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1 s primarily dependent on endocytosis via the low density lipoprotein receptor.
2 e expression for lipoprotein lipase and very-low-density lipoprotein receptor.
3 id not bind to the frizzled (Fz) receptor or low-density lipoprotein receptor.
4 esis, and inhibits cholesterol uptake by the low-density lipoprotein receptor.
5 t mice (0.162 cm(2)+/-0.023 [n=9], P2X7(-/-) low density lipoprotein receptor(-/-) : 0.084 cm(2)+/-0.
6 tack complex domain (FIMAC), CD5 domain, and low density lipoprotein receptor 1 (LDLr1) and LDLr2 dom
7 and (99m)Tc-labeled anti-lectinlike oxidized low-density lipoprotein receptor 1 antibody, which detec
8 ibody, which detects the lectinlike oxidized low-density lipoprotein receptor 1 that is overexpressed
12 Hepatic clearance of remnants occurs via low density lipoprotein receptors and the heparan sulfat
16 Reversa mice, which are deficient in the low-density lipoprotein receptor and in which hyperchole
17 lesterol lowering, with the discovery of the low-density lipoprotein receptor and its physiology and
18 role for both a t-PA receptor, most likely a low-density lipoprotein receptor, and a plasminogen rece
19 h ER stress and aortic lesion development in low-density lipoprotein receptor- and AMPKalpha2-deficie
20 rotein, plasma for high-density lipoprotein; low-density lipoprotein receptor, APOE and APOB for low-
21 n that the longer Sepp1 isoforms bind to the low density lipoprotein receptor apoER2, but the mechani
23 che within macrophage by modulating oxidized low-density lipoprotein receptor CD36, phagolysosomal ma
24 forms showed that the amino-terminal modular low-density lipoprotein receptor class A (LA) domains wi
25 thylglutaryl-coenzyme A reductase, and human low-density lipoprotein receptor), compared to uninfecte
26 the inflamed aorta in atherosclerosis-prone low-density lipoprotein receptor deficient (Ldlr(-/-)) m
27 arrow-restricted deletion of DNGR-1 in Ldlr (low-density lipoprotein receptor)-deficient mice (Ldlr(-
28 y of Nur77 on atherosclerosis was studied in low density lipoprotein receptor-deficient (Ldlr(-/-)) m
30 tic lesions and spleens of high-fat diet-fed low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
31 herosclerotic lesions from high-fat diet-fed low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
32 Lethally irradiated, atherosclerosis-prone, low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
34 Tet2-mutant cells in atherosclerosis-prone, low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
36 ate senescent cells in atherosclerosis-prone low-density lipoprotein receptor-deficient (Ldlr(-/-)) m
37 od vessels invading photoreceptors: the very low-density lipoprotein receptor-deficient (Vldlr(-/-) )
42 mplement pathways have been shown to protect low-density lipoprotein receptor-deficient mice (Ldlr(-/
43 the liver of diet-induced insulin-resistant low-density lipoprotein receptor-deficient mice and of g
44 lammation and reduced steatosis in livers of low-density lipoprotein receptor-deficient mice fed a We
45 results in decreased hepatic inflammation in low-density lipoprotein receptor-deficient mice on a Wes
46 ress as prime response pathways in livers of low-density lipoprotein receptor-deficient mice on a Wes
49 erosclerosis and insulin resistance in mice, low-density lipoprotein receptor-deficient, S100A9-defic
50 subtilisin/kexin type 9 (PCSK9) binds to the low-density lipoprotein receptor, escorting it to its de
51 lipoproteins depends on heparan sulfate and low density lipoprotein receptors expressed on the basal
53 -related protein 1 (LRP1) is a member of the low density lipoprotein receptor family and plays import
54 n, and alpha-AP-2 and directs endocytosis of low density lipoprotein receptor family members by recog
