戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 al for this sustained VLDL-TAG secretion and lipid homeostasis.
2 nalogous effects on both liver and intestine lipid homeostasis.
3 PROX1 control expression of genes regulating lipid homeostasis.
4 DL) play a major role in maintaining overall lipid homeostasis.
5 om the TGN to the PM through its function in lipid homeostasis.
6 rotein that functions in innate immunity and lipid homeostasis.
7 nd peroxisomes for organelle maintenance and lipid homeostasis.
8 in genes that modulate synaptic signaling or lipid homeostasis.
9 een characterized and shown to play roles in lipid homeostasis.
10 on, parasite defense, epithelial repair, and lipid homeostasis.
11 otein (SREBP) transcription factors regulate lipid homeostasis.
12 solic folding environment through changes in lipid homeostasis.
13  represents a novel regulatory mechanism for lipid homeostasis.
14 d oxidation in muscle and impair glucose and lipid homeostasis.
15 he important role of PARP-1 on LXR-regulated lipid homeostasis.
16 isms evaluate oxygen availability to control lipid homeostasis.
17 metabolism in the germline with whole-animal lipid homeostasis.
18  regulators of genes involved in cholesterol/lipid homeostasis.
19 d cancer, which display prominent defects in lipid homeostasis.
20 2 crosstalk is essential to maintain hepatic lipid homeostasis.
21 cating a direct effect of HCV replication on lipid homeostasis.
22 anscriptional activity in regulating hepatic lipid homeostasis.
23 REBP), the master regulator of intracellular lipid homeostasis.
24 s demonstrated benefits for both glucose and lipid homeostasis.
25 lar signaling, cell survival and protein and lipid homeostasis.
26 nd other membranes help to maintain membrane lipid homeostasis.
27 ese relations to the maintenance of systemic lipid homeostasis.
28 siological function of MGAT3 and its role in lipid homeostasis.
29 insulinopenic conditions to maintain minimal lipid homeostasis.
30 t play a key role in cellular and organismal lipid homeostasis.
31 ein-folding environment and maintain hepatic lipid homeostasis.
32 xpression of miR-802 to maintain glucose and lipid homeostasis.
33  to uncover new players in the regulation of lipid homeostasis.
34 iption factors in the context of glucose and lipid homeostasis.
35 g cellular metabolism, including glucose and lipid homeostasis.
36 ochondrial sirtuin, SIRT4, as a regulator of lipid homeostasis.
37 d carbohydrate metabolism and FXR-controlled lipid homeostasis.
38  results establish a role for calcineurin in lipid homeostasis.
39 activity and expression of genes involved in lipid homeostasis.
40 role in maintaining intracellular sterol and lipid homeostasis.
41 as aeruginosa to decode ORF PA0919-dependent lipid homeostasis.
42 n, chemical transport, energy metabolism and lipid homeostasis.
43 in regulating both normal and FXR-controlled lipid homeostasis.
44 r this enzyme in membrane lipid turnover and lipid homeostasis.
45  play an important role in the regulation of lipid homeostasis.
46  and improves several aspects of glucose and lipid homeostasis.
47 nsulin sensitivity and maintains glucose and lipid homeostasis.
48  of several key intestinal genes involved in lipid homeostasis.
49 dyslipidemia and deranged maternal and fetal lipid homeostasis.
50 ink ABCG1 to diseases of dysregulated tissue lipid homeostasis.
51 cular links between bile acid metabolism and lipid homeostasis.
52 s and tissues to provide energy and maintain lipid homeostasis.
53 c metabolism as well as hormone, energy, and lipid homeostasis.
54 ipids for energy and are central to cellular lipid homeostasis.
55  platelets with functions in glutathione and lipid homeostasis.
56  the insulin signaling pathway in regulating lipid homeostasis.
57 ects the dynamics of cellular and whole-body lipid homeostasis.
58  of functional CYP4V2 in HepG2 cells altered lipid homeostasis.
59  complex diseases, including those affecting lipid homeostasis.
60  critical strategy used by cells to maintain lipid homeostasis.
61 Scly in a mouse affected hepatic glucose and lipid homeostasis.
62 onality and for maintenance of mitochondrial lipid homeostasis.
