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1 , high levels of triglycerides and decreased high-density lipoprotein).
2 the anti-atherogenic functions attributed to high density lipoprotein.
3 poprotein A-I (ApoA-I), a major component of high-density lipoprotein.
4  in duplicate for glucose, triglyceride, and high-density lipoprotein.
5  result of compensatory increases in ApoE on high-density lipoprotein.
6 nd APOE, respectively) and the generation of high density lipoproteins.
7  form lipid-protein particles reminiscent of high-density lipoproteins.
8 ome to control body mass, triglycerides, and high-density lipoproteins.
9 nd low-density lipoproteins whereas increase high-density lipoproteins.
10 teolysis and misfolding by binding to plasma high-density lipoproteins.
11 n, very-low-density lipoprotein (VLDL), LDL, high-density lipoprotein].
12 cholesterol efflux to apolipoprotein A-I and high-density lipoprotein-3 were qualitatively and quanti
13 des (84 versus 77 mg/dL, P = 0.01) and lower high-density lipoprotein (46 versus 60 mg/dL, P = 0.004)
14 ycerides (-53.7 +/- 116.4 mg/dL, P < 0.001), high-density lipoprotein (8.2 +/- 12.9 mg/dL, P < 0.001)
15 tly associated with higher concentrations of high-density lipoprotein (9%) and sex-hormone binding gl
16          In Abca1 knockout mice (Abca1(ko)), high density lipoproteins and ApoA-I are virtually lacki
17 n under shear stress can be modulated by the high-density lipoprotein and apolipoprotein A-I (HDL/Apo
18 ce, triglycerides, type-2 diabetes mellitus, high-density lipoprotein and low-density lipoprotein cho
19                                              High-density lipoprotein and triglyceride values rapidly
20 17 coincided with a significant QTL for HDL (high-density lipoprotein) and a suggestive QTL for non-H
21 ts and increase in hsCRP, total cholesterol, high-density lipoprotein, and low-density lipoprotein le
22 n E levels were also measured in serum, LDL, high-density lipoprotein, and red blood cell membranes a
23 ure, triglycerides, low-density lipoprotein, high-density lipoprotein, and total cholesterol were not
24  Total cholesterol, low-density lipoprotein, high-density lipoprotein, and triglyceride levels all si
25 C-reactive protein, low-density lipoprotein, high-density lipoprotein, and triglyceride single-nucleo
26 , low-density lipoprotein (LDL) cholesterol, high-density lipoprotein, and triglycerides], lipoprotei
27 ) low-density lipoprotein oxidizability, (2) high-density lipoprotein antioxidant/anti-inflammatory c
28 tion to previously reported triglyceride and high-density lipoprotein associations, the variant was a
29 xed to glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) on
30 point to understand the molecular details of high density lipoprotein biogenesis.
31 (Apo)A-I, the major lipid-binding protein of high-density lipoprotein, can prevent autoimmunity and s
32 triglycerides, but was associated with lower high density lipoprotein cholesterol (-0.014 standard de
33                         We predicted height, high density lipoprotein cholesterol (HDL) and body mass
34 nterestingly, significantly higher levels of high density lipoprotein cholesterol (HDLc) were observe
35 enzymatic activity and a 35% increase of the high density lipoprotein cholesterol that was observed u
36 een duration of moderate hyperlipidemia (non-high-density lipoprotein cholesterol >/= 160 mg/dL) in e
37 oprotein cholesterol (LDL-C) <160 mg/dl, and high-density lipoprotein cholesterol >/=40 mg/dl.
38 events and control of 6 RFs (no smoking, non-high-density lipoprotein cholesterol <130 mg/dl, triglyc
39 lesterol (1.6 [1.1-2.1]), and borderline low high-density lipoprotein cholesterol (1.4 [1.0-1.8]) rem
40 lipoprotein cholesterol (27.9 to 60.0%), non-high-density lipoprotein cholesterol (10.0 to 36.6%), ap
41  statistically significantly increased serum high-density lipoprotein cholesterol (13 trials; net cha
42  showed nominal significant association with high-density lipoprotein cholesterol (2 SNPs), low-densi
43 e saw a small increase in rate of change for high-density lipoprotein cholesterol (beta = 0.28 mg/dL;
44  associated in opposite directions with both high-density lipoprotein cholesterol (beta coefficient=-
45 carriers, carriers of PTV at CETP had higher high-density lipoprotein cholesterol (effect size, 22.6
46 s of total cholesterol (TC) (>/= 200 mg/dL), high-density lipoprotein cholesterol (HDL-C) (<40 mg/dL)
47 rs have been shown to substantially increase high-density lipoprotein cholesterol (HDL-C) and apolipo
48     Although the inverse association between high-density lipoprotein cholesterol (HDL-C) and risk of
49 y artery disease (CAD), but the relevance of high-density lipoprotein cholesterol (HDL-C) and triglyc
50                                Low levels of high-density lipoprotein cholesterol (HDL-C) are common
51                 The prognostic importance of high-density lipoprotein cholesterol (HDL-C) as a specif
52  LDL-c from 155 to 128 mg/dL (P < .001), and high-density lipoprotein cholesterol (HDL-c) from 50.3 t
53 ational epidemiologic studies, higher plasma high-density lipoprotein cholesterol (HDL-C) has been as
54 cause of ischemic stroke, and a low level of high-density lipoprotein cholesterol (HDL-C) is also con
55 diet only), red wine significantly increased high-density lipoprotein cholesterol (HDL-C) level by 0.
56 ubfamily A, member 1 (ABCA1) and circulating high-density lipoprotein cholesterol (HDL-C) levels in v
57 -density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C) were either
58                          Differences in mean high-density lipoprotein cholesterol (HDL-C), LDL-C, and
59 ol levels, including total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-densit
60                 Levels of serum cholesterol, high-density lipoprotein cholesterol (HDL-C), low-densit
61  a small, and chitosan an impressive rise in high-density lipoprotein cholesterol (HDL-C).
62 variants at the GALNT2 locus associated with high-density lipoprotein cholesterol (HDL-C).
63  NAFLD, such as hypertriglyceridemia and low high-density lipoprotein cholesterol (HDL-C).
64 vels of TRAP, was positively associated with high-density lipoprotein cholesterol (HDL-C; beta = 8.36
65 ated locus associated with triglycerides and high-density lipoprotein cholesterol (HDL-C; cg27243685;
66                                Low levels of high-density lipoprotein cholesterol (HDLc) have been as
67 lesterol (decreased in LFHC group only), and high-density lipoprotein cholesterol (increased in VHFLC
68  cholesterol (LDL-C), triglycerides, and non-high-density lipoprotein cholesterol (non-HDL-C) present
69 t also LDL-related biomarkers, including non-high-density lipoprotein cholesterol (non-HDL-C), apolip
70 nsity lipoprotein cholesterol (LDL-C) or non-high-density lipoprotein cholesterol (non-HDL-C).
71 ith >/= 5 births had the highest odds of low high-density lipoprotein cholesterol (OR, 1.5; 95% confi
72 lipoprotein cholesterol, and HbA1c and lower high-density lipoprotein cholesterol (P < 0.001 for all)
73 sedentary time was associated with decreased high-density lipoprotein cholesterol (P=0.04), and incre
74 and years of schooling (rG=0.18, s.e.=0.03), high-density lipoprotein cholesterol (rG=0.28, s.e.=0.05
75  CI, 1.11-1.94]), an elevated serum level of high-density lipoprotein cholesterol (RR per 1-SD increa
76                     The total cholesterol to high-density lipoprotein cholesterol (TC/HDL-C) ratio, e
77 notypes: V(G)/V(p)=31.4%, P<3.1x10(-11)) and high-density lipoprotein cholesterol (V(G)/V(p)=26.4%, P
78 low-density lipoprotein cholesterol [LDL-C], high-density lipoprotein cholesterol [HDL-C], and trigly
79 asting lipid fractions (triglycerides [TGs], high-density lipoprotein cholesterol [HDL-C], low-densit
80 ed for LDL-C were observed with achieved non-high-density lipoprotein cholesterol and apolipoprotein
81 t association was found for higher levels of high-density lipoprotein cholesterol and decreased preva
82  adjusted models, women had higher levels of high-density lipoprotein cholesterol and high-density li
83 cational attainment, exercise, levels of non-high-density lipoprotein cholesterol and high-sensitivit
84 e MetS components and CA, except for reduced high-density lipoprotein cholesterol and nonfasting gluc
85 oprotein cholesterol, and ratios of total to high-density lipoprotein cholesterol and triglycerides t
86 terol; lipoprotein(a), apolipoprotein B, and high-density lipoprotein cholesterol are largely unaffec
87 for other cardiac risk factors including non-high-density lipoprotein cholesterol at 55 years of age
88 mprove clinical outcomes, despite increasing high-density lipoprotein cholesterol by 30%.
89 re, body mass index, apolipoprotein A-1, and high-density lipoprotein cholesterol concentration (beta
90 ted fasting blood glucose concentration, low high-density lipoprotein cholesterol concentration, hype
91 rapy, body mass index, heart rate, total and high-density lipoprotein cholesterol concentrations, smo
92 pectroscopy and a validated ex vivo assay of high-density lipoprotein cholesterol efflux capacity.
93                             Neither low- nor high-density lipoprotein cholesterol GRS was significant
94                              Total serum and high-density lipoprotein cholesterol have been considere
95  exposure to even moderate elevations in non-high-density lipoprotein cholesterol have elevated risk
96 ansaminase, white blood cell count and lower high-density lipoprotein cholesterol in men, and with hi
97 ), triglyceride level (-40%, -29%, and -8%), high-density lipoprotein cholesterol level (32%, 30%, an
98 f at least 70 mg/dL or a final screening non-high-density lipoprotein cholesterol level of at least 1
99  physical activity, total cholesterol level, high-density lipoprotein cholesterol level, systolic blo
100 ely associated with treated hypertension and high-density lipoprotein cholesterol level.
101 ted to physical or mental stress; and higher high-density lipoprotein cholesterol level.
102 ice lacking T39 (T39(-/-)) display increased high-density lipoprotein cholesterol levels associated w
103 iglyceride levels greater than 204 mg/dL and high-density lipoprotein cholesterol levels less than 34
104 s were also more likely to smoke, have lower high-density lipoprotein cholesterol levels, and have hi
105 rglycemia, elevated triglyceride levels, low high-density lipoprotein cholesterol levels, high blood
106 s in total, low-density lipoprotein, and non-high-density lipoprotein cholesterol levels, in triglyce
107 ompared with controls, despite no changes in high-density lipoprotein cholesterol or other circulatin
108 leukin-10 remained persistently elevated and high-density lipoprotein cholesterol persistently depres
109 h ARIC metabolic phenotypes, including total:high-density lipoprotein cholesterol ratio (rG=-0.44, P=
110 vents, digoxin use, and total cholesterol to high-density lipoprotein cholesterol ratio were associat
111 ded risk factors were body mass index, total:high-density lipoprotein cholesterol ratio, and systolic
112                                    Total and high-density lipoprotein cholesterol similarly increased
113  gene, TEAD2, is found to be associated with high-density lipoprotein cholesterol through gene-based
114 than in WT mice (2.6 versus 0.4 mmol/L), and high-density lipoprotein cholesterol was significantly l
115                               High levels of high-density lipoprotein cholesterol were associated wit
116 lipoprotein cholesterol and triglycerides to high-density lipoprotein cholesterol were calculated.
117  of higher systolic blood pressure and lower high-density lipoprotein cholesterol with Carotid artery
118 nce, blood pressure, triglycerides, glucose, high-density lipoprotein cholesterol) at 15 (n=512), 16
119  7 (low-density lipoprotein cholesterol), 8 (high-density lipoprotein cholesterol), 14 (triglycerides
120 epatitis A), biochemical (e.g., carotenoids, high-density lipoprotein cholesterol), physiological (e.
121  largely explained by lowering of non-HDL-C (high-density lipoprotein cholesterol), rather than incre
122 ait (for example, rs7115089, miR-125b-5p and high-density lipoprotein cholesterol).
123 rol, 109.23 mg/dL (103.68-114.79 mg/dL); for high-density lipoprotein cholesterol, 42.80 mg/dL (39.84
124 erol, 71 single-nucleotide polymorphisms for high-density lipoprotein cholesterol, and 40 single-nucl
125 olesterol, the ratio of total cholesterol to high-density lipoprotein cholesterol, and 8-OHdG levels.
126 e relationship between additional LDL-C, non-high-density lipoprotein cholesterol, and apolipoprotein
127 r age, sex, hypertension, smoking, diabetes, high-density lipoprotein cholesterol, and body mass inde
128 c biomarkers, including glycated hemoglobin, high-density lipoprotein cholesterol, and C-reactive pro
129 diastolic blood pressure, total cholesterol, high-density lipoprotein cholesterol, and glucose levels
130 lic abnormalities (high fasting glucose, low high-density lipoprotein cholesterol, and high triglycer
131     Low-density lipoprotein cholesterol, non-high-density lipoprotein cholesterol, and ratios of tota
132 ia, neuroticism, educational attainment, and high-density lipoprotein cholesterol, and significant ne
133                           Total cholesterol, high-density lipoprotein cholesterol, and triglycerides
134         Lipid traits (total, low-density and high-density lipoprotein cholesterol, and triglycerides)
135 were also observed in total cholesterol, non-high-density lipoprotein cholesterol, apolipoprotein B,
136 ding hypertension, hypertriglyceridemia, low high-density lipoprotein cholesterol, central obesity, a
137 -regression for various covariates including high-density lipoprotein cholesterol, each 1 unit of nat
138 ssure, ratio of fasting total cholesterol to high-density lipoprotein cholesterol, estimated glomerul
139 abolic biomarkers (diastolic blood pressure, high-density lipoprotein cholesterol, fasting and 2-hour
140 dominal obesity, elevated triglycerides, low high-density lipoprotein cholesterol, high blood pressur
141 ent for low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, lipoprotein(a), tr
142                                              High-density lipoprotein cholesterol, low-density lipopr
143 ture mapping analysis for total cholesterol, high-density lipoprotein cholesterol, low-density lipopr
144 e-mapping analysis that were associated with high-density lipoprotein cholesterol, low-density lipopr
145 -wide DNA methylation and blood lipid levels high-density lipoprotein cholesterol, low-density lipopr
146 rs, carriers of PTV at CETP displayed higher high-density lipoprotein cholesterol, lower low-density
147 ences were found for fasting plasma glucose, high-density lipoprotein cholesterol, or triglycerides w
148 s such as waist circumference, triglyceride, high-density lipoprotein cholesterol, systolic and diast
149 and fasting blood sample (total cholesterol, high-density lipoprotein cholesterol, triglycerides, glu
150 actors: low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, typ
151 rable objective biomarkers (concentration of high-density lipoprotein cholesterol, vitamin D and C-re
152 cholesterol and triglyceride, and increasing high-density lipoprotein cholesterol.
153 effect estimate as large as that of total or high-density lipoprotein cholesterol.
154 s of low-density lipoprotein cholesterol and high-density lipoprotein cholesterol.
155 density lipoprotein cholesterol families) or high-density lipoprotein cholesterol.
156 n part owing to hypertriglyceridemia and low high-density lipoprotein cholesterol.
157 may preferentially improve triglycerides and high-density lipoprotein cholesterol.
158 tolic blood pressure, total cholesterol, and high-density lipoprotein cholesterol.
159 h diabetes with hypertriglyceridemia and low high-density lipoprotein cholesterol.
160 ity lipoprotein cholesterol; lower levels of high-density lipoprotein cholesterol; and, to a lesser e
161 or remnant cholesterol, and -8 mg/dl for non-high-density lipoprotein cholesterol; lipoprotein(a), ap
162 s of total, low-density lipoprotein, and non-high-density lipoprotein cholesterol; lower levels of hi
163 ntly associated with total cholesterol (TC), high-density-lipoprotein cholesterol (HDL-C), low-densit
164 d alcohol and was positively associated with high-density-lipoprotein cholesterol and intakes of poly
165 lin resistance), serum-triglyceride-to-serum-high-density lipoprotein-cholesterol ratio TG/HDL-C, or
166 sterol, low-density lipoprotein-cholesterol, high-density lipoprotein-cholesterol, or triglyceride, 4
167 ypes of MDD with changes of fasting glucose, high-density lipoprotein-cholesterol, triglycerides, sys
168 tion between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expre
169 ted QT interval, HR-corrected QT interval or high-density lipoprotein-cholesterol.
170 lesterol, 2) low-density lipoprotein, and 3) high-density lipoprotein compared to group C.
