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1 e in the YS mice is exacerbated by brown fat adaptive thermogenesis.
2 ody weight), resting energy expenditure, and adaptive thermogenesis.
3  maintaining BAT function, especially during adaptive thermogenesis.
4 zed for energy expenditure, a process called adaptive thermogenesis.
5 alpha 2 subunit (CHRNA2) signaling to induce adaptive thermogenesis.
6  EC-KO mice have normal body composition and adaptive thermogenesis.
7  is dissipated as heat in a process known as adaptive thermogenesis.
8  by basal metabolism, physical activity, and adaptive thermogenesis.
9 resistance to the LPS-induced suppression of adaptive thermogenesis.
10 ory responses are key regulators to suppress adaptive thermogenesis.
11 iation with increased energy expenditure and adaptive thermogenesis.
12 involved in energy expenditure, most notably adaptive thermogenesis.
13 otecting critical organs from hypothermia by adaptive thermogenesis.
14 diture in small mammals and neonates through adaptive thermogenesis.
15  in WAT that drove uncoupled respiration and adaptive thermogenesis.
16 pecific roles for NT-PGC-1alpha in basal and adaptive thermogenesis.
17 gram of alternative macrophage activation in adaptive thermogenesis.
18 etic input to the transcriptional program of adaptive thermogenesis.
19  and oxidative metabolism, and essential for adaptive thermogenesis.
20 of mitochondrial uncoupling and nonshivering adaptive thermogenesis.
21 c responsiveness does not limit cold-induced adaptive thermogenesis.
22 cription factors to orchestrate a program of adaptive thermogenesis.
23 that plays a major role in the regulation of adaptive thermogenesis.
24 relation to classical physiological views of adaptive thermogenesis.
25 ays a major role in regulating lipolysis and adaptive thermogenesis.
26  receptors to the transcriptional program of adaptive thermogenesis.
27 tant second messengers for the regulation of adaptive thermogenesis.
28 ave a direct role in adipocyte metabolism or adaptive thermogenesis.
29 A (miR)-33 in the brain is indispensable for adaptive thermogenesis.
30 fatty acid uptake, oxidative metabolism, and adaptive thermogenesis.
31  model and this response is dissociated from adaptive thermogenesis.
32 ments in rodent models designed to stimulate adaptive thermogenesis, a long-term increase in metaboli
33 xpenditure through heat generation is termed adaptive thermogenesis, a process carried out by thermog
34 kable under basal conditions and show normal adaptive thermogenesis, a process previously suggested t
35               Juvenile king penguins develop adaptive thermogenesis after repeated immersion in cold
36 esults demonstrate that NRDC in BAT controls adaptive thermogenesis and body temperature homeostasis
37              LCN2(-/-) mice exhibit impaired adaptive thermogenesis and cold intolerance.
38  Brown adipose tissue (BAT) is essential for adaptive thermogenesis and dissipation of caloric excess
39 portance of this energy-dissipating cycle in adaptive thermogenesis and energy expenditure in animals
40 (TrkB) neurons leads to a robust increase in adaptive thermogenesis and energy expenditure without al
41 brown adipose tissue, which is essential for adaptive thermogenesis and energy expenditure.
42 n resistance, and fatty liver due to reduced adaptive thermogenesis and energy expenditure.
43                                              Adaptive thermogenesis and fatty acid oxidation were enh
44  several other oxidative processes including adaptive thermogenesis and fatty acid oxidation.
45 lpha (PGC-1alpha) has been shown to regulate adaptive thermogenesis and glucose metabolism.
46 s as an essential mediator for LN-controlled adaptive thermogenesis and highlight its potential to co
47 the preponderant determinant of the impaired adaptive thermogenesis and hypothermia in cold-exposed D
48 verexpression of Foxp1 in adipocytes impairs adaptive thermogenesis and promotes diet-induced obesity
49 specific PGRMC2-null mice unable to activate adaptive thermogenesis and prone to greater metabolic de
50 eficient for OPA1 in adipocytes had impaired adaptive thermogenesis and reduced cold-induced browning
51                            Nevertheless, the adaptive thermogenesis and the expression of uncoupling
52 an receptor GPR50 plays an important role in adaptive thermogenesis and torpor.
53 urthermore, SPC(DeltaIl33) mice had impaired adaptive thermogenesis and were unresponsive to leptin-i
54   Brown adipocytes (BAs) are specialized for adaptive thermogenesis and, upon sympathetic stimulation
55 c (appetite-suppressing) pathway, peripheral adaptive thermogenesis, and fatty acid oxidation.
