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1  that triglyceride levels causally influence low-density lipoprotein.
2 re typically present in oxidatively modified low-density lipoprotein.
3 inds both high-density lipoprotein (HDL) and low-density lipoprotein.
4 blood pressure 51.2%; body mass index 33.8%; low-density lipoprotein 31.4%; and waist-to-hip ratio 29
5 ces, -0.35 kg/m(2); 95% CI, -0.62 to -0.07), low-density lipoprotein (4 studies; mean differences, -0
6            Exposure of monocytes to oxidized low-density lipoprotein, 7-ketocholesterol, phorbol 12-m
7  preventing inflammation induced by oxidized low-density lipoprotein and promoting apoptotic cell cle
8 ned significant after adjusting for baseline low-density lipoprotein and statin dose (beta=-0.27; P=0
9 ss 6 to 12 months, including blood pressure, low-density lipoprotein and total cholesterol levels, an
10 tween noncoding rare variants in SLC22A3 and low-density lipoprotein and total cholesterol, associati
11 tiology via extensive associations with very-low-density lipoprotein and triglyceride metabolism.
12 isease who require further reduction in LDL (low-density lipoprotein) and non-HDL-C.
13 tivity and total HDL antioxidant capacity on low-density lipoproteins), and HDL vasodilatory capacity
14 biomarkers, namely, fibrinogen, adiponectin, low-density lipoprotein, and 8-isoprostane.
15 ciated with a significant increase in total, low-density lipoprotein, and high-density lipoprotein (H
16  Serum levels of total cholesterol (TC), TG, low-density lipoprotein, and high-density lipoprotein we
17 resulted in significant reductions in total, low-density lipoprotein, and non-high-density lipoprotei
18 ncreased high-density lipoprotein, decreased low-density lipoprotein, and reduced atherosclerosis.
19  IHD, systolic and diastolic blood pressure, low-density lipoprotein- and total cholesterol, triglyce
20 ocumab had no effects on FCRs or PRs of very low-density lipoproteins-apoB and very low-density lipop
21 is tempers triglyceride availabiity for very low density lipoprotein assembly and allows homeostatic
22 the CC-genotype was associated with elevated low density lipoprotein cholesterol (LDLc) and total cho
23  burden related to phenotypic FH, defined by low-density lipoprotein cholesterol >/=190 mg/dL, is lik
24 h a third who had residual cholesterol risk (Low-density lipoprotein cholesterol >100 mg/dL).
25    Children with HeFH (age, 6-<18 years) and low-density lipoprotein cholesterol >4.9 mmol/L or >4.1
26 ntion parameters-aspirin use, lipid control (low-density lipoprotein cholesterol <70 mg/dL or statin
27 ncomitant therapies, including patients with low-density lipoprotein cholesterol <70 mg/dl.
28 d with the highest versus lowest quartile of low-density lipoprotein cholesterol (>/= 146 versus </=
29 idence interval, 18-27; P<1.0x10(-4)), lower low-density lipoprotein cholesterol (-12.2 mg/dL; 95% co
30 ipoprotein cholesterol (1.6 [1.2-2.2]), high low-density lipoprotein cholesterol (1.6 [1.1-2.1]), and
31 ]), obesity (3.7 [2.0-7.0]), borderline high low-density lipoprotein cholesterol (1.6 [1.2-2.2]), hig
32 63.1%), LDL cholesterol (1.3 to 32.9%), very-low-density lipoprotein cholesterol (27.9 to 60.0%), non
33 oach using only childhood lipid measures for low-density lipoprotein cholesterol (area under the rece
34                          Pravastatin lowered low-density lipoprotein cholesterol (change in SD units
35 A and NPHSII, respectively; both p < 0.001), low-density lipoprotein cholesterol (correlation coeffic
36 t showed differential responses in total and low-density lipoprotein cholesterol (decreased in LFHC g
37                                          For low-density lipoprotein cholesterol (LDL) of 130-159 mg/
38          Patients with primary elevations of low-density lipoprotein cholesterol (LDL-C) >/=190 mg/dL
39 se <126 mg/dl, total cholesterol <240 mg/dl, low-density lipoprotein cholesterol (LDL-C) <160 mg/dl,
40 iglycerides (TGs), high-density (HDL-C), and low-density lipoprotein cholesterol (LDL-C) (n=627).
