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1 matory response, early/late E2-response, and cholesterol homeostasis.
2 plays an important role in the regulation of cholesterol homeostasis.
3 iptional repressor to regulate bile acid and cholesterol homeostasis.
4 cells, is involved in maintaining organismal cholesterol homeostasis.
5 oth the enteroviral life cycle and host cell cholesterol homeostasis.
6 ngs related to the impact of SLU pathways in cholesterol homeostasis.
7 oplasmic reticulum is essential for cellular cholesterol homeostasis.
8 rption of bile acids and plays a key role in cholesterol homeostasis.
9 mportance of hepatic LXRalpha for whole body cholesterol homeostasis.
10 ol directly on major molecular parameters of cholesterol homeostasis.
11 d that statins only modestly affected cancer cholesterol homeostasis.
12 ligomeric Abeta(42) (oAbeta(42)) in neuronal cholesterol homeostasis.
13 ors (LXRs) are nuclear receptors involved in cholesterol homeostasis.
14 tic circulation of bile acids, as well as in cholesterol homeostasis.
15 iption factors involved in the regulation of cholesterol homeostasis.
16 terol that serve a central role in mediating cholesterol homeostasis.
17 ression plays an important role in adipocyte cholesterol homeostasis.
18 iological regulator of both triglyceride and cholesterol homeostasis.
19 of bile acid signaling in regulating overall cholesterol homeostasis.
20  inflammatory responses by altering cellular cholesterol homeostasis.
21 al program, which includes genes involved in cholesterol homeostasis.
22  mechanism for how these oxysterols regulate cholesterol homeostasis.
23 nd lysosomes (Ly) (LE/Ly) to globally manage cholesterol homeostasis.
24 iological set-point levels, thereby ensuring cholesterol homeostasis.
25 udies define DHR96 as a central regulator of cholesterol homeostasis.
26 o control an important regulatory pathway in cholesterol homeostasis.
27 y play a role in the oxysterol regulation of cholesterol homeostasis.
28 r (ASBT), a key membrane protein involved in cholesterol homeostasis.
29  may provide novel approaches for regulating cholesterol homeostasis.
30 feration through the maintenance of cellular cholesterol homeostasis.
31 1 inhibition and subsequent dysregulation of cholesterol homeostasis.
32 o major pathways by which the body regulates cholesterol homeostasis.
33 ole in lipoprotein metabolism and macrophage cholesterol homeostasis.
34 ng in all three of these important routes of cholesterol homeostasis.
35  density lipoproteins and plays key roles in cholesterol homeostasis.
36 ceptor (LDLR) family and functions in plasma cholesterol homeostasis.
37  LDLR SNPs may alter splicing efficiency and cholesterol homeostasis.
38  in systemic and hepatic glucose, lipid, and cholesterol homeostasis.
39 ceptor function in maintenance of whole body cholesterol homeostasis.
40  addition, bile acids play a crucial role in cholesterol homeostasis.
41 nterferes with its role in regulating plasma cholesterol homeostasis.
42  important role in maintaining bile acid and cholesterol homeostasis.
43 yl esters, regulating a key step in cellular cholesterol homeostasis.
44 ions and represents a consequence of altered cholesterol homeostasis.
45 em for the maintenance of total body fat and cholesterol homeostasis.
46 R) signaling pathway regulates bile acid and cholesterol homeostasis.
47 ellular sterol trafficking and regulation of cholesterol homeostasis.
48 polipoprotein E (apoE) is a key regulator of cholesterol homeostasis.
49  is crucial for regulating genes involved in cholesterol homeostasis.
50 ce the toxic effects of arsenic on lipid and cholesterol homeostasis.
51         It plays important roles in cellular cholesterol homeostasis.
52  crucial roles in lipoprotein metabolism and cholesterol homeostasis.
53  These findings identified a novel lncRNA in cholesterol homeostasis.
54 st in part, through the regulation of plasma cholesterol homeostasis.
55 l and phytosterols and plays a major role in cholesterol homeostasis.
56 chanisms by which PPARs influence macrophage cholesterol homeostasis.
57 ile acids, which is critical for maintaining cholesterol homeostasis.
58 retroendocytic transporter for regulation of cholesterol homeostasis.
59 or (FXR), which is an important regulator of cholesterol homeostasis.
60 R) to signal cholesterol excess and maintain cholesterol homeostasis.
61 r importance to the regulation of whole body cholesterol homeostasis.
62 totoxic death as a result of changes in cell cholesterol homeostasis.
63  that contain sterol sensors are involved in cholesterol homeostasis.
64  in transcytosis, and in regulating cellular cholesterol homeostasis.
65 oid X receptors (FXR), which are involved in cholesterol homeostasis.
66 ous literature suggests that LRP-1 regulates cholesterol homeostasis.
67 ent and synthesis rate while preserving host cholesterol homeostasis.
68 ing GM-CSF signalling, immune modulation and cholesterol homeostasis.
69 , including PCSK9, an important regulator of cholesterol homeostasis.
70 accumulation defects in cells with disrupted cholesterol homeostasis.
71 is plays a key role in regulating whole body cholesterol homeostasis.
72 f the unfolded protein response, and altered cholesterol homeostasis.
73 1, an enzyme involved in regulating cellular cholesterol homeostasis.
74 g protein recently found to be implicated in cholesterol homeostasis.
75 scription factor SREBP2, master regulator of cholesterol homeostasis.
76  and over time causes disruption in cellular cholesterol homeostasis.
77 hile LXRalpha has its most marked effects on cholesterol homeostasis.
78 multiple pan-coronavirus factors involved in cholesterol homeostasis.
79  development of mechanisms for intracellular cholesterol homeostasis.
80 iptional regulators of cellular and systemic cholesterol homeostasis.
81 ne expression associated with the control of cholesterol homeostasis.
82 , as well as phosphoinositide signalling and cholesterol homeostasis.
83 ular Loop1-Loop7 binding, a central event in cholesterol homeostasis.
84 e diet to characterize the role in lipid and cholesterol homeostasis.
85 fflux from cells and regulates intracellular cholesterol homeostasis.
86  engulfment of apoptotic cells [8-13] and to cholesterol homeostasis [14].
87  the ER and thereby has an essential role in cholesterol homeostasis(2,3).
88 levels in cell cultures requires normal cell cholesterol homeostasis; 2) HA degradation may contribut
89                         They are crucial for cholesterol homeostasis, a major lipid constituent of my
90 rmacologic approaches in an attempt to alter cholesterol homeostasis across the CNS.
91 ed LDL/cholesterol and altered intracellular cholesterol homeostasis also causes chromosomal instabil
92 rosclerosis, we have asked whether disrupted cholesterol homeostasis alters HA accumulation in low de
93     This assay provides a new tool to assess cholesterol homeostasis among tissues in humans.
94 d with I1061T-NPC1 leading to restoration of cholesterol homeostasis, an effect that is largely drive
95  These findings reveal Nrf1 as a guardian of cholesterol homeostasis and a core component of adaptive
96 ts a mechanistic link between apoE-regulated cholesterol homeostasis and Abeta degradation.
97 ings identify ABCG1 as a novel integrator of cholesterol homeostasis and adaptive immune programs.
98  demonstrates that adipose LAL drives tissue-cholesterol homeostasis and affects BAT metabolism, sugg
99 ernative splicing as a modulator of cellular cholesterol homeostasis and as an underlying mechanism o
100                  However, its role in plasma cholesterol homeostasis and atherosclerosis has not been
101 ase (ACAT) is an enzyme involved in cellular cholesterol homeostasis and atherosclerosis.
102 he critical role of beta-cell ABCA1 in islet cholesterol homeostasis and beta-cell function and highl
103                 LXRs play a critical role in cholesterol homeostasis and bile acid metabolism.
104 n the tumour, and illustrates a link between cholesterol homeostasis and cancer.
105 phan nuclear receptor (NR5A2) that regulates cholesterol homeostasis and cell plasticity in endoderma
106                             The link between cholesterol homeostasis and cleavage of the amyloid prec
107 y lipoprotein receptor (LDLR) is crucial for cholesterol homeostasis and deficiency in LDLR functions
108 et al. here identify effects of Wolbachia on cholesterol homeostasis and dengue virus replication in
109 rogenitor cells (OPCs), Lrp1 is required for cholesterol homeostasis and differentiation into mature
110 ation-defective RID-alpha mutant deregulates cholesterol homeostasis and elicits lysosomal storage ab
111 lators of lipid metabolism genes involved in cholesterol homeostasis and fatty acid oxidation.
112 e Tangier disease characterized by defective cholesterol homeostasis and high density lipoprotein (HD
113 ors or LXRs are key modulators of macrophage cholesterol homeostasis and immune responses.
