ライフサイエンスコーパス: RQ

1 RQ and carbohydrate oxidation were inversely related to

2 RQ is also found in several eukaryotic species that util

3 RQ is an aminoquinone that is structurally similar to ub

4 RQ is not found in humans or other mammals, and therefor

5 RQ is not found in humans or other mammals, and therefor

6 RQ is structurally similar to ubiquinone (coenzyme Q or

7 RQ was unaffected by sleep restriction.

8 roup had a slightly higher (0.807 +/- 0.006) RQ than the control group (0.791 +/- 0.005, P = 0.05).

9 ction into the PVN (n = 10) or PFH (n = 10), RQs and locomotor activity were monitored over three hou

10 iture (24-EE), 24-h respiratory quotient (24-RQ), and the oxidation rates of fat and carbohydrate wer

11 At this time, 24-RQ was lowered (P < 0.001), corresponding to a 23% incre

12 with synaptic transmission, Syt1-R398/399Q (RQ), in syt1 null mutant cells.

13 (29 months after imatinib mesylate; median 6 RQ-PCR assays), 23 patients (27%) had disease progressio

14 05] and down-regulation of Cyclin D1 (n = 7; RQ 1 vs. 0.61, P < 0.05) in mesenchymal tissue.

15 0-40 min of treatment, PFH NPY did not alter RQ at any of the doses tested.

16 CA-CF, but fruit stored under DCA-RQ 1.5 and RQ 2.0 also showed higher amounts of key volatile compou

17 8.2+/-5.0 to 35.4+/-9.5 microgram/beat, and RQ increased by 23% (all P<0.05).

18 ain outcome measures included resting EE and RQ (ventilated hood technique), body composition (dual-e

19 Measures included EE and RQ during the sleep episode on day 2 and continuously ov

20 sma GLP-1 concentrations with resting EE and RQ.

21 RMR and RQ did not change significantly from baseline to day 21,

22 based genome-wide autosomal scans on RMR and RQ phenotypes, obtained from indirect calorimetry, were

23 ) contributing to the variability in RMR and RQ.

24 In lean adolescents, 24-h RQ and RQ during SEE decreased (both P < 0.01) and fat oxidatio

25 es in EE (EEchamber), sleeping EE (SEE), and RQ.

26 ed (VO2), carbon dioxide produced (VCO2) and RQ (VCO2/VO2).

27 refore, a real-time quantitative TRAP assay (RQ-TRAP) was optimized in the present study and evaluate

28 (FRET) between 605QD and Cy5 and Iowa Black RQ, we develop a single-QD-based aptameric sensor that i

29 tive correlation with GDR regardless of BMI, RQ, or sex but became nonsignificant in T2DM.

30 e significantly from baseline to day 21, but RQ decreased on day 22 (P < 0.001), which resulted in an

31 ated conditions (lower postprandial or clamp RQ).

32 In conclusion, RQ-TRAP provides a new tool for the rapid and reliable q

33 e monitored by respiratory quotient 1.3 (DCA-RQ 1.3) showed lower ethylene production, respiration ra

34 e monitored by respiratory quotient 1.5 (DCA-RQ 1.5) increased the acetaldehyde, ethanol and ethyl ac

35 The apples were stored in DCA-RQ, a new technology for storing fruits, and were compar

36 cence (DCA-CF) and respiratory quotient (DCA-RQ) on the quality and volatile profile of 'Royal Gala'

37 phere monitored by respiratory quotient (DCA-RQ) with three fruit maturity stages at harvest (early h

38 The storage of 'Galaxy' apple under DCA-RQ 1.3 is efficient in keeping quality regardless of the

39 red under DCA-CF, but fruit stored under DCA-RQ 1.5 and RQ 2.0 also showed higher amounts of key vola

40 (89 +/- 14 kcal/d, P < 0.0001) and decreased RQ (-0.111 +/- 0.003, P < 0.0001).

41 at all times studied and reliably decreased RQ within 30 min of infusion.

42 diabetic versus nondiabetic subjects (Delta RQ 0.06 +/- 0.01 vs. 0.10 +/- 0.01, respectively, P < 0.

43 ASTRO-D2KO mice also exhibited lower diurnal RQ and greater contribution of fatty acid oxidation to e

44 However, NPY reliably enhanced RQs from 30 to 120 min of testing.

45 protonated semiquinone (i.e., k(2)AB = k(ET)(RQ) = 2 x 10(4) s(-)(1)).

46 When we adjusted fasting RQ for percentage body fat and age, the reduced-obese gr

47 lower fasting fat oxidation (higher fasting RQ) and/or an impaired ability to oxidize carbohydrate d

48 To identify a gene specifically required for RQ biosynthesis, we determined the complete genome seque

49 t gene to be discovered that is required for RQ biosynthesis.

50 further validate the requirement of rquA for RQ biosynthesis, we generated a deletion mutant from wil

51 d REE (R(2) ~ 0.9) but were unacceptable for RQ (R(2) = 0.3), Gox, and Fox (R(2) = 0.2).

