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1 terium tracing studies of redox cofactor and fatty acid metabolism.
2 zation, extracellular matrix attachment, and fatty acid metabolism.
3 ) regulate genes involved in cholesterol and fatty acid metabolism.
4  AMPK in turn promotes glycolysis and alters fatty acid metabolism.
5 CoA synthetase 1 (ACSL1) plays a key role in fatty acid metabolism.
6 luding glycerophospholipid, glycerolipid and fatty acid metabolism.
7  esters and triglycerides, SCD is pivotal in fatty acid metabolism.
8 tion factor that regulates genes involved in fatty acid metabolism.
9 e enzyme stearoyl-CoA desaturase-1 (SCD1) in fatty acid metabolism.
10  little is known about cafestol's effects on fatty acid metabolism.
11 nase/insulin pathway and an up-regulation of fatty acid metabolism.
12 fatty acid transport protein, CD36, altering fatty acid metabolism.
13 liver is a major metabolic organ involved in fatty acid metabolism.
14 0) T antigens and oncogenic Ras(12V), affect fatty acid metabolism.
15 1(-/-) mice was associated with altered free fatty acid metabolism.
16 r in lipotoxic diseases due to modulation of fatty acid metabolism.
17 acking its DNA-binding-dependent activity on fatty acid metabolism.
18 s well as SCD1, the rate-limiting enzyme for fatty acid metabolism.
19 of the hepatic genes involved in glucose and fatty acid metabolism.
20 ) is an essential facet in the regulation of fatty acid metabolism.
21 he tricarboxylic acid cycle (TCA) cycle, and fatty acid metabolism.
22 neogenesis, glyoxylate cycle, and long-chain fatty acid metabolism.
23 ys important roles in whole-body glucose and fatty acid metabolism.
24  evidence that CTRP1 is a novel regulator of fatty acid metabolism.
25 d the relation between GIP, 11beta-HSD1, and fatty acid metabolism.
26 d its application to (13)C-tracer studies of fatty acid metabolism.
27  novel and complex connection between PD and fatty acid metabolism.
28 ng emergent activities in and dependences on fatty acid metabolism.
29 luding the citric acid cycle, polyamine, and fatty acid metabolism.
30 hould be broadly applicable to investigating fatty acid metabolism.
31 rial DNA depletion, mutation, or a defect of fatty acid metabolism.
32 that serve as key determinants of myocardial fatty acid metabolism.
33 ay major roles in regulating cholesterol and fatty acid metabolism.
34 lation of pathways involved in mitochondrial fatty acid metabolism.
35 reflect tissue-specific aspects of lipid and fatty acid metabolism.
36 ty acids to acyl-CoAs in the initial step of fatty acid metabolism.
37 it altered expression of genes that regulate fatty acid metabolism.
38 ynthesis and for A2B receptors in decreasing fatty acid metabolism.
39 poptosis, reactive oxygen species (ROS), and fatty acid metabolism.
40 strating diabetes-induced changes in retinal fatty acid metabolism.
41 ll development after infection by modulating fatty acid metabolism.
42 ion levels of representative marker genes in fatty acid metabolism.
43 ivation of genes involved in cholesterol and fatty acid metabolism.
44 dentified fadR, which encodes a regulator of fatty acid metabolism.
45  in addition to possessing fas genes used in fatty acid metabolism.
46 the natriuretic peptides influence lipid and fatty acid metabolism.
47 cell proliferation and altered mitochondrial fatty acid metabolism.
48 metabolites associated with carbohydrate and fatty acid metabolism.
49 evel and altered metabolites associated with fatty acid metabolism.
50 ls contain an unexplored plasticity in their fatty acid metabolism.
51 ession that is important for cholesterol and fatty acid metabolism.
52 ice through physiologic functions apart from fatty acid metabolism.
53           Bile acid (BA) signaling regulates fatty acid metabolism.
54 ates well with their downregulated amino and fatty acid metabolism.
55 ofiles, consistent with severe disruption of fatty acid metabolism.
