ライフサイエンスコーパス: second reaction

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1 continuous double helix that facilitates the second reaction.

2 but lacks the ability to participate in the second reaction.

3 In the second reaction, a forwarding primer containing as 5' ov

4 . krusei and C. lusitaniae are detected in a second reaction, also with two probe sets.

5 In a second reaction, AsbC catalyzes transfer of the activate

6 multimeric complex, which then catalyzes the second reaction, Bax-dependent pore formation.

7 A second reaction between 2-aminothiazole and peroxide-oxi

8 Following either rearrangement, a second reaction, between MeReO(SCH(2)C(6)H(4)S)Y and Y,

9 In the second reaction channel, addition of ozone to the carbon

10 The decay to the ground state occurs along a second reaction coordinate associated with decarboxylati

11 In the second reaction, diphosphate ester ionization-initiated

12 ic double-hairpin oligonucleotides while the second reaction explains the ability of the RecA protein

13 In the second reaction, galactose-1-phosphate (gal-1-P) is boun

14 e 5'-end of nascent mRNA with GMP during the second reaction in a set of three enzymatic reactions th

15 aldehyde dehydrogenase (ASADH) catalyzes the second reaction in the aspartate pathway, a pathway requ

16 O1, which is known to be associated with the second reaction in the pathway.

17 ate-4-hydroxylase (C4H), which catalyzes the second reaction in the phenylpropanoid pathway.

18 LPAT1 encodes the enzyme that catalyzes the second reaction in the prokaryotic pathway.

19 5'-phosphosulfate (APS) kinase catalyzes the second reaction in the two-step conversion of inorganic

20 5'-phosphosulfate (APS) kinase catalyzes the second reaction in the two-step, ATP-dependent conversio

21 ylates the substrate and is transformed to a second reaction intermediate, a C(4a)-FMN-hydroxy specie

22 FabA, however, carries out a second reaction involving isomerization of trans-2-enoyl

23 The second reaction is faster than the first reaction since

24 These experiments indicate that the second reaction is nearly one order of magnitude faster

25 The second reaction joins the two exons with a 3'-5' phospho

26 cofactor 6R-tetrahydrobiopterin (H4B) in the second reaction of NO synthesis, which is conversion of

27 version of l-NHA to NO and citrulline in the second reaction of the NOS.

28 phatidic acid acyltransferase catalyzing the second reaction of the pathway was reduced by RNAi in th

29 The second reaction proceeds via iridium-mediated C-H activa

30 ate to the high affinity receptor state (the second reaction) ranges from 10(-4) to 10(-2) s-1.

31 action was not significantly faster than the second reaction sequence.

32 at the impaired reactivities occurred in the second reaction step in which a non-covalent AT-thrombin

33 er by K60fA thrombin occurs primarily in the second reaction step in which a noncovalent AT-thrombin

34 inases are primarily due to an effect in the second reaction step in which a noncovalent serpin-prote

35 s both substrate binding and the rate of the second reaction step increase.

36 n in the presence of TM was localized in the second reaction step, as reflected by an approximately 2

37 a metal ion-leaving group interaction in the second reaction step, suggesting that the two steps of s

38 roduct yields, specifically by enhancing the second reaction step.

39 a remarkable 55% yield of fructose after the second reaction step.

40 ate for cleavage of the scissile bond in the second reaction step.

41 In the second reaction the hydrazone linkage was reduced with s

42 on, which provided a variable (up to several seconds) reaction time.

43 vents the adoption of a conformation for the second reaction to repair the AGT-oligo complex.

44 This alpha-hydroxyketone is oxidized, in a second reaction, to the alpha,beta-diketone (1R,5R)-6,6-

45 and cyclopentane ring formation, and then a second reaction with molecular oxygen in the S configura

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