55 olecular chaperone that binds LRP1 and other low density lipoprotein receptor family members in the e
58 oprotein receptor (VLDLR) is a member of the low-density lipoprotein receptor family that binds multi
59 ined that ER liposomes utilize scavenger and low-density lipoprotein receptors for endocytosis and en
60 -related protein 1 (LRP1) is a member of the low-density lipoprotein receptor gene family found in ne
61 levels by raising the expression of SREBP2, low-density lipoprotein receptor, HMGCo-A reductase, and
62 nvertase subtilisin kexin 9 (PCSK9) binds to low-density lipoprotein receptors, increasing serum LDL-
63 the in vivo models of C57BL/6 wild-type and low density lipoprotein receptor knock-out (LDLR(-/-)) m
64 when Foxo1(KR/KR) mice are intercrossed with low density lipoprotein receptor knock-out mice (Ldlr(-/
65 ow density lipoprotein cholesterol (LDLc) in low density lipoprotein receptor knockout (LDLR(-/-)) mi
66 of G5-PEG and PB-NLCs were investigated in a low density lipoprotein receptor knockout (LDLr-/-) mous
67 vels by 22 and 31%, respectively, in fasting low-density lipoprotein receptor knockout (LDLR(-/-)) mi
69 hages in advanced atherosclerotic lesions of low-density lipoprotein receptor knockout (LDLR(-/-)) mi
70 found that genetic deletion of AMPKalpha2 in low-density lipoprotein receptor knockout (LDLr(-/-)) st
72 in ovalbumin- (OVA-) sensitized C57BL/6 and low-density lipoprotein receptor knockout mice (LDLr(-/-
73 of atherogenesis by mPGES-1 deletion in the low-density lipoprotein receptor knockout mice (n=17-21)
76 and vascular leakage in the eyecups of very low-density lipoprotein receptor knockout mice, a model
79 on in lymphatic organs, and atherogenesis in low-density lipoprotein receptor knockouts were unaltere
82 moxifen exerts an atheroprotective action on low density lipoprotein receptor (LDL-r(-/-)) female mic
84 K9) down-regulates surface expression of the low-density lipoprotein receptor (LDL-R), increasing ser
85 ls was transplanted into lethally irradiated low density lipoprotein receptor Ldlr(-/-) mice on an at
86 a1(-/-) mice to mice that do not express the low density lipoprotein receptor (Ldlr(-/-)), which are
87 3 ubiquitin ligase-inducible degrader of the low density lipoprotein receptor (LDLR) (Idol) as a post
89 epidermal growth factor-like-A domain of the low density lipoprotein receptor (LDLR) and mediates LDL
90 ted sdAbs efficiently blocked PCSK9-mediated low density lipoprotein receptor (LDLR) degradation in c
91 at CCP size and dynamic behavior varies with low density lipoprotein receptor (LDLR) expression level
92 bind heparin and receptors belonging to the low density lipoprotein receptor (LDLR) family, known to
98 Mice fed a Western-type diet and lacking low-density lipoprotein receptor (Ldlr(-/-)T39(-/-)) sho
99 because of loss-of-function mutations in the low-density lipoprotein receptor (LDLR) and homozygous f
100 The effect of the treatments on cellular low-density lipoprotein receptor (LDLR) and proprotein c
101 in genetically deficient iPSC utilizing the low-density lipoprotein receptor (LDLR) deficiency Famil
103 ent-type ligand-binding repeats (CRs) in the low-density lipoprotein receptor (LDLR) family are thoug
105 PSCs from JD a patient with mutations in the low-density lipoprotein receptor (LDLR) gene that result
106 le nucleotide polymorphism in exon 12 of the low-density lipoprotein receptor (LDLR) gene, rs688, has
107 which cystathionine beta-synthase (CBS) and low-density lipoprotein receptor (LDLr) genes were defic
108 of cholesterol and an overexpression of the low-density lipoprotein receptor (LDLR) in pancreatic tu
114 ime in atherosclerotic lesion macrophages of low-density lipoprotein receptor (Ldlr) knockout mice fe
115 e crossed Gsk3a/GSK3alpha-knockout mice with low-density lipoprotein receptor (Ldlr) knockout mice.
