks of feeding, the high fat/high cholesterol diet, wild type, and CEL(-/-) mice gain
73 pigs were fed either a normal (NORM, n=6) or high cholesterol diet, with (HICHOL-ARG, n=6) or without
74 ice markedly increased the susceptibility to high cholesterol diet-induced liver injury and abolished
75  E-null (ApoE(-/-)) and wild-type mice fed a high cholesterol diet.
76 mption of comparable amounts of the high fat/high cholesterol diet.
77  mice, and these effects were exacerbated by high cholesterol diet.
78 asal low fat diet or a western-type high fat/high cholesterol diet.
79 lesterol content induced by consumption of a high cholesterol diet.
80 Similar results were obtained on a high fat, high cholesterol diet.
81 d their plasma cholesterol level following a high cholesterol diet.
82 de genetically deficient for MCP-1 and fed a high cholesterol diet.
83 D68) in the aortas of LDLR knockout mice fed high cholesterol diet.
84                       All animals were fed a high-cholesterol diet (1.25%) for 6 or 12 weeks.
85 -) mice on either chow (314 +/- 41 cells) or high-cholesterol diet (395 +/- 53 cells).
86 ion was highest in hypertensive animals on a high-cholesterol diet (43.9+/-0.7%, versus 12.0+/-2.0% f
87  aorta after both chow (503 +/- 67 cells) or high-cholesterol diet (648 +/- 81 cells).
88 d on either regular mouse chow (ApoE-R) or a high-cholesterol diet (ApoE-C) for 25 weeks.
89 ow, normal chow plus nitro-L-arginine (LNA), high-cholesterol diet (Chol), or high-cholesterol diet s
90 randomized to three groups: normal diet (N), high-cholesterol diet (HC) and HC diet plus simvastatin
91 ivate a homeostatic program in response to a high-cholesterol diet (HCD) and regulate both the differ
92 )H oxidase placed on either a normal diet or high-cholesterol diet (HCD) for 2 weeks.
93 , and Abca1(-/-)Abcg1(-/-) mice fed either a high-cholesterol diet (HCD) or a Western diet (WTD).
94 that feeding adult zebrafish (Danio rerio) a high-cholesterol diet (HCD) resulted in hypercholesterol
95                                    Feeding a high-cholesterol diet (HCD) supplemented with a red fluo
96 nd premature deaths in response to high-fat, high-cholesterol diet (HFC).
97 mice (Apoe(-/-) ) challenged with a high-fat high-cholesterol diet affirmed the use of NR in other in
98 5 kg) were made atherosclerotic by feeding a high-cholesterol diet after endothelial aortic injury.
99 ractions in apoE(-/-) mice fed a normal or a high-cholesterol diet after short-term (ie, 18 hours) si
100 ate that psychosocial stress and a high-fat, high-cholesterol diet aggravate cardiovascular disease,
101 us 12.0+/-2.0% for normotensive animals on a high-cholesterol diet and 4.7+/-4.7% for animals on stan
102                              Mice were fed a high-cholesterol diet and killed 24 weeks after transpla
103 ection in vivo, we analyzed the effects of a high-cholesterol diet and reduced apolipoprotein E (apoE
104  lesions in pigs that have been induced by a high-cholesterol diet and stenosis, and the effect of th
105 andomized to receive a normal (control) or a high-cholesterol diet and treated with vehicle or rosigl
106  wild-type (WT) females consuming a high-fat/high-cholesterol diet and tumor growth was evaluated.
107  hepatic cholesterol in wild-type mice fed a high-cholesterol diet but is not effective in FXR-null m
108 hown that C57BL/6J mice exposed to CIH and a high-cholesterol diet develop dyslipidemia, atherosclero
109 oE-deficient background or challenged with a high-cholesterol diet developed autoantibodies.
110 ring the second half of a 26-week regimen of high-cholesterol diet did not regress, but did significa
111                The mice received a high-fat, high-cholesterol diet during the last 3 weeks to induce
112                         ApoE(-/-) mice fed a high-cholesterol diet exhibited higher blood cholesterol
113  Breast tumors from animals fed the high-fat/high-cholesterol diet exhibited the fastest progression.
114 is induced in response to LXR activation and high-cholesterol diet feeding.
115 r atherosclerotic lesions after high-fat and high-cholesterol diet feeding.