114 mechanism by which perturbation of beta-cell cholesterol homeostasis and impaired insulin secretion i
115  regulating both macrophage inflammation and cholesterol homeostasis and implicate IL-19 as a link be
116  the physiological significance of UBIAD1 in cholesterol homeostasis and indicate inhibition of HMGCR
117 icates coordinated and reciprocal control of cholesterol homeostasis and inflammatory pathways.
118  with OSBP, thereby disrupting intracellular cholesterol homeostasis and inhibiting viral entry.
119 ay also be important in regulating beta-cell cholesterol homeostasis and insulin secretion.
120 s an important role in controlling lipid and cholesterol homeostasis and is a potential target for th
121  in high density lipoprotein (HDL) regulates cholesterol homeostasis and is protective against athero
122 for participation of small noncoding RNAs in cholesterol homeostasis and is the first to implicate a
123 preclinical data, focusing on alterations in cholesterol homeostasis and its consequent effect on pat
124  role of microbiota in regulating whole-body cholesterol homeostasis and its response to a cholestero
125     We conclude that PP2A activity regulates cholesterol homeostasis and LDL-C uptake.
126 able insights into the mechanisms regulating cholesterol homeostasis and LDLR trafficking.
127                    Despite central roles for cholesterol homeostasis and lipid metabolism, their func
128 iption factors that induce genes controlling cholesterol homeostasis and lipogenesis.
129 s; however, a potential link between altered cholesterol homeostasis and platelet production has not
130 a and beta are transcriptional regulators of cholesterol homeostasis and potential targets for the de
131 epatic FXR by FGF15/19-induced Src maintains cholesterol homeostasis and protects against atheroscler
132 These results reveal a new facet of cellular cholesterol homeostasis and provide a potential explanat
133 ing how SHP interacts with LRH-1 to regulate cholesterol homeostasis and provide new insights into ho
134  obesity is associated with abnormal hepatic cholesterol homeostasis and resistance to leptin action.
135 concert with the SREBP host genes to control cholesterol homeostasis and suggest that miR-33 may repr
136 development of atherosclerosis by regulating cholesterol homeostasis and suppressing inflammatory gen
137 ificance of hepatic CPR-dependent enzymes in cholesterol homeostasis and systemic drug clearance, and
138 ion in caveolae via actions on both membrane cholesterol homeostasis and the level of activation of t
139  have been implicated in regulating cellular cholesterol homeostasis and therefore play critical role
140                                              Cholesterol homeostasis and trafficking are critical to
141  Cyp7a1 plays a critical role in maintaining cholesterol homeostasis and underscores the importance o
142 , type I (SR-BI) in the modulation of global cholesterol homeostasis and vascular cell function, and
143 rter ABCG1 has an essential role in cellular cholesterol homeostasis, and dysregulation has been asso
144 oxidation of fatty acids, fatty acid uptake, cholesterol homeostasis, and lipogenesis.
145 ng their own biosynthesis, lipid absorption, cholesterol homeostasis, and local mucosal defenses in t
146 ous biochemical processes such as secretion, cholesterol homeostasis, and regulation of chromatin str
147 ear receptors that are central regulators of cholesterol homeostasis, and synthetic LXR agonists have
148 trol of growth signaling pathways, lipid and cholesterol homeostasis, and the breakdown of xenobiotic
149  targets the Golgi complex and disrupts cell cholesterol homeostasis, and this action of Abeta-(1-42)
150 lipoproteins, how it helps maintain cellular cholesterol homeostasis, and, finally, how it is catabol
151 ctions, including autophagosome degradation, cholesterol homeostasis, antigen presentation, and cell
152 of Wwox involve multiple pathways, including cholesterol homeostasis, ApoA-I/ABCA1 pathway, and fatty
153 tion of lipofuscin bisretinoids and abnormal cholesterol homeostasis are implicated in macular degene
154       Our genetic screen therefore points to cholesterol homeostasis as a potential target for the tr
155 sphatidylinositol phosphate biosynthesis and cholesterol homeostasis as critical host pathways suppor
156 eptor agonists, which regulate intracellular cholesterol homeostasis, augment PKA agonist- or high ph
157 erferes with normal human cell life, such as cholesterol homeostasis, blood coagulation, EGFR binding
158 ole for Aup1 in maintenance of intracellular cholesterol homeostasis, but they also highlight the clo
159 ts demonstrate that changes in intracellular cholesterol homeostasis by ABCG1 profoundly impact iNKT