116 r risk for patients who already have reduced low-density lipoprotein receptor (LDLR) levels, such as
122 erized a novel mouse model, middle-aged male low-density lipoprotein receptor (LDLR)(-/-) mice fed a
124 we demonstrate that modulating levels of the low-density lipoprotein receptor (LDLR), a cell surface
125 2 (Dab2) recruits its cargoes, including the low-density lipoprotein receptor (LDLR), and mediates en
127 at for one of the identified substrates, the low-density lipoprotein receptor (LDLR), ERdj5 is requir
128 audin-1 (CLDN1), Occludin (OCLN), SR-BI, and low-density lipoprotein receptor (LDLR), function mainly
129 tercellular adhesion molecule-1 (ICAM-1) and low-density lipoprotein receptor (LDLR), inter- and intr
130 s, we identified 2 nonsynonymous variants in low-density lipoprotein receptor (LDLR), namely p.G116S
131 ceptor/coreceptor molecules CD81, claudin-1, low-density lipoprotein receptor (LDLr), occludin, and S
132 ertase subtilisin/kexin type 9 (PCSK9) binds low-density lipoprotein receptor (LDLR), preventing its
134 rmone (PTH) inhibits aortic calcification in low-density lipoprotein receptor (LDLR)-deficient mice f
135 mice, apolipoprotein E (apoE)-deficient and low-density lipoprotein receptor (LDLR)-deficient mice t
136 receptor tyrosine-protein kinase), and Lrp4 (low-density lipoprotein receptor (LDLR)-related protein
137 We previously demonstrated that macrophage low-density lipoprotein receptor (LDLR)-related protein
138 ACAT), ACAT2, small heterodimer partner, and low-density lipoprotein receptor (LDLR)-related proteins
142 n (MYLIP, aka IDOL and inducible degrader of low-density lipoprotein receptor [LDLR]), with LDL chole
144 els through a mechanism that is dependent on low-density lipoprotein receptors (LDLRs) and LDLR-relat
146 eased plasma PCSK9 levels, increased hepatic low-density lipoprotein receptor levels, and decreased p
147 binding assay showed that SERPINA3K binds to low-density lipoprotein receptor-like protein 6 (LRP6) w
149 xpression was analyzed in aortic arches from low density lipoprotein receptor(-/-) mice consuming a h
151 were transplanted into irradiated recipient low-density lipoprotein receptor(-/-) mice, and atherosc
153 in apolipoprotein-deficient (apoE(-/-)) and low-density lipoprotein receptor negative (LDLR(-/-)) mi
156 clerotic lesion size was found in Ldlr(-/-) (low-density lipoprotein receptor null) mice transplanted
157 hages worsened atherosclerosis in irradiated low-density lipoprotein receptor null-recipient mice and
159 en by a SM22Cre-IKKbeta-flox system rendered low density lipoprotein receptor-null mice resistant to
160 eficiency on experimental atherosclerosis in low-density lipoprotein receptor-null mice (Ldlr(-/-)).
162 n the vascular smooth muscle lineage of male low-density lipoprotein receptor-null mice, a background
164 APP chimeras harboring targeting motifs from low-density lipoprotein receptor or neuron-glia cell-adh
165 ncrease in permeability, whereas blockade of low-density lipoprotein receptors or exposed lysine resi
166 d via the liver provided that an intact apoE-low-density lipoprotein receptor pathway is present.