116    ApoE(-/-) BL/6 and BALB/c mice consumed a high-cholesterol diet for 10, 16, and 24 weeks with equi
117 n E-deficient (apoE-/-) mice that consumed a high-cholesterol diet for 12 weeks and age-matched apoE+
118  low-density lipoprotein that had been fed a high-cholesterol diet for 12 weeks.
119 ld-type cells, and provided them a high-fat, high-cholesterol diet for 14 weeks.
120 a chow diet (Low group, n=10) or a continued high-cholesterol diet for 16 months (High group, n=5).
121 The remaining rabbits continued to consume a high-cholesterol diet for 16 months (High group, n=5).
122 +; or BL:TG:Ealpha, IA(b)+IE(k)+, were fed a high-cholesterol diet for 16 weeks and evaluated histomo
123 poprotein E-deficient (Apoe(-/-)) mice fed a high-cholesterol diet for 16 wk developed more severe at
124             Experimental animals placed on a high-cholesterol diet for 2 or more weeks exhibit an inf
125  arteries of normal pigs that had been fed a high-cholesterol diet for 4 weeks.
126 tor-deficient (LDLR-/-) mice maintained on a high-cholesterol diet for 6 weeks with either a HD-Ad co
127 ittermate controls were placed on a high-fat/high-cholesterol diet for 7 weeks beginning at 17 months
128 cient mice, and the chimeric mice were fed a high-cholesterol diet for 8 weeks.
129 d one carotid artery, and animals were fed a high-cholesterol diet for two months to create various s
130 poE(-/-), wild-type (Agtr2+) mice consumed a high-cholesterol diet from 4 weeks of age.
131                         Diabetic mice on the high-cholesterol diet had accelerated development of dia
132                        TTR-Abcb11 mice fed a high-cholesterol diet had greater increases in plasma an
133                    We noted that a high-fat, high-cholesterol diet increased expression of the Notch
134                                            A high-cholesterol diet leads to significant increases in
135                      The effects of high-fat/high-cholesterol diet on body composition, plasma lipids
136       This was exacerbated by feeding mice a high-cholesterol diet or, more dramatically, by inactiva
137                                  Moreover, a high-cholesterol diet resulted in up to 3-fold increase
138                                            A high-cholesterol diet significantly facilitated A. phago
139 nine (LNA), high-cholesterol diet (Chol), or high-cholesterol diet supplemented with L-arginine (Arg)
140 ty lipoprotein receptor(-/-) mice were fed a high-cholesterol diet to investigate the functional role
141                        Yorkshire swine fed a high-cholesterol diet underwent left circumflex ameroid
142 osclerotic lesion development in response to high-cholesterol diet was enhanced in Panx1 (del) Apoe (
143      The induction of Cyp7A1 expression by a high-cholesterol diet was impaired in NCoA6(L2m/L2m) mic
144 ate lesion development in mice if a high-fat/high-cholesterol diet was started after infection, indic
145 orally treated for 1 week with HSP-65, and a high-cholesterol diet was started after the last treatme
146       Thirty-five apo E-deficient mice fed a high-cholesterol diet were included in the study.
147 gh-fat diet and C57BL/6 mice fed a high-fat, high-cholesterol diet were injected with recombinant Nef
148 standard chow, a high-cholesterol diet, or a high-cholesterol diet with hypertension induced by angio
149 on of rat-IgG or saline; 13 weeks, continued high-cholesterol diet).
150 rd diet/periodontally healthy); 2) group Hc (high-cholesterol diet); 3) group HcP (high-cholesterol d
151  suppressed by cholesterol enrichment and by high-cholesterol diet, and facilitated following cholest
152  diet, followed by LDLR(-/-) that were fed a high-cholesterol diet, ApoE(-/-) that were fed normal ch