41 haracterized by extremely elevated levels of low-density lipoprotein cholesterol (LDL-C) and accelera
42 ma concentrations of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and apolipop
43                                        Serum low-density lipoprotein cholesterol (LDL-C) and high-den
44 ontinuous relationship between reductions in low-density lipoprotein cholesterol (LDL-C) and major ad
45                    Increased serum levels of low-density lipoprotein cholesterol (LDL-C) are an indep
46 oring nonfasting lipid assessment may affect low-density lipoprotein cholesterol (LDL-C) estimation.
47 elected individuals with increased levels of low-density lipoprotein cholesterol (LDL-C) have shown m
48 tients with elevated 10-year risk (>5%) or a low-density lipoprotein cholesterol (LDL-C) level of 4.9
49 y statins and targeting or using a threshold low-density lipoprotein cholesterol (LDL-C) level of les
50 cluding 511 adult patients with uncontrolled low-density lipoprotein cholesterol (LDL-C) levels and h
51 noclonal antibody against PCSK9 that reduces low-density lipoprotein cholesterol (LDL-C) levels by 55
52 itors in patients with persistently elevated low-density lipoprotein cholesterol (LDL-C) levels despi
53 ter transfer protein (CETP) inhibitors lower low-density lipoprotein cholesterol (LDL-C) levels witho
54                  The primary outcome was the low-density lipoprotein cholesterol (LDL-C) levels.
55 amination of the effects of lifetime reduced low-density lipoprotein cholesterol (LDL-C) on cardiovas
56  was shown that intraindividual variation in low-density lipoprotein cholesterol (LDL-C) predicts bot
57                                              Low-density lipoprotein cholesterol (LDL-C) reductions w
58 exin type 9 monoclonal antibodies can reduce low-density lipoprotein cholesterol (LDL-C) to very low
59                             Median untreated low-density lipoprotein cholesterol (LDL-C) was 239 mg/d
60 vestigated whether the relative reduction in low-density lipoprotein cholesterol (LDL-c) was a good i
61 igh-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglyc
62 igh-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and triglyc
63           Elevated cholesterol, particularly low-density lipoprotein cholesterol (LDL-C), is frequent
64                                  Importance: Low-density lipoprotein cholesterol (LDL-C)-lowering all
65 orin Efficacy International Trial, intensive low-density lipoprotein cholesterol (LDL-C)-reducing the
66 preventing cardiovascular events by reducing low-density lipoprotein cholesterol (LDL-C).
67  key role in regulating the levels of plasma low-density lipoprotein cholesterol (LDL-C).
68  could be useful for treating high levels of low-density lipoprotein cholesterol (LDL-C).
69 imarily expressed in the liver and regulates low-density lipoprotein cholesterol (LDL-C).
70  one of the scavenger receptors for oxidized low-density lipoprotein cholesterol (ox-LDL), plays a cr
71 l/L, LF = -0.31 +/- 0.10 mmol/L; P = 0.024), low-density lipoprotein cholesterol (PY = -0.35 +/- 0.10
72  patients after acute coronary syndrome with low-density lipoprotein cholesterol 50 to 125 mg/dL were
73 igh-density lipoprotein cholesterol [HDL-C], low-density lipoprotein cholesterol [LDL-C], total chole
74 e subtilisin/kexin type 9), markedly reduces low-density lipoprotein cholesterol across diverse patie
75 n/kexin type 9) inhibitor evolocumab reduced low-density lipoprotein cholesterol and cardiovascular e
76 me-wide significant variants associated with low-density lipoprotein cholesterol and coronary heart d
77                      The interaction between low-density lipoprotein cholesterol and IHD genetic load
78 creased body mass index, active smoking, and low-density lipoprotein cholesterol and lipoprotein(a) l
79 nsistent relationship between lower achieved low-density lipoprotein cholesterol and lower risk of li
80 s and cumulative exposure to lower levels of low-density lipoprotein cholesterol are not associated w
81 atment to placebo in individuals with normal low-density lipoprotein cholesterol but increased C-reac
82                        Unregulated uptake of low-density lipoprotein cholesterol by circulating monoc
