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1                                              Fleming Fund, UK Aid, and US Centers for Disease Control
2                                              Fleming oxidation of the related, very functionalized si
3                                            A Fleming phase II trial was designed.
4 ino bicyclo[2.2.1]heptane intermediate 23, a Fleming-Tamao oxidation for the conversion of dimethyl(p
5                   The study was planned as a Fleming two-stage design, enabling one to assess the eff
6                               According to a Fleming 2-stage phase 2 design, monotherapy was consider
7            More than 70 years ago, Alexander Fleming discovered lysozyme and proposed that nonpathoge
8                            Just as Alexander Fleming's penicillin, and the myriad other bioactive nat
9 ird edge was already recognized by Alexander Fleming in 1945 in his Nobel acceptance speech, which wa
10 eport the draft genome sequence of Alexander Fleming's original fungal isolate behind the discovery o
11  Almost 90 years have passed since Alexander Fleming discovered the antimicrobial activity of lysozym
12 m analysis was applied using the O'Brien and Fleming boundaries.
13 ial alkyne hydrosilylation, epoxidation, and Fleming-Tamao oxidation.
14 nt and graft survival using Kaplan-Meier and Fleming-Harrington weighted log-rank test and examined s
15 e chronostratigraphy of the dinosaur-bearing Fleming Fjord Group of central East Greenland and, with
16                                  The O'Brien Fleming boundary at this analysis corresponded to a two-
17                                  The O'Brien-Fleming and Peto group sequential stopping methods are e
18 (.02) did not cross the prespecified O'Brien-Fleming boundary (.00116) for the interim analysis.
19   Planned interim analysis using the O'Brien-Fleming boundary was crossed for improvement in OS.
20 og-rank test was carried out with an O'Brien-Fleming efficacy boundary of P 0.0161.
21 ed on a group sequential design with O'Brien-Fleming spending function.
22 n-DeMets monitoring boundary with an O'Brien-Fleming stopping rule.
23  sequential testing procedure and an O'Brien-Fleming-type alpha-spending function.
24 ce level of 0.20, power of 0.80, and O'Brien-Fleming-type cumulative error spending function), the 83
25 ling with aryl and vinyl halides followed by Fleming-Tamao oxidation enables generation of anti,syn-s
26             In this issue of Molecular Cell, Fleming et al. show that histone H2B ubiquitylation and
27 ent Health, Health Outlook, Health Distress, Fleming Self-Esteem, Bergner Physical Appearance, and Se
28 undation, Courtney Meningioma Research Fund, Fleming Meningioma Research Fund, and the Gray Family Fo
29 ctions and an intramolecular hydrosilylation/Fleming-Tamao oxidation sequence to establish seven of t
30 instock, J.S., Yanek, L.R., Lane, J., Miller-Fleming, T.W., Brody, J.A., Raffield, L.M. et al.
31               Micrococcus luteus (NCTC2665, "Fleming strain") has one of the smallest genomes of free
32 cleaving C-Si bonds under mild conditions of Fleming-Tamao oxidation.
33 The one-sample multiple testing procedure of Fleming was applied at the predetermined recruitment sta
34 erim OS futility analysis was planned as per Fleming design.
35  consider an alternative model, the spatial -Fleming-Viot process ( FV), which has recently gained po
36  Diels-Alder cycloaddition, and a late-stage Fleming-Tamao oxidation.
37 imary end point, evaluated using a one-stage Fleming design for detecting a true success rate of at l
38                                  A two-stage Fleming statistical design was used.
39                                        Tamao-Fleming oxidation of selected 3-silylproline derivatives
40 Prior removal of the silicon moiety by Tamao-Fleming oxidation proceeded in excellent yield and provi
41  via a trans-selective hydrosilylation/Tamao-Fleming oxidation sequence, complementary to the existin
42 o gamma-amino alcohols with a modified Tamao-Fleming oxidation strategy followed by two additional st
43  mild and practical alternative to the Tamao-Fleming oxidation of vinylsilanes and the Arndt-Eistert
44 olanes are suitable substrates for the Tamao-Fleming oxidation to form cyclopropanols with conservati
45 ital Foundation, the Wellcome Trust, and the Fleming Fund.
46 enDE) show amino acid divergence between the Fleming strain and both industrial strains, whereas a su
47  displayed amino acid divergence between the Fleming strain and industrial strains.
48 ial Care using UK aid funding managed by the Fleming Fund.
49 Social Care using aid funding managed by the Fleming Fund.