153               Here we show that in rats on a high-cholesterol diet, cholesterol levels in hippocampal
154 CXCR2, in the spleen in apoE(-/-) mice fed a high-cholesterol diet, compared with the other 3 groups.
155 rta was highest in ApoE(-/-) that were fed a high-cholesterol diet, followed by LDLR(-/-) that were f
156 red to 2 groups of Sprague-Dawley rats fed a high-cholesterol diet, ie, one group received MCT concom
157                             In response to a high-cholesterol diet, IRA B cell numbers increase prefe
158 andomly assigned to receive standard chow, a high-cholesterol diet, or a high-cholesterol diet with h
159                          After 16 weeks of a high-cholesterol diet, P2X7-deficient mice showed smalle
160                     In Abcg1(-/-) mice fed a high-cholesterol diet, plasma levels of 7-ketocholestero
161                      When fed on a high-fat, high-cholesterol diet, PON1-null mice were more suscepti
162                 In LDLR-deficient mice fed a high-cholesterol diet, T cell-specific ABCG1 deficiency
163                                Finally, on a high-cholesterol diet, Tcad/ApoE-DKO mice increased athe
164 cholesterol after maintenance on a high-fat, high-cholesterol diet, the MPO-Tg animals developed a 2-
165                   At the end of 8 weeks of a high-cholesterol diet, the rabbits were killed, and the
166 lpha/beta-deficient bone marrow and fed on a high-cholesterol diet, they had markedly decreased early
167 ere fed either a normal (NORM group; n=7) or high-cholesterol diet, with (CHOL-ATR group; n=7) or wit
168 be (cholesterol-lowering drug), and high-fat/high-cholesterol diet, with or without ezetimibe.
169                                            A high-cholesterol diet, with or without periodontitis, re
170 arginase II gene (Arg II(-/-) mice) prevents high-cholesterol diet-dependent decreases in vascular NO
171 on area and cholesterol content of high-fat, high-cholesterol diet-induced atherosclerotic lesions.
172 in L-TGH KO mice challenged with a high-fat, high-cholesterol diet.
173 d atherosclerosis was induced with a 16-week high-cholesterol diet.
174 nal biglycan content in diabetic mice on the high-cholesterol diet.
175 late excess cholesterol when maintained on a high-cholesterol diet.
176   Seven ApoE(-/-) and 7 LDLR(-/-) received a high-cholesterol diet.
177 ndotheliazation of the abdominal aorta and a high-cholesterol diet.
178 L receptor-deficient mice and administered a high-cholesterol diet.
179 eptor-deficient C57BL/6J mice fed a high-fat/high-cholesterol diet.
180 (-1) for 5 weeks beginning 3 weeks after the high-cholesterol diet.
181 -/-)) mice that develop atherosclerosis on a high-cholesterol diet.
182 e receptor for LDL that were maintained on a high-cholesterol diet.
183 ifestyle that includes a uniformly high-fat, high-cholesterol diet.
184 more than 2-fold in the livers of mice fed a high-cholesterol diet.
185 apolipoprotein E (apoE)-deficient mice fed a high-cholesterol diet.
186 ury in apoE-deficient (apoE(-/-)) mice fed a high-cholesterol diet.
187 land White rabbits were fed normal chow or a high-cholesterol diet.
188 bbits (n=31) using aortic balloon injury and high-cholesterol diet.
189  in pigs at baseline and after 12 weeks of a high-cholesterol diet.
190 n 35 rabbits by air desiccation injury and a high-cholesterol diet.
191 tion in plaque burden in Ldlr(-/-) mice on a high-cholesterol diet.
192 oliferating cells from mice fed the high-fat/high-cholesterol diet.
193  but not in Senp2(+/+)/Ldlr(-/-), mice fed a high-cholesterol diet.
194 when maintained on a Western-type, high-fat, high-cholesterol diet.
195  the liver in response to both fasting and a high-cholesterol diet.
196 up Hc (high-cholesterol diet); 3) group HcP (high-cholesterol diet/periodontitis); and 4) group P (st
197 nduction through de-endothelialization and a high-cholesterol diet; 14 were then thrombus triggered.
198  compared with wild type mice under high fat/high cholesterol dietary conditions (80.1 +/- 3.7 versus
199 ant reduction (54%, P<0.01) of the high-fat, high-cholesterol dieteninduced atherosclerotic plaques w
200                                     High fat/high cholesterol diets exacerbate beta-amyloidosis in mo
201                     In response to high fat, high cholesterol diets, both MUT1-CETP and MUT2-CETP tra
202           On both regular chow and high fat, high cholesterol diets, expression of CETP in LCAT-Tg mi
203 further, mice were challenged with high fat, high cholesterol diets.
204  profiles between regular basal and high fat/high cholesterol diets.
205                     On both the low- and the high-cholesterol diets, whole liver and isolated hepatoc
206 s of Mexico and Americans consuming low- and high-cholesterol diets.
207 and variations in the environment due to the high-cholesterol disease state.
208 racteristics similar to wild type CCK1R in a high cholesterol environment.
209  from atherosclerotic lesions because of the high-cholesterol environment.