63 nounsaturated fatty acids and is crucial for lipid homeostasis.
64 A negated the HCV-induced alteration of host lipid homeostasis.
65  gene expression required for normal hepatic lipid homeostasis.
66 ant role in MAPK-mediated control of hepatic lipid homeostasis.
67 es have highlighted mTORC1 as a regulator of lipid homeostasis.
68 that is critically relevant to pneumonia and lipid homeostasis.
69 ites act in independent pathways to maintain lipid homeostasis.
70 ther lipids and are critical for maintaining lipid homeostasis.
71  the regulation of xenobiotic metabolism and lipid homeostasis.
72 utant mice exhibit associated alterations in lipid homeostasis.
73  an important hormone regulating glucose and lipid homeostasis.
74 n to be involved in VLDL assembly or hepatic lipid homeostasis.
75 spholipid composition and the maintenance of lipid homeostasis.
76 an important role in maintaining glucose and lipid homeostasis.
77 and highlights the role of adipose tissue in lipid homeostasis.
78 y are fundamental to our understanding of OM lipid homeostasis.
79 regulator of autophagy that controls hepatic lipid homeostasis.
80 ential role in the regulation of glucose and lipid homeostasis.
81 crophages exceeds their capacity to maintain lipid homeostasis.
82  dysregulating peroxisomal and mitochondrial lipid homeostasis.
83 um stress and impairments in cholesterol and lipid homeostasis.
84  due to their ability to improve glucose and lipid homeostasis.
85 s and is crucial for controlling LD size and lipid homeostasis.
86 NDS exposure induces profound alterations in lipid homeostasis.
87 ed in mitochondrial fission, morphology, and lipid homeostasis.
88 egulate the hepatic acute-phase response and lipid homeostasis.
89 se metabolic pathways, including glucose and lipid homeostasis.
90  developed alveolar proteinosis with altered lipid homeostasis.
91 egulated genes, and dysregulation of hepatic lipid homeostasis.
92 in the ctl1 mutant, linking CTL1 function to lipid homeostasis.
93 d KLF6 as mediator of hepatocyte glucose and lipid homeostasis.
94 trophin (CT)-1 is a regulator of glucose and lipid homeostasis.
95 is pathway may link outer membrane fusion to lipids homeostasis.
96 reveals fundamental mechanisms that maintain lipid homeostasis across metabolic states and leverages
97 f RNA polymerase (pol) III and intracellular lipid homeostasis across species.
98 peptides toward normalization of glucose and lipid homeostasis after duodenal bypass surgery.
99             Agents or therapies that restore lipid homeostasis among neurons, astrocytes, and microgl
100  fluid lipid domains (RIFs) perturbs overall lipid homeostasis and affects membrane protein localizat
101  critical role for LRP1 in maintaining brain lipid homeostasis and associated synaptic and neuronal i
102 involved in Endoplasmic Reticulum (ER)-based lipid homeostasis and autophagy.
103 pase A (OmpLA) is involved in outer-membrane lipid homeostasis and bacterial virulence.
104 ein factors, critically influencing systemic lipid homeostasis and biochemically contributing many me
105  be an alternate pathway leading to improved lipid homeostasis and controlled downstream insulin sign
106 a structural protein of caveolae involved in lipid homeostasis and endocytosis.
107 ator of PPARgamma activation and function in lipid homeostasis and energy expenditure.
108  PGC-1alpha expression in the maintenance of lipid homeostasis and glucose metabolism.
109 provided new insights into the regulation of lipid homeostasis and has revealed new molecular pathway
110                      Notably, alterations in lipid homeostasis and immune impairment are independent
111 er X receptors (LXRs) exert key functions in lipid homeostasis and in control of inflammation.
112 se benefits might result from regulations of lipid homeostasis and increased faecal bile-acid outputs
113 at mediates bidirectional cross-talk between lipid homeostasis and inflammation.
114 n 6, SIRT6, is critical for both glucose and lipid homeostasis and is involved in maintaining genomic
115 lism plays an important role for glucose and lipid homeostasis and its alterations contribute to meta
116 7 is a nutrient-sensing component of glucose/lipid homeostasis and may be a target in insulin resista
117  that have a well-defined role in regulating lipid homeostasis and metabolic diseases.