83 sult in lifelong exposure to lower levels of low-density lipoprotein cholesterol can provide informat
84 ificantly lower median time-weighted average low-density lipoprotein cholesterol compared with placeb
85        In secondary analyses conditioning on low-density lipoprotein cholesterol concentration, the e
86 t-day humans, including variants involved in low-density lipoprotein cholesterol concentrations, schi
87 s for neurocognitive impairment per 20 mg/dL low-density lipoprotein cholesterol decrements were 1.02
88 s in the face of lower levels of circulating low-density lipoprotein cholesterol in mice lacking miR-
89 A1c was -0.022 +/- 0.53%; however, total and low-density lipoprotein cholesterol increased significan
90 CI, -0.82 to -0.16]; 23 trials [n = 58022]), low-density lipoprotein cholesterol level (-2.58 mg/dL [
91 , but approval rates did not vary by patient low-density lipoprotein cholesterol level nor statin use
92                             The overall mean low-density lipoprotein cholesterol level was 26.5% lowe
93 ter publication) in the cohort with elevated low-density lipoprotein cholesterol levels (ie, >/=190 m
94 , including reductions in blood pressure and low-density lipoprotein cholesterol levels and improveme
95  atherosclerotic cardiovascular disease with low-density lipoprotein cholesterol levels of at least 7
96 counted net price of $10311 in patients with low-density lipoprotein cholesterol levels of at least 8
97            Individuals with elevated fasting low-density lipoprotein cholesterol levels were also ran
98                                       Higher low-density lipoprotein cholesterol levels were not asso
99 sment of the efficacy and safety of lowering low-density lipoprotein cholesterol levels with atorvast
100 iagnoses, lipid-lowering medication use, and low-density lipoprotein cholesterol levels.
101 levels and increases in serum creatinine and low-density lipoprotein cholesterol levels.
102  24% (95% CI, 8-37; P=0.004) despite similar low-density lipoprotein cholesterol lowering.
103  on the potential long-term effects of lower low-density lipoprotein cholesterol on neurocognitive im
104  of early initiation of statin treatment for low-density lipoprotein cholesterol reduction in childre
105 NA that regulates LDLR and may contribute to low-density lipoprotein cholesterol response to statin t
106 eye examination, hemoglobin A1c testing, and low-density lipoprotein cholesterol testing), prescribin
107 eye examination, hemoglobin A1c testing, and low-density lipoprotein cholesterol testing), prescribin
108 sed on benefits estimated from reductions in low-density lipoprotein cholesterol that occurred in PCS
109                Low-fat diets tend to improve low-density lipoprotein cholesterol the most, while lowe
110                                    Intensive low-density lipoprotein cholesterol therapy with ezetimi
111 ing family history, more stringent age-based low-density lipoprotein cholesterol thresholds, or alter
112 herosclerotic Cardiovascular Risk in Adults, low-density lipoprotein cholesterol treatment thresholds
113                         The median admission low-density lipoprotein cholesterol was lower among pati
114 s coronary intervention, and higher level of low-density lipoprotein cholesterol were independent pre
115                        Moreover, lowering of low-density lipoprotein cholesterol with evolocumab redu
116                                              Low-density lipoprotein cholesterol(LDL-C) is a well est
117 (A), biomarkers (B) (NT-proBNP, hs-cTnT, and low-density lipoprotein cholesterol), and clinical varia
118 -8 mg/dl for total cholesterol, -8 mg/dl for low-density lipoprotein cholesterol, +8 mg/dl for remnan
119 ed on 58 single-nucleotide polymorphisms for low-density lipoprotein cholesterol, 71 single-nucleotid
120 nt of saturated with unsaturated fats lowers low-density lipoprotein cholesterol, a cause of atherosc
121 ype natriuretic peptide, and lower levels of low-density lipoprotein cholesterol, adiponectin, lipopr
122 with progressively higher levels of glucose, low-density lipoprotein cholesterol, and blood pressure.
