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1 lic regulators (e.g., Lipoprotein lipase and Uncoupling protein 2).
2 tty-acid-induced activation of mitochondrial uncoupling protein 2.
3 by scavenging of the ROS or by inhibition of uncoupling protein 2.
4 nd -4, catalase, superoxide dismutase-2, and uncoupling protein-2.
5 ssigned to chromosome 12) in the area of the uncoupling protein 2/3 gene cluster.
6  and activators of transcription 1alpha, and uncoupling protein 2, among others.
7 is increased the expression of mitochondrial uncoupling protein 2 and raised the AMP-to-ATP ratio, th
8        Cardiac transcripts of genes encoding uncoupling proteins 2 and 3 are up-regulated in parallel
9 nction of the cardiac enriched mitochondrial uncoupling proteins 2 and 3 during delayed ischemic prec
10 a(2+) fluxes, have been described: the novel uncoupling proteins 2 and 3, the leucine zipper-EF-hand
11 ase in the expression of the transcripts for uncoupling proteins-2 and -3 also accompanied this incre
12 ruvate kinase, hormone-sensitive lipase, and uncoupling proteins-2 and -3.
13 almitoyltransferase-I, acyl-CoA oxidase, and uncoupling protein-2) and their coordinating transcripti
14 ation of neuropeptide expression, as well as uncoupling protein 2, and abnormal responses to a metabo
15  to chemotherapy, increase the expression of uncoupling protein 2, and decrease the entry of pyruvate
16             In the cytoprotective hierarchy, uncoupling protein-2 appears to play a greater role than
17 ochondria, ATP-hydrolyzing mitochondria, and uncoupling protein 2 are not significant contributors to
18 nzymes involved in ROS scavenging, including uncoupling protein 2, catalase, and copper zinc superoxi
19                                              Uncoupling protein-2 depletion alone significantly atten
20 ed uncoupling protein depletion and isolated uncoupling protein-2 depletion augments ROS production i
21 iac derived myoblasts is abolished following uncoupling protein-2 depletion by RNA-interference.
22 tor gamma co-activator alpha (Pgc1alpha) and uncoupling protein 2 expression, suggesting mechanisms f
23 ypes of mice with targeted disruption of the uncoupling protein-2 gene (Ucp2-/-) is greater macrophag
24 ransgenic mice engineered to overexpress the uncoupling protein 2 in hypocretin neurons (Hcrt-UCP2) h
25  agouti-related peptide, neuropeptide Y, and uncoupling protein 2 in the hypothalamus, but no increas
26         Adenosine triphosphate decreased and uncoupling protein 2 increased in fa/fa rats treated wit
27      Previous work in our lab has shown that uncoupling protein-2 is a major mediator of I/R in steat
28 is hypothesis, we see a dramatic increase in uncoupling protein-2 levels in the combination treated a
29                           Here, we show that uncoupling protein-2-mediated mitochondrial reprogrammin
30 r-activated receptor-gamma, adiponectin, and uncoupling protein-2 mRNA levels in adipose, indicating
31 anoxia and reoxygenation tolerance following uncoupling protein 2 or 3 and combined 2 and 3 RNAi show
32 ion through the AMP-activated protein kinase-uncoupling protein 2 pathway.
33 ism for modified bioenergetics that involves uncoupling protein-2 that is up-regulated in aged cells
34 tion in muscle cells through an induction of uncoupling protein 2 (UCP-2) and through regulation of t
35  modest increases in the expression level of uncoupling protein 2 (UCP-2) leads to a rapid and dramat
36                                              Uncoupling protein 2 (UCP-2) was increased as were other
37 vity (which peaks at 30 minutes post-PH) and uncoupling protein-2 (UCP-2) (which begins around 30 min
38 bility to replenish ATP due to overexpressed uncoupling protein-2 (UCP-2) or (2) induction of growth
39  Quantitative RT-PCR indicated that mRNA for uncoupling protein-2 (UCP-2) was increased in the cPLA(2
40 ng enzymes of free fatty acid metabolism and uncoupling protein-2 (UCP-2).
41 trated that global deletion of mitochondrial uncoupling protein 2 (UCP2(-/-)) in mice impaired glucag
42 (PPARy) and promotes the PPARy-mitochondrial uncoupling protein 2 (UCP2) cascade.
