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1 t play a key role in cellular and organismal lipid homeostasis.
2 ein-folding environment and maintain hepatic lipid homeostasis.
3  to uncover new players in the regulation of lipid homeostasis.
4 iption factors in the context of glucose and lipid homeostasis.
5 g cellular metabolism, including glucose and lipid homeostasis.
6 ochondrial sirtuin, SIRT4, as a regulator of lipid homeostasis.
7 d carbohydrate metabolism and FXR-controlled lipid homeostasis.
8 se metabolic pathways, including glucose and lipid homeostasis.
9  results establish a role for calcineurin in lipid homeostasis.
10 activity and expression of genes involved in lipid homeostasis.
11 role in maintaining intracellular sterol and lipid homeostasis.
12 as aeruginosa to decode ORF PA0919-dependent lipid homeostasis.
13 n, chemical transport, energy metabolism and lipid homeostasis.
14  developed alveolar proteinosis with altered lipid homeostasis.
15 in regulating both normal and FXR-controlled lipid homeostasis.
16 r this enzyme in membrane lipid turnover and lipid homeostasis.
17  play an important role in the regulation of lipid homeostasis.
18  and improves several aspects of glucose and lipid homeostasis.
19 nsulin sensitivity and maintains glucose and lipid homeostasis.
20  of several key intestinal genes involved in lipid homeostasis.
21 ink ABCG1 to diseases of dysregulated tissue lipid homeostasis.
22 cular links between bile acid metabolism and lipid homeostasis.
23 s and tissues to provide energy and maintain lipid homeostasis.
24 c metabolism as well as hormone, energy, and lipid homeostasis.
25  platelets with functions in glutathione and lipid homeostasis.
26  the insulin signaling pathway in regulating lipid homeostasis.
27 ects the dynamics of cellular and whole-body lipid homeostasis.
28  of functional CYP4V2 in HepG2 cells altered lipid homeostasis.
29  complex diseases, including those affecting lipid homeostasis.
30  critical strategy used by cells to maintain lipid homeostasis.
31 Scly in a mouse affected hepatic glucose and lipid homeostasis.
32 egulated genes, and dysregulation of hepatic lipid homeostasis.
33 onality and for maintenance of mitochondrial lipid homeostasis.
34 nounsaturated fatty acids and is crucial for lipid homeostasis.
35 A negated the HCV-induced alteration of host lipid homeostasis.
36  gene expression required for normal hepatic lipid homeostasis.
37 ant role in MAPK-mediated control of hepatic lipid homeostasis.
38 in the ctl1 mutant, linking CTL1 function to lipid homeostasis.
39 es have highlighted mTORC1 as a regulator of lipid homeostasis.
40 that is critically relevant to pneumonia and lipid homeostasis.
41 ther lipids and are critical for maintaining lipid homeostasis.
42 egulate the hepatic acute-phase response and lipid homeostasis.
43  the regulation of xenobiotic metabolism and lipid homeostasis.
44 utant mice exhibit associated alterations in lipid homeostasis.
45  an important hormone regulating glucose and lipid homeostasis.
46 n to be involved in VLDL assembly or hepatic lipid homeostasis.
47 an important role in maintaining glucose and lipid homeostasis.
48 and highlights the role of adipose tissue in lipid homeostasis.
49 d KLF6 as mediator of hepatocyte glucose and lipid homeostasis.
50 n of sPLA(2) and subsequent local changes in lipid homeostasis.
51  these beneficial effects of zinc on hepatic lipid homeostasis.
52 ceride transfer protein in plasma and tissue lipid homeostasis.
53 ent fashion, implicating a role of LPCAT3 in lipid homeostasis.
54 ges and plays an important role in pulmonary lipid homeostasis.
55 emodeling may potentially impact glucose and lipid homeostasis.
56 phan nuclear receptors in their mediation of lipid homeostasis.
57 etabolic transcription factors that regulate lipid homeostasis.
58  whereas LXRs are sterol sensors that affect lipid homeostasis.
59 ranscription factors that play a key role in lipid homeostasis.
60 by this protein functions to modulate plasma lipid homeostasis.
61 sors and regulate whole-body cholesterol and lipid homeostasis.