123 ntrol subjects and had higher triglycerides, low-density lipoprotein cholesterol, and HbA1c and lower
124 pe 9 (PCSK9) inhibitors substantially reduce low-density lipoprotein cholesterol, but it is presently
125 nic profile scores for BMI, HDL cholesterol, low-density lipoprotein cholesterol, coronary artery dis
126 ng insulin, triglyceride, total cholesterol, low-density lipoprotein cholesterol, fasting glucose, di
127  diabetes duration, systolic blood pressure, low-density lipoprotein cholesterol, hemoglobin A1c, alb
128 ated to cardiovascular disease risk factors: low-density lipoprotein cholesterol, high-density lipopr
129  high-density lipoprotein cholesterol, lower low-density lipoprotein cholesterol, lower triglycerides
130                             Current smoking, low-density lipoprotein cholesterol, multivessel CAD, di
131                                              Low-density lipoprotein cholesterol, non-high-density li
132 In multivariable analysis, older age, higher low-density lipoprotein cholesterol, pack per year of sm
133                     Also, total cholesterol, low-density lipoprotein cholesterol, triacylglycerol, gl
134 Application of SCOPA to two GWAS of high-and low-density lipoprotein cholesterol, triglycerides and b
135 1 microbe intervention in rats reduced serum low-density lipoprotein cholesterol, triglycerides and t
136 ex, fasting plasma glucose, glycohemoglobin, low-density lipoprotein cholesterol, triglycerides, high
137 ensitivity cardiac troponin T (hs-cTnT), and low-density lipoprotein cholesterol, where NT-proBNP and
138 acebo, in addition to effective statin-based low-density lipoprotein cholesterol-lowering treatment.
139 is-methylation quantitative trait loci for a low-density lipoprotein cholesterol-related differential
140 n, blood pressure, albuminuria, smoking, and low-density lipoprotein cholesterol.
141 ulating triglycerides and a 12% reduction in low-density lipoprotein cholesterol.
142 ent-specific ratios of triglycerides to very low-density lipoprotein cholesterol.
143 lycerols, apolipoproteins A-I and B, or very low-density lipoprotein cholesterol.
144 29) for triglycerides, and 95.0% (19/20) for low-density lipoprotein cholesterol.
145  that includes potent statin therapy and low low-density lipoprotein cholesterol.
146 igh-density-lipoprotein cholesterol (HDL-C), low-density-lipoprotein cholesterol (LDL-C), and/or trig
147         There was a significant reduction in low density lipoprotein-cholesterol (LDL-C), an increase
148  Plasma levels of total cholesterol (T-CHL), low density lipoprotein-cholesterol (LDL-CHL), and resis
149 and cardiovascular disease (CVD) context and low density lipoprotein-cholesterol concentrations withi
150 xcept for an inverse association of FT4 with low-density lipoprotein-cholesterol.
151 ed back into the cellular media, whereas the low-density lipoprotein component was localized to the l
152 n DCs on atherosclerosis were examined using low-density lipoprotein-deficient (Ldlr(-/-)) bone marro
153 players in the endosomal/lysosomal egress of low-density lipoprotein-derived cholesterol.
154          Exposure of macrophages to oxidized low-density lipoprotein downregulated LKB1 in vitro.
155                          Low cholesterol and low-density lipoprotein have been associated with greate
156 with cholesterol concentrations in high- and low-density lipoproteins (HDL and LDL) particles measure
157               Blood pressure, triglycerides, low-density lipoprotein, high-density lipoprotein, and t
158                           Total cholesterol, low-density lipoprotein, high-density lipoprotein, and t
159  CAD as a function of their association with low-density lipoprotein, high-density lipoprotein, trigl
160 tein component, indicating their origin from low-density lipoprotein, intermediate-density lipoprotei
161 a (FH) is characterized by severely elevated low density lipoprotein (LDL) cholesterol.
162  contributes to atherosclerosis by targeting low density lipoprotein (LDL) receptor (LDLR) degradatio
163  show that alpha2delta-1 is a ligand for the Low Density Lipoprotein (LDL) Receptor-related Protein-1
164  kinetics of key biological proteins, namely Low Density Lipoprotein (LDL), Tissue Necrosis Factor al
165                                     Egg yolk low density lipoprotein (LDL)/polysaccharide nanogels ar
166     Although EC are in constant contact with low density lipoproteins (LDL), how EC process LDL and w
167                            Uptake of labeled low-density lipoprotein (LDL) and cholesterol was measur
168 gnificantly lowers blood pressure as well as low-density lipoprotein (LDL) and high-density lipoprote
169 95% CI, 0.80-0.95, per mmol/l increase), and low-density lipoprotein (LDL) cholesterol (OR, 0.83; 95%
170 btilisin/kexin type 9 (PCSK9), lowers plasma low-density lipoprotein (LDL) cholesterol and apolipopro
171 e cardiometabolic risk-factor profile [lower low-density lipoprotein (LDL) cholesterol and triglyceri
172 e subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by appr
173 was found to produce sustained reductions in low-density lipoprotein (LDL) cholesterol levels over th
174  despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels.
