ライフサイエンスコーパス: oxygen consumption rate

1 se, surgery, or topical drugs on the corneal oxygen consumption rate.

2 relationship between oxygen supply rate and oxygen consumption rate.

3 sufficient to decrease the maximal cellular oxygen consumption rate.

4 ting of the wines studied according to their oxygen consumption rate.

5 cose metabolism, without impacting the basal oxygen consumption rate.

6 P/ADP ratio, CO2 and lactate production, and oxygen consumption rate.

7 xidative phosphorylation on the basis of the oxygen consumption rate.

8 yzed using Fick's law to obtain the per-cell oxygen consumption rate.

9 ex I of the respiratory chain, decreased the oxygen consumption rate.

10 arly in relation to the body mass scaling of oxygen consumption rates.

11 ased basal, spare, and maximal mitochondrial oxygen consumption rates.

12 , with a complimentary reduction in cellular oxygen consumption rates.

13 on-contraction coupling, [Ca(2+)](rest), and oxygen consumption rates.

14 tilage thickness, cell density, and cellular oxygen consumption rates.

15 VEGF+ and Vec cells had equivalent oxygen consumption rates.

16 ited before it affects maximal mitochondrial oxygen consumption rates.

17 owed reduced lean mass (-12%), reduced total oxygen consumption rate (-8%), improved glucose toleranc

18 e metabolic disturbances as shown by reduced oxygen consumption rates after application of topical an

19 O-induced basal leak respiration and overall oxygen consumption rate, along with increased triglyceri

20 Changes in the cellular impedance, oxygen consumption rate and acidification rate can be re

21 Compared to M-MO, GM-MO displayed higher oxygen consumption rate and aerobic glycolysis (extracel

22 individuals, together with markedly reduced oxygen consumption rate and hyperfragmentation of the mi

23 cells (E10) induced a drop in mitochondrial oxygen consumption rate and impairment of cellular bioen

24 e presence of oxygen, profoundly reduced the oxygen consumption rate and increased the extracellular

25 expression in tumor cells regulated cellular oxygen consumption rate and metabolism.

26 observed that TSPO deficiency decreased the oxygen consumption rate and mitochondrial membrane poten

27 The oxygen consumption rate and NAD(P)H oxidation levels inc

28 ived, and from this the relationship between oxygen consumption rate and oxygen partial pressure is d

29 inoma cells overexpressing TIGAR have higher oxygen consumption rates and ATP levels when exposed to

30 evels showed that exposure to SSRI increased oxygen consumption rates and decreased carbohydrate leve

31 I assembly, higher complex I-linked state 3 oxygen consumption rates and decreased superoxide produc

32 As a consequence, oxygen consumption rates and intracellular ATP concentra

33 hese hypoxic "non-Warburg" cells had highest oxygen consumption rates and mitochondrial capacity cons

34 hondrial levels of RMRP, in turn suppressing oxygen consumption rates and modestly reducing mitochond

35 The Mcl-1 transgene increased oxygen consumption rates and mROS expression in mock-inf

36 We have investigated the oxygen consumption rates and oxygen concentration in wil

37 MB increases cellular oxygen consumption rates and reduces anaerobic glycolysi

38 instrument can also be used to measure cell oxygen consumption rates and thereby calculate glycolyti

39 iffusion, have been linked to differences in oxygen consumption rates and/or aerobic activity levels

40 (BV), blood oxygen saturation, tissue pO(2), oxygen consumption rate, and hypoxic fraction.

41 succinate dehydrogenase activity, succinate oxygen consumption rates, and heart adenosine triphospha

42 ted in significantly increased mitochondrial oxygen consumption rates, ATP production rates, and enha

43 production consumed, and (iii) bottom-water oxygen consumption rates become less dependent on relati

44 In vitro study of the cellular oxygen consumption rate before and after PDT treatment i

45 lts showed no significant differences in the oxygen consumption rate between white and red wines, and

46 thermogenic activation of EPA by increasing oxygen consumption rate, brown-specific marker genes, an

47 radual but significant reduction in cellular oxygen consumption rate by 6 hours, corresponding with u

48 reases of brown-specific signature genes and oxygen consumption rate by EPA were concurrent with up-r

49 The lower oxygen consumption rate, changes in lipid and metabolite

50 sensitive, and using a population of cells, oxygen consumption rates could be calculated down to a s

51 Mitochondrial quantity and oxygen consumption rates decrease with aging, although m

52 d the measurement volume biases the measured oxygen consumption rate depending on the actual [O(2)] g

53 edicted from biomechanical modeling, and the oxygen consumption rate during dives decreased with dept

54 wever, M-MO exhibited a significantly higher oxygen consumption rate/ECAR ratio.

55 que imaging system for GSCs, we assessed the oxygen consumption rate, extracellular acidification rat

56 The results indicate that the oxygen consumption rate follows second-order kinetics de

57 tion algorithm to deconvolute the biological oxygen consumption rate from the measured [O(2)].