56 rate-limiting enzyme for omega-3 and omega-6 fatty acid metabolism.
57 artners of ABCD2 involved in polyunsaturated fatty-acid metabolism.
58 cardiolipin, phosphonolipid, amino acid, and fatty acid metabolism; a partial Kreb's cycle; a reduced
59  and skeletal muscle, an accelerated rate of fatty acid metabolism, abnormal glucose metabolism, cons
60 olism', 'ceramides', 'creatine metabolism', 'fatty acid metabolism (acyl carnitine, polyunsaturated)'
61 tabolism and expression of genes involved in fatty acid metabolism, additional studies in differentia
62 anges in phenylpropanoid, glucosinolate, and fatty acid metabolism, although the nature and timing of
63 s, some of which include sucrose metabolism, fatty acid metabolism, amino acid metabolism, carbon fix
64 mediated ripening, including AOX, TCA cycle, fatty acid metabolism, amino acid metabolism, organic ac
65 rgy metabolism, (2) protein degradation, (3) fatty acid metabolism and (4) antioxidant system are alt
66 in pathways of branched-chain amino acid and fatty acid metabolism and (b) increased maximal capacity
67    Acylcarnitines (ACs) play a major role in fatty acid metabolism and are potential markers of metab
68 is of IL-6 in males may inadvertently affect fatty acid metabolism and augment aging-related neuroinf
69 ik Inuit, particularly in pathways involving fatty acid metabolism and cellular adhesion (CPNE7, ICAM
70 s involved in vesicle trafficking transport, fatty acid metabolism and cellular component biogenesis.
71 erall, this work demonstrates a link between fatty acid metabolism and E3 ligase activities in plants
72 d obesity and exhibit enhanced mitochondrial fatty acid metabolism and elevated oxidative capacity of
73                            Palmitate induced fatty acid metabolism and endoplasmic reticulum (ER) str
74 gs identify an intimate relationship between fatty acid metabolism and ER proteostasis that influence
75 fect of dietary Pi excess on skeletal muscle fatty acid metabolism and exercise capacity that is inde
76 P) functions both intracellularly as part of fatty acid metabolism and extracellularly as diazepam bi
77 t cycle, the diet-induced effects on growth, fatty acid metabolism and final eating quality were asse
78            We therefore examined glucose and fatty acid metabolism and hepatic glucose production in
79                FadR is a master regulator of fatty acid metabolism and influences virulence in certai
80 tial for the expression of genes involved in fatty acid metabolism and ingestion-associated stress re
81 R-33a and -b also regulate genes involved in fatty acid metabolism and insulin signaling.
82 l-CoA carboxylase (ACC) has crucial roles in fatty acid metabolism and is an attractive target for dr
83 like acetyl-CoA, is a high energy product of fatty acid metabolism and is produced through a similar
84 T liver biopsies, intrahepatic expression of fatty acid metabolism and lipid transport genes was lowe
85 cated in regulating cholesterol homeostasis, fatty acid metabolism and lipogenesis.
86 tional signature without normal increases in fatty acid metabolism and mitochondrial biogenesis genes
87                       Whether derailments in fatty acid metabolism and mitochondrial dysfunction are
88 ide hydrolase (sEH), opening a new branch of fatty acid metabolism and providing an additional site f
89              These genes are associated with fatty acid metabolism and represent mechanistic targets
90                                Consequently, fatty acid metabolism and ROS production were enhanced,
91 le insights into the regulatory mechanism of fatty acid metabolism and seed size determination, and s
92 e compatible with a multilevel impairment of fatty acid metabolism and significant mitochondrial dysf
93 ipate in myogenesis, neurogenesis, lipid and fatty acid metabolism and skeletal muscle structure or c
94 receptor (GPCR) pathways control glucose and fatty acid metabolism and the onset of obesity and diabe
95                                Regulation of fatty acid metabolism and the physiological effects of f
96 e pathways for fuel excess, the glycerolipid/fatty acid metabolism and the polyol pathway, were found
97 ately connected to intracellular pathways of fatty acid metabolism and therefore uniquely poised to c
98 e, mitochondrial capacity around glucose and fatty acid metabolism and thermogenesis is found to decl
99 , and echium oil affects the biochemistry of fatty acid metabolism and thus the balance of proinflamm
100 amily in tomato is important both to primary fatty acid metabolism and to responses to biotic stress.