175 oncern that these drugs or the low levels of low-density lipoprotein (LDL) cholesterol that result fr
176 l3 mRNA, Angptl3 protein, triglycerides, and low-density lipoprotein (LDL) cholesterol, as well as re
177 mes were: blood pressure, total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density
178 nstrated to be associated with at least 1 of low-density lipoprotein (LDL) cholesterol, high-density
179 n-kexin type 9 (PCSK9) and reduces levels of low-density lipoprotein (LDL) cholesterol.
180 isin-kexin type 9 (PCSK9), reduces levels of low-density lipoprotein (LDL) cholesterol.
181 tal role in clearing atherogenic circulating low-density lipoprotein (LDL) cholesterol.
182 type 9 (PCSK9), a target for the lowering of low-density lipoprotein (LDL) cholesterol.
183 protein and known for the endocytosis of the low-density lipoprotein (LDL) family receptors.
184         Incubation of plasma electronegative low-density lipoprotein (LDL) from UNx rats with normal
185                              Electronegative low-density lipoprotein (LDL) has been shown to increase
186 ly, hepatic vigilin knockdown decreases VLDL/low-density lipoprotein (LDL) levels and formation of at
187                                          The low-density lipoprotein (LDL) receptor (LDLR) is a centr
188                Although sequence analysis of low-density lipoprotein (LDL) receptor (LDLR) mRNA did n
189                             To this end, the low-density lipoprotein (LDL) receptor was targeted for
190 isin/kexin type 9 (PCSK9) down-regulates the low-density lipoprotein (LDL) receptor, elevating LDL ch
191 iosynthesis thereby upregulating the hepatic low-density lipoprotein (LDL) receptors and increasing t
192       Our data indicate that electronegative low-density lipoprotein (LDL) shows SMase activity, whic
193                           Increased level of low-density lipoprotein (LDL) strongly correlates with i
194                         Carbamylation alters low-density lipoprotein (LDL) structure and is thought t
195 ins, such as high-density lipoprotein (HDL), low-density lipoprotein (LDL), and very-low density lipo
196 ther the most electronegative subfraction of low-density lipoprotein (LDL), L5, is correlated with QT
197                                              Low-density lipoprotein (LDL), one of the four major gro
198 ipid traits (high-density lipoprotein (HDL), low-density lipoprotein (LDL), plasma concentrations of
199  9 (PCSK9), such as evolocumab, lower plasma low-density lipoprotein (LDL)-cholesterol concentrations
200 CDP) on the role of non-statin therapies for low-density lipoprotein (LDL)-cholesterol lowering in th
201 HT) and its derivatives in olive oil protect low-density lipoproteins (LDL) against oxidation.
202 lied with cholesterol derived from uptake of low-density lipoproteins (LDL) and synthesis.
203 rin Efficacy International Trial by reducing low-density-lipoprotein (LDL) cholesterol levels more th
204                                              Low-density lipoproteins (LDLs) are a class of nanocarri
205 hages ingest high levels of damaged modified low-density lipoproteins (LDLs), generating macrophage f
206           Even after accounting for baseline low-density lipoprotein level, statin exposure continued
207 ffect persists after accounting for baseline low-density lipoprotein level.
208  (-250.19 g; 95% CI, -459.9 to -40.5 g), and low-density lipoprotein levels (-15.4 mg/dL; 95% CI, -23
209 n-1(Sort1), a known regulator of circulating low-density lipoprotein levels in humans, as a novel tar
210                After accounting for baseline low-density lipoprotein levels, persons who filled presc
211       RATIONALE: Lipoprotein(a) [Lp(a)] is a low-density lipoprotein-like lipoprotein and important c
212 gh-density lipoprotein lipids and lower very-low-density lipoprotein lipids, glucose levels, branched
213 tein, intermediate-density lipoprotein, very-low-density lipoprotein, lipoprotein (a), or chylomicron
214          No changes in plasma levels of very low-density lipoprotein/low-density lipoprotein, high-de
215 ystemic treatment with anti-inflammatory and low-density lipoprotein-lowering drugs are currently bei
216 terol (MD -8.5 mg/dl, 95% CI -9.5, -7.4) and low-density lipoprotein (MD -2.4 mg/dl, 95% CI -3.4, -1.
