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1 ce calcium hydroxide as a byproduct of their hydration reaction.
2 tion prior to malate release in the fumarate hydration reaction.
3 id, respectively, compared to the unassisted hydration reaction.
4 n metalloenzymes that catalyze hydrolysis or hydration reactions.
5 eous activation of both substrates in alkyne hydration reactions.
6 rbon where proton donation occurs during the hydration reaction and a larger increase in electron den
7 nd activates the metal-ligated water for the hydration reaction and His-164 acts as a catalytic acid.
8 significant catalytic activity in the CO(2) hydration reaction and was inhibited by sulfonamides, su
9 f Inelastic Neutron Scattering to assess the hydration reactions and the interactions between natural
10 s a very high catalytic activity for the CO2 hydration reaction, being similar kinetically to the hum
11 s in rapid equilibrium with HCO(3)(-)via the hydration reaction catalyzed by carbonic anhydrases.
13 ity and first-order rate constant for the CA hydration reaction from 10 degrees C to 40 degrees C usi
14 ACP resulted in the reverse enzyme-catalyzed hydration reaction, giving an approximately 3:1 equilbri
15 , the catalytic water, which is added in the hydration reaction, has been modeled into well-defined e
16 .e., Lys345-NH(2), Glu211-COOH), whereas the hydration reaction is catalyzed by a larger fraction of
22 n of Martian crust suggests that metamorphic hydration reactions played a critical part in the seques
25 crosomal epoxide hydrolase (EPHX1) catalyzes hydration reactions that determine the cellular disposit
26 e via a short sequence ending in a Mukaiyama hydration reaction to establish the key tertiary alcohol
28 arkovnikov reductive amination and oxidative hydration reactions to access linear amines and carboxyl
29 ses effective catalytic activity for the CO2 hydration reaction, with kcat of 9.35 x 10(5) s(-1) and
30 le and overall rate-determining steps in the hydration reaction, with two potential mechanisms propos