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1 lly dispersed on the support surface (Pt/Al3+penta = 1), whereas two-dimensional Pt rafts form at hig
2 oncentrations of 14 PBDE congeners including penta (28, 47, 99, 100, 153, 154), octa (183, 196, 197,
3 etected in the CCC fractions (12 tetra-, 117 penta-, 81 hexa-, and 17 heptachlorinated OH-CTTs), whic
4  of di-(AG/CT), tri-(AGG/CTT), tetra-(AAAT), penta-(AGAGG), and hexa-(AGAGGG) repeats was 34.9%, 7.0%
5  with the synthesis of enkephalin-like model penta- and decapeptides, then octreotate amide and final
6 tional study on amino- and nitro-substituted penta- and heptafulvenes reveals the interplay between t
7 rocyclic and linear isomers were detected in penta- and heptameric assemblies; in the larger octa- an
8 utants retain the ability to synthesize some penta- and hexa-acylated lipid A molecules because of li
9 d lipopolysaccharide (LPS) with a variety of penta- and hexa-acylated lipid A structures under differ
10         Specifically, caspase-11 responds to penta- and hexa-acylated lipid A, whereas tetra-acylated
11 ogeneous mixture of lipid A structures, with penta- and hexa-acylated structures containing one and t
12 orewater concentrations, by >90% for tetra-, penta- and hexa-clorinated congeners to 60-70% for octac
13 d NO(-), respectively, to yield a mixture of penta- and hexa-coordinate nitrosylated cyt c.
14                                 In contrast, penta- and hexa-O-galloyl-glucose induced greatest and m
15                    These strains accumulated penta- and hexaacylated free lipid A containing a second
16 LpxL and LpxM, resulting in the synthesis of penta- and hexaacylated lipid A, which is optimal for th
17 akthrough of high-volume sampler filters for penta- and hexachlorobenzene and semiquantitative values
18             Benchmarking of PAHs relative to penta- and hexachlorobenzene confirmed that the most rem
19 .042) for most groups, with the exception of penta- and hexachlorobiphenyls, DDE and mirex.
20 eflecting changes in the equilibrium between penta- and hexacoordinate heme species in the enzyme.
21 The concept of planar hypercoordinate (e.g., penta- and hexacoordinate) carbons is intriguing as it i
22  in multiple bonding and the ability to form penta- and hexacoordinated structures, that mean that ch
23 glutamate analogue) and 36% of D1694 (mostly penta- and hexaglutamates) remained in the cells.
24 s for cytotoxicity, was anabolized mostly to penta- and hexaglutamates, whereas approximately 80% of
25 ed in very strong amplification of the large penta- and hexameric macrocycles.
26 mes cleave tri- and tetramers of GlcNAc from penta- and hexameric oligomers and are unable to cleave
27 F in a stepwise sequential manner, but novel penta- and hexapeptides as well as tri- and tetrapeptide
28                          However, for larger penta- and hexasaccharides (LNF-1 and LND-1), the anisot
29  of 2013, which may reflect the phase-out of penta- and octa-BDE mixtures has led to significant decl
30                          A mass inventory of penta- and octa-BDEs in Toronto was estimated to be 200
31 al trends are consistent with the removal of penta- and octa-PBDEs from the global market.
32  emissions of 0.4-4 tonnes.y(-1) for each of penta- and octaBDE and 0.35-3.5 tonnes.y(-1) for decaBDE
33                                The stocks of penta- and octaBDE peaked in in-use products at 17,000 (
34           Acute 48-h nominal LC50 values for penta- and octabromodiphenyl ether (pentaBDE, octaBDE),
35  A structural heterogeneity, containing both penta- and tetra-acylated lipid A structures.
36                                 Although the penta- and tetra-CNs (predominantly CN-52/60 and CN-42)
37 emistry is described with a system involving penta- and tetracationic intermediates.
38 ated by the signalling nucleotides guanosine penta- and tetraphosphate ((p)ppGpp).
39 iated by the signaling nucleotides guanosine penta- and tetraphosphate (ppGpp).
40  and tetraphosphate [(p)ppGpp] and adenosine penta- and tetraphosphate [(p)ppApp] have distinct funct
41 hemically similar, the nucleotides guanosine penta- and tetraphosphate [(p)ppGpp] and adenosine penta
42  PBP2a can cross-link glycan strands bearing penta- and triglycine, but not monoglycine, and experime
43  and diazenes for the oxidative synthesis of penta- and trisubstituted pyrroles: a nitrenoid analogue
44 By contrast, serum concentrations of tetra-, penta-, and hexa-BDEs were lowest in the youngest childr
45 alyzes the hydrolysis of diadenosine tetra-, penta-, and hexa-phosphates with a preference for diaden
46 he most hydrophobic compounds (i.e., tetra-, penta-, and hexachlorobenzene), 1.5% organic matter by m
47                           The planar tetra-, penta-, and hexacoordinate boron are the prevalent struc
48             A large number of planar tetra-, penta-, and hexacoordinate carbon (local-minimum) struct
49 ost abundant, followed by di-, tri-, tetra-, penta-, and hexanucleotide repeat motifs.
50 of microsatellite (mono-, di-, tri-, tetra-, penta-, and hexanucleotide repeats) are found in excess,
51          PnhA hydrolyzes diadenosine tetra-, penta-, and hexaphosphates with a preference for diadeno
52 ient conditions for the synthesis of tetra-, penta-, and hexasubstituted derivatives of 1,4-dihydropy
53  MOS-IV, MOS-V and MOS-VI consist of tetra-, penta-, hexa-, and hepta-saccharides with molecular weig
54  small molecule of natural origin, 1,2,3,4,6-penta- O-galloyl-beta-d-glucopyranose (PGG), binds to ca
55 at one of our synthetic analogues (1,2,3,4,6-penta- O-galloyl-beta-d-mannopyranose (PGM)), with manno
56                         Total consumption of penta-, octa-, and decaBDE from 1970 to 2020 in products
57  10-150, and 200-2000 g.capita(-1).y(-1) for penta-, octa-, and decaBDE, respectively, over the time
58 be transported as efficiently by MsbA as are penta- or hexa-acylated lipid A species.
59                                          The penta- or hexa-coordinate thiolate heme (9 pH 11) and th
60                                          The penta- or hexa-coordinate thiolate heme (9<=pH<=11) and
61 n involves two types of building units where penta- or hexa-coordinated Al is present.
62 sumption that MsbA is optimized to transport penta- or hexaacylated lipid A, we overexpressed the lau
63 ol with boric acid and are likely to contain penta- or hexacoordinated vanadium rather than tetracooo
64 erial species synthesize (p)ppