ライフサイエンスコーパス: respiration rate

1 threshold for ecosystem function (i.e. soil respiration rate).

2 sponsive down to 0.01x the culture's maximum respiration rate.

3 d ICP response to changes in head-of-bed and respiration rate.

4 d pressure but did not change heart rate and respiration rate.

5 ng blood pressure, increasing heart rate and respiration rate.

6 fibroblasts exhibited an exceptionally high respiration rate.

7 ion as being responsible for the decrease in respiration rate.

8 e for Bcl-2 does not prevent the decrease in respiration rate.

9 th thermodynamic and kinetic controls on the respiration rate.

10 tween its resource assimilation rate and its respiration rate.

11 ange in membrane potential despite increased respiration rate.

12 t to that required to support the endogenous respiration rate.

13 associated metabolic demands by altering its respiration rate.

14 en formal mindfulness practice and decreased respiration rate.

15 ctivity, but rather by greater reductions in respiration rate.

16 consistently showed a reduced ADP-stimulated respiration rate.

17 starch, and glutathione levels and a reduced respiration rate.

18 ey functional enzymes could be used to infer respiration rates.

19 s, or that physiological acclimation reduces respiration rates.

20 MP stimulation with high UCP1 expression and respiration rates.

21 soil temperatures and potentially lower soil respiration rates.

22 ly was due to an increase (27%) in leaf dark-respiration rates.

23 ation occurred without a concomitant rise in respiration rates.

24 additive and comparable effects on microbial respiration rates.

25 potassium levels, and reduced mitochondrial respiration rates.

26 tect ferrocyanide or which affected cellular respiration rates.

27 that the 3460A mutation reduced the maximal respiration rate 20-28%, the 11778A mutation 30-36%, and

28 17 times that of forest soil-based MFCs and respiration rates about 10 times higher than forest soil

29 mRNA target levels plateaued or declined at respiration rates above 5 mueeq/L-hr.

30 ming and magnitude of seasonal heterotrophic respiration rates, again reflecting structural uncertain

31 toheterotrophic conditions and exhibited low respiration rate, although the mutant grew normally unde

32 V3 or PIV3 and adenovirus, with an increased respiration rate and body temperature late in the course

33 ch defined by differing parameter values for respiration rate and crop palatability.

34 drial [NADH] ([NADH]m) may regulate cellular respiration rate and energetic state, it is not clear ho

35 . tuberculosis arrests growth, decreases its respiration rate and is resistant to isoniazid, rifampic

36 native gel assay), decrease in mitochondrial respiration rate and reduction of mitochondrial membrane

37 elf life at room conditions by reducing cell respiration rate and water evaporation.

38 hypothermic (30 degreesC) reperfusion, both respiration rates and all enzyme activities remained at

39 Respiration rates and cell concentrations in subseafloor

40 2 millimoles O2 per liter had higher state 3 respiration rates and decreased percentages of alternati

41 der to regulate photosynthetic gas exchange, respiration rates and defend against pathogen entry.

42 ADP/ATP recycling mechanism to maintain high respiration rates and low electron leak.

43 The measurement of low respiration rates and low ethylene production during gro

44 Complex I respiration rates and protein levels were 33% lower in h

45 se lines were characterized by no changes in respiration rates and TCA cycle flux, which together wit

46 Because of the low respiration rates and the thinness of the sediment, inte

47 ies revealed differential changes in overall respiration rates and tricarboxylic acid (TCA) cycle flu

48 d allow realistic estimates of cell-specific respiration rates and turnover times for living bacteria

49 hlorophyll content, photosynthetic activity, respiration rate, and antioxidant capacity.

50 amate and alpha-ketoglutarate, mitochondrial respiration rate, and GSH levels and decreases reactive

51 ity, pupil diameter, electrodermal activity, respiration rate, and phase) or alpha power was observed

52 capacity relative to the residual endogenous respiration rate, and, correspondingly, a higher COX inh

53 ting community composition, enzyme activity, respiration rates, and residual organic matter reactivit

54 rameters (weight loss, firmness, and color), respiration rate, antioxidant activity and phenolics (me

55 ydrostatic pressure on lethal and sublethal (respiration rate, antioxidant enzyme activity) toxicity

56 to stably express full-length ATM, exhibited respiration rates approaching those of wild-type cells.

57 timulation of lymphocytes, with steady-state respiration rate as a convenient marker of metabolic sti

58 These results reject respiration rate as the sole factor impacting the tempo

59 e delay, by a decrease in overall endogenous respiration rate, as measured in vivo in the whole cell

60 Ca content was accompanied by reductions in respiration rate, ascorbic acid degradation, and membran

61 We measured respiration rates associated with leaf litter, wood, and

62 will decrease owing to higher soil and plant respiration rates associated with warming temperatures.

63 ms showed a delay in ethylene production and respiration rate at 20 degrees C and during cold storage

64 -acclimated individuals had lower growth and respiration rates at intermediate temperatures than cold

65 e characteristics are known to regulate soil respiration rates at plot scales within certain biomes,

66 signs, such as body temperature, heart rate, respiration rate, blood pressure, pulse oxygenation, and

67 FeCl(2) addition initially increased respiration rates, but not the total amount of hydrocarb

68 es in HS pigs increased by 1.6 degrees C and respiration rates by 2-fold (P<0.05).

69 rhizal roots and hyphae decrease soil carbon respiration rates by up to 67% under field conditions in

70 reflected by increased hepatic mitochondrial respiration rates, changes in hepatic gene expression, a

71 xpression of Delta13RAP2.12 led to decreased respiration rates, changes in the levels of tricarboxyli

72 Respiration rates, complex I protein and activity, prote

73 ces of variability for in vivo data included respiration rate, degree of user experience, and animal

74 inkage or indirectly by decreasing microbial respiration rates due to lower redox levels in the soil.

75 imals often exhibited long periods of steady respiration rate during either immobility or running, wh

76 Here we present field measurements, respiration rate estimates and a steady-state model that

77 Respiration rates, ETC protein levels, mitochondrial den

78 ring storage, visual quality, physiological (respiration rate, ethylene production, ammonium content)

79 tial, mitochondrial fragmentation, increased respiration rates, exacerbated PINK1/Parkin-dependent mi

80 ng of the Baltic Sea will enhance planktonic respiration rates faster than it will for planktonic pri

81 duced, which reduced ethylene production and respiration rate; however, it did not increase physiolog

82 temperature during cold challenges, enhanced respiration rates, improved glucose homeostasis, and red

83 chondrial structure, number, and the maximal respiration rate in Acsl1(T-/-) hearts, but did not impr

84 n by increasing glycolysis and mitochondrial respiration rate in C2C12 muscle cells.

85 RNA and protein biomarkers with chloroethene respiration rate in Dehalococcoides.

86 e causes an early decrease in the endogenous respiration rate in intact 143B.TK(-) cells.

87 The cys-c1 mutation produces a reduction in respiration rate in leaves, an accumulation of reactive

88 erved an increase of maximum coupled state 3 respiration rate in mitochondria isolated from the place

89 nsistent with the previously reported higher respiration rate in mmdh1mmdh2 leaves.

90 CO2 ), and increased precipitation - on soil respiration rates in an annual-dominated Mediterranean g

91 States 3, 4, and 5 respiration rates in extraocular muscle mitochondria wer

92 rmocline that have multiplicative effects on respiration rates in low-O(2) water.

93 on isotopes, 'omics' analyses and surveys of respiration rates in mesocosms or ecosystems.

94 neous specific substrate uptake, growth, and respiration rates in response to a continuous-to-batch s

95 nderscoring the requirement to maintain high respiration rates in the heart.

96 f intermittent contractions on mitochondrial respiration rates in the human diaphragm following surge

97 Numerous studies have demonstrated that soil respiration rates increase under experimental warming, a

98 Respiration rate increased during the stressful part of

99 pressure, and rate of pressure increase) and respiration rate increased during the stressful part of

100 Respiration rates increased under nutrient-enriched cond

101 Microbial biomass-specific respiration rates increased with incubation temperature,

102 Over the study period, base respiration rates increased with leaf productivity, but

103 Detrital mass-specific respiration rates increased with temperature, exhibiting

104 In freely moving mice, instantaneous respiration rate is extremely variable, and respiration

105 Respiration rate is known to correlate with aspects of p

106 rature, Topt ), the temperature at which the respiration rate is most sensitive to changes in tempera

107 This caused increased respiration rates, leading to the observed higher levels

108 nt exposure caused an immediate reduction in respiration rate, likely due to reduced pumping to preve

109 unstable clones, which along with decreased respiration rates may explain the increased levels of ce

110 CA-RQ 1.3) showed lower ethylene production, respiration rate, mealiness and higher flesh firmness in

111 n increasing, unchanging, or even decreasing respiration rates observed in soils.

112 e) oxidase activity, ethylene production and respiration rate of apples stored for 9months at 1.0 deg

113 OA-treatment reduced the respiration rate of artichokes and led to higher total h

114 The respiration rate of mmdh1mmdh2 seeds was significantly e

115 ion-selective electrode (Ag(+)-ISE) and the respiration rates of E. coli cells were measured by oxyg

116 The authors measured respiration rates of isolated mitochondria using a Clark

117 ved a small but significant reduction in the respiration rates of mitochondria.

118 us to calculate realistic, species-specific respiration rates of root branches.

119 acclimation occur generally, the increase in respiration rates of terrestrial plants in response to c

120 The per-cell respiration rates of this community are about 2 orders o

121 Climate warming is expected to increase respiration rates of tropical forest trees and lianas, w

122 son's r of 0.89 and 0.88, respectively) with respiration rates on log-log plots between 1.5 and 280 m

123 terial oxygen saturation, end-tidal CO2, and respiration rate (P>0.05).

124 and thawed permafrost endmember OC sources, respiration rates per unit dissolved OC were 1.3-1.6 tim

125 State III mitochondrial respiration rates (pmol O2/s/mg wet weight) were 15.05 +

126 cted than required to support the endogenous respiration rate, pointing to a tighter in vivo control

127 ned high sedimentation caused an increase in respiration rate, potentially due to the energetic cost

128 The decrease in the endogenous respiration rate precedes the release of cytochrome c fr

129 sehip oil (RO) at 2% on ethylene production, respiration rate, quality parameters, bioactive compound

130 rcA, R = 0.91 for MvrD; n = 7) or calculated respiration rate (R = 0.81 for FrcA, R = 0.62 for MvrD;

131 al H2 uptake was correlated with rhizosphere respiration rates (r = 0.8, P < 0.001), and H2 metabolis

132 Corresponding net respiration rates (R) are obtained from a net organic ca

133 Reich et al. report that the whole-plant respiration rate, R, in seedlings scales linearly with p

134 se was mainly due to a decreased autotrophic respiration rate (Ra).

135 Intriguingly, however, day respiration rates remained unaffected.

136 onverted into oxygen units, the computed net respiration rate represents less than half the oxygen ut

137 rial function, with markedly reduced maximum respiration rate, reserve respiration capacity, and mito

138 Respiration rates responded weakly to gradients in N or

139 The analysis of endogenous respiration rate revealed a significant decrease in the

140 rease in mitochondrial protein synthesis and respiration rates, revealed, in comparison, a significan

141 Restricted changes were recorded in respiration rate, ripening index, and instrumental colou

142 revealed 2-fold variation in nighttime leaf respiration rate (RN) among mature leaves from an Arabid

143 assess underlying ischemia, and estimate the respiration rate (RR) and tidal volume (TV) from analysi

144 On average, LTMs showed slower baseline respiration rate (RR) than Controls.

145 ned the effects of fire severity on the soil respiration rate (Rs) and its component change in a Dahu

146 d four experiments, we show that whole-plant respiration rate scales approximately isometrically (sca

147 prominent during immobility and running with respiration rates slower than theta oscillations.

148 In its absence, respiration rate slows and the lack of this electron sin

149 response to increased irradiance, low tissue respiration rate, small amounts of stem and root tissue

150 ved effects of TCS on bacterial abundance or respiration rates, suggesting that bacterial density and

151 Shrub vegetation had the highest respiration rates, suggesting that despite higher rates

152 AL displayed a higher baseline mitochondrial respiration rate than SAL.

153 Higher increases in respiration rates than in production may lead to the dep

154 nic substrates is a more dominant control of respiration rates than low temperature.

155 rom KLF4-deficient hearts revealed a reduced respiration rate that is likely due to defects in electr

156 ificantly more than brown ones; both possess respiration rates that are greater than those of higher

157 he dominant hydrocarbon controlling the bulk respiration rates, that the rates peaked around 11 July,

158 intensity fire increased growing-season soil respiration rates through a combination of three mechani

159 at the cause of the high sensitivity of soil respiration rate to changes in snow depth is a unique so

160 re was an initial delay in the return of the respiration rate to normal.

161 al scaling, isometric scaling of whole-plant respiration rate to total nitrogen content is observed w

162 ha lipoic acid (ALA), restored mitochondrial respiration rates to levels approaching those of wild-ty

163 clude that the immediate initial increase in respiration rate upon elevation of work is not activated

164 t there are limits to our ability to predict respiration rates using environmental drivers at the glo

165 ., fungal) drivers of detrital mass-specific respiration rates using the metabolic theory of ecology,

166 report that SOM decomposition or soil basal respiration rate was significantly affected by changes i

167 State IV mitochondrial respiration rates were 3.59 +/- 1.25 and 2.11 +/- 0.97 i

168 Photosynthesis and respiration rates were also reduced in the DeltaCpcC1C2:

169 Interestingly, both pyruvate and glutamate respiration rates were decreased in TG mice.

170 three years, total microbial cell counts and respiration rates were highest in the GAC amended soil.

171 nd gene expression levels, calcification and respiration rates were measured relative to pHT 8.1 cont

172 atory differences became nonsignificant when respiration rates were normalized to the number of respi

173 Maximum mitochondrial respiration rates were significantly (p < 0.001) higher

174 NADH- and FADH(2)-linked maximal respiration rates were similar between lean and obese in

175 In contrast, state 3 respiration rates were similar in ob/ob and control mito

176 t mitochondrial number, size, and fatty acid respiration rates were unchanged.

177 Inactivation of cytosolic PEPCK affected the respiration rate, which suggests that an excess of oxalo

178 arming (1-2 degrees C) had no effect on soil respiration rates, while +N addition and elevated CO2 co

179 ort the maximum NADH dehydrogenase-dependent respiration rate, with no upregulation of translation oc

180 oxygen concentrations suggest that microbial respiration rates within the plume were not appreciably

181 nied by increases in both photosynthesis and respiration rates, without affecting the activity of pho