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1 ant of 1.58 x 10(5) M(-)(1) s(-)(1) for this irreversible reaction.
2 otentials, and is a one-electron, one-proton irreversible reaction.
3 h equilibrium over 24 h, as well as for fast irreversible reactions.
4 e reversible and compare them to essentially irreversible reactions.
5 mer would be present if dissociation were an irreversible reaction and if dimer formation required GT
6 sopentenyl 5-diphosphate in an ATP-dependent irreversible reaction and is therefore an attractive tar
9 ts the potential of this method for studying irreversible reactions at sub-microsecond timescales usi
10 functional rationale for the positioning of irreversible reactions at the beginning of unbranched bi
11 nd the rate constant for the physiologically irreversible reaction between [P]IICB(Glc) and Glc was 3
12 activity inhibition and uses a specific and irreversible reaction between phosphoryl halides and a f
15 We systematically varied the position of the irreversible reaction in model pathways and compared the
16 than an otherwise equivalent pathway with an irreversible reaction located at any step other than the
18 hesized from all-trans-retinal (atRAL) in an irreversible reaction mainly catalyzed by retinal dehydr
19 s preserved for a class of complex, strongly irreversible reaction mechanisms and determine the corre
20 t most unbranched biosynthetic pathways have irreversible reactions near their beginning, many times
22 one site to adjacent sites, and k(trap), for irreversible reaction of the radical cation with H(2)O o
23 und a cyclic molecular track when powered by irreversible reactions of a chemical fuel, 9-fluorenylme
24 ere the redox moieties are ionic, and (2) an irreversible reaction on two different types of enzymes
27 and as the oxidation of retinaldehyde is an irreversible reaction, RA production has to be considere
28 hey encounter mercury ions, which promote an irreversible reaction that converts the dyes to fluoresc
29 of apo and different holo forms of Fet3p are irreversible reactions that depend on the scan rate.
30 nated N-hydroxysulfenamide intermediate, two irreversible reactions that lead to either the disulfide
31 reasons for this fact, then one would expect irreversible reactions to be equally distributed among a
34 nic O6-alkylguanine lesions within DNA in an irreversible reaction which results in inactivation of t
35 C/EBPbeta by helenalin acetate is not due to irreversible reaction with cysteine residues of C/EBPbet
36 1-pyrrolidinyloxy (I) is shown to undergo an irreversible reaction with peroxyl radicals and other ra
38 yme (K1=8.5 microM. 5.2 microM) prior to the irreversible reaction, with maximum rate constants of 0.
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