101 nvestigated the role of FABP4 in endothelial fatty acid metabolism and tumour angiogenesis.
102 , stem cell maintenance and differentiation, fatty acid metabolism and type-2 diabetes.
103 I an association of downregulated genes with fatty acid metabolism and upregulated genes with inflamm
104 hich acts as a molecular brake that inhibits fatty acid metabolism and WAT browning.Histone deacetyla
105 ells are sensitive to approaches that target fatty acid metabolism and, in particular, fatty acid des
106 o pathways are traditionally associated with fatty acid metabolism and, unexpectedly, we found that i
107 oxoglutaric acid (citrate cycle), carnitine (fatty acid metabolism), and pyroglutamic acid (glutathio
108 cate that (i) MUC1 regulates cholesterol and fatty acid metabolism, and (ii) activation of these path
109 uding changes in biomarkers of inflammation, fatty acid metabolism, and bile acids.
110 BMAT including insulin resistance, decreased fatty acid metabolism, and enhanced contributions to loc
111 thway, related to oxidative phosphorylation, fatty acid metabolism, and glycolysis.
112 val effects, primarily through angiogenesis, fatty acid metabolism, and hemopoesis pathways.
113  oxidative phosphorylation, drug metabolism, fatty acid metabolism, and intestinal maturation, events
114 its of respiratory complexes, ATP machinery, fatty acid metabolism, and Krebs cycle, which further de
115 nsferase, a mitochondrial enzyme involved in fatty acid metabolism, and MED13, a component of the Med
116 and n6), eicosanoids, lysolipid, dipeptides, fatty acid metabolism, and purine metabolism [(hypo) xan
117 EBP target genes, selective reprogramming of fatty acid metabolism, and suppression of inflammatory-r
118 gamma coactivator 1alpha, a key regulator of fatty acid metabolism, and that proliferator-activated r
119 luding amino acid, iron, and polyunsaturated fatty acid metabolism, and the biosynthesis of glutathio
120 ode connecting carbohydrate, amino acid, and fatty acid metabolism, and the regulation of pyruvate fl
121  metabolism-particularly the polyunsaturated fatty acids metabolism, and purine metabolism-that were
122  lipid metabolism pathways in pan-cancer are fatty acid metabolism, arachidonic acid metabolism, chol
123 indicate that variants in genes important in fatty acid metabolism are associated with SCA survival i
124      We conclude that fadR and regulation of fatty acid metabolism are essential for V. vulnificus to
125 trophic acetate, propionate and longer chain fatty acid metabolism are mostly understood, but key ste
126 lved in lipid metabolism, especially omega-6 fatty acid metabolism, are up-regulated in livers of mic
127  EAE susceptibility, implicating short-chain fatty acid metabolism as a key element conserved across
128 dipose and skeletal muscle biopsies revealed fatty acid metabolism as a key pathway modified by weigh
129                         Our results indicate fatty acid metabolism as a target for tumour-specific ap
130  derivative, which is an essential factor in fatty acid metabolism as acyltransferase cofactor and in
131                                  A switch to fatty acid metabolism as an energy source and an enhance
132 ogether, our studies identify HIF control of fatty acid metabolism as essential for ccRCC tumorigenes
133 or-activated receptor alpha and dysregulated fatty acid metabolism as potential therapeutic targets.
