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1 s in response to physiologic stimuli (termed metabolic flexibility).
2 al Ca(2+) uptake during activity and achieve metabolic flexibility.
3 nsulin and positively correlated with IS and metabolic flexibility.
4 e context of cellular thiamine synthesis and metabolic flexibility.
5 increased reliance on glycolysis and reduced metabolic flexibility.
6 and opportunists is strongly associated with metabolic flexibility.
7 st, we found that the heart had considerable metabolic flexibility.
8 on of mitochondrial respiration with limited metabolic flexibility.
9 tion, dysfunction, and global impairments in metabolic flexibility.
10 g metabolic memory, despite achieving modest metabolic flexibility.
11 the TCA cycle, providing further evidence of metabolic flexibility.
12 ment, this process provides tumor cells with metabolic flexibility.
13 alcium signaling, which are crucial for TNBC metabolic flexibility.
14 h mutant plants, demonstrating their lack of metabolic flexibility.
15 r are unavailable, thereby ensuring neuronal metabolic flexibility.
16 h the evolution of mammalian hibernation and metabolic flexibility.
17 ile type of immune cells exhibits remarkable metabolic flexibility.
18 ar phagocytes which occurs at the expense of metabolic flexibility.
19 ulated molecular architecture for hepatocyte metabolic flexibility.
20 lic adaptation to this stressor and maintain metabolic flexibility.
21 not done so constitutively, consistent with metabolic flexibility.
22 This may also affect one's metabolic flexibility.
23 activity levels are a primary determinant of metabolic flexibility.
24 he PDK isoform that is a potent modulator of metabolic flexibility.
25 lular energy metabolism, suggesting neuronal metabolic flexibility.
26 sired metabolic cross-talk while maintaining metabolic flexibility.
27 acyclic terpenes, suggesting a reduction of metabolic flexibility.
28 hways, and improving insulin sensitivity and metabolic flexibility.
29 rs from metabolic bystander to key driver of metabolic flexibility.
30 in the fed state, contributing to a loss of metabolic flexibility.
31 may thus participate in the preservation of metabolic flexibility.
32 r to IPGR, but less active while maintaining metabolic flexibility.
33 reby allowing the heart to maintain its full metabolic flexibility.
34 ulin sensitive, and active while maintaining metabolic flexibility.
35 is for how NAD(+) homeostasis factors confer metabolic flexibility.
36 mental approaches to studying the concept of metabolic flexibility across a range of activity and ina
38 ineered cell lines, which revealed a lack of metabolic flexibility and a contribution of the 3q29 gen
39 ompensatory fashion, which may contribute to metabolic flexibility and a growth advantage to sustain
40 r levels of thiamin vitamers for the plant's metabolic flexibility and ability to acclimate to an alt
41 es a potential mechanism for the increase in metabolic flexibility and enhanced insulin sensitivity p
42 eview, we provide a contemporary view of the metabolic flexibility and functional plasticity of skele
44 High fat feeding impairs skeletal muscle metabolic flexibility and induces insulin resistance, wh
48 hat the gene ech-6 is potential modulator of metabolic flexibility and may be a target for promoting
50 acterium stems from its genomic variability, metabolic flexibility and phenotypic diversity, enabling
51 ibility was inversely correlated with IS and metabolic flexibility and positively correlated with bod
52 the importance of muscle PDH in maintaining metabolic flexibility and preventing the development of
54 dial glucose uptake and oxidation reduce the metabolic flexibility and render the heart susceptible t
56 ify how OPA1 up-regulation allows AML cells' metabolic flexibility and survival and nominates specifi
58 eight loss, improved glucose homeostasis and metabolic flexibility, and better mobility and strength.
59 because of their small genome size, reduced metabolic flexibility, and high worldwide abundance in f
60 ice, abolished diurnal rhythms in whole body metabolic flexibility, and increased markers of adverse
61 he regulatory mechanisms and significance of metabolic flexibility are not completely understood.
62 re, BEZ-treated mice also exhibited improved metabolic flexibility as well as an enhanced mitochondri
63 ricted feeding partially restored whole body metabolic flexibility, as well as day-night differences
64 sion of pyruvate transport induces a form of metabolic flexibility associated with the use of lipids
66 organisms that have substantial genetic and metabolic flexibility, can resist multiple classes of an
69 e most salient feature of the network is the metabolic flexibility demonstrated in response to variou
70 onnected through homologous recombination, a metabolic flexibility despite a small genome size, and a
73 and aquatic) green alga that has significant metabolic flexibility for balancing redox equivalents an
85 We will also discuss how the ETC enhances metabolic flexibility in methanogens and can even permit
87 ectively, our study identified a key role of metabolic flexibility in modulating the effect of FGFR s
89 xposure in early pregnancy programs impaired metabolic flexibility in offspring, which may increase s
90 glucose metabolism, insulin sensitivity, and metabolic flexibility in overweight adults (aged 45-65 y
91 ncoded in the genome, suggesting significant metabolic flexibility in oxidizing NADH under a variety
92 al muscle mitochondrial substrate choice and metabolic flexibility in part by regulating PDH function
93 reen alga Chlamydomonas reinhardtii displays metabolic flexibility in response to a changing environm
95 fatty acid oxidation, glucose oxidation and metabolic flexibility in soleus muscle cells from ABA-tr
98 ndings reveal how microbial interactions and metabolic flexibility -including using alternative energ
100 sal fatty acid oxidation, maintained glucose metabolic flexibility, increased nonoxidative glucose di
102 performance and glucoregulation, and greater metabolic flexibility independent of diet composition.