171 ciated with very low-density lipoprotein and high-density lipoprotein composition measures, other cho
172 .30 and 0.14, respectively; both p < 0.001), high-density lipoprotein (correlation coefficient 0.16 a
173    We validate our method using a real mouse high-density lipoprotein data (HDL) and show that CAVIAR
174 (-/-)) show decreased fatty liver, increased high-density lipoprotein, decreased low-density lipoprot
175 es mellitus, serum potassium, serum albumin, high-density lipoprotein, estimated glomerular filtratio
176 )particles to indicate their relationship to high-density lipoproteins formed by human apolipoprotein
177               Cholesterol efflux capacity of high-density lipoproteins from J774 macrophages after cA
178 omain protein 39B (Ttc39b, C9orf52) (T39), a high-density lipoprotein gene discovered in human genome
179 resistance, insulin, hemoglobin A1c, and low high-density lipoprotein had significant shared gene eff
180 resistance, insulin, hemoglobin A1c, and low high-density lipoprotein had significant shared gene eff
181         Structural and functional aspects of high-density lipoproteins have been studied for over hal
182 ed from the circulation and transferred from high density lipoprotein (HDL) - a main carrier of chole
183 ups and assessed for total cholesterol (TC), high density lipoprotein (HDL) and low density lipoprote
184 body fat -0.00516 (95% CI -0.00761--0.0027), high density lipoprotein (HDL) cholesterol 0.00179 (95%
185 ipid transfer protein (PLTP) participates in high density lipoprotein (HDL) metabolism.
186                    Paraoxonase 1 (PON1) is a high density lipoprotein (HDL)-associated protein with a
187 all to the liver) is terminated by selective high density lipoprotein (HDL)-cholesteryl ester (CE) up
188               SR-BI is the main receptor for high density lipoproteins (HDL) and mediates the bidirec
189 s designed for the analysis of lipoproteins, high density lipoproteins (HDL), apoproteins, and lipid
190 and function of the potent anti-inflammatory high-density lipoprotein (HDL) and accelerated atheroscl
191 A1 (apoA1) is the major protein component of high-density lipoprotein (HDL) and has well documented a
192              We identified that component as high-density lipoprotein (HDL) and its major apolipoprot
193 1, is a lipoprotein receptor that binds both high-density lipoprotein (HDL) and low-density lipoprote
194             Associations were independent of high-density lipoprotein (HDL) and non-HDL cholesterol,
195                   Insulin resistance and low high-density lipoprotein (HDL) are associated with pulmo
196 ng of apolipoprotein A-I (apoA1) and nascent high-density lipoprotein (HDL) assembly is not well unde
197 6, 0.154; P = 0.007) and the ratio of TGs to high-density lipoprotein (HDL) cholesterol (beta = 2.689
198 eceptor BI (SR-BI) is the major receptor for high-density lipoprotein (HDL) cholesterol (HDL-C).
199 = 16.4 mg/dL, 95% CI: 11.2, 21.5), and lower high-density lipoprotein (HDL) cholesterol (MD = -2.1 mg
200 tein B were higher after VA than after iTFA; high-density lipoprotein (HDL) cholesterol and apolipopr
201                              Serum levels of high-density lipoprotein (HDL) cholesterol and apolipopr
202 observing associations between low levels of high-density lipoprotein (HDL) cholesterol and cardiovas
203                           The causal role of high-density lipoprotein (HDL) cholesterol in cardioprot
204 l attainment, openness to new experience and high-density lipoprotein (HDL) cholesterol levels are mo
205         Recent failures of drugs that raised high-density lipoprotein (HDL) cholesterol levels to red
206 reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels.
207 known to have effects on serum levels of non-high-density lipoprotein (HDL) cholesterol that alter th
208 iglycerides were 13% lower and the levels of high-density lipoprotein (HDL) cholesterol were 7% highe
209 rease in total, low-density lipoprotein, and high-density lipoprotein (HDL) cholesterol, but not in t
210 d body mass index (BMI), C-reactive protein, high-density lipoprotein (HDL) cholesterol, forced expir
211 e cardiometabolic risk-factor profile [lower high-density lipoprotein (HDL) cholesterol, higher total
212 ed circulating lipid profiles, in particular high-density lipoprotein (HDL) cholesterol, in overweigh
213 fasting glucose, insulin, total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density
214 ns of abnormal values for total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density
215 f low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, or triglycer
216  the median (n = 83) was older and had lower high-density lipoprotein (HDL) cholesterol, phospholipid
217 s such as waist circumference, triglyceride, high-density lipoprotein (HDL) cholesterol, systolic and
218 , low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triacylglyce
219  mass index (BMI), waist circumference (WC), high-density lipoprotein (HDL) cholesterol, triglyceride
220 as well as low-density lipoprotein (LDL) and high-density lipoprotein (HDL) cholesterol.