168 se subtilisin/kexin type 9 (PCSK9) regulates low density lipoprotein receptor protein levels by diver
170 L mice showed dramatic reductions in hepatic low-density lipoprotein receptor protein and increased p
171 ntibodies developed in these mice, LDLR(-/-)/low-density lipoprotein receptor Rag 1 double-knockout m
173 IDOL pathway in the liver can override other low-density lipoprotein receptor regulatory pathways lea
174 endent internalization of Abeta bound to the low density lipoprotein receptor related protein-1, a ke
175 complex formation involves Frizzled4 (Fz4), low-density lipoprotein receptor related protein 5/6 (Lr
176 ckkopf2 (Dkk1/2), to their cognate receptor, low-density-lipoprotein-receptor related protein 6 (LRP6
180 und that ADAMTS-5 is rapidly endocytosed via low density lipoprotein receptor-related protein 1 (LRP1
181 In addition to its endocytic function, the low density lipoprotein receptor-related protein 1 (LRP1
184 ndocytic clearance by the scavenger receptor low density lipoprotein receptor-related protein 1 (LRP1
185 htly to the clearance and signaling receptor low density lipoprotein receptor-related protein 1 (LRP1
188 ent increases mRNA and protein expression of low density lipoprotein receptor-related protein 2 and a
189 served amino acid position (p.R1188W) in the low density lipoprotein receptor-related protein 5 (LRP5
190 ted Wnt with its receptors Frizzled (Fz) and low density lipoprotein receptor-related protein 5/6 (LR
191 morphogenesis gene 2, as well as coreceptor low density lipoprotein receptor-related protein 6 (LRP6
192 ay genes, such as frizzled homolog 7 (FZD7), low density lipoprotein receptor-related protein 6 and t
193 receptor-associated protein (an inhibitor of low density lipoprotein receptor-related protein functio
194 tic receptor alpha(2)-macroglobulin receptor/low density lipoprotein receptor-related protein in the
195 hosphorylation of eNOS was decreased by anti-low density lipoprotein receptor-related protein-1 (LRP)
196 es, and we found that the endocytic receptor low density lipoprotein receptor-related protein-1 (LRP-
198 oligomers was dependent on the transmembrane low density lipoprotein receptor-related protein-1 (LRP1
201 ent and activation of beta1 integrin via the low density lipoprotein receptor-related protein-1 (LRP1
203 g to two receptors, the single transmembrane low density lipoprotein receptor-related proteins 5 and
204 bind to two distinct receptors, namely, the low-density lipoprotein receptor-related protein (LRP) a
206 We previously reported that RanBP9 binds low-density lipoprotein receptor-related protein (LRP),
207 ng phospholipids, von Willebrand factor, and low-density lipoprotein receptor-related protein (LRP).
208 e largest member of the LDL receptor family, low-density lipoprotein receptor-related protein (LRP1).
212 llaries was associated with its reduction in low-density lipoprotein receptor-related protein 1 (LRP1
213 t portion of apoE and sAbeta compete for the low-density lipoprotein receptor-related protein 1 (LRP1
216 e has demonstrated significant roles for the low-density lipoprotein receptor-related protein 1 (LRP1
217 , the receptors for these secreted proteins, low-density lipoprotein receptor-related protein 1 (LRP1
218 he deletion of a major lipoprotein receptor, low-density lipoprotein receptor-related protein 1 (LRP1
219 ed MvEC required expression of GRP78 and the low-density lipoprotein receptor-related protein 1 (LRP1
221 tween BKCaand both alpha2M and its receptor, low-density lipoprotein receptor-related protein 1 (LRP1
222 ction with the endocytic scavenger receptor, low-density lipoprotein receptor-related protein 1 (LRP1
223 pericytes also requires the function of the low-density lipoprotein receptor-related protein 1 (LRP1
224 s isoform-specific interactions of apoE with low-density lipoprotein receptor-related protein 1 on br
225 ASA-ApoE-II, uptake was partially due to the low-density lipoprotein receptor-related protein 1.
226 jects have identified autoantibodies against low-density lipoprotein receptor-related protein 4 (LRP4
227 tenance of neuromuscular synapses, and (iii) low-density lipoprotein receptor-related protein 4 (Lrp4
228 ctin, a protein acting downstream from agrin/low-density lipoprotein receptor-related protein 4 (LRP4
229 se in the brain was impaired in mice lacking low-density lipoprotein receptor-related protein 4 (Lrp4
230 We identified previously in vitro LRP4 (low-density lipoprotein receptor-related protein 4) as a
231 -derived protein, which interacts with LRP4 (low-density lipoprotein receptor-related protein 4) to a
232 ancer have identified novel functions of the low-density lipoprotein receptor-related protein 4-muscl
233 e human skeleton is affected by mutations in low-density lipoprotein receptor-related protein 5 (LRP5