43 se core temperature and white adipose tissue uncoupling protein 2 (UCP2) expression in aP2-agouti tra
44 ciation between alleles of the mitochondrial uncoupling protein 2 (UCP2) gene and obesity because UCP
45  Additionally, intracellular glutathione and uncoupling protein 2 (UCP2) gene expressions were quanti
46                                              Uncoupling protein 2 (UCP2) has been shown to conduct ca
47 sion of the mitochondrial uncoupling protein uncoupling protein 2 (UCP2) in Foxa1-deficient islets, r
48                                              Uncoupling protein 2 (UCP2) is a mitochondrial protein t
49                                Mitochondrial uncoupling protein 2 (UCP2) is an integral membrane prot
50            Here we report that mitochondrial uncoupling protein 2 (UCP2) is expressed discretely in n
51                                              Uncoupling protein 2 (UCP2) is involved in various physi
52                                              Uncoupling protein 2 (UCP2) maps to a region on distal m
53 Here we show that voluntary exercise induces uncoupling protein 2 (UCP2) mRNA expression and mitochon
54                                              Uncoupling protein 2 (UCP2) plays a regulating role in h
55                Mechanistically, ROS promoted uncoupling protein 2 (UCP2) protein expression and phosp
56                            The mitochondrial uncoupling protein 2 (UCP2) relieves oxidative and neuro
57 ostin 23 epistatically relies on a HIF1A-LEP-Uncoupling Protein 2 (UCP2) signaling axis lowering cell
58                                              Uncoupling protein 2 (UCP2) uncouples respiration from o
59 atty acids (FFAs) and elevated expression of uncoupling protein 2 (UCP2) without concomitant increase
60                                              Uncoupling protein 2 (UCP2), a mitochondrial anion carri
61  of glucose sensing in POMC neurons involves uncoupling protein 2 (UCP2), a mitochondrial protein tha
62  factor, CARP, and beta-myosin heavy chain), uncoupling protein 2 (UCP2), a protein involved in the c
63 ) and a concurrent increase in expression of uncoupling protein 2 (Ucp2), a regulator of mitochondria
64 ICU1), mitochondrial Ca(2+) uniporter (MCU), uncoupling protein 2 (UCP2), and leucine zipper EF-hand-
65                                              Uncoupling protein 2 (UCP2), by virtue of its mitochondr
66 pendent on the mitochondrial redox state via uncoupling protein 2 (UCP2)-dependent alterations in mit
67 n evoke strong upregulation of mitochondrial uncoupling protein 2 (UCP2).
68 PPARalpha target gene encoding mitochondrial uncoupling protein 2 (UCP2).
69  MAF BZIP transcription factor A (MafA), and uncoupling protein 2 (Ucp2).
70 d was accompanied by increased expression of uncoupling protein 2 (UCP2).
71 al respiration in mice that are dependent on uncoupling protein 2 (UCP2).
72 f proton transport mediated by mitochondrial uncoupling protein 2 (UCP2).
73 ty from inflammation via upregulation of the uncoupling protein 2 (UCP2).
74 elated peptide 1 (DRP1) under the control of uncoupling protein 2 (UCP2).
75 ation of the anaerobic metabolism-associated uncoupling protein 2 (UCP2).
76        Endoplasmic reticulum (ER) stress and uncoupling protein-2 (UCP2) activation are opposing modu
77 nscription factor-3 (Atf3) and mitochondrial uncoupling protein-2 (Ucp2) are highly induced in Tsc2-d
78         We show that genetic manipulation of uncoupling protein-2 (UCP2) directly affects substantia
79  our group showed an increased expression of uncoupling protein-2 (UCP2) in pancreas from rats with B
80               Current evidence suggests that uncoupling protein-2 (UCP2) is a regulator of insulin se
81                                Mitochondrial uncoupling protein-2 (UCP2) is highly expressed in steat
82                                              Uncoupling protein-2 (UCP2) is present in many tissues w
83                                              Uncoupling protein-2 (UCP2) mediates mitochondrial proto
84 Here, we demonstrated that the mitochondrial uncoupling protein-2 (UCP2) regulates NLRP3-mediated cas
85       Lipid-laden hepatocytes highly express uncoupling protein-2 (UCP2), a mitochondrial carrier tha
86 to preventing insulin release, ROS activates uncoupling protein-2 (UCP2), a mitochondrial inner membr
87 ive response in cancer cells to be linked to uncoupling protein-2 (UCP2), a mitochondrial suppressor
88 amined how liver regeneration is affected by uncoupling protein-2 (UCP2), an inner mitochondrial memb
89                  The endocrine regulation of uncoupling protein-2 (UCP2), an inner mitochondrial prot
90 developmental and nutritional programming of uncoupling protein-2 (UCP2), glucocorticoid receptor (GR
91 ation in the TCA cycle, and independently of uncoupling protein-2 (UCP2), sirtuin-2 (SIRT2), the G pr
92                                          The uncoupling protein 2, UCP2, is a member of a family of i
93 zed as proapoptotic; however others, such as uncoupling protein 2, were not previously known to be ap
94 itochondrial superoxide production activates uncoupling protein 2, which decreases the ATP/ADP ratio