62 ivation, airspace remodeling, and surfactant lipid homeostasis.
63 dentify ABCG1 as a key regulator of cellular lipid homeostasis.
64 trophin (CT)-1 is a regulator of glucose and lipid homeostasis.
65 spectively, act together to maintain hepatic lipid homeostasis.
66 ontrolling both systemic and tissue-specific lipid homeostasis.
67  role in regulating cellular cholesterol and lipid homeostasis.
68 function as a metabolic sensor in regulating lipid homeostasis.
69 hat ABCG1 plays essential roles in pulmonary lipid homeostasis.
70 cids and that mutations in this locus affect lipid homeostasis.
71 al for this sustained VLDL-TAG secretion and lipid homeostasis.
72 at PXR plays an endobiotic role by impacting lipid homeostasis.
73 han nuclear receptors in their regulation of lipid homeostasis.
74 ping metabolic effects in the maintenance of lipid homeostasis.
75 nalogous effects on both liver and intestine lipid homeostasis.
76 at encode proteins critical to intracellular lipid homeostasis.
77 h-density lipoprotein (HDL) biosynthesis and lipid homeostasis.
78 esponsible for regulating genes that control lipid homeostasis.
79  to control bile acid synthesis and maintain lipid homeostasis.
80 ests a link between lipid-droplet motion and lipid homeostasis.
81 unique adaptation associated with vertebrate lipid homeostasis.
82 PROX1 control expression of genes regulating lipid homeostasis.
83 erilipin, LSD2 is responsible for regulating lipid homeostasis.
84 e insulin sensitizers with the regulation of lipid homeostasis.
85 nsulin sensitization/glucose homeostasis and lipid homeostasis.
86 es and hepatocytes is pivotal for whole-body lipid homeostasis.
87 DL) play a major role in maintaining overall lipid homeostasis.
88 om the TGN to the PM through its function in lipid homeostasis.
89 rotein that functions in innate immunity and lipid homeostasis.
90 nd peroxisomes for organelle maintenance and lipid homeostasis.
91 een characterized and shown to play roles in lipid homeostasis.
92 on, parasite defense, epithelial repair, and lipid homeostasis.
93 otein (SREBP) transcription factors regulate lipid homeostasis.
94 solic folding environment through changes in lipid homeostasis.
95  represents a novel regulatory mechanism for lipid homeostasis.
96 d oxidation in muscle and impair glucose and lipid homeostasis.
97 he important role of PARP-1 on LXR-regulated lipid homeostasis.
98 isms evaluate oxygen availability to control lipid homeostasis.
99 metabolism in the germline with whole-animal lipid homeostasis.
100  regulators of genes involved in cholesterol/lipid homeostasis.
101 d cancer, which display prominent defects in lipid homeostasis.
102 2 crosstalk is essential to maintain hepatic lipid homeostasis.
103 cating a direct effect of HCV replication on lipid homeostasis.
104 anscriptional activity in regulating hepatic lipid homeostasis.
105 REBP), the master regulator of intracellular lipid homeostasis.
106 s demonstrated benefits for both glucose and lipid homeostasis.
107 lar signaling, cell survival and protein and lipid homeostasis.
108 nd other membranes help to maintain membrane lipid homeostasis.
109 ese relations to the maintenance of systemic lipid homeostasis.
110 siological function of MGAT3 and its role in lipid homeostasis.
111 insulinopenic conditions to maintain minimal lipid homeostasis.
112 is pathway may link outer membrane fusion to lipids homeostasis.
113 f RNA polymerase (pol) III and intracellular lipid homeostasis across species.
114 peptides toward normalization of glucose and lipid homeostasis after duodenal bypass surgery.
115  fluid lipid domains (RIFs) perturbs overall lipid homeostasis and affects membrane protein localizat
116  critical role for LRP1 in maintaining brain lipid homeostasis and associated synaptic and neuronal i
117 pase A (OmpLA) is involved in outer-membrane lipid homeostasis and bacterial virulence.
118 ein factors, critically influencing systemic lipid homeostasis and biochemically contributing many me
119  conclude that SWS is essential for membrane lipid homeostasis and cell survival in both neurons and
120    Overall, chronic CETP deficiency disrupts lipid homeostasis and compromises the TG storage functio
121  be an alternate pathway leading to improved lipid homeostasis and controlled downstream insulin sign
122 a structural protein of caveolae involved in lipid homeostasis and endocytosis.
