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1 b use and associated postural adjustments (, companion article).
2 ystallographic protomers as described in the companion article.
3 low, presented in greater detail in a second companion article.
4 4E10HL mice are described in the companion article.
5 ations of platelet aggregation explored in a companion article.
6 rimental validation will be presented in the companion article.
7 reement with the experiments reported in the companion article.
8 ions with experimental observations from the companion article.
9 asome towards oligopeptides described in the companion article.
10 the identity of this trypanosome prompt this companion article.
11 Ross Sea (Andrill-2A) that is presented in a companion article.
12 ation was developed and characterized in our companion article.
13 Unlike b12 knock-in mice, described in the companion article, 4E10HL mice were found to undergo pro
16 ified model to explain measurements from the companion article and from previously published experime
17 l results of W. Y. Yang and M. Gruebele (see companion article) and T. G. Oas and co-workers on the l
18 nded molecular dynamics simulations from the companion article by Beaven et al. in this issue of Biop
19 Integrating genome-scan results from the companion article by Ghosh et al., we identify several r
22 ative models such as the one proposed in the companion article can be used to study cellular network
27 brane unbinding from the cytoskeleton in our companion article I, we focus in this article on the reg
30 ine simulation and experimental results (see companion article in this issue) to achieve a comprehens
36 ote that similar effects are reported in the companion article on fragment ions from electron capture
41 ation with the kinetic data presented in the companion article, provide insight into the rate-limitin
42 th those on enzyme homologs described in the companion articles, reveal conserved biochemical and bio
46 nal octapetides of the alpha-subunits in the companion article, suggesting that the Mtb proteasome ha
47 findings are consistent with results in the companion article that suggest that inducer allows the T
49 dynamics in RAW 264.7 cells developed in the companion article, the calcium response to complement 5a
52 D47) as estimated in a Burns and colleagues' companion Article to obtain the total costs of blood dis
71 f infectious factors is discussed here; in a companion article, we will examine the possible role of
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