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4 Using pyridine as a nucleophilic probe, we have demonstrated both experimentally and computationally
19 sity of states with density functional theory calculations, we have demonstrated that hydrogen atoms preferentially occup
20 On the background of TH 2 inflammation, we have demonstrated that innate immune cells (notably, airwa
21 the cytoplasmic changes of iron concentration dynamics and we have demonstrated that iron oxide NPs, but not zerovalent
28 ombin microinjection in the mesenteric circulation of mice, we have demonstrated that the fibrin network of thrombi progr
31 Collectively, for the first time to our knowledge, we have demonstrated that the noninvasive measurement of hypo
32 Without losses of the structural advantages, we have demonstrated that the permeation properties of the ho
33 endent counterregulation of MyD88 tyrosine phosphorylation, we have demonstrated that the scaffolding function of recepto
34 odels and sera from clinically well-characterized patients, we have demonstrated that there are dynamic changes in HMGB1
35 ry important outcome of this work is the knowledge that now we have demonstrated that these devices can be successfully o
37 Using a number of complementary techniques, we have demonstrated that these responses are dependent on in
38 a case in point for the physiological roles of the system, we have demonstrated that this multitasking system can be exp
39 Y neurons expressing agouti-related peptide (AgRP) in mice, we have demonstrated that this neuronal population tonically
45 By combining isotope-tracing and genetic experiments, we have demonstrated the presence of an intact de novo biosyn
46 omain peptides are one such assembler, and in previous work we have demonstrated the reversibility of their assembly unde
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