160  that selected dietary plant sterols disrupt cholesterol homeostasis by affecting two critical regula
161 n receptor (LDLR) plays a key role in plasma cholesterol homeostasis by binding and internalizing lip
162 plasmic reticulum that play crucial roles in cholesterol homeostasis by inhibiting excessive choleste
163 he gallbladder may have a role in regulating cholesterol homeostasis by modulating the physical forms
164  and pro-oxidative factor, alters macrophage cholesterol homeostasis by repressing ABCA1 to promote f
165 the endoplasmic reticulum (ER) that controls cholesterol homeostasis by transporting sterol regulator
166 tion that MDCKII cells respond to changes in cholesterol homeostasis by up-regulating a pathway for c
167      Moreover, drug-induced perturbations of cholesterol homeostasis cause mitochondrial DNA disorgan
168                             Impaired hepatic cholesterol homeostasis causes intracellular free choles
169 n localization with such varied processes as cholesterol homeostasis, cell signalling and cytokinesis
170 F therefore plays a central role in cellular cholesterol homeostasis coordinating Rab7 activation, en
171 f CETP biosynthesis in cells alters cellular cholesterol homeostasis, demonstrating an intracellular
172 tion, the extent to which it impacts hepatic cholesterol homeostasis depends on cholesterol intake.
173 tors function as bidirectional regulators of cholesterol homeostasis, driving efflux when cholesterol
174 ancy outcome, with possible implications for cholesterol homeostasis during human pregnancy.
175 R-125a-5p have been implicated in regulating cholesterol homeostasis, fatty acid metabolism and lipog
176 l in cancer, with several demonstrating that cholesterol homeostasis genes can modulate development.
177  differential expression of inflammatory and cholesterol homeostasis genes in the macrophage subpopul
178                   Daidzein also elevated the cholesterol homeostasis genes in the poststroke brain wi
179                                              Cholesterol homeostasis genes that require LXR for expre
180 odeling, we found that daidzein enhanced the cholesterol homeostasis genetic program, including Lxr a
181 ant roles in the regulation of bile acid and cholesterol homeostasis, glucose metabolism, and insulin
182                                Altered brain cholesterol homeostasis has been implicated in Huntingto
183                                    Disrupted cholesterol homeostasis has been reported in Alzheimer d
184 s (LXRs), one cellular mechanism to regulate cholesterol homeostasis, has been found to alter Abeta l
185    Apolipoprotein E (ApoE), a key ligand for cholesterol homeostasis, has been shown to interact with
186           Apolipoprotein E, a key ligand for cholesterol homeostasis, has been shown to interact with
187                  Their beneficial effects on cholesterol homeostasis have made these transporters imp
188                                       Intact cholesterol homeostasis helps to maintain hematopoietic
189 d its apolipoproteins in regulating cellular cholesterol homeostasis, highlighting recent advances on
190             Whether mTOR is also affected by cholesterol homeostasis, however, has remained unknown.
191  the products of which control bile acid and cholesterol homeostasis; however, the role of DRIP205 in
192 get of oAbeta(42), directly linking Abeta to cholesterol homeostasis impairment.
193 rovided evidence for the alteration of brain cholesterol homeostasis in 129.Mecp2-null mice, an exper
194 ion in the developing pancreas and maintains cholesterol homeostasis in adults.
195 loping brain may be due to the disruption of cholesterol homeostasis in astrocytes.
196 direct evidence of a role for maintenance of cholesterol homeostasis in bone health.
197   We found that CtBP regulates intracellular cholesterol homeostasis in breast cancer cells by formin
198 ypes suggested a potential role of disrupted cholesterol homeostasis in cancer development but additi
199            In this report, we have evaluated cholesterol homeostasis in Cav1 knock-out mice.
200 -apoE interactions may contribute to overall cholesterol homeostasis in cells and tissues that expres
201 ke-induced behavioral deficits via enhancing cholesterol homeostasis in chronic stroke, and this occu
202 n-2 and -1 genes, respectively, and regulate cholesterol homeostasis in concert with their host genes
203                                  It restores cholesterol homeostasis in cultured NPC1 mutant fibrobla
204 hanism of bile acid signaling in maintaining cholesterol homeostasis in Cyp7a1-tg mice.
205  tractable tool to explore the complexity of cholesterol homeostasis in eukaryotic cells and to devel
206 ive of oxidative stress and dysregulation of cholesterol homeostasis in fish from polluted sites.