217 % confidence interval 3.48-6.78), other very-low-density lipoprotein measures, and branched-chain ami
218  inhibition of PCSK9 has any effects on very low-density lipoprotein or intermediate-density lipoprot
219 induced by cholesterol crystals and oxidized low-density lipoproteins (ox-LDL), potentially by increa
220 xidative stress were measured in plasma: (1) low-density lipoprotein oxidizability, (2) high-density
221                                              Low-density lipoprotein oxidizability, indicative of the
222 d leads to the uptake of native and oxidized low-density lipoprotein (oxLDL) by macrophages (Mvarphis
223                                     Oxidized low-density lipoprotein (oxLDL) is known to activate inf
224  CD36 recognizes oxidized lipids in oxidized low-density lipoprotein (oxLDL) particles, a process tha
225                            Retained oxidized low-density lipoprotein (oxLDL), in turn, stimulated myo
226  that internalize lipids, including oxidized low-density lipoprotein (oxLDL).
227 Procollagens, pre-chylomicrons, and pre-very low-density lipoproteins (pre-VLDLs) are too big to fit
228 macrophage LKB1 reduction caused by oxidized low-density lipoprotein promotes foam cell formation and
229 icantly improved high-density lipoprotein to low-density lipoprotein ratios in high fat-fed mice with
230 n signals via the lipoprotein receptors very low density lipoprotein receptor (VLDLR) and apolipoprot
231 t mice (0.162 cm(2)+/-0.023 [n=9], P2X7(-/-) low density lipoprotein receptor(-/-) : 0.084 cm(2)+/-0.
232 xpression was analyzed in aortic arches from low density lipoprotein receptor(-/-) mice consuming a h
233                      P2X7(+/+) and P2X7(-/-) low density lipoprotein receptor(-/-) mice were fed a hi
234                                              Low density lipoprotein receptor-null (Ldlr(-/-)) mice o
235                                          The low density lipoprotein receptor-related protein 1 (LRP1
236 ent increases mRNA and protein expression of low density lipoprotein receptor-related protein 2 and a
237 ent and activation of beta1 integrin via the low density lipoprotein receptor-related protein-1 (LRP1
238     Mice fed a Western-type diet and lacking low-density lipoprotein receptor (Ldlr(-/-)T39(-/-)) sho
239                                       Female low-density lipoprotein receptor (Ldlr) deficient mice w
240                                          The low-density lipoprotein receptor (LDLR) plays a pivotal
241 audin-1 (CLDN1), Occludin (OCLN), SR-BI, and low-density lipoprotein receptor (LDLR), function mainly
242 ertase subtilisin/kexin type 9 (PCSK9) binds low-density lipoprotein receptor (LDLR), preventing its
243       As proof-of-principle, we targeted the low-density lipoprotein receptor (Ldlr), which when dele
244  the inflamed aorta in atherosclerosis-prone low-density lipoprotein receptor deficient (Ldlr(-/-)) m
245 element binding protein 2 and downregulating low-density lipoprotein receptor expression.
246  of atherogenesis by mPGES-1 deletion in the low-density lipoprotein receptor knockout mice (n=17-21)
247  inhibits atherosclerosis development in the low-density lipoprotein receptor knockout mouse.
248 with mPges-1 on a hyperlipidemic background (low-density lipoprotein receptor knockouts).
