ライフサイエンスコーパス: oxygen transfer

1 tonation of uric acid, activating it for the oxygen transfer.

2 ound I, followed by hydrogen abstraction and oxygen transfer.

3 p-hydroxybenzoate in the transition state of oxygen transfer.

4 and electrochemical, high surface area, and oxygen transfer ability, which have attracted considerab

5 ncy, maternal position significantly affects oxygen transfer across the placenta and may in part prov

6 with reduced utero-placental blood flow and oxygen transfer across the placenta with an average 6.2%

7 yond electron transfer and electron transfer-oxygen transfer aerobic transformations, there a few exa

8 that harnesses the potential of N(2)O as an oxygen transfer agent onto sp(3)-hybridized carbons.

9 tricted fetuses due to 13.5% lower placental oxygen transfer and 26% lower fetal oxygen delivery comp

10 e areas: bioreactor designs for increases in oxygen transfer and decreases in shear stress; bioreacto

11 ntal and fetoplacental blood flow, placental oxygen transfer and fetal oxygenation in FGR and healthy

12 high catalytic activity and surface area to oxygen transfer and fluorescent quenching capabilities a

13 2NC10H6)2TeO with acetonitrile proceeds with oxygen transfer and gives rise to the formation of the n

14 Oxygen transfer and hydrogen migration almost coincide i

15 longation of food shelf life by limiting the oxygen transfer and the reactivity of free radicals, whi

16 olvement of placental BPGM in maternal-fetal oxygen transfer, and in the pathophysiology of FGR.

17 mechanistic peculiarities of stereoselective oxygen transfer are given attention.

18 lavin-dependent halogenases, and an array of oxygen transfer catalysts.

19 used by the FeTPP and P450 systems, with all oxygen transfers coming from an FeO entity.

20 The effect of villi density on oxygen transfer efficiency is assessed by numerically so

21 solved oxygen (DO) concentration can improve oxygen transfer efficiency, thereby reducing energy use.

22 al lineO](2+) occurs by an electron transfer-oxygen transfer (ET-OT) mechanism as supported by the ob

23 O-Au-->Au-OOH-->Au-OH-->Au-H, via successive oxygen-transfer events.

24 pentacoordinate heme sites capable of inert oxygen transfer evolved from hexacoordinate hemoglobins

25 The reaction cascade is initiated by an oxygen transfer from a N-oxide onto a gold-activated alk

26 mation is suggested following intermolecular oxygen transfer from a peroxythiocarbonyl intermediate t

27 manipulated interfaces facilitate the atomic oxygen transfer from adsorbed carbon dioxide molecules t

28 The previously obtained ICR data of oxygen transfer from NO(2)(+) to the aromatic ring are a

29 As the (FeO) content increases in slag, the oxygen transfer from slag to steel is evident, and the i

30 nylamidines readily undergo enantioselective oxygen transfer from sulfur to carbon atom in the presen

31 As a biomarker for oxygen transfer from the lungs into the blood, the oxyge

32 sulfide-containing peptide cation results in oxygen transfer from the reagent anion to the peptide ca

33 The Gibbs free energies of oxygen transfer from these heterocyclic hydroperoxides t

34 surface Bronsted acidity, and rate-limiting oxygen transfer from this intermediate to alkenes, favor

35 transfer from the lungs into the blood, the oxygen transfer function ( OTF oxygen transfer function

36 he blood, the oxygen transfer function ( OTF oxygen transfer function ) was calculated.

37 om oxygen-enhanced MRI T1 mapping (including oxygen transfer function [OTF], delta T1 oxygenated volu

38 OTF oxygen transfer function and volume over threshold are n

39 orrelation (r = 0.65, P = .0001) and the OTF oxygen transfer function at 6 hours showed an inverse co

40 Oxygen transfer function may serve as an early marker fo

41 with the standard dose of allergen, the OTF oxygen transfer function was decreased at 6 hours in ast

42 The oxygen transfer function was significantly lower in pati

43 alues at room air and at 100% oxygen and the oxygen transfer function were calculated.

44 Consequently Au-OH compounds are capable of oxygen-transfer generating gold hydrides, a key reaction

45 may not be sufficient to accurately describe oxygen transfer in the BMHC.

46 thways with more efficient activation of key oxygen-transfer intermediates.