235 ptions of tryptophan hydroxylase 1 (Tph1) or low-density lipoprotein receptor-related protein 5 (Lrp5
236 Wnt signaling ligand or receptors, including low-density lipoprotein receptor-related protein 5 (LRP5
237 in Lrp5(ACT) mice in which a mutation in the low-density lipoprotein receptor-related protein 5 Wnt c
238 riched around the Wnt-activated Frizzled and low-density lipoprotein receptor-related protein 5/6 rec
241 a critical chaperone for the Wnt coreceptor low-density lipoprotein receptor-related protein 6 (LRP6
243 ation, where it binds to the Wnt co-receptor low-density lipoprotein receptor-related protein 6 (LRP6
244 quires caveolin-dependent internalization of low-density lipoprotein receptor-related protein 6 (LRP6
245 nin signaling pathway by down-regulating the low-density lipoprotein receptor-related protein 6 (LRP6
246 ical Wnt ligand Wnt3a and the Wnt coreceptor low-density lipoprotein receptor-related protein 6 (LRP6
248 t signaling by binding to the Wnt coreceptor low-density lipoprotein receptor-related protein 6 (LRP6
249 to determine contributions of Wnt coreceptor low-density lipoprotein receptor-related protein 6 (LRP6
250 ecific for the E1E2 domain of Wnt coreceptor low-density lipoprotein receptor-related protein 6, Mab2
251 itatory synapse number were mediated via the low-density lipoprotein receptor-related protein and sub
252 se domain 9 (ADAM9), reticulon 4 (RTN4), and low-density lipoprotein receptor-related protein associa
253 eted frizzled-related protein, Dickkopf, and low-density lipoprotein receptor-related protein gene fa
255 sense substitutions within LRP1B, encoding a low-density lipoprotein receptor-related protein tied to
256 nt of interaction of mutants with either the low-density lipoprotein receptor-related protein, Lrp4 (
258 ple receptors including mannose receptor and low-density lipoprotein receptor-related protein-1 (LRP1
260 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
262 (LPS) by a pathway that apparently requires low-density lipoprotein receptor-related protein-1 (LRP1
263 the neurovascular hypothesis, impairment of low-density lipoprotein receptor-related protein-1 (LRP1
265 rocytic thrombospondin-1 (TSP1) and synaptic low-density lipoprotein receptor-related protein-1 (LRP1
267 alytic hemopexin domain of MMP9 binds to the low-density lipoprotein receptor-related protein-1, trig
268 sis and lysosome-dependent degradation in an low-density lipoprotein receptor-related protein-1-depen
269 -dependent PDGFRbeta protein degradation via low-density lipoprotein receptor-related protein-1.
270 y, we show that Wnt receptors (Frizzled4 and low-density lipoprotein receptor-related protein5 [Lrp5]
271 n (RAP), a ligand-binding antagonist for the low-density lipoprotein receptor-related proteins (LRPs)
272 1 (DKK-1), a ligand for the WNT coreceptors low-density lipoprotein receptor-related proteins 5 and
273 receptors frizzled 1-10 and the co-receptors low-density lipoprotein receptor-related proteins 5 and
275 e frizzled receptor (FZD) and the coreceptor low-density lipoprotein-receptor-related protein 5 (LRP5
276 loci, rs1466535, located within intron 1 of low-density-lipoprotein receptor-related protein 1 (LRP1
278 Here we show that the soluble form of the low-density lipoprotein receptor relative, LR11/SorLA (s
279 via apolipoprotein E receptor 2 and the very low density lipoprotein receptor, resulting in the phosp
280 Drosophila vitellogenin receptor Yolkless, a low density lipoprotein receptor superfamily member, occ
282 teraction with the RELN receptor VLDLR (very low-density lipoprotein receptor); this was confirmed by
283 These antibodies prevent the degradation of low density lipoprotein receptor, thus lowering serum le
284 thereby preventing the recirculation of the low-density lipoprotein receptor to the hepatocyte cell
285 ch region (aa 95-141) that separates the two low-density lipoprotein receptor type A (LDLR-A) domains
287 n signals via the lipoprotein receptors very low density lipoprotein receptor (VLDLR) and apolipoprot
288 polipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is internal
289 We discovered that miR-200c targets the very low density lipoprotein receptor (Vldlr) and its ligand
293 ed choroidal neovascularization and the very low density lipoprotein receptor (Vldlr)-knockout mouse]
297 thways including through the receptors, Very low-density lipoprotein receptor (Vldlr), Apolipoprotein
298 e deficient in another Reelin receptor, very low-density lipoprotein receptor (VLDLR), had normal rod
300 nopathy and another angiogenic model of very-low-density lipoprotein receptor (Vldlr)-deficient (Vldl
301 ion disrupts an interaction with VLDLR (very low-density lipoprotein receptor), while the APOER2 sign
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