134 ly fewer copies of several genes involved in fatty acid metabolism as well as AMY1B, the salivary amy
135 e Hippo pathway in lung cancer, and point to fatty acids metabolism as a key regulator of lung cancer
136 iferator-activated receptor signalling' and 'fatty acid metabolism' as the three most enriched pathwa
137 ive and respiratory capacities, nitrogen and fatty acid metabolism, as well as the first complete ele
138 ly suppressed TCA cycle, altered glucose and fatty acids metabolism, as well as nucleic acids metabol
139 implications in the chronic abnormalities of fatty acid metabolism associated with obesity and diabet
140  weight (BW) ratio, and higher expression of fatty acid metabolism-associated genes ( Acot1, Fabp1, a
141            Effects of PERC on kidney weight, fatty acid metabolism-associated genes [ Acot1 (Acyl-CoA
142 dge of the complex mechanisms of peroxisomal fatty acid metabolism at a molecular level and elucidate
143 al DOCK gene, regulates postprandial TAG and fatty acid metabolism by controlling activation of its p
144 urrent knowledge regarding the regulation of fatty acid metabolism by distinct cell autonomous circad
145                 Experimental manipulation of fatty acid metabolism by drug treatment turns a mouse in
146                       In contrast, restoring fatty acid metabolism by genetic or pharmacological meth
147 diator co-activator subunit in regulation of fatty acid metabolism by nuclear receptor-like transcrip
148 DT-15 plays a critical role in regulation of fatty acid metabolism by the nematode PPAR-like nuclear
149  of mitochondrial oxidative phosphorylation, fatty acid metabolism, calcium handling, and sarcomere f
150 cyclic and acyclic products generated during fatty acid metabolism can also function as important che
151 with type 1 diabetes, myocardial glucose and fatty acid metabolism can be manipulated by altering pla
152 l-intrinsic lipid profile and changes in the fatty acid metabolism can dictate the cell's response to
153 lestatic disease progression because altered fatty acid metabolism can enhance reactive oxygen specie
154  odds ratio, 2.04; P = 1.24 x 10(-7)) with a fatty acid metabolism; confirmation of PDE4DIP was obser
155 lved in cholesterol efflux (ABCA1 and NPC1), fatty acid metabolism (CROT and CPT1a), and insulin sign
156 riants of genes that control polyunsaturated fatty acid metabolism (CYP4F3, FADS1, and FADS2), along
157 thways for steroid biosynthesis, cell cycle, fatty acid metabolism, DNA replication, and biosynthesis
158  where they have been postulated to regulate fatty acid metabolism due to their ability to form stabl
159 in muscle during contracture, alterations in fatty acid metabolism during cardiac ischemia and postis
160  in coordinately regulating carbohydrate and fatty acid metabolism during the progression from fastin
161 centrations was not clear because of complex fatty acid metabolism dynamics in soil.
162 seases known for abnormalities in long-chain fatty acid metabolism, e.g., the Sjogren-Larsson syndrom
163  an uncharacterized branch of polyketide and fatty acid metabolism, encoding a large diversity of bio
164 R)alpha is known primarily as a regulator of fatty acid metabolism, energy balance, and inflammation,
165 ease in gene expression of mitochondrial and fatty acid metabolism enzymes in hepatocytes with reduce
166       It was demonstrated that, by impacting fatty acid metabolism, ETF and ETFDH mutations led to se
167 tionship between iron, oxidative injury, and fatty acid metabolism exists, but transduction mechanism
168 gulation (ZMIZ1), genome maintenance (FEN1), fatty acid metabolism (FADS1 and FADS2), cancer cell mot
169  molecular signatures indicative of enhanced fatty acid metabolism (FAM).
170 1 diabetes, the myocardium relies heavily on fatty acid metabolism for energy.