118                                              Lipid homeostasis and metabolism are closely related to
119 r regeneration (ALR) protein is critical for lipid homeostasis and mitochondrial function.
120 mino acid metabolism, its endogenous role in lipid homeostasis and muscle physiology is unknown.
121 ied differential actions of ILP7 and ILP8 in lipid homeostasis and ovarian development.
122         Our results prioritize the disturbed lipid homeostasis and oxidative stress as potential mech
123  to increase bile acid synthesis to maintain lipid homeostasis and prevent nonalcoholic fatty liver d
124 ER) membrane proteins play a central role in lipid homeostasis and protein quality control.
125 perturbed but critical switch in controlling lipid homeostasis and provide a new hope for the develop
126 ion yeast Schizosaccharomyces pombe regulate lipid homeostasis and the hypoxic response under conditi
127  findings have highlighted the complexity of lipid homeostasis and the important role that miRNAs pla
128 he complex interrelation between LD-mediated lipid homeostasis and the regulation of autophagy potent
129 e suggests an important relationship between lipid homeostasis and the UPR.
130 SCs led to abnormalities in nerve energy and lipid homeostasis and to increased lactate release.
131              ER-Golgi contact sites regulate lipid homeostasis and trafficking across the trans-Golgi
132 ssfully identified known kinases involved in lipid homeostasis and uncovered new ones.
133 otein convertase with essential functions in lipid homeostasis and unfolded protein response pathways
134 drial protein and lipid import with cellular lipid homeostasis and whole plant stress responses.
135                                       Hence, lipid-homeostasis and antioxidant abilities of CLHs in t
136 lex relationship between acetate metabolism, lipid homeostasis, and autophagy and propose Acc1-depend
137 bolic functions such as ER-PM communication, lipid homeostasis, and Ca(2+) influx.
138 activates genes involved in drug metabolism, lipid homeostasis, and cell proliferation.
139  Glucocorticoids are important regulators of lipid homeostasis, and chronically elevated glucocortico
140 rvival, intracellular signaling, protein and lipid homeostasis, and clotting processes.
141  the expression of a gene program regulating lipid homeostasis, and hepatic-specific ablation of eith
142 scoveries in bacterial lipid trafficking, OM lipid homeostasis, and host recognition of microbial pat
143 BP activity is tightly regulated to maintain lipid homeostasis, and is modulated upon extracellular s
144                     Here, choline transport, lipid homeostasis, and mitochondria function were analyz
145 ovel role for Lrp1 in peroxisome biogenesis, lipid homeostasis, and OPC differentiation during white
146  communication, ER stress, viral maturation, lipid homeostasis, and others.
147 ritical role in the regulation of energy and lipid homeostasis, and promotes the development of metab
148 nt axis for coordinating pathogen responses, lipid homeostasis, and survival and identify transcripti
149 we have identified several critical genes in lipid homeostasis (Apoa1, Apoa2 and ApoF) that are repre
150 ory pathways required to maintain eukaryotic lipid homeostasis are largely unknown.
151 normal cellular function, and disruptions in lipid homeostasis are linked to the progression of sever
152  are altered and cholesterol trafficking and lipid homeostasis are perturbed.