123 ator of PPARgamma activation and function in lipid homeostasis and energy expenditure.
124  PGC-1alpha expression in the maintenance of lipid homeostasis and glucose metabolism.
125  Lipin-1 and lipin-2 are required for normal lipid homeostasis and have unique physiological roles.
126 tional role for both HSL and ATGL in hepatic lipid homeostasis and identifies these enzymes as potent
127 er X receptors (LXRs) exert key functions in lipid homeostasis and in control of inflammation.
128 se benefits might result from regulations of lipid homeostasis and increased faecal bile-acid outputs
129 in respiratory epithelial cells altered lung lipid homeostasis and induced compensatory lipid accumul
130                                              Lipid homeostasis and inflammation are key determinants
131 at mediates bidirectional cross-talk between lipid homeostasis and inflammation.
132 lism plays an important role for glucose and lipid homeostasis and its alterations contribute to meta
133 ensity alters blood pressure and glucose and lipid homeostasis and limits adaption to obesogenic diet
134 l to explore regulatory mechanisms governing lipid homeostasis and lipid trafficking in plants.
135 sterol sensors that regulate cholesterol and lipid homeostasis and macrophage functions.
136  that have a well-defined role in regulating lipid homeostasis and metabolic diseases.
137                                              Lipid homeostasis and metabolism are closely related to
138  of energy metabolism, including glucose and lipid homeostasis and mitochondrial oxidative metabolism
139 mino acid metabolism, its endogenous role in lipid homeostasis and muscle physiology is unknown.
140 ied differential actions of ILP7 and ILP8 in lipid homeostasis and ovarian development.
141 for an important physiologic role for GIP in lipid homeostasis and possibly in the pathogenesis of ob
142  to increase bile acid synthesis to maintain lipid homeostasis and prevent nonalcoholic fatty liver d
143 ER) membrane proteins play a central role in lipid homeostasis and protein quality control.
144 perturbed but critical switch in controlling lipid homeostasis and provide a new hope for the develop
145 gression of liver regeneration by modulating lipid homeostasis and regulating hepatocyte proliferatio
146 ion yeast Schizosaccharomyces pombe regulate lipid homeostasis and the hypoxic response under conditi
147  findings have highlighted the complexity of lipid homeostasis and the important role that miRNAs pla
148 he complex interrelation between LD-mediated lipid homeostasis and the regulation of autophagy potent
149 ed, Lp-PLA2 may be an important link between lipid homeostasis and the vascular inflammatory response
150 SCs led to abnormalities in nerve energy and lipid homeostasis and to increased lactate release.
151 ssfully identified known kinases involved in lipid homeostasis and uncovered new ones.
152 otein convertase with essential functions in lipid homeostasis and unfolded protein response pathways
153                                       Hence, lipid-homeostasis and antioxidant abilities of CLHs in t
154 C mice had reduced adiposity, impaired serum lipid homeostasis, and a higher respiratory exchange rat
155 bolic functions such as ER-PM communication, lipid homeostasis, and Ca(2+) influx.
156 target genes involved in metabolic pathways, lipid homeostasis, and carcinogenesis.
157  Glucocorticoids are important regulators of lipid homeostasis, and chronically elevated glucocortico
158 rvival, intracellular signaling, protein and lipid homeostasis, and clotting processes.
159  the expression of a gene program regulating lipid homeostasis, and hepatic-specific ablation of eith
160 BP activity is tightly regulated to maintain lipid homeostasis, and is modulated upon extracellular s
161                     Here, choline transport, lipid homeostasis, and mitochondria function were analyz
162 ovel role for Lrp1 in peroxisome biogenesis, lipid homeostasis, and OPC differentiation during white
163 ritical role in the regulation of energy and lipid homeostasis, and promotes the development of metab
164 we have identified several critical genes in lipid homeostasis (Apoa1, Apoa2 and ApoF) that are repre
165 in vitro and in vivo functions of apoA-I and lipid homeostasis are discussed.
166 ory pathways required to maintain eukaryotic lipid homeostasis are largely unknown.