52 ncy virus strain SIVmac239 were changed from RQ to YE, the resultant virus was able to replicate in p

53 l strain SIVmac239 bearing the mutation from RQ to YE (YE-Nef) both induce an acute lethal disease in

54 In lean adolescents, 24-h RQ and RQ during SEE decreased (both P < 0.01) and fat o

55 The 24-h respiratory quotient (24-h RQ) and 24-h carbohydrate balance (24-h CHO-Bal) are pre

56 The 24-h RQ, 24-h carbohydrate oxidation (24-h CHO-Ox), and 24-h

57 erved region is as follows: block I, [NX]-H-[RQ]-S-X-[LYIM]-D; block II, G-X-[IF]-F-I-[RD]-R; block I

58 gotes (C/C) for the ADIPOR1 SNP had a higher RQ (P = 0.003) and greater overall (P < 0.03) and abdomi

59 KI to minimize Hg(2+) interference; however, RQ-2 selectively detects Au(3+) without any interference

60 ction < 0.001) in relation to 2-y changes in RQ.

61 s seizure, and sudden death were detected in RQ/+ mutant mice in vivo; however, when provoked, cortic

62 cantly associated with a greater increase in RQ (P = 0.01) but was not related to changes in RMR and

63 Similarly, UCN blocked the increase in RQ elicited by NPY alone.

64 mouse exhibited sustained (24 h) increase in RQ values, increased food intake, tolerance to glucose,

65 o the PVN evoked dose-dependent increases in RQ within 30-40 min of treatment, PFH NPY did not alter

66 ted feeding and evoked reliable increases in RQ.

67 antly associated with a greater reduction in RQ (P = 0.03) and a greater increase in RMR and RMR/kg (

68 EE were observed, nor were there changes in RQs after NE or MUS.

69 Both ghrelin and NPY increased RQ, indicating enhanced utilization of carbohydrates and

70 QTL influencing RQ were found on chromosomes 12q13 (1.65) and 14q22 (1.8

71 x kg(-1) x d(-1) with epinephrine infusion; RQ: 0.832 +/- 0.012 with saline infusion and 0.879 +/- 0

72 Increased resting fat metabolism (i.e., low RQ) and obesity were observed to independently promote a

73 ADIPOR1 T and ADIPOR2 G alleles) had a lower RQ than did the rare homozygotes.

74 equired intermediate for the biosynthesis of RQ in R. rubrum.

75 d assays were monitored for the formation of RQ(3).

76 ith R. rubrum used for the identification of RQ biosynthetic intermediates.

77 ith BCR-ABL, and underline the importance of RQ-PCR monitoring to guide management using molecularly

78 uffered soils had the greatest proportion of RQs > 1.0.

79 eating and blocked the peptide's effects on RQ.

80 ) potentiated the effect of NPY (25 pmol) on RQ and food intake, these responses were inhibited by pr

81 Sensitive MRD detection using MFC and/or RQ-PCR has become feasible in virtually all AML patients

82 age-related changes in energy expenditure or RQ.

83 ent of optimized real-time quantitative PCR (RQ-PCR) assays for WT1 (commonly overexpressed and a put

84 ethods including real-time quantitative PCR (RQ-PCR) for abnormal fusion transcripts, RQ-PCR for prot

85 Protein tyrosine phosphatase RQ (PTPRQ) was initially identified as a protein tyrosin

86 hrine infusion ended, but the postabsorptive RQ remained modestly elevated.

87 1 (sFRP-1) [n = 12; relative quantification (RQ) 1 vs. 2.33, P < 0.05] and down-regulation of Cyclin

88 Analysis of relative quantification (RQ) ratios of mGlu2 and mGlu3 mRNA expression revealed a

89 reflected an apparent respiratory quotient (RQ) < 1.

90 Respiratory quotient (RQ) and resting metabolic rate (RMR) were measured.

91 In obese adolescents, respiratory quotient (RQ) and substrate oxidation also did not change.

92 ved measurement of the respiratory quotient (RQ) by indirect calorimetry during the fasted to fed tra

93 ailment on 24-h EE and respiratory quotient (RQ) by using whole-room indirect calorimetry under fixed

94 tabolic rate (RMR) and respiratory quotient (RQ) represent candidate genes for obesity, type 2 diabet

95 d on the nitrogen-free respiratory quotient (RQ) revealed fat oxidation to be significantly increased

96 aluate the appropriate respiratory quotient (RQ) value to achieve a safe lowest oxygen limit (LOL), d

97 Respiratory quotient (RQ) was calculated as V(CO2)/V(O2).

98 REE and the respiratory quotient (RQ) were measured by indirect calorimetry in the postabs

99 esting metabolic rate, respiratory quotient (RQ), and adiposity-related phenotypes.

100 ed with changes in EE, respiratory quotient (RQ), and body composition.

101 or body mass (AEE/BM), respiratory quotient (RQ), and carbohydrate oxidation with QS and SWS during n

102 rgy expenditure (REE), respiratory quotient (RQ), glucose/carbohydrate oxidation (Gox), and fat oxida

103 ed by BMI, the resting respiratory quotient (RQ), T2DM, and sex.

104 metabolic rate (RMR), respiratory quotient (RQ), temperature, fasting serum glucose, insulin, free f

105 ubstrate oxidation-ie, respiratory quotient (RQ).