153 The hormone FGF21 regulates carbohydrate and lipid homeostasis as well as body weight, and increasing
154 wn/beige adipocyte formation and glucose and lipid homeostasis, as well as the involvement of retinoi
155 e Dicer1 cKO epididymis displayed an altered lipid homeostasis associated with a 0.6-fold reduction i
156 vestigate the effects of alcohol exposure on lipid homeostasis at the white adipose tissue (WAT)-live
157 d the effects of Miltefosine on macrophage's lipid homeostasis, autophagy, and NLRP3 inflammasome ass
158 ogically associated proteins are involved in lipid homeostasis, be it in lipid transport, incorporati
159 mportant beneficial regulator of glucose and lipid homeostasis but its levels are also abnormally inc
160 degeneration is also connected to changes in lipid homeostasis, but how these are related to PINK1-in
161 22) is abundant in the liver and involved in lipid homeostasis, but its relevance to the long-term ri
162  and have emerged as important modulators of lipid homeostasis, but the extent of their role has not
163 that CD36 plays an important role in hepatic lipid homeostasis, but the results have been conflicting
164  acting as a myokine that regulates systemic lipid homeostasis by activating TOR in hepatocyte-like c
165                           The disturbance of lipid homeostasis by altered sphingolipid levels may be
166                 We show that MeCP2 regulates lipid homeostasis by anchoring the repressor complex con
167 ly members (A, B and FSP27) regulate hepatic lipid homeostasis by controlling lipid droplet growth an
168 aromyces cerevisiae, plays a crucial role in lipid homeostasis by controlling the relative proportion
169 but also lead to a more complex imbalance in lipid homeostasis by disturbing PI4P metabolism.
170                            The regulation of lipid homeostasis by insulin is mediated in part by the
171                            The regulation of lipid homeostasis by insulin is mediated in part by the
172                    LPCAT3 maintains systemic lipid homeostasis by regulating lipid absorption in inte
173 s that CREBH plays a key role in maintaining lipid homeostasis by regulating the expression of the ge
174 lue lupin proteins appear to affect cellular lipid homeostasis by up-regulating SREBP-2 and CYP7A1 ge
175                              CTD also alters lipid homeostasis, cell wall integrity, endocytosis, adh
176 e maturation with alterations in glucose and lipid homeostasis characterized by reduced glycogen stor
177 g1 or Insig2 did not alter SREBP activity or lipid homeostasis, deletion of both genes (Insig1/2(Delt
178                               Maintaining ER lipid homeostasis despite these fluctuations is crucial
179 free fatty acids have key roles in governing lipid homeostasis during exercise.
180 ve SHs, and thus for deciphering the role of lipid homeostasis during rice seed germination.
181 n to be one of the major drivers of impaired lipid homeostasis during the pathogenesis of non-alcohol
182 ains carrying mutations in genes involved in lipid homeostasis enhanced sterility phenotypes, while m
183  indicated that ABCG1 was crucial for tissue lipid homeostasis, especially in the lung.
184 lation of HO-1 (heme oxygenase-1; HMOX1) and lipid homeostasis genes.
185 parable to those attributed to variations in lipid homeostasis genes.
186 ers the circadian oscillation of glucose and lipid homeostasis genes.
187 ndance for genes associated with glucose and lipid homeostasis (GLUT4, IRS1, FASN, ACACA, FATP2, CD36
188 t programs of gene expression and control of lipid homeostasis has been unclear.
189                              Altered hepatic lipid homeostasis, hepatocellular injury, and inflammati
190 his review we elucidate the role of PCSK9 in lipid homeostasis, highlight the impact of PCSK9 on athe
191  macrophages respond to loss of tissue-level lipid homeostasis, highlighting Trem2 as a key sensor of
192  (FOXOs) have been implicated in glucose and lipid homeostasis; however, the role of FOXOs in the dev
193 an610-Quad and an iSelect panel enriched for lipid homeostasis, hypertension, and drug metabolism gen
194 LS; however, it is unclear whether disrupted lipid homeostasis (i.e., lipid cacostasis) occurs proxim
195 lucidates SIRT4 as an important regulator of lipid homeostasis, identifies MCD as a SIRT4 target, and
196 osure, independent of nicotine, altered lung lipid homeostasis in alveolar macrophages and epithelial
197                                              Lipid homeostasis in animal cells is maintained by stero
198  modulates both LD size and cellular neutral lipid homeostasis in both leaves and seeds.
199  factor of the zinc finger family, regulates lipid homeostasis in clear cell renal cell carcinoma (cc
200 REBP)-encoding genes and control cholesterol/lipid homeostasis in concert with their host gene produc
201 tively, have recently been shown to regulate lipid homeostasis in concert with their host genes.
202 aims to investigate the effects of 25HC3S on lipid homeostasis in diet-induced NAFLD mouse models.
203 nelles via the proteasome and contributes to lipid homeostasis in eukaryotic cells.