207 xpression of NRs and other genes involved in cholesterol homeostasis in freshly isolated and cultured
208 As in lipid- associated DNA regions regulate cholesterol homeostasis in hepatocytes.
209 eased cholesterol activates LXRs to maintain cholesterol homeostasis in highly-dense glioblastoma cel
210 tical role for pancreatic beta cell-specific cholesterol homeostasis in insulin secretion as well as
211 pha and LXRbeta) are important regulators of cholesterol homeostasis in liver and macrophages.
212 the function of Insig proteins in regulating cholesterol homeostasis in mammalian cells.
213                                              Cholesterol homeostasis in mammals involves pathways for
214 SORT1 may be beneficial in improving hepatic cholesterol homeostasis in metabolic and inflammatory li
215 BP-dependent gene regulation governing lipid/cholesterol homeostasis in metazoans in response to fast
216 ptor protein expression, and restored plasma cholesterol homeostasis in mice lacking a functional liv
217 vious studies suggest that AHR ligands alter cholesterol homeostasis in mice through repression of ge
218                     We have now investigated cholesterol homeostasis in NPC1-deficient cells of the b
219  developmental myelination through targeting cholesterol homeostasis in OLCs.
220             However, 0.1 and 1 mm CD altered cholesterol homeostasis in opposite directions.
221 ent of lipoproteins that plays a key role in cholesterol homeostasis in plasma and in brain.
222 ivity and support the importance of cellular cholesterol homeostasis in regulating beta-cell insulin
223 ced block on cholesterol efflux and restores cholesterol homeostasis in RPE cells.
224 ma levels of 24S-OHC as a biomarker of brain cholesterol homeostasis in RTT.
225 ritical role for PMP22 in the maintenance of cholesterol homeostasis in Schwann cells.
226 and ABCG8 (G5G8-/- mice) profoundly perturbs cholesterol homeostasis in the adrenal gland.
227                                              Cholesterol homeostasis in the body is controlled mainly
228 holesterol absorption and the maintenance of cholesterol homeostasis in the body.
229 gest that, in addition to the involvement in cholesterol homeostasis in the brain, this enzyme may pa
230          However, complete understandings of cholesterol homeostasis in the cell remains elusive, par
231 anizing principle for signaling pathways and cholesterol homeostasis in the cell, relatively little i
232  an essential role in maintaining peripheral cholesterol homeostasis in the context of hypercholester
233 sm suggests that TTF-1 may be a modulator of cholesterol homeostasis in the lung.
234 hat peroxisomes are critical for maintaining cholesterol homeostasis in the neonatal mouse.
235 ng cassette transporter G1 (ABCG1) regulates cholesterol homeostasis in thymocytes and peripheral CD4
236 he first report that cowpea peptides inhibit cholesterol homeostasis in vitro in two distinct routes,
237 s to beta-cell function by maintaining islet cholesterol homeostasis in vivo.
238 patic TFEB nuclear localization and improves cholesterol homeostasis in Western diet-fed mice.
239 n ileal FGF15/19 to hepatocyte FGFR4 axis in cholesterol homeostasis, in metabolic homeostasis in viv
240  the integration of mitochondria in cellular cholesterol homeostasis, in which ATAD3 plays a critical
241 lic disorders associated with aberrant lipid/cholesterol homeostasis, including metabolic syndrome an
242 s of CYP27A1 led to dysregulation of retinal cholesterol homeostasis, including unexpected upregulati
243  role of the intestine in the maintenance of cholesterol homeostasis increasingly is recognized.
244 eport validation of Usf1 as a causal gene of cholesterol homeostasis, insulin sensitivity and body co
245 d the potential of therapeutically targeting cholesterol homeostasis is a controversial area in the c
246 atients and mice models of AD suggested that cholesterol homeostasis is altered in neurons that accum
247                  Thus, proper control of LDL-cholesterol homeostasis is critical for organismal healt
248                                     Cellular cholesterol homeostasis is important for normal beta-cel
249                                     Cellular cholesterol homeostasis is maintained by Scap, an endopl
250                                              Cholesterol homeostasis is maintained through concerted
251    In light of our findings we postulate how cholesterol homeostasis is maintained within the cell an
252                                              Cholesterol homeostasis is mediated by Scap, a polytopic
253                       This demonstrates that cholesterol homeostasis is modified in BPDCN and can be
254 the role of NPC1L1 in maintaining whole body cholesterol homeostasis is not known.