210 D was induced by 5/6 nephrectomy in high-fat high-cholesterol fed apolipoprotein E-deficient mice.
211                                              High cholesterol-fed, 26-week-old apoE-deficient mice re
212 approach to prepare supported membranes with high cholesterol fractions close to the cholesterol solu
213                          The odds ratios for high cholesterol (&gt;/=240 mg/dL), by increasing quartile
214 ociated with decreased serum cholesterol and high cholesterol has been associated with increased like
215  coronary heart disease and with and without high cholesterol have demonstrated consistently that sta
216  were studied after a 3-mo normal (n = 7) or high cholesterol (HC) (n = 7) diet, HC diet supplemented
217 ere randomized to 3 groups fed a normal (N), high cholesterol (HC), or HC+simvastatin (HC+S) diet for
218  weeks: control (4% fat and 0% cholesterol); high cholesterol (HC; 4% fat and 1% cholesterol); high f
219 s of age, were randomized to a normal (N) or high-cholesterol (HC) diet (2% cholesterol, 15% lard) wi
220               Mice were fed a normal (ND) or high-cholesterol (HC) diet beginning at 5 weeks postinfe
221  mice were placed on either a normal (ND) or high-cholesterol (HC) diet for 2 weeks.
222 ApoE(-/-) mice fed a low-cholesterol (LC) or high-cholesterol (HC) diet were infected with approximat
223 lar brain damage in old ApoE(-/-) mice fed a high-cholesterol (HC) diet with dietary controlled intak
224 on of double-balloon injury and a nine-month high-cholesterol (HC) diet.
225  and zebrafish exposed to high-fat (HFDs) or high-cholesterol (HCDs) diets develop acute innate infla
226 is of asthma, high blood pressure, diabetes, high cholesterol, heart problems, or any other physical
227 w that in 9-month-old APP23 mice, a high-fat/high-cholesterol (HF) diet provided for 4 months exacerb
228 ce dietary atherosclerosis in mice, high-fat/high-cholesterol (HF) diets are frequently supplemented
229  following four diets: control (C), high-fat/high-cholesterol (HF), control and 1% cholate (CA) and H
230  were fed either regular chow or a high-fat, high-cholesterol (HFC) diet for 3 months.
231 ; 15% fat and 0% cholesterol); and high fat, high cholesterol (HFHC; 15% fat and 1% cholesterol).
232       We explored the effects of a high-fat, high-cholesterol (HFHC) diet on vascular responses in ba
233 18 men, 20 to 90 years of age, without known high cholesterol, high triglycerides, cardiovascular dis
234                 Adjustment for self-reported high cholesterol, high triglycerides, high blood pressur
235            We examined the hypothesis that a high-cholesterol, high-fat (HCHF) diet can directly caus
236 e on the LDLR knockout background were fed a high-cholesterol/high-fat diet containing cholate, howev
237 ); RRs for obese men with diabetes mellitus, high cholesterol, hypertension, smoking, and low fitness
238  high cholesterol typically progress to full high cholesterol in 2-3 years, and pre-diabetic patients
239  mental disorder, hypertension, obesity, and high cholesterol in parents and those same conditions in
240 e Y140A construct also behaved like CCK1R in high cholesterol in regard to its internalization, sensi
241 ve effects on cardiac apoptosis in rats with high cholesterol intake.
242 e metastatic effects of hypercholesterolemia.High cholesterol is a risk factor for breast cancer recu
243 than 90%, except for high blood pressure and high cholesterol level (negative predictive values, 33%
244 ent for reported hypertension, diabetes, and high cholesterol level, a WHR of 0.76 or higher or waist
245 sence of diagnosed hypertension or diagnosed high cholesterol level, and menopausal status.
246 hol use, history of hypertension, history of high cholesterol level, and other covariates, the relati
247 cular disease, fasting plasma glucose level, high cholesterol level, overweight, current smoking, hig
248 ry risk factors, eg, high blood pressure and high cholesterol level.
