ライフサイエンスコーパス: oxygen dissociation

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1 en structure population controls the rate of oxygen dissociation.

2 mpeting reaction pathways involving nitrogen-oxygen dissociation and alpha-hydrogen deprotonation for

3 dissociation by providing proximal sites for oxygen dissociation and attachment.

4 ion (TPD) was used to quantify the amount of oxygen dissociation and to study the stability of the ox

5 suggests that the growth edge autocatalyzes oxygen dissociation by providing proximal sites for oxyg

6 The ability to right-shift the oxygen dissociation curve was retained across the spectr

7 moglobin associated with a left-shift in the oxygen dissociation curve, profound ascorbate deficiency

8 tions, and temperature-induced shifts in the oxygen dissociation curve.

9 rying concentrations of NO up to 80 ppm, and oxygen dissociation curves (ODCs) were measured.

10 Wyman, and Changeux to simulate whole-blood oxygen dissociation curves and red cell sickling in the

11 Oxygen dissociation on metal oxides is a key reaction st

12 Direct observation of the oxygen dissociation process is described, quantitatively

13 is confirmed by the dramatic decrease in the oxygen dissociation rate compared with sperm whale myogl

14 rate oxygen affinity, and a relatively rapid oxygen dissociation rate constant.

15 te heme iron, high oxygen affinity, and slow oxygen dissociation rate constant.

16 from each other only in oxygen affinity and oxygen dissociation rate constants, two factors key to t

17 arable stability to autoxidation and similar oxygen dissociation rate.

18 More importantly, our modeling of in vivo oxygen dissociation, sickling, and oxygen delivery sugge

19 le method is presented for separation of the oxygen dissociation step from the overall ORR.

20 (ORR) makes it difficult to investigate the oxygen dissociation step independently.

21 a0.6 Sr0.4 Co0.2 Fe0.8 O3-delta is better at oxygen dissociation than (La0.8 Sr0.2 )0.95 MnO3+/-delta