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1 ter by co-precipitation with barium or other alkaline earth metals.
2 ly relevant concentrations of the alkali and alkaline earth metals.
3 sitive ion mode CAD with/without alkaline or alkaline earth metal adduction, the ratio of product ion
4 r chalcogen (Se, Te) of the type AFFeAs (A = alkaline-earth metal), AFe(2)As(2), AFeAs (A = alkali me
7 ed understanding of the interactions between alkaline earth metals and DOM under conditions that are
10 e to calcium(ii) (such as the lanthanides or alkaline earth metals), and in a few key cases this targ
12 s possessing disulfide bonds with sodium and alkaline earth metal are generated using electrospray io
13 rgan and others is that fluxes of alkali and alkaline earth metals are required for signaling, but tr
14 rigid 7 K argon matrix containing alkali or alkaline earth metal atoms and NO(2) isolated from each
15 asis for analyzing the binding of alkali and alkaline earth metal atoms over a broad range of systems
16 e" structure of stoichiometry AeTiO(2) (AE = alkaline earth metal, Be, Mg, Ca, Sr, and Ba), we find s
18 ionophore-facilitated transfer of a smaller alkaline earth metal cation with higher hydrophilicity a
22 rference effects from other alkali metal and alkaline earth metal cations and has good stability and
23 est in free energy in complexes with smaller alkaline earth metal cations and that zwitterionic forms
25 an indeed function as ligands for alkali and alkaline earth metal cations in a manner similar to that
26 tions to compare the solvation of alkali and alkaline-earth metal cations in water and liquid CO(2) a
28 vation of singly charged cationic alkali and alkaline earth metal complexes, which results in the hig
30 tal amidoborane compounds of the alkali- and alkaline earth metals have in recent years found applica
32 model systems for understanding the roles of alkaline earth metal ions in nucleic acid processing.
34 cated that Cd(II) and the heavier and larger alkaline earth metal ions Sr(II) and Ba(II) were effecti
40 cleavage was detected in the presence of the alkaline-earth metal ions Mg(2+), Ca(2+), Sr(2+), and Ba
43 infinite-layer compound ACuO2 (where A is an alkaline earth metal)-is an excellent way of investigati
44 robe is selective for Hg(II) over alkali and alkaline earth metals, most divalent first-row transitio
45 ite general phenomenon: among the alkali and alkaline earth metals, Na and Mg generally have the weak
46 ither a preferential accumulation of heavier alkaline earth metals nor core-shell structures in the c
50 This indicated that fractionation between alkaline earth metals was not inherent to intracellularl
51 as facilitated through the use of alkali and alkaline-earth metals, which selectively fill the availa
52 own SHG active AMCO3F (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) materials indicates
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