171 translocation, DNA binding, and induction of fatty acid metabolism genes acyl coenzyme A oxidase and
172                                              Fatty acid metabolism governs multiple intracellular sig
173                                              Fatty acid metabolism has received significant attention
174                                 Hypothalamic fatty acid metabolism has recently been implicated in th
175 oA carboxylases (ACCs), a crucial enzyme for fatty acid metabolism, has been shown to promote fatty a
176 alities such as metabolic acidosis, abnormal fatty acid metabolism, hyperlipidemia, and hyperglycemia
177 creen of the genes that regulate glucose and fatty acid metabolism identified an ACC necessary for sa
178                    Consistent with a role in fatty acid metabolism in cells, MBLAC2 was cross-linked
179       This study determined retinal-specific fatty acid metabolism in control and diabetic animals.
180 r, there are no experimental data on retinal fatty acid metabolism in diabetes.
181  determine the functional effects of altered fatty acid metabolism in experimental models.
182        This proliferative barrier imposed by fatty acid metabolism in hCOs could be rescued by simult
183          Insight into how the liver controls fatty acid metabolism in health and how these processes
184 eficiency did not alter hepatic ceramide and fatty acid metabolism in high cholesterol atherogenic di
185 ipoxygenase (12/15-LOX)-mediated unsaturated fatty acid metabolism in HSC function.
186 etabolic syndrome due to positive effects on fatty acid metabolism in liver and white adipose tissue.
187 al expression of genes involved in lipid and fatty acid metabolism in men with insulin resistance.
188                         FGF21 also regulates fatty acid metabolism in mice consuming a diet that prom
189 ined body composition as well as glucose and fatty acid metabolism in mice rendered deficient of Lrp4
190 dies demonstrate a pivotal role of essential fatty acid metabolism in myocardial phospholipid remodel
191  These data show that ACOT7 counterregulates fatty acid metabolism in neurons and protects against ne
192 ism; however, the basic metabolic control of fatty acid metabolism in neurons remains enigmatic.
193 al oxygen consumption (MVo(2)), glucose, and fatty acid metabolism in nondiabetic subjects and three
194 ide evidence for the importance of lipid and fatty acid metabolism in OC and serve as the foundation
195                       We discuss the role of fatty acid metabolism in Plasmodium and why we believe t
196 chanism parallels a phenotypic disruption in fatty acid metabolism in SIRT6 null mice as revealed by
197 d body composition, glucose homeostasis, and fatty acid metabolism in Sost(-/-) mice as well as mice
198 me functional prediction supported decreased fatty acid metabolism in the gut microbiome of subjects
199 ctional intracellular protein that regulates fatty acid metabolism in the nucleus via interactions wi
200 -regulated genes involved in the glucose and fatty acid metabolism in the primary hepatocytes.
201 rtance of a previously unrecognized sRNA for fatty acid metabolism in this major human pathogen.
202 hetase (ACSL) family that plays key roles in fatty acid metabolism in various tissues in an isozyme-s
203 been documented to play an important role in fatty acid metabolism in vivo and subsequently may be in
204  the importance of Clk2 in the regulation of fatty acid metabolism in vivo and suggest that inhibitio
205 yrate is used to measure carbohydrate versus fatty acid metabolism in vivo.
206 ncoding genes, emphasizing the importance of fatty-acid metabolism in neurological diseases.
207           It is likely that abnormalities in fatty acid metabolism, in conjunction with adipose tissu
208 ly for the tryptophan-kynurenine pathway and fatty acid metabolism, in the peripheral system of MDD p
209 nase plays a central role in polyunsaturated fatty acid metabolism, inaugurating the biosynthesis of
210 n of expression of numerous genes modulating fatty acid metabolism, including ADIPOR1 (adiponectin re
211  was strongly associated with markers of n-3 fatty acid metabolism, including degree of unsaturation
212 e used (13)C tracers and lipidomics to probe fatty acid metabolism, including desaturation, as a func
213 display features indicative of altered lipid/fatty acid metabolism, including differential adiposity
214 rular gene expression of enzymes involved in fatty acid metabolism, including induction of stearoyl-C
215 olic disorders characterized by dysregulated fatty acid metabolism, including nonalcoholic steatohepa
216 gested that enhanced capacity for energy and fatty acid metabolism, increased protein degradation, re
217     CD36 is a scavenger receptor involved in fatty acid metabolism, innate immunity and angiogenesis.
218 uggest that Rv1075c is involved in ester and fatty acid metabolism inside host cells.