249 st common (grade 1 or 2) adverse events were high cholesterol levels (14 of 30 patients), nausea (11
250                                              High cholesterol levels also lead to overproduction of A
251 ompared with normal HSFs, EEs in NPFs showed high cholesterol levels and an altered organization of r
252                                              High cholesterol levels greatly increase the risk of car
253  death, and only one quarter of persons with high cholesterol levels have attained recommended levels
254                                              High cholesterol levels in circulating immune complexes
255 eports of high blood pressure, diabetes, and high cholesterol levels in fathers were accurate: Positi
256                                              High cholesterol levels in the blood increase the risk o
257                                              High cholesterol levels increase APP and apoE expression
258                                     In mice, high cholesterol levels mobilize HSPCs into the bloodstr
259 rmal C57BL6 mice and failed to normalize the high cholesterol levels of apoE-deficient mice due to in
260  ameliorate the negative effects of high fat/high cholesterol levels on cognition and amyloid patholo
261 e prevalence or diagnosis of hypertension or high cholesterol levels or on the use of medication for
262 er, after adjustment for age, race, smoking, high cholesterol levels requiring medication, body mass
263 vascular disease, diabetes, hypertension, or high cholesterol levels were followed through 2009.
264  blood pressure, 1.88 (95% CI,1.67-2.13) for high cholesterol levels, 2.72 (95% CI, 2.38-3.12) for as
265 ns between perfluorooctanoic acid (PFOA) and high cholesterol levels, but studies of hypertension and
266 s were reliable, except for hypertension and high cholesterol levels.
267 than the RRs for obese men who smoked or had high cholesterol levels.
268 r =10 years, hypertension, macroalbuminuria, high cholesterol, low high-density lipoprotein, high C-r
269                             Diets containing high cholesterol markedly increased the expression of AB
270 ood and cerebrovasculature and combined with high cholesterol may be a key component to the accumulat
271  P=0.03 for males and P<10(-4) for females), high cholesterol medication use in runners (P<10(-4) for
272  reductions in the odds for hypertension and high cholesterol medication use per METhr/d run or per M
273 stive CHRNA3-CHRNA5 findings with respect to high-cholesterol-medication use and distrustful attitude
274                         Tumors from high-fat/high-cholesterol mice had significantly higher microvess
275    Canalicular BSEP, mostly present in raft (high cholesterol) microdomains in control rats, was larg
276                                     Thus, at high cholesterol mole fraction, this unfavorable free en
277                                   At similar high cholesterol mole fractions, the in-plane elasticity
278 higher proportion of hypertension, diabetes, high cholesterol, obesity, and lower education, income,
279 g, still one of two people with diabetes has high cholesterol, one of three has high blood pressure,
280                    Mice fed diets containing high cholesterol or an LXR-selective agonist exhibited a
281 stment for covariates including a history of high cholesterol or coronary artery disease.
282 utants can be partially rescued on a diet of high cholesterol or one that includes the insect steroid
283 y lipoprotein receptor(-/-) mice consuming a high-cholesterol or chow diet.
284 bcb11) and FVB/NJ mice (controls) were fed a high-cholesterol or high-fat diet for 12 weeks.
285 R [odds ratio] 1.43; heart disease: OR 1.68; high cholesterol: OR 1.26; stroke: OR 1.99; arthritis; O
286                  More than 90% of borderline high cholesterol patients are retested within the 3 year
287 cal bilayered membrane with an exceptionally high cholesterol/phospholipid ratio.
288 tion; history of hypertension, diabetes, and high cholesterol; postmenopausal hormone use; alcohol in
289 y, low high-density lipoprotein cholesterol, high cholesterol ratio, high C-reactive protein, hyperte
290 cardiac threat posed by high blood pressure, high cholesterol, smoking, obesity, physical inactivity,
291     We examined hypertension, heart disease, high cholesterol, stroke, arthritis, asthma, chronic obs
292 sion on 2 visits, prediabetes, diabetes, and high cholesterol than eczema alone.
293 limoles per liter, multiply by 0.0259) and a high cholesterol to triglycerides ratio (1.52) in very l
294  obesity (body mass index >/= 30 kg/m2), and high cholesterol (total blood cholesterol >/= 240 mg/dL
295                     Patients with borderline high cholesterol typically progress to full high cholest
296  A and B included volunteers with borderline-high cholesterol values [5.2-6.2 mmol total cholesterol/
297 infected patients who required treatment for high cholesterol were given 20 mg atorvastatin per day.
298 , alcohol, tobacco, high blood pressure, and high cholesterol were major causes of disease burden.
299                A total of 7594 patients with high cholesterol were studied, along with 2764 patients
300 -, and gld.apoE-/- mice were maintained on a high cholesterol Western diet and received daily simvast
301                                              High cholesterol, which induced beta-sheets, promoted fu

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