106 ing and alterations in respiratory quotient (RQ).

107 ected in reductions in respiratory quotient (RQ).

108 iratory exchange rate (respiratory quotient [RQ]) and decreases food intake.

109 to glucose (change in respiratory quotient [RQ]) was mainly related to insulin-stimulated glucose di

110 nt changes in resting respiratory quotients (RQs) in normal (Baseline: 0.78+/-0.03; Depleted: 0.69+/-

111 expenditure (EE) and respiratory quotients (RQs) in the absence of food were made over 2 h in parall

112 ting and postprandial respiratory quotients (RQs), or rate of lipolysis.

113 d in order to compute respiratory quotients (RQs).

114 l have significant pollution risk quotients (RQs > 1), indicating ecotoxicological concerns.

115 Risk quotients (RQs) were calculated on the basis of a dietary Hg exposu

116 ind that a human leaky RyR2 mutation, R176Q (RQ), alters neurotransmitter release probability in mice

117 ing an internationally standardized PML-RARA RQ-PCR assay has been successfully used to guide molecul

118 2 polymorphisms with resting metabolic rate, RQ, and body mass index, percentage body fat, sum of 6 s

119 time quantitative polymerase chain reaction (RQ-PCR) analysis to determine whether frequent monitorin

120 time quantitative polymerase chain reaction (RQ-PCR) assays to detect leukemia-specific transcripts (

121 time quantitative-polymerase chain reaction (RQ-PCR) assays were developed and evaluated in samples a

122 time quantitative polymerase chain reaction (RQ-PCR) measurement of Epstein-Barr viral load, we used

123 time quantitative polymerase chain reaction (RQ-PCR) provides information for patient stratification

124 time quantitative polymerase chain reaction (RQ-PCR)-based MRD detection via antigen-receptor rearran

125 time quantitative polymerase chain reaction (RQ-PCR); 186 were found to have the bcl-2 rearrangement

126 with resistance near the quantum resistance RQ = h/e2, where h is Planck's constant and e is the ele

127 Rhodoquinone (RQ) is a required cofactor for anaerobic respiration in

128 Rhodoquinone (RQ) is an important cofactor used in the anaerobic energ

129 hain; and a laterally acquired rhodoquinone (RQ) biosynthesis enzyme.

130 ve Q(10) in the Q(B) site with rhodoquinone (RQ), which has a higher pK(a), we were able to observe t

131 Rigorous sequential RQ-PCR monitoring provides the strongest predictor of RF

132 ety profile and relative risks of [(18)F]SPA-RQ with 3 different methods of image analysis.

133 P antagonist-receptor quantifier ([(18)F]SPA-RQ) [2-fluoromethoxy-5-(5-trifluoromethyl-tetrazol-1-yl)

134 f 192 +/- 7 MBq (5.2 +/- 0.2 mCi) [(18)F]SPA-RQ.

135 sma were useful as material for EBV-specific RQ-PCR in immunosuppressed patients and nonimmunosuppres

136 hcKO mice also had higher (P<0.05) fed state RQ values than WT animals at 22 degrees C, consistent wi

137 UcnI alone suppressed RQ responses.

138 t grow anaerobically and does not synthesize RQ, and compared it with that of a spontaneous revertant

139 and has recovered the ability to synthesize RQ.

140 smid-complemented F11 was able to synthesize RQ.

141 trastructural morphometry revealed that Syt1-RQ fully restored the docking defect observed previously

142 However, unlike Syt1-wt, Syt1-RQ-induced docking was strictly PI(4,5)P2-dependent.

143 he most common spider species using targeted RQ-PCR to quantify the potential efficiency of spiders a

144 The latter observation suggests that RQ is an electron carrier of a fumarate reductase-type c

145 for this increase in REE, determined by the RQ, was from increased carbohydrate oxidation, not from

146 and were thus eligible for inclusion in the RQ-PCR analysis.

147 antly increased REE by 12% and increased the RQ.

148 Finally, overexpressing the RQ-mutant in wild type cells produced no effect on eithe

149 In vitro studies revealed that the RQ mutation selectively strengthened excitatory, but not

150 and 48% lower, respectively, in men with the RQ genotype than in men with the RR genotype but increas

151 ients with sensitivities at least similar to RQ-PCR (</=10(-5)), if sufficient cells (>4 x 10(6), pre

152 CR (RQ-PCR) for abnormal fusion transcripts, RQ-PCR for proteins known to be overexpressed in AML suc

153 and caspase-3 expression was evaluated using RQ-PCR, immunohistochemistry, or Western blot.

154 s and aging on EE and substrate utilization (RQ) in p66 Shc-/- (ShcKO) and wild-type (WT) mice.

155 R2 (ie, IVS1 -1352G-->A) was associated with RQ (P = 0.03 and 0.04, respectively), and the associatio

156 Comparison with RQ-PCR-based MRD data showed a clear positive relation b

157 composition) and negatively correlated with RQ (after adjustment for age, sex, and percentage body f

158 sults confirm the PAET mechanism in RCs with RQ and give strong support that this mechanism is active