255 ossible mechanism for HD neurotoxicity where cholesterol homeostasis is perturbed.
256 olesterol is present in the plasma membrane, cholesterol homeostasis is principally regulated through
257                                              Cholesterol homeostasis is regulated by a family of tran
258                                              Cholesterol homeostasis is required to maintain normal c
259 erol synthesis and uptake are repressed, and cholesterol homeostasis is restored.
260  of seminiferous epithelium, and disorder of cholesterol homeostasis, is uniformly accelerated upon i
261  >300 variants in the NPC1 gene that disrupt cholesterol homeostasis leading to the rapid onset and p
262  a number of biological processes, including cholesterol homeostasis, lipid metabolism, and keratinoc
263                                      Because cholesterol homeostasis may have an essential role in ce
264 ctions related to nucleoid and mitochondrial cholesterol homeostasis, modified the distribution of ch
265 perfamily whose members function in cellular cholesterol homeostasis (Niemann-Pick C1) and Hedgehog s
266 ite the significance of this interaction for cholesterol homeostasis, no structure of either ARH or t
267 uclear liver X receptor (LXR) helps maintain cholesterol homeostasis, not only through promotion of c
268         As a sensor regulating intracellular cholesterol homeostasis, nuclear receptor LXR-alpha was
269  These results suggested that intrapulmonary cholesterol homeostasis, other than systematic cholester
270  proteins, extending the known repertoire of cholesterol homeostasis players.
271 ignaling plays a role in modulating cellular cholesterol homeostasis, PM biophysical properties, and
272 regulatory mechanism contributes to maintain cholesterol homeostasis preventing excessive cholesterol
273 ovel, cell cycle mechanism by which aberrant cholesterol homeostasis promotes neurodegeneration and a
274                                 Dysregulated cholesterol homeostasis promotes the pathology of athero
275 hibition of phosphatidylinositol kinases and cholesterol homeostasis reduced replication of all three
276                                     Cellular cholesterol homeostasis regulates endoproteolytic genera
277 d by STARD4 is an important component of the cholesterol homeostasis regulatory machinery.
278 regulate variant trafficking, stability, and cholesterol homeostasis, results consistent with the rol
279 ntified a dysregulation of genes involved in cholesterol homeostasis, some of them being liver X rece
280 leviates mitochondrial dysfunction, aberrant cholesterol homeostasis, striatal atrophy, impaired dopa
281 idence support the notion that alteration of cholesterol homeostasis strongly predisposes to Alzheime
282 decrease in ubiquinone levels and changes in cholesterol homeostasis suggest that mevalonate pathway
283       Here, I offer personal perspectives on cholesterol homeostasis that reflect my belief that cert
284  receptors are involved in the regulation of cholesterol homeostasis, the combination of higher chole
285  Treatment with 5-AzaC disturbed subcellular cholesterol homeostasis, thereby impeding activation of
286    In contrast, wild-type animals maintained cholesterol homeostasis through basal expression of gene
287  HIV-1 transcription in T cells is linked to cholesterol homeostasis through control of TFII-I expres
288 through which the biological clock regulates cholesterol homeostasis through its regulation of non-rh
289 olecules that play a major role in mediating cholesterol homeostasis through mechanisms which have no
290  post-transcriptional mechanisms that assure cholesterol homeostasis through their sterol-induced bin
291 ntial role in LDL-C (low-density lipoprotein cholesterol) homeostasis through regulating the PCSK9 (p
292          Thus, IFITM3 disrupts intracellular cholesterol homeostasis to block viral entry, further un
293 olecular basis for the link between Arf6 and cholesterol homeostasis using an inducible knockout (KO)
294 volved in cholesterol synthesis and cellular cholesterol homeostasis using comprehensive two-dimensio
295                  Rexinoids affect intestinal cholesterol homeostasis via two receptors: retinoic acid
296 ons contribute to the regulation of cellular cholesterol homeostasis, we synthesized the enantiomer o
297 ith 0.1 to 10 mm CD after which survival and cholesterol homeostasis were monitored.
298 renatal growth and nutrition influence adult cholesterol homeostasis, whether prenatal growth modifie
299 inding protein (OSBP) regulate intracellular cholesterol homeostasis, which is required for many viru
300 nistically link the regulation of macrophage cholesterol homeostasis with defective efferocytosis.

 
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