58 ired glucose uptake, mitochondrial function, oxygen consumption rates, glycolysis, lactic acid, and A

59 ondrial bioenergetic parameters, such as the oxygen consumption rate in cell cultures, enzyme activit

60 -coated microRNA-211 partially augmented the oxygen consumption rate in PIG3V cells.

61 nd two-photon excited fluorescence data, the oxygen consumption rate in the stratum basale is estimat

62 We measured pO(2) and the oxygen consumption rate in vivo by electron paramagnetic

63 ombine to match oxygen diffusion capacity to oxygen consumption rates in both air- and water-breathin

64 nadione sodium bisulfite (MSB) increased the oxygen consumption rates in both cell lines, whereas CCC

65 PCMB (p-chloromercurobenzoate) inhibited the oxygen consumption rates in both WT and rho(0) cells, wh

66 tiproliferative activities and inhibition of oxygen consumption rates in cells were distinctly differ

67 at match the reduced hindlimb blood flow and oxygen consumption rates in IUGR fetal sheep.

68 rates match reduced hindlimb blood flow and oxygen consumption rates in the IUGR fetus.

69 timulation conditions induced increased OCR (oxygen consumption rate) in the presence of Ca2+, which

70 Mitochondrial oxygen consumption rate increases early and decreases du

71 errucosus continuously showed 15-36% reduced oxygen consumption rates indicating metabolic depression

72 Mechanistically, SCH772984 increased the oxygen consumption rate, indicating that these cells rel

73 rial respiratory chain enzyme activities and oxygen consumption rates indistinguishable from controls

74 eases glucose uptake, lactate secretion, and oxygen consumption rates; inhibition of glucose consumpt

75 They also confirm that the oxygen consumption rate is influenced by temperature in

76 Net flux (oxygen consumption rate) is determined by demand for ATP

77 scavenging DPPH, and, even without modifying oxygen consumption rate, it protected quite well wine co

78 ho developed BPD or died had a lower maximal oxygen consumption rate (mean +/- SEM, 107 +/- 8 vs. 235

79 Het and Hom oxygen consumption rates measured in intact myotubes usi

80 the mutant did not exhibit major changes in oxygen consumption rate, mitochondrial membrane potentia

81 roduces cells with gene expression profiles, oxygen consumption rates, nitric oxide production levels

82 depletion from serum blunts the induction of oxygen consumption rate observed in tubule cells treated

83 Results indicate that MPP(+)-induced loss in oxygen consumption rate (OCR) and ATP production by mito

84 lecting an increased production of NADH, and oxygen consumption rate (OCR) by 0.32 nmol/min/100 islet

85 The mitochondrial oxygen consumption rate (OCR) increased in 1alpha,25(OH)

86 urs, we conduct a high-throughput screen for oxygen consumption rate (OCR) reduction and identify a n

87 rat islets by acetylcholine and response of oxygen consumption rate (OCR), NAD(P)H, cytosolic Ca2+,

88 etabolites (glucose, lactate, pyruvate), and oxygen consumption rate (OCR).

89 nover and proton leak to basal mitochondrial oxygen consumption rate (OCR).

90 Oxygen consumption rate (OCR, aerobic respiration) and e

91 Oxygen Consumption Rates (OCRs) are faster with higher c

92 d mitochondrial dysfunction evidenced by low oxygen consumption rates (OCRs), complex activities, ATP

93 riate data techniques identify six different Oxygen-Consumption-Rates (OCRs) as required to completel

94 oxic conditions, decreased the mitochondrial oxygen consumption rate of cultured cells and mice.

95 analyze the onset of the pathology, maximal oxygen consumption rate of left ventricular permeabilize

96 oxygen behaviour in upper basement suggests oxygen consumption rates of 1 nmol cm(-3)ROCK d(-1) or l

97 In particular, the substantially lower oxygen consumption rates of ectotherms of a given body m

98 lls, whereas potassium cyanide decreased the oxygen consumption rates only in WT Molt-4 cells.

99 nide m-chlorophenylhydrazone) stimulated the oxygen consumption rates only in WT Molt-4 cells.

100 sed to measure pO2 profiles and to calculate oxygen consumption rates (Q(O2)) in tumors.

101 Significant oxygen-consumption-rate/reactive oxygen species cause dr

102 Extracellular acidification and oxygen consumptions rates, respective measures of glycol

103 For varying tissue oxygen consumption rates, the importance of the frequenc

104 The algorithm increases the useful range of oxygen consumption rates, the temporal resolution, and d

105 erently dampened and thus underestimates the oxygen consumption rate; the discrepancy is much larger

106 exercise at an intensity of 85 % of the peak oxygen consumption rate (V(O(2))).

107 The circadian rhythmicity of oxygen consumption rate (Vo2) was disrupted in aged obes

108 Oxygen consumption rate was clearly related to the level

109 Oxygen consumption rate was measured in NIH1286/VEGF+ [V

110 Whole-body or cellular oxygen consumption rate was not altered, suggesting MTZ

111 from capillary networks in muscle at a high oxygen consumption rate was simulated using a computatio

112 Oxygen consumption rates were relatively independent of

113 Wild-type Molt-4 cells have moderate oxygen consumption rates, which were significantly reduc