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1 tituted pyridines, chiral, and silicon-based tripods.
2 CsNO3 with 0.1 mM HNO3 in the aqueous phase, tripods 1, 2, and 9 enhance CsNO3 extraction by factors
5 we report the crystal structures of several tripod amphiphiles that contain an N-oxide hydrophilic g
6 mpensation for insulin resistance across the TRIPOD and PIPOD studies revealed that pioglitazone stop
7 structures that resemble a spinning top on a tripod and revealed that the two XB co-crystals are isom
8 ween an inward-projecting C-terminal helical tripod and the crossing of two 'ankle' segments; it also
9 density, a compound consisting of a triallyl tripod attached via a p-phenylene unit to a porphyrin (1
14 artz crystal microbalance (QCM) to show that tripod-bound Concanavalin A retains its affinity for pol
15 yridine, phen is 1,10-phenanthroline, and Ad-tripod-bpy (phen) and C-tripod-bpy (phen) are tripod-sha
16 enanthroline, and Ad-tripod-bpy (phen) and C-tripod-bpy (phen) are tripod-shaped bpy (phen) ligands b
17 y)(2)(Ad-tripod-phen)(2+) (1), Ru(bpy)(2)(Ad-tripod-bpy)(2+) (2), Ru(bpy)(2)(C-tripod-phen)(2+) (3),
18 (2)(C-tripod-phen)(2+) (3), and Ru(bpy)(2)(C-tripod-bpy)(2+) (4) (where bpy is 2,2'-bipyridine, phen
27 e identical sulfur-containing termini as the tripod feet, 4-acetylsulfanylmethylphenyl units in the c
29 We show that the model has stable double-tripod gaits over the animal's speed range, that its dyn
30 ution data revealed that 7.9% ID/g of RGD-Au-tripods had accumulated in the U87MG tumor after 24 h po
31 model for Individual Prognosis Or Diagnosis (TRIPOD) Initiative developed a set of recommendations fo
34 sts of three oligophenylene heptamers as the tripod legs and one bromophenyl group as the functional
35 bend between domains 1 and 2 of ICAM-2 and a tripod-like arrangement of N-linked glycans in the membr
41 porates a surface attachment group (triallyl tripod or vinyl monopod) and a distal functional group (
42 Four tripodal sensitizers, Ru(bpy)(2)(Ad-tripod-phen)(2+) (1), Ru(bpy)(2)(Ad-tripod-bpy)(2+) (2),
43 bpy)(2)(Ad-tripod-bpy)(2+) (2), Ru(bpy)(2)(C-tripod-phen)(2+) (3), and Ru(bpy)(2)(C-tripod-bpy)(2+) (
44 of the heterohexameric receptor-binding and tripod protein complexes within its baseplate about an a
45 ults in disruption of the interaction of the tripod proteins with the tail sheath, hence triggering i
46 -Asp-d-Phe-Cys (RGDfC) peptide conjugated Au-tripods (RGD-Au-tripods) to U87MG tumor-bearing mice sho
48 ripod-bpy (phen) and C-tripod-bpy (phen) are tripod-shaped bpy (phen) ligands based on 1,3,5,7-tetrap
51 of the hexaphenylene boronate to provide the tripod-shaped oligophenylene, composed of 22 phenylene a
52 -targeting moiety, and 1,3,5-triazine as the tripod splitter module, were designed and synthesized.
60 similarity of findings between the PIPOD and TRIPOD studies support a class effect of thiazolidinedio
61 hat occurred during placebo treatment in the TRIPOD study and maintained the stability of beta-cell f
63 omen who were not diabetic at the end of the TRIPOD study, 89 enrolled in the PIPOD study, 86 complet
67 RGDfC) peptide conjugated Au-tripods (RGD-Au-tripods) to U87MG tumor-bearing mice showed PAI contrast
71 double bond in each of the three legs of the tripod upon the hydrosilylation process accompanying att
74 tropic, branched, gold nanoarchitectures (Au-tripods) with predetermined composition and morphology f
75 ted through a benzene spacer to an isobutane tripod, with each arm of the tripod ending in a methylth
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