ライフサイエンスコーパス: mitochondrial uncoupling protein

1 d uncoupling protein 3 (UCP3), a thermogenic mitochondrial uncoupling protein.

2 n trophozoites similar to that produced by a mitochondrial uncoupling protein.

3 CP3L; UCP3L does not function primarily as a mitochondrial uncoupling protein.

4 ty acid homeostasis, lipoprotein lipase, the mitochondrial uncoupling protein 1 (UCP1) and sterol reg

5 This occurs despite normal basal mitochondrial uncoupling protein 1 (UCP1) concentration.

6 Mitochondrial uncoupling protein 1 (UCP1) is responsible

7 and that cAMP-dependent transcription of the mitochondrial uncoupling protein 1 (UCP1) promoter by be

8 e tissue (BAT) thermogenesis, which requires mitochondrial uncoupling protein 1 (UCP1).

9 uirrels (Ictidomys tridecemlineatus) express mitochondrial uncoupling protein 1 (UCP1).

10 l as large extramembraneous segments and the mitochondrial uncoupling protein 1, which is a transmemb

11 this serves to up-regulate and activate the mitochondrial uncoupling protein 1, which mediates a pro

12 y in the form of heat through the actions of mitochondrial uncoupling protein 1.

13 ype of thermogenic fat cell that express the mitochondrial uncoupling protein-1 and thus represent a

14 xpression, which encodes the key thermogenic mitochondrial uncoupling protein-1.

15 viously demonstrated that global deletion of mitochondrial uncoupling protein 2 (UCP2(-/-)) in mice i

16 amine the association between alleles of the mitochondrial uncoupling protein 2 (UCP2) gene and obesi

17 Mitochondrial uncoupling protein 2 (UCP2) is an integral

18 Here we report that mitochondrial uncoupling protein 2 (UCP2) is expressed d

19 l proliferation evoke strong upregulation of mitochondrial uncoupling protein 2 (UCP2).

20 uction of the PPARalpha target gene encoding mitochondrial uncoupling protein 2 (UCP2).

21 This increased the expression of mitochondrial uncoupling protein 2 and raised the AMP-to

22 ly enhanced fatty-acid-induced activation of mitochondrial uncoupling protein 2.

23 ulation and function of the cardiac enriched mitochondrial uncoupling proteins 2 and 3 during delayed

24 activating transcription factor-3 (Atf3) and mitochondrial uncoupling protein-2 (Ucp2) are highly ind

25 Mitochondrial uncoupling protein-2 (UCP2) is highly expr

26 Here, we demonstrated that the mitochondrial uncoupling protein-2 (UCP2) regulates NLRP

27 We and others have shown previously that mitochondrial uncoupling protein 3 (UCP3) improves funct

28 Ralpha expression, fatty acid oxidation, and mitochondrial uncoupling protein 3 (UCP3) levels, while

29 and associated with a 38-58% decrease in the mitochondrial uncoupling protein 3 (UCP3) levels.

30 so increased hepatic transcripts for UCP2, a mitochondrial uncoupling protein, and the protein itself

31 In conclusion, mitochondrial uncoupling proteins are necessary componen

32 Mitochondrial uncoupling proteins dissociate ATP synthes

33 in brown adipose tissue, in particular, the mitochondrial uncoupling protein gene (Ucp1).

34 inactivation of the brown adipocyte-specific mitochondrial uncoupling protein gene, Ucp1.

35 Mitochondrial uncoupling proteins have been implicated i

36 orted the identification of a brain-specific mitochondrial uncoupling protein homologue, UCP4.

37 Evidence for the presence of a mitochondrial uncoupling protein in P. berghei was also

38 Fatty acids are known to enhance mitochondrial uncoupling protein (UCP) activity.

39 tative DAF-16-regulated gene ucp-4, the sole mitochondrial uncoupling protein (UCP) in nematodes.

40 we generated transgenic mice expressing the mitochondrial uncoupling protein (Ucp) in skeletal muscl

41 The mitochondrial uncoupling protein (UCP) in the mitochondr

42 and, upon sympathetic stimulation, activate mitochondrial uncoupling protein (UCP)-1 and oxidize fat

43 f AMPK phosphorylation and the expression of mitochondrial uncoupling protein (UCP)-2.

44 Fatty acids induce mitochondrial uncoupling proteins (UCP) 2 and 3 in muscl

45 tty-acid concentrations were raised, cardiac mitochondrial uncoupling proteins (UCP) increased (isofo

46 hanism of fatty acid-dependent uncoupling by mitochondrial uncoupling proteins (UCP) is still in deba

47 ments did not affect protein levels of brain mitochondrial uncoupling proteins (UCP-2, 4, and 5).

48 Brown fat generates heat via the mitochondrial uncoupling protein UCP1, defending against

49 The availability of mice lacking the mitochondrial uncoupling protein UCP1, has provided an o

50 rgy as heat via the unique expression of the mitochondrial uncoupling protein UCP1.

51 e expends energy in the form of heat via the mitochondrial uncoupling protein UCP1.

52 wo major thermogenic pathways encoded by the mitochondrial uncoupling protein (Ucp1) and mitochondria

53 The mRNA levels for the mitochondrial uncoupling protein (UCP1) in fat tissues o

54 ologues of the brown adipose tissue-specific mitochondrial uncoupling protein (UCP1) vary from 29% to

55 occurs in brown adipose tissue (BAT) through mitochondrial uncoupling protein (UCP1).

56 By stimulating proton leak, mitochondrial uncoupling proteins (UCP1-3) increase mito

57 eonatal brain, because of high levels of the mitochondrial uncoupling protein (UCP2).

58 Mitochondrial uncoupling proteins (UCPs) are involved in

59 Mitochondrial uncoupling proteins (UCPs) are transporter

60 be explained by increased expression of the mitochondrial uncoupling protein uncoupling protein 2 (U