47 An oxygen transfer mechanism can explain the formation of N

48 ing hydrogen-abstraction (H-abstraction) and oxygen-transfer (O-transfer) reactivity of a series of n

49 complex (heme) is an important cofactor for oxygen transfer, oxygen storage, oxygen activation, and

50 Pump performance, oxygen transfer, oxygenator resistance, and hematologic

51 es (IIAs) and umbilical vein (UV), placental oxygen transfer (placental flux), fetal oxygen saturatio

52 esmethyl-TRA (ca. 40%), whereas the proposed oxygen transfer prevails for O(3) attack resulting in N-

53 ces matrix size and bandwidth of the coupled oxygen transfer problem.

54 ng involved also in the catalytically-driven oxygen transfer process, and they suggest that oxygen re

55 O-labeling studies revealed that the S-to-C2 oxygen-transfer process involves initial formation of a

56 o identify specific chemical markers of cork oxygen transfer rate (OTR) influence.

57 Four oxygen transfer rate conditions (0.8, 1.9, 8.0, and 11.9

58 The cork oxygen transfer rate emerged as a pivotal factor and had

59 The system achieved an average oxygen transfer rate of 116.4 +/- 5.5 mL/min, with an av

60 bottled into clear bottles, closed with low oxygen transfer rate stoppers, and stored for three mont

61 assessed for their colour, water vapour and oxygen transfer rate, textural, functional groups and se

62 oppers, ranging from 0.2 to 1.8 mg/L/year of oxygen transfer rate.

63 Studies were then conducted into a unique oxygen transfer reaction between O6-(benzotriazol-1-yl)i

64 The oxygen transfer reaction pathway was determined to be th

65 Kinetic analysis revealed that the oxygen transfer reaction to the phosphetane is rate dete

66 highly regioselective gold-catalyzed single oxygen transfer reaction, involving internal trifluorome

67 positional selectivity, as well as observed oxygen transfer reactions in the gas phase.

68 its analogues can mediate electron transfer-oxygen transfer reactions where oxygen atoms are transfe

69 ivity toward cysteine and methionine through oxygen-transfer reactions and limited reactivity for oth

70 nctional theory (DFT) studies and allows for oxygen-transfer reactions with electron-deficient organi

71 2,3-Dichloropyridine N-oxide, a novel oxygen transfer reagent, allows the conductance of the g

72 building blocks, N(2)O is able to act as an oxygen-transfer reagent that allows the formation of car

73 into carbonyl compounds using nitroarenes as oxygen transfer reagents under visible light.

74 rticipate in hydroxylation, the mechanism of oxygen transfer remains controversial.

75 Most innovations addressed either oxygen transfer, shear induced by stirring, control of w

76 t in stabilizing the transition state of the oxygen transfer step by forming a hydrogen bond between

77 B substrate and to properly align it for the oxygen transfer step.

78 he catalyst surface, for which the selective oxygen-transfer step becomes feasible.

79 After additional proton transfer and oxygen transfer steps, benzylic alcohols are formed that

80 electron fills a vacancy in the 2s state of oxygen, transferring sufficient energy to allow electron

81 f the model that considers tradeoffs between oxygen transfer to eggs versus water loss from them.

82 rin consumption vary 6-fold, consistent with oxygen transfer to the amino acid being partially or ful

83 The reductions in oxygen transfer to the fetus, termed delivery flux, of 1

84 iron-oxo double bond of CYP3A4, resulting in oxygen transfer to the ortho position, is proposed.

85 N-methylquinolinium are used, while in cage oxygen transfer to the photoexcited (thio)pyrylium deriv

86 to the flavin-C4a-hydroxide with concomitant oxygen transfer to the substrate, and the dehydration of

87 Under this paradigm, oxygen transfer to tissues is perfusion-limited.

88 ng the vast respiratory surface across which oxygen transfers to the blood(1).

89 s transfer, while the borate species enables oxygen transfer toward O-O bond formation.

90 of maternal supine positioning on placental oxygen transfer was not independent of the effect of FGR

91 d imaging and T2 relaxometry, blood flow and oxygen transfer were estimated in the maternal, fetal an

92 , experience a relatively greater decline in oxygen transfer when mothers lie supine in late gestatio

93 mbination of electron-transfer mediation and oxygen transfer which was related to the acid/base chemi

94 ascorbic acid degradation was related to the oxygen transfer with higher losses in standard PET (53%)