56 HB1) in adipocyte mitochondrial respiration, adaptive thermogenesis, and long-chain fatty acid (LCFA)
57                Systemic insulin sensitivity, adaptive thermogenesis, and serum metabolic and lipid pr
58 ed hepatic insulin sensitivity and increased adaptive thermogenesis, and Them2-/- mice are also resis
59                       Weight loss results in adaptive thermogenesis, and there is no indication for a
60                                They regulate adaptive thermogenesis as well as glucose and fat oxidat
61                                              Adaptive thermogenesis (AT) is currently defined as the
62                                              Adaptive thermogenesis (AT) is the fat-free mass (FFM)-i
63                      TRX2 deficiency impairs adaptive thermogenesis by suppressing fatty acid oxidati
64  variant N terminal (NT)-PGC-1alpha regulate adaptive thermogenesis by transcriptional induction of t
65                                              Adaptive thermogenesis has attracted much attention beca
66                            Recent studies of adaptive thermogenesis have shown how mitochondrial prol
67 en-group differences in body composition and adaptive thermogenesis; however, the change in resting e
68   Diet-induced weight loss is accompanied by adaptive thermogenesis, ie, a disproportional or greater
69 nk beta(3)-androgenic receptor activation to adaptive thermogenesis in adipose tissue.
70  mouse to assess the effects of UCP1 loss on adaptive thermogenesis in adult mice.
71                                     Although adaptive thermogenesis in BAT increases energy expenditu
72 f browning in inguinal WAT and activation of adaptive thermogenesis in brown adipose tissue (BAT).
73 dered a central transcriptional regulator of adaptive thermogenesis in brown adipose tissue (BAT).
74             PGC-1alpha plays a vital role in adaptive thermogenesis in brown adipose tissue and stimu
75 ria functions and plays an important role in adaptive thermogenesis in brown adipose.
76  metabolism, particularly certain aspects of adaptive thermogenesis in brown fat and skeletal muscle,
77 (beta-AR) signaling is a pathway controlling adaptive thermogenesis in brown or beige adipocytes.
78  a recently identified candidate mediator of adaptive thermogenesis in humans.
79                                   Therefore, adaptive thermogenesis in juvenile king penguins is link
80  and reveal GPR50 to be a novel component of adaptive thermogenesis in mammals.
81 r mechanisms responsible for the compromised adaptive thermogenesis in obese subjects have not yet be
82                        This may be a form of adaptive thermogenesis in response to an inability to st
83     Possible functions include 1) control of adaptive thermogenesis in response to cold exposure and
84 re thought to be significant contributors to adaptive thermogenesis in skeletal muscle and can act as
85 ates energy expenditure through an efficient adaptive thermogenesis in the BAT.
86 f C14-C18 in wild-type animals also impaired adaptive thermogenesis in the BAT.
87  a master regulator of energy metabolism and adaptive thermogenesis in the brown fat cell.
88                                              Adaptive thermogenesis in the resting component of total
89 protein viral protein R (Vpr) contributes to adaptive thermogenesis in two mouse models and human adi
90 investigate the mitochondrial basis of avian adaptive thermogenesis in vitro.
91                                A decrease in adaptive thermogenesis is a contributing factor to obesi
92                                              Adaptive thermogenesis is an energy-demanding process th
93                                              Adaptive thermogenesis is an important component of ener
94                                              Adaptive thermogenesis is essential for survival, and th
95 aim of this study was to investigate whether adaptive thermogenesis is sustained during weight mainte
96                                              Adaptive thermogenesis is the cellular process transform
97                                              Adaptive thermogenesis is the process of heat generation
98    Interleukin-33 acts perinatally to ensure adaptive thermogenesis lifelong.
99 (+) biosynthesis is essential for regulating adaptive thermogenesis, lipolysis, and whole-body energy
100 s a major site of energy dissipation through adaptive thermogenesis mediated by uncoupling protein 1
101                  Heart rate and cold-induced adaptive thermogenesis, mediated by thyroid hormone-cate
102 iple aspects of energy metabolism, including adaptive thermogenesis, mitochondrial biogenesis, and fa
103 portant regulators of energy expenditure and adaptive thermogenesis, notably through their action in
104  leads to a marked reduction of BAT-mediated adaptive thermogenesis, obesity and systemic insulin res
105                                              Adaptive thermogenesis of BAT was impaired in HFD offspr
106                                              Adaptive thermogenesis, or the regulated production of h
107  via type 2 deiodinase (D2) is necessary for adaptive thermogenesis, such that mice lacking D2 (D2KO)
108       Our data reveal surprising deficits of adaptive thermogenesis that drive metabolic inefficiency
109 press energy expenditure, a process known as adaptive thermogenesis, the mechanistic underpinnings of
110 rrant BAT mitochondria and fail to carry out adaptive thermogenesis under cold stress.
111 , and there is no indication for a change in adaptive thermogenesis up to 1 y, when weight loss is ma
112 dipose-derived cytokine in the regulation of adaptive thermogenesis via a non-adrenergic pathway.
113 ermine by a pharmacological approach whether adaptive thermogenesis was TR isoform--specific.
114 zed determinants of adipocyte plasticity and adaptive thermogenesis, which may have potential therape
115 ting adipocyte differentiation and enhancing adaptive thermogenesis within adipocytes, and siRNA targ

 
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