219 ly represented categories included lipid and fatty acid metabolism, insulin action, and cell-cycle re
220  influence of genetics and the microbiome on fatty acid metabolism is also discussed.
221                                              Fatty acid metabolism is perturbed in atherosclerotic le
222                        Thus, monounsaturated fatty acid metabolism is pivotal for alphaS-induced neur
223 etic heart, glycolysis is suppressed whereas fatty acid metabolism is promoted.
224 dings of this study suggest that unsaturated fatty acid metabolism is significantly dysregulated in t
225  transcription factor involved in sustaining fatty acid metabolism, is upregulated in Salmonella-infe
226 n metabolic pathways, carbon metabolism, and fatty acid metabolism, likely descriptive of the epigene
227 rains related to increased lipid metabolism, fatty acid metabolism, lipid and fatty acid processing,
228 associated with glycolysis (Warburg effect), fatty acid metabolism (lipogenesis, oxidation, lipolysis
229 eficiency primarily affected very long chain fatty acid metabolism, mutant fibroblasts also showed re
230 ociated with the escalated regulation of the fatty acid metabolism network.
231 d-dependent transcription factor involved in fatty acid metabolism, obesity, wound healing, inflammat
232 nvolved in amino sugar, nucleotide sugar and fatty acid metabolism, one carbon pool for folate metabo
233           Our findings indicate that altered fatty acid metabolism or utilization is present in CD an
234  the acetyl-proteins are enzymes involved in fatty acid metabolism, oxidative phosphorylation or the
235 tified several perturbed pathways, including fatty acid metabolism-particularly the polyunsaturated f
236 nregulation of oxidative phosphorylation and fatty acid metabolism pathway genes.
237 inflammation, oxidative phosphorylation, and fatty acid metabolism pathways as well as cell death and
238 of the mitochondrial biogenesis, glucose and fatty acid metabolism pathways that lack in near homopla
239 We investigated whether genetic variation in fatty acid metabolism pathways was associated with SCA s
240 owed that photosynthesis/photoprotection and fatty acid metabolism pathways were specifically enriche
241 ed involvement of amino acid and short-chain fatty acid metabolism pathways.
242 alterations in the tryptophan-kynurenine and fatty acid metabolism pathways.
243 , oxidative response and protein, carbon and fatty acid metabolism pathways.
244 genes involved in oxidative phosphorylation, fatty acid metabolism, peroxisome, bile acid metabolism,
245 uding protein-glycosylation, polyunsaturated fatty acid metabolism, phospholipid modeling, and glucos
246                       Given that deregulated fatty acid metabolism plays a key role in kidney fibrosi
247 t in branched-chain amino acid catabolism or fatty acid metabolism possessed altered susceptibility t
248 iated with dysregulation of intramyocellular fatty acid metabolism, possibly because of an inherited
249     PPAR-delta agonists are known to enhance fatty acid metabolism, preserving glucose and physical e
250  target of azole antifungals) and a putative fatty acid metabolism protein (and a potential azole dru
251 c bile acid transporters and cholesterol and fatty acid metabolism proteins, including Scp2/x, Abcg5/
252 ls of 15 acylcarnitines, suggesting abnormal fatty acid metabolism related to mitochondrial dysfuncti
253 ntified oxidative stress and polyunsaturated fatty acid metabolism-related pathways, as well as tryps
254 pression of cardiac Ppara and its downstream fatty acid metabolism-related targets.