167 normal cellular function, and disruptions in lipid homeostasis are linked to the progression of sever
168 The hormone FGF21 regulates carbohydrate and lipid homeostasis as well as body weight, and increasing
169 s sterol sensors that impact cholesterol and lipid homeostasis, as well as inflammation.
170 wn/beige adipocyte formation and glucose and lipid homeostasis, as well as the involvement of retinoi
171 e Dicer1 cKO epididymis displayed an altered lipid homeostasis associated with a 0.6-fold reduction i
172  superfamily members, IFNs and caspases; (b) lipid homeostasis associated with the transcription fact
173 vestigate the effects of alcohol exposure on lipid homeostasis at the white adipose tissue (WAT)-live
174 ogically associated proteins are involved in lipid homeostasis, be it in lipid transport, incorporati
175 mportant beneficial regulator of glucose and lipid homeostasis but its levels are also abnormally inc
176 degeneration is also connected to changes in lipid homeostasis, but how these are related to PINK1-in
177 22) is abundant in the liver and involved in lipid homeostasis, but its relevance to the long-term ri
178  and have emerged as important modulators of lipid homeostasis, but the extent of their role has not
179 that CD36 plays an important role in hepatic lipid homeostasis, but the results have been conflicting
180                           The disturbance of lipid homeostasis by altered sphingolipid levels may be
181                 We show that MeCP2 regulates lipid homeostasis by anchoring the repressor complex con
182 aromyces cerevisiae, plays a crucial role in lipid homeostasis by controlling the relative proportion
183 but also lead to a more complex imbalance in lipid homeostasis by disturbing PI4P metabolism.
184                            The regulation of lipid homeostasis by insulin is mediated in part by the
185                            The regulation of lipid homeostasis by insulin is mediated in part by the
186 s that CREBH plays a key role in maintaining lipid homeostasis by regulating the expression of the ge
187 lue lupin proteins appear to affect cellular lipid homeostasis by up-regulating SREBP-2 and CYP7A1 ge
188 e maturation with alterations in glucose and lipid homeostasis characterized by reduced glycogen stor
189 alpha (PPARalpha), in addition to regulating lipid homeostasis, controls the level of tissue damage a
190 g1 or Insig2 did not alter SREBP activity or lipid homeostasis, deletion of both genes (Insig1/2(Delt
191 free fatty acids have key roles in governing lipid homeostasis during exercise.
192 ains carrying mutations in genes involved in lipid homeostasis enhanced sterility phenotypes, while m
193  indicated that ABCG1 was crucial for tissue lipid homeostasis, especially in the lung.
194 ers the circadian oscillation of glucose and lipid homeostasis genes.
195 ndance for genes associated with glucose and lipid homeostasis (GLUT4, IRS1, FASN, ACACA, FATP2, CD36
196 t programs of gene expression and control of lipid homeostasis has been unclear.
197                              Altered hepatic lipid homeostasis, hepatocellular injury, and inflammati
198 his review we elucidate the role of PCSK9 in lipid homeostasis, highlight the impact of PCSK9 on athe
199  (FOXOs) have been implicated in glucose and lipid homeostasis; however, the role of FOXOs in the dev
200 an610-Quad and an iSelect panel enriched for lipid homeostasis, hypertension, and drug metabolism gen
201 lucidates SIRT4 as an important regulator of lipid homeostasis, identifies MCD as a SIRT4 target, and
202 teins in the regulatory system that mediates lipid homeostasis in animal cells.
203  modulates both LD size and cellular neutral lipid homeostasis in both leaves and seeds.
204  To test the hypothesis that perturbation of lipid homeostasis in cardiomyocytes contributes to cardi
205 REBP)-encoding genes and control cholesterol/lipid homeostasis in concert with their host gene produc
206 tively, have recently been shown to regulate lipid homeostasis in concert with their host genes.
207 aims to investigate the effects of 25HC3S on lipid homeostasis in diet-induced NAFLD mouse models.
208      Circulating AKH levels in turn regulate lipid homeostasis in fat body/adipose and the intestine.
209 patocellular uptake of LCFAs, and thus liver lipid homeostasis in general, is largely a protein-media
210 d be broadly applied to investigate neuronal lipid homeostasis in healthy and diseased brains.
