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