255 idome and demonstrate immediate responses in fatty acid metabolism represented by increases in eicosa
256       Cellular imbalances of cholesterol and fatty acid metabolism result in pathological processes,
257         BMIPP SPECT detects abnormalities in fatty acid metabolism resulting from myocardial ischemia
258  and the edge of the tumor undergo different fatty acid metabolism, resulting in different chemical e
259 ndrial dysfunction is linked to dysregulated fatty acid metabolism, resulting in increased levels of
260                  Gene expression profiles of fatty acid metabolism show commonalities across pan-canc
261 othesis that TNT exposure affected lipid and fatty acid metabolism, showing that hormetic effects cou
262 eir toxic levels in peroxisomal disorders of fatty acid metabolism, such as adrenoleukodystrophy and
263               Pctp(-/-) mice exhibit altered fatty acid metabolism that is accompanied by reduced hep
264                                   Endogenous fatty acid metabolism that results in elongation and des
265 eotide-dependent deacetylase SIRT1 regulates fatty acid metabolism through multiple nutrient sensors.
266 ysaccharides implicated in the modulation of fatty acid metabolism, thus critical players in cell env
267                              The response of fatty acid metabolism to administration of bifidobacteri
268 ase, which together convert intermediates of fatty acid metabolism to alkanes and alkenes.
269  signaling in macrophages links dysregulated fatty acid metabolism to oxidative stress from the mitoc
270 ional regulation of suberin deposition, from fatty acid metabolism to phenylpropanoid biosynthesis, i
271 pha coordinately regulates mitochondrial and fatty acid metabolism to promote tumor growth.
272  substrate utilization from oxygen-consuming fatty acid metabolism toward oxygen-sparing glycolysis a
273 hysiological processes including glucose and fatty acid metabolism, transcription, cell growth, mitoc
274 lant infection in M. oryzae by regulation of fatty acid metabolism, turgor establishment and inductio
275 about how LRH-1 controls hepatic glucose and fatty acid metabolism under physiological conditions.
276 decrease in expression of enzymes related to fatty acid metabolism, urea cycle, cell replication, and
277 oal was to investigate cafestol's effects on fatty acid metabolism using Caenorhabditis elegans.
278                            However, blocking fatty acid metabolism using inhibitors to prevent acyl-a
279 in human umbilical vein endothelial cells on fatty acid metabolism, viability and angiogenesis.
280 r characterization revealed that a switch to fatty acid metabolism was a central driver of cardiac ma
281 ssure has affected the genetic regulation of fatty acid metabolism, we assessed 233 serum metabolic p
282  action of nuclear receptors, in glucose and fatty acid metabolism, we generated skeletal muscle-spec
283                     The alterations in brain fatty acid metabolism were concomitant with a loss of le
284  Several genes involved in lipid droplet and fatty acid metabolism were differentially expressed in I
285 wn to have a central role in regulating free fatty acid metabolism were downregulated in the livers,
286 itric acid cycle, amino acid metabolism, and fatty acid metabolism were found to be highly enriched h
287  demonstrated that hallmark genes related to fatty acid metabolism were highly expressed in samples w
288 l known PPARalpha target genes involved with fatty acid metabolism were observed, reflecting the expe
289 c glycolysis, oxidative phosphorylation, and fatty acid metabolism, were also reduced in T cells lack
290 ression of genes involved with oogenesis and fatty acid metabolism when on its host.
291 mitochondrial oxidative phosphorylation, and fatty acid metabolism, whereas the late-phase 4-1BBL-med
292 sis by coordinated regulation of glucose and fatty acid metabolism, which provide a molecular basis f
293 nd decreased expression of genes involved in fatty acid metabolism, which was prevented by blockade o
294 ncoupling of LDs from mitochondria, reducing fatty acid metabolism while increasing LD-bacterial cont
295  by increasing protein and RNA synthesis and fatty acid metabolism, while decreasing autophagy.
296          Therefore, V. cholerae co-ordinates fatty acid metabolism with 1-acyl G3P synthesis.
297     To examine the association of endogenous fatty acid metabolism with future development of metabol
298                These cells exhibited altered fatty acid metabolism with increased rates of beta-oxida
299 tyl-CoA carboxylase (ACC) is a key enzyme of fatty acid metabolism with multiple isozymes often expre
300 remodeling resulted in profound increases in fatty acid metabolism within this tissue.

 
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