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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 the second reaction, APOBEC3A deaminates unmodified cytosine
6                                         In a second reaction, AsbC catalyzes transfer of the activate
7 multimeric complex, which then catalyzes the second reaction, Bax-dependent pore formation.
8                                            A second reaction between 2-aminothiazole and peroxide-oxi
9            Following either rearrangement, a second reaction, between MeReO(SCH(2)C(6)H(4)S)Y and Y,
10                                       In the second reaction channel, addition of ozone to the carbon
11 aired and mechanistically intertwined with a second reaction class.
12 The decay to the ground state occurs along a second reaction coordinate associated with decarboxylati
13 e) of a new vibrational coherence along this second reaction coordinate in a mode associated with the
14 he bacterial P450 isozyme that can trigger a second reaction cycle with molecular oxygen.
15                                       In the second reaction, diphosphate ester ionization-initiated
16 ic double-hairpin oligonucleotides while the second reaction explains the ability of the RecA protein
17                                       In the second reaction, galactose-1-phosphate (gal-1-P) is boun
18 e 5'-end of nascent mRNA with GMP during the second reaction in a set of three enzymatic reactions th
19 aldehyde dehydrogenase (ASADH) catalyzes the second reaction in the aspartate pathway, a pathway requ
20 O1, which is known to be associated with the second reaction in the pathway.
21 ate-4-hydroxylase (C4H), which catalyzes the second reaction in the phenylpropanoid pathway.
22  LPAT1 encodes the enzyme that catalyzes the second reaction in the prokaryotic pathway.
23 5'-phosphosulfate (APS) kinase catalyzes the second reaction in the two-step conversion of inorganic
24 5'-phosphosulfate (APS) kinase catalyzes the second reaction in the two-step, ATP-dependent conversio
25 ylates the substrate and is transformed to a second reaction intermediate, a C(4a)-FMN-hydroxy specie
26                 FabA, however, carries out a second reaction involving isomerization of trans-2-enoyl
27                                          The second reaction is faster than the first reaction since
28          These experiments indicate that the second reaction is nearly one order of magnitude faster
29                                          The second reaction is the C17-C20 bond scission, which is s
30                                            A second reaction is the demonstration that HIFU irradiati
31                                          The second reaction joins the two exons with a 3'-5' phospho
32 cofactor 6R-tetrahydrobiopterin (H4B) in the second reaction of NO synthesis, which is conversion of
33 version of l-NHA to NO and citrulline in the second reaction of the NOS.
34 phatidic acid acyltransferase catalyzing the second reaction of the pathway was reduced by RNAi in th
35                                          The second reaction proceeds via iridium-mediated C-H activa
36 ate to the high affinity receptor state (the second reaction) ranges from 10(-4) to 10(-2) s-1.
37                Nitrogen donation reduces the second reaction rate, making the mono squaramide a mild
38 action was not significantly faster than the second reaction sequence.
39  dose; most (10 patients) also developed the second reaction sooner as compared with the first-dose r
40 at the impaired reactivities occurred in the second reaction step in which a non-covalent AT-thrombin
41 er by K60fA thrombin occurs primarily in the second reaction step in which a noncovalent AT-thrombin
42 inases are primarily due to an effect in the second reaction step in which a noncovalent serpin-prote
43 s both substrate binding and the rate of the second reaction step increase.
44 n in the presence of TM was localized in the second reaction step, as reflected by an approximately 2
45 a metal ion-leaving group interaction in the second reaction step, suggesting that the two steps of s
46 roduct yields, specifically by enhancing the second reaction step.
47 ate for cleavage of the scissile bond in the second reaction step.
48 a remarkable 55% yield of fructose after the second reaction step.
49                                       In the second reaction the hydrazone linkage was reduced with s
50                                   During the second reaction, the olefin installed in situ enables C-
51                                       In the second reaction, the oxyferryl intermediate oxidizes the
52 on, which provided a variable (up to several seconds) reaction time.
53 vents the adoption of a conformation for the second reaction to repair the AGT-oligo complex.
54   This alpha-hydroxyketone is oxidized, in a second reaction, to the alpha,beta-diketone (1R,5R)-6,6-
55  and cyclopentane ring formation, and then a second reaction with molecular oxygen in the S configura