204      Circulating AKH levels in turn regulate lipid homeostasis in fat body/adipose and the intestine.
205 a critical role for mitochondrial fusion and lipid homeostasis in GSC maintenance, providing insight
206 d be broadly applied to investigate neuronal lipid homeostasis in healthy and diseased brains.
207  C-associated inflammation and alteration of lipid homeostasis in infected cells.
208  intermediates, thereby maintaining membrane lipid homeostasis in leaves.
209 gest that myonectin links skeletal muscle to lipid homeostasis in liver and adipose tissue in respons
210 the effect of the loss of TAK1 expression on lipid homeostasis in liver and adipose tissues.
211                            Here, we examined lipid homeostasis in mice lacking calcineurin Abeta (CnA
212 PLIN2 expression, steatosis, and glucose and lipid homeostasis in mice with alcoholic steatosis and i
213 sent an adaptive response that preserves WAT lipid homeostasis in obese and insulin-resistant states.
214 te-derived hormone that restores glucose and lipid homeostasis in obesity-induced diabetes.
215 pids resemble previously reported effects on lipid homeostasis in other species.
216 scription factors regulate oxygen-responsive lipid homeostasis in the fission yeast Schizosaccharomyc
217 tance of SERCA2b in dysregulated glucose and lipid homeostasis in the liver of obese mice and suggest
218 t is required for mitochondrial function and lipid homeostasis in the liver.
219 ides insights into the mechanisms underlying lipid homeostasis in the liver.
220 roplet protein perilipin 2 (PLIN2) modulates lipid homeostasis in the liver.
221                                Consistently, lipid homeostasis in the Mwk cerebellum was found to be
222 red for proper biogenesis of LDs and neutral lipid homeostasis in vegetative tissues.
223                                              Lipid homeostasis in vertebrates is regulated by 3 stero
224 hat SKN-1 plays a direct role in maintaining lipid homeostasis in which it is activated by lipids.
225 epresents a coordinated mechanism to achieve lipid homeostasis in which plants couple the transcripti
226  metabolism is a key aspect of intracellular lipid homeostasis in yeast and mammals, but its role in
227  previously unappreciated deep remodeling of lipid homeostasis, including extreme changes to phosphol
228 s (LDs), organelles specialized for cellular lipid homeostasis, increase in size and number at the on
229 nce suggests that alterations of glucose and lipid homeostasis induced by obesity are associated with
230 r receptor CD36 contributes significantly to lipid homeostasis, inflammation, and amyloid deposition,
231                     The effects of 25HC3S on lipid homeostasis, inflammatory responses, and insulin s
232                             Dysregulation of lipid homeostasis is a common feature of several major h
233                             Dysregulation of lipid homeostasis is a precipitating event in the pathog
234 ring disease; however, it is unclear whether lipid homeostasis is adversely affected in the in the sp
235          The pivotal role of LDs in cellular lipid homeostasis is clearly established, but processes
236 gnals required for the regulation of hepatic lipid homeostasis is complex.
237 nce and disturbed homeostasis and shows that lipid homeostasis is essential to maintain adult skin ba
238                Previously, it was shown that lipid homeostasis is important in rotavirus replication.
239 dependent regulation of membrane and storage lipid homeostasis is only rudimentary.
240 nd adipokine gene transcription, its role in lipid homeostasis is poorly understood.
241                A key component of eukaryotic lipid homeostasis is the esterification of sterols with
242 /ATG2B KO cells, implying that regulation of lipid homeostasis is the major autophagy-dependent activ
243 as the role of adipose tissue in glucose and lipid homeostasis is widely recognized, its role in syst
244 ent conferred multiple effects on macrophage lipid homeostasis leading to increased cholesterol relea
245  VAP-ligand binding couples proteostasis and lipid homeostasis leading to observed phenotypes of lipi
246  photosynthetic apparatus and changes in the lipid homeostasis, leading to accumulation of triacylgly
247 ipocyte hypertrophy and improved glucose and lipid homeostasis, marked by increased glucose and insul
248 neration and developing therapies to restore lipid homeostasis may lead to a treatment for ALS.SIGNIF
249       Studies have shown that disturbance in lipid homeostasis may represent a critical determinant i
250 2A or C2C failed to rescue two defects in PM lipid homeostasis observed in E-Syts KO cells, delayed d
251  that the participation of CGI-58 in neutral lipid homeostasis of nonfat-storing tissues is similar,
252  results suggest a dependence of glucose and lipid homeostasis on Scly activity.