249        METHODS AND Paradoxically, Ldlr(-/-) (low-density lipoprotein receptor null) mice deficient in
250 clerotic lesion size was found in Ldlr(-/-) (low-density lipoprotein receptor null) mice transplanted
251 ion disrupts an interaction with VLDLR (very low-density lipoprotein receptor), while the APOER2 sign
252 arrow-restricted deletion of DNGR-1 in Ldlr (low-density lipoprotein receptor)-deficient mice (Ldlr(-
253 teraction with the RELN receptor VLDLR (very low-density lipoprotein receptor); this was confirmed by
254                         Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), one of the s
255  Tet2-mutant cells in atherosclerosis-prone, low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
256 ate senescent cells in atherosclerosis-prone low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
257 od vessels invading photoreceptors: the very low-density lipoprotein receptor-deficient (Vldlr(-/-) )
258                                         In a low-density lipoprotein receptor-deficient atherosclerot
259 results in decreased hepatic inflammation in low-density lipoprotein receptor-deficient mice on a Wes
260 ress as prime response pathways in livers of low-density lipoprotein receptor-deficient mice on a Wes
261                                              Low-density lipoprotein receptor-related protein 1 (LRP-
262                                              Low-density lipoprotein receptor-related protein 1 (LRP1
263 , the receptors for these secreted proteins, low-density lipoprotein receptor-related protein 1 (LRP1
264 ction with the endocytic scavenger receptor, low-density lipoprotein receptor-related protein 1 (LRP1
265 ctin, a protein acting downstream from agrin/low-density lipoprotein receptor-related protein 4 (LRP4
266 ancer have identified novel functions of the low-density lipoprotein receptor-related protein 4-muscl
267 ptions of tryptophan hydroxylase 1 (Tph1) or low-density lipoprotein receptor-related protein 5 (Lrp5
268                                              Low-density lipoprotein receptor-related protein 6 (LRP6
269 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
270                                              Low-density lipoprotein receptor-related protein-1 (LRP1
271  (LPS) by a pathway that apparently requires low-density lipoprotein receptor-related protein-1 (LRP1
272 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
273 receptors frizzled 1-10 and the co-receptors low-density lipoprotein receptor-related proteins 5 and
274                             In parallel, the low-density-lipoprotein receptor plays a predominant rol
275 els through a mechanism that is dependent on low-density lipoprotein receptors (LDLRs) and LDLR-relat
276 ntiplatelet therapy, blood pressure control, low-density lipoprotein reduction, and lifestyle modific
277                        Blocking hepatic very low-density lipoprotein secretion through genetic or pha
278 echanisms and consequences of defective very low-density lipoprotein secretion.
279 inadequate increases in IHTG export via very low-density lipoprotein secretion.
280 free fatty acid oxidation, or decreased very-low-density lipoprotein secretion.
281 (standardized estimate, 0.07; P = .003), and low-density lipoprotein (standardized estimate, 0.04; P
282 links to the apolipoprotein B component of a low-density lipoprotein through a disulfide bridge to fo
283 rporation into palmitate of circulating very low-density lipoprotein triglyceride.
284 tions were observed for extremely large very-low-density lipoprotein triglycerides (odds ratio [OR] =
285  very low-density lipoproteins-apoB and very low-density lipoproteins triglycerides or on postprandia
286 sion of SRA (scavenger receptor A), modified low-density lipoprotein uptake and foam cell formation,
287 DL), low-density lipoprotein (LDL), and very-low density lipoprotein (VLDL), play a critical role in
288 notion that HCV coopts the secretion of very-low-density lipoprotein (VLDL) for its egress.
289 impaired ER-to-Golgi trafficking of pre-very low-density lipoprotein (VLDL) particles.
290 tic triglycerides (TAG) associated with very-low-density lipoprotein (VLDL) play a major role in main
291 nuation of hepatic steatosis, increased very low-density lipoprotein (VLDL) secretion, and improved g
292  prevents fructose-induced increases in very-low-density lipoprotein (VLDL) triglycerides by decreasi
293 ) for 8 weeks on the plasma kinetics of very-low-density lipoprotein (VLDL)-apolipoprotein B-100 (apo
294 d proteomic profiles implicated these 3 very-low-density lipoprotein (VLDL)-associated apolipoprotein
295 ortant for HCV cell-to-cell spread, but very-low-density lipoprotein (VLDL)-containing mouse serum di
296 erved strong positive associations with very-low-density lipoprotein (VLDL)-lipoproteins, VLDL-choles
297                                         Very-low-density lipoproteins (VLDL) is a hallmark of metabol
298 in (HDL) yields 4-6% of the LDL signal, very-low-density-lipoprotein (VLDL) yields 1-3%, and human se
299 lisin/kexin type 9 (PCSK9) selectively binds low-density lipoprotein; we hypothesized that it can als
300 d the hope that additional agents that lower low-density lipoprotein will decrease risk of atheroscle

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