104 nergy homeostasis, and dysregulation of this metabolic flexibility is a dominant cause of several met
109 mulate physiological cardiac remodeling, and metabolic flexibility is important for maintaining mitoc
112 aired systolic function, significant cardiac metabolic flexibility is retained, including the ability
117 iac retinoic acid insufficiency and impaired metabolic flexibility linked to a compromised PDK4/PDH p
118 t-chain alkane metabolism suggests that such metabolic flexibility may be important in many environme
121 hanges in macronutrient composition of diet (metabolic flexibility) may be informative of individuals
122 on acceptors, which together with methanogen metabolic flexibility, may explain peat microbiome compo
123 in energy expenditure, glucose homeostasis, metabolic flexibility, mobility, and strength, excessive
124 cular dissection of its functions, providing metabolic flexibility needed for dietary adaptation.
125 Overall, our study uncovers a mechanism of metabolic flexibility occurring during ccRCC progression
127 t adiponectin is a factor that increases the metabolic flexibility of adipose tissue, enhancing its a
129 Decreasing glycolysis aims to combat the metabolic flexibility of both primary and secondary tumo
131 of HIF-1 or metabolic enzymes may impair the metabolic flexibility of cancer cells and make them more
133 d culture GEO12CF provides insights into the metabolic flexibility of Dehalococcoides and could be us
136 f polycations and vemurafenib diminishes the metabolic flexibility of melanoma cells, making them una
141 res and the protein complement highlight the metabolic flexibility of Picochlorum SE3 that encodes ge
144 elative to fatty acids, thereby limiting the metabolic flexibility of the heart that is critically in
145 Relieving this inhibition can increase the metabolic flexibility of the hyperthyroid heart and redu
146 f the MTP family in Leishmania increased the metabolic flexibility of these protists and contributed
148 during a 6-wk period had a neutral effect on metabolic flexibility or postprandial glucose metabolism
150 hought to be one of the main contributors to metabolic flexibility-promoting mitochondrial energy pro
151 in ATP levels; however, beta cells lack this metabolic flexibility, resulting in a nitric oxide-depen
152 nglycosylatable SIRT1 in the liver abrogated metabolic flexibility, resulting in systemic insulin res
154 s and laboratory experiments revealed a high metabolic flexibility, suggesting a considerable capacit
155 y contribute to the dynamic, tissue-specific metabolic flexibility that enables growth and survival i
157 compared to controls and displayed a loss of metabolic flexibility that was not observed in fibroblas
158 glucose oxidation and is closely linked with metabolic flexibility, the importance of muscle PDH duri
160 demonstrate that the diabetic heart retains metabolic flexibility to adapt to hypoxia, but is hinder
161 In conclusion, type 2 diabetic hearts retain metabolic flexibility to adapt to hypoxia, with normal H
163 We integrate macronutrient regulation and metabolic flexibility to elucidate how wild orangutans (
170 llular compartments provides plants with the metabolic flexibility to maintain physiological levels o
171 nitiating cells display stress tolerance and metabolic flexibility to survive in a harsh environment
172 using different nutrient sources, cells gain metabolic flexibility to survive periods of starvation.
173 ility of sleep/wake states and providing the metabolic flexibility to transition between states.
178 its on and evolutionary consequences of this metabolic flexibility, we developed a coarse-grained mat
179 connection between phenotypic switching and metabolic flexibility, where metabolic specialization of
180 et-induced obesity disrupts cardiac "diurnal metabolic flexibility", which is normalized by time-of-d
181 rtant regulator of HIF-driven glycolysis and metabolic flexibility, which influences the development
182 g had no effect on weight gain but increased metabolic flexibility while reducing body fat and liver
183 hat high levels of physical activity predict metabolic flexibility, while physical inactivity and sed
184 of plasma glucose and insulin, and a loss of metabolic flexibility with decreased lipid oxidation.
185 s are equipped with a somewhat unappreciated metabolic flexibility with important implications for th
186 eliminating glucotoxicity, which reinstates metabolic flexibility with restored preprandial lipid ox
189 At the same time, a great potential for metabolic flexibility within this group is uncovered, wi
190 ities in high Candida samples display higher metabolic flexibility yet lower contributional diversity