211  C-associated inflammation and alteration of lipid homeostasis in infected cells.
212  intermediates, thereby maintaining membrane lipid homeostasis in leaves.
213 gest that myonectin links skeletal muscle to lipid homeostasis in liver and adipose tissue in respons
214 the effect of the loss of TAK1 expression on lipid homeostasis in liver and adipose tissues.
215 ta/delta function as important regulators of lipid homeostasis in mammals, it becomes important to as
216  (DAG) kinase that is essential for membrane lipid homeostasis in many Gram-positive pathogens.
217 s regulating expression of genes controlling lipid homeostasis in many tissues.
218 EBP-dependent gene regulation and control of lipid homeostasis in metazoans.
219                            Here, we examined lipid homeostasis in mice lacking calcineurin Abeta (CnA
220 PLIN2 expression, steatosis, and glucose and lipid homeostasis in mice with alcoholic steatosis and i
221 sent an adaptive response that preserves WAT lipid homeostasis in obese and insulin-resistant states.
222 te-derived hormone that restores glucose and lipid homeostasis in obesity-induced diabetes.
223 in, TNF-alpha, IL-6, and apolipoproteins, on lipid homeostasis in several nonadipose tissues, includi
224 scription factors regulate oxygen-responsive lipid homeostasis in the fission yeast Schizosaccharomyc
225 tance of SERCA2b in dysregulated glucose and lipid homeostasis in the liver of obese mice and suggest
226 ative stress and, potentially, a function in lipid homeostasis in the liver.
227 t is required for mitochondrial function and lipid homeostasis in the liver.
228 roplet protein perilipin 2 (PLIN2) modulates lipid homeostasis in the liver.
229                                Consistently, lipid homeostasis in the Mwk cerebellum was found to be
230 red for proper biogenesis of LDs and neutral lipid homeostasis in vegetative tissues.
231                                              Lipid homeostasis in vertebrates is regulated by 3 stero
232 hat SKN-1 plays a direct role in maintaining lipid homeostasis in which it is activated by lipids.
233  metabolism is a key aspect of intracellular lipid homeostasis in yeast and mammals, but its role in
234 y pathway is required for maintaining proper lipid homeostasis in yeast, especially when cells are gr
235  previously unappreciated deep remodeling of lipid homeostasis, including extreme changes to phosphol
236 s (LDs), organelles specialized for cellular lipid homeostasis, increase in size and number at the on
237 nce suggests that alterations of glucose and lipid homeostasis induced by obesity are associated with
238                     The effects of 25HC3S on lipid homeostasis, inflammatory responses, and insulin s
239                             Dysregulation of lipid homeostasis is a common feature of several major h
240          The pivotal role of LDs in cellular lipid homeostasis is clearly established, but processes
241 gnals required for the regulation of hepatic lipid homeostasis is complex.
242                Previously, it was shown that lipid homeostasis is important in rotavirus replication.
243 dependent regulation of membrane and storage lipid homeostasis is only rudimentary.
244 nd adipokine gene transcription, its role in lipid homeostasis is poorly understood.
245                A key component of eukaryotic lipid homeostasis is the esterification of sterols with
246                                              Lipid homeostasis is transcriptionally regulated by thre
247 as the role of adipose tissue in glucose and lipid homeostasis is widely recognized, its role in syst
248  VAP-ligand binding couples proteostasis and lipid homeostasis leading to observed phenotypes of lipi
249 d RAR target genes involved in regulation of lipid homeostasis, leading to weight loss and improved i
250       Studies have shown that disturbance in lipid homeostasis may represent a critical determinant i
251 t may participate in functions as diverse as lipid homeostasis, membrane traffic, and signaling.
252 2A or C2C failed to rescue two defects in PM lipid homeostasis observed in E-Syts KO cells, delayed d
253  that the participation of CGI-58 in neutral lipid homeostasis of nonfat-storing tissues is similar,
254  results suggest a dependence of glucose and lipid homeostasis on Scly activity.
255                 We identify an age-dependent lipid homeostasis pathway in Caenorhabditis elegans that
256 k between growth control and the cholesterol/lipid homeostasis pathway.
