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1 /ionization (MALDI) source after the solvent is evaporated.
2                After separation, the solvent is evaporated and the microchip is ready for MALDI-MS an
3 organic eluate containing extracted analytes was evaporated and reconstituted for LC-MS/MS analysis.
4                   Individual iron (Fe) atoms were evaporated and coadsorbed with CO molecules on a si
5 rimer, and tetramer) with beta-O-4 linkages, were evaporated and deprotonated using negative-ion mode
6           Aqueous solution plutonium samples were evaporated and encapsulated inside of a gold foil a
7             The circumstellar accretion disk was evaporated by ultraviolet radiation from the star wh
8                    In thermal dealloying, Hg was evaporated due to the use of a high-energy electron
9 with 10(2)-10(6) microbial propagules/mL and were evaporated for at least 24 hours.
10 % more sunlight than when volatile chemicals are evaporated from the mixture, and state that "many cl
11 drules come to equilibrium with the gas that was evaporated from other chondrules, and which explains
12     With this approach the analyte molecules are evaporated in a very fast process, comparable to a s
13                                  A gold film was evaporated on top of the CH(3)NH(3)PbI(3) as a back
14 core with a SiO(2) shell, where the core can be evaporated or sublimated from the open end of the she
15 yde, guanidine hydrochloride, and 0.5 M NaCl were evaporated over varying periods of time.
16                         Solutions must often be evaporated prior to analysis either to preconcentrate
17 mmonium bicarbonate is used, the samples can be evaporated rather than desalted, preventing substanti
18                   The organic enriched phase was evaporated, reconstituted in 25muL acetonitrile and
19                           The final extracts are evaporated to dryness, redissolved in 10:90 or 20:80
20  was also observed when the reaction mixture was evaporated to dryness and redissolved in water.
21                  The enriched phase obtained was evaporated to dryness and the residue reconstituted
22                            The organic layer was evaporated to dryness and the residue was reconstitu
23        Water samples containing TDG and TDGO were evaporated to dryness under nitrogen, dissolved in
24                                      Solvent was evaporated under nitrogen stream and lipid content w
25 solutions and SRM soil and tissue digestates were evaporated using a hot plate method and a newly dev
26 ol, 3/2-methyl-1-butanol and ethyl octanoate were evaporated whereas the other volatile compounds inc

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