253                 We identify an age-dependent lipid homeostasis pathway in Caenorhabditis elegans that
254                      In the Golgi apparatus, lipid homeostasis pathways are coordinated with the biog
255 ce of miRNAs in regulating key signaling and lipid homeostasis pathways that alter the balance of ath
256 ) assembly and secretion impact intrahepatic lipid homeostasis, plasma lipoprotein profile, and energ
257 ple PFAS, were implicated in growth (RPTOR), lipid homeostasis (PON1, PON3, CIDEB, NR1H2), inflammati
258 synthesis by 5-AzaC disturbs cholesterol and lipid homeostasis, probably through the glycerolipid bio
259                           Here, we show that lipid homeostasis regulated by Caenorhabditis elegans Me
260                                These include lipid homeostasis, regulation of Ca(2+) dynamics, and co
261                                    Mammalian lipid homeostasis requires proteolytic activation of mem
262 own-regulation of ARV1 disturbs membrane and lipid homeostasis, resulting in a disruption of ER integ
263 uced body mass and improved both glucose and lipid homeostasis similarly in wild-type mice compared w
264  were associated with functions in redox and lipid homeostasis, suggesting potential negative impacts
265 ion pathways involved in hepatic glucose and lipid homeostasis, suggesting that this coactivator may
266 ors (LXRs) are transcriptional regulators of lipid homeostasis that also have potent anti-inflammator
267 ght loss accompanied by improved glucose and lipid homeostasis that are hallmarks of RYGB.
268 known as C1QBP) as an important regulator of lipid homeostasis that regulates both aerobic and anaero
269             Despite its importance in plasma lipid homeostasis, the regulation of Lmf1 remains unexpl
270 KI-1)/site-1 protease (S1P) is implicated in lipid homeostasis, the unfolded protein response, and ly
271 ch fasting or glucagon stimulation modulates lipid homeostasis through acetylation of CREBH.
272 al membrane plays a crucial role in cellular lipid homeostasis through biosynthesis of the non-bilaye
273 serve as intracellular receptors that couple lipid homeostasis through interactions with two phenylal
274 IGF2BP2 has an important role in maintaining lipid homeostasis through its modulation of ABCA1 expres
275 ver an important role for NCoR in regulating lipid homeostasis through the coordinated control of dif
276 -1 may maternally regulate LD biogenesis and lipid homeostasis to orchestrate the formation of the pe
277 to MICOS, combining functions in protein and lipid homeostasis to preserve mitochondrial structure an
278  thus identify Bif-1 as a novel regulator of lipid homeostasis to prevent the pathogenesis of obesity
279 germline-deficient C. elegans by maintaining lipid homeostasis to prolong life span.
280  and elevated PAP activity, which maintained lipid homeostasis under basal conditions, but led to die
281 ibonuclease, is required to maintain hepatic lipid homeostasis under ER stress conditions through rep
282 nesis for the purpose of maintaining hepatic lipid homeostasis under nutritional stress or circadian
283 ation, plays an important regulatory role in lipid homeostasis upon energy demands.
284 se results demonstrate that THs can regulate lipid homeostasis via autophagy and help to explain how
285 duces cellular membrane fluidity and impairs lipid homeostasis via rate-limiting metabolic processes
286 d by Kv2 channel-VAP pairing regulate PtdIns lipid homeostasis via VAP-associated PtdIns transfer pro
287  ablation and the consequent deregulation of lipid homeostasis was also shown to attenuate hepatocell
288  [CDCA]) play major roles in cholesterol and lipid homeostasis, we examined the effects of bile acids
289    Hepatic insulin signaling and glucose and lipid homeostasis were investigated.
290 et (40% kcal fat), parameters of glucose and lipid homeostasis were measured.
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

 
Page Top