257                      In the Golgi apparatus, lipid homeostasis pathways are coordinated with the biog
258 ce of miRNAs in regulating key signaling and lipid homeostasis pathways that alter the balance of ath
259 ) assembly and secretion impact intrahepatic lipid homeostasis, plasma lipoprotein profile, and energ
260 synthesis by 5-AzaC disturbs cholesterol and lipid homeostasis, probably through the glycerolipid bio
261                                These include lipid homeostasis, regulation of Ca(2+) dynamics, and co
262 stributing lipids among CNS cells for normal lipid homeostasis, repairing injured neurons, maintainin
263  various organelles, and maintenance of cell lipid homeostasis requires nimble regulation and coordin
264                                    Mammalian lipid homeostasis requires proteolytic activation of mem
265 own-regulation of ARV1 disturbs membrane and lipid homeostasis, resulting in a disruption of ER integ
266  the influencing feature of both glucose and lipid homeostasis showing case-control heterogeneity.
267 uced body mass and improved both glucose and lipid homeostasis similarly in wild-type mice compared w
268 ion pathways involved in hepatic glucose and lipid homeostasis, suggesting that this coactivator may
269 ors (LXRs) are transcriptional regulators of lipid homeostasis that also have potent anti-inflammator
270 ght loss accompanied by improved glucose and lipid homeostasis that are hallmarks of RYGB.
271 n TRAIL signaling and alteration of membrane lipid homeostasis that occurs in parallel to apical casp
272 known as C1QBP) as an important regulator of lipid homeostasis that regulates both aerobic and anaero
273    We describe a unique relationship between lipid homeostasis, the lipid-sensitive transcription fac
274             Despite its importance in plasma lipid homeostasis, the regulation of Lmf1 remains unexpl
275 KI-1)/site-1 protease (S1P) is implicated in lipid homeostasis, the unfolded protein response, and ly
276 ch fasting or glucagon stimulation modulates lipid homeostasis through acetylation of CREBH.
277 al membrane plays a crucial role in cellular lipid homeostasis through biosynthesis of the non-bilaye
278  cholesterol biosynthetic pathway regulating lipid homeostasis through both the LXR and sterol respon
279 serve as intracellular receptors that couple lipid homeostasis through interactions with two phenylal
280 al role in lipoprotein metabolism and plasma lipid homeostasis through its high-affinity binding to t
281 ver an important role for NCoR in regulating lipid homeostasis through the coordinated control of dif
282 to MICOS, combining functions in protein and lipid homeostasis to preserve mitochondrial structure an
283  thus identify Bif-1 as a novel regulator of lipid homeostasis to prevent the pathogenesis of obesity
284 germline-deficient C. elegans by maintaining lipid homeostasis to prolong life span.
285  and elevated PAP activity, which maintained lipid homeostasis under basal conditions, but led to die
286 ibonuclease, is required to maintain hepatic lipid homeostasis under ER stress conditions through rep
287 se results demonstrate that THs can regulate lipid homeostasis via autophagy and help to explain how
288  ablation and the consequent deregulation of lipid homeostasis was also shown to attenuate hepatocell
289  [CDCA]) play major roles in cholesterol and lipid homeostasis, we examined the effects of bile acids
290    Hepatic insulin signaling and glucose and lipid homeostasis were investigated.
291 s describe a novel gene involved in cellular lipid homeostasis, which effects may impact atherosclero
292 ceptor alpha (PPARalpha), a key regulator of lipid homeostasis whose transcriptional targets include
293  control membrane biogenesis by coordinating lipid homeostasis with protein quality control.
294  surprising phenotype, as it links cutaneous lipid homeostasis with whole body energy balance.
295   Circadian clocks play an important role in lipid homeostasis, with impact on various metabolic dise
296 ral role in controlling energy, glucose, and lipid homeostasis, with specialized neurons within nucle
297 nd is thought to be related to dysfunctional lipid homeostasis within those cells.
298  highlights a novel mechanism that regulates lipid homeostasis without profoundly affecting the activ
299 e kinase beyond biomineralization, including lipid homeostasis, wound healing, and cell migration and
300 mmalian liver processes, such as glucose and lipid homeostasis, xenobiotic metabolism, and regenerati

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