221 ], and a positive association was shown with high-density lipoprotein (HDL) cholesterol.
222 ents whether obesity-induced endothelial and high-density lipoprotein (HDL) dysfunction is rapidly im
223 erse cholesterol transport (RCT) and reduces high-density lipoprotein (HDL) function in vivo.
224 nder LPS challenge, leading to modulation of high-density lipoprotein (HDL) in animals.
225                                              High-density lipoprotein (HDL) is a heterogeneous popula
226        There is though a hypothesis that low high-density lipoprotein (HDL) levels in this group of p
227 rotein A-I (apoA-I) plays a critical role in high-density lipoprotein (HDL) maturation.
228 othesis that cholesterol efflux capacity and high-density lipoprotein (HDL) particle concentration pr
229 P is bound to apolipoprotein M (ApoM) in the high-density lipoprotein (HDL) particle, the immunologic
230                                              High-density lipoprotein (HDL) particles are involved in
231 DL, very low-density lipoprotein (VLDL), and high-density lipoprotein (HDL) particles.
232 mational reorganization during remodeling of high-density lipoprotein (HDL) particles.
233 low very-low-density lipoprotein (VLDL)/high high-density lipoprotein (HDL) profile.
234 that functions as a physiologically relevant high-density lipoprotein (HDL) receptor whose primary ro
235    Twenty-four hours post-MI measurements of high-density lipoprotein (HDL) triglycerides (HDL-TG) pr
236 line (PBS) without significant interference: high-density lipoprotein (HDL) yields 4-6% of the LDL si
237 ified AH is 4%-23% in eQTLs, 35% in GWASs of high-density lipoprotein (HDL), and 23% in GWASs of schi
238 rides, and strong negative associations with high-density lipoprotein (HDL), HDL-diameter, HDL-C, HDL
239 ared with the SSGWAS for blood lipid traits (high-density lipoprotein (HDL), low-density lipoprotein
240                        Lipoproteins, such as high-density lipoprotein (HDL), low-density lipoprotein
241           The CHEESE diet caused a 5% higher high-density lipoprotein (HDL)-cholesterol concentration
242 r HCV entry) and also blocks SR-BI-dependent high-density lipoprotein (HDL)-mediated enhancement of v
243  LPS binding protein, competitively inhibits high-density lipoprotein (HDL)-mediated LPS association
244 , is known to cause a dramatic rise in small high-density lipoprotein (HDL).
245 ]sitostanol- and [(14) C]cholesterol-labeled high-density lipoprotein (HDL).
246  particularly when present on the surface of high-density lipoprotein (HDL).
247  to cholesterol, promoting the maturation of high-density lipoproteins (HDL) from discoidal to spheri
248 etabolism and anti-atherogenic properties of high-density lipoproteins (HDL) is unknown.
249                        Beneficial effects of high-density lipoproteins (HDL) seem altered in patients
250 gosine-1-phosphate (S1P) is a constituent of high-density lipoproteins (HDL) that contributes to thei
251 holesterol esters (CE) from atheroprotective high-density lipoproteins (HDL) to atherogenic low-densi
252                               Early forms of high-density lipoproteins (HDL), nascent HDL, are formed
253 id rafts, is a receptor for cholesterol-rich high-density lipoproteins (HDL).
254 justed follow-up blood lipid concentrations (high-density lipoprotein [HDL] and low-density lipoprote
255  cholesterol, low-density lipoprotein [LDL], high-density lipoprotein [HDL], and triglycerides [TGs])
256 eins including brain (apoE) and circulating (high-density lipoprotein, HDL) synergize to facilitate A
257                  The biological functions of high-density lipoproteins (HDLs) contribute to explainin
258                      We recently showed that high-density lipoproteins (HDLs) enhance ischemia-mediat
259 h a genetic variant previously correlated to high-density lipoprotein in a human genome-wide associat
260 nsity lipoprotein is causal for CHD, whereas high-density lipoprotein is not.
261 lectrochemical responses of purified low and high density lipoproteins (LDL and HDL, respectively) we
262 predicting height, body mass index (BMI) and high-density lipoprotein level (HDL) in two data cohorts
263 ounder population sequences: chr16:70790626 (high-density lipoprotein levels beta -1.71 (SE 0.25), P=
264                                   Increasing high-density lipoprotein levels in Apoa1bp(-/-) mice by
265 either prevalent CVD or CVD risk factors and high-density lipoprotein levels less than 50 mg/dL (<55
266 glyceride, very low-density lipoprotein, and high-density lipoprotein levels, as well as risk of coro
267 ating adiponectin was associated with higher high-density lipoprotein lipids and lower very-low-densi
268 trong inverse associations were observed for high-density lipoprotein measures, e.g., high-density li
269 tein A-I (apoA-I) has been shown to increase high-density lipoprotein-mediated cholesterol efflux cap
270                     Here we demonstrate that high-density lipoprotein-mimicking nanodiscs coupled wit
271 e, 2-h glucose and insulin, haemoglobin A1c, high-density lipoprotein or blood pressure.
272 oriasis (OR, 3.90; 95% CI, 1.57-9.66); lower high-density lipoprotein (OR, 0.99; 95% CI, 0.98-0.99);
273  of high-density lipoprotein cholesterol and high-density lipoprotein particle concentration, leptin,
274 logical samples, with a special focus on non-high-density-lipoprotein particle concentrations (non-HD
275                       TLF-1 is a subclass of high density lipoprotein particles defined by two primat
276 s (72.4 vs. 64.6; P = 0.02), decreased large high-density lipoprotein particles (5.3 vs. 6.7; P < 0.0
277 ipid transfer protein, and incorporated into high-density lipoprotein particles.
278 hway as well as the extracellular matrix and high-density lipoprotein pathways in the aetiology of AM
279                            Despite the lower high-density lipoprotein plasma levels, both transgenic
280 ved as danger signals; efflux cholesterol to high-density lipoprotein; proliferate and migrate; under
281 g/dL; 95% CI: 0.9, 9.7 mg/dL) and the LDL to high-density lipoprotein ratio (5 trials; net change: 0.
282 tatus; alcohol intake; SBP; DBP; cholesterol:high-density lipoprotein ratio; diabetes; body mass inde
283 er receptors BI (SR-BI) and BII (SR-BII) are high-density lipoprotein receptors that recognize variou
284          ApoA-I, the major protein of plasma high-density lipoprotein, removes cellular cholesterol a
285 otein cholesterol ratio (rG=-0.44, P=0.005), high-density lipoprotein (rG=-0.48, P=0.005), systolic b
286 we describe the development of reconstituted high-density lipoprotein (rHDL)-facilitated TAM PET imag
287 ree clinically relevant nanomedicines, i.e., high-density lipoprotein ([S]-HDL), polymeric micelles (
288 eptide nanoparticles that mimic native human high density lipoproteins significantly increases peptid
289 for high-density lipoprotein measures, e.g., high-density lipoprotein size (OR = 0.36, 0.30-0.42) and
290 tal (standardized estimate, 0.06; P = .050), high-density lipoprotein (standardized estimate, 0.07; P
291 ipoprotein subclasses, with the exception of high-density lipoprotein subclasses, which displayed a m
292        Fenugreek also significantly improved high-density lipoprotein to low-density lipoprotein rati
293 density lipoprotein/low-density lipoprotein, high-density lipoprotein, triglycerides, cytokines or bi
294 D and at least 1 of low-density lipoprotein, high-density lipoprotein, triglycerides, type 2 diabetes
295 ir association with low-density lipoprotein, high-density lipoprotein, triglycerides, type 2 diabetes
296 ng the gut microbiome explained </= 25.9% of high-density lipoprotein variance, significantly outperf
297 her (95% confidence interval, 1.71-2.97) and high-density lipoprotein was 1.62 mg/dL lower (95% confi
298 micelles, and nanocrystal-core reconstituted high-density lipoproteins, we have shown the approach's
299 terol (TC), TG, low-density lipoprotein, and high-density lipoprotein were measured.
300 rary's nanoparticles are based on endogenous high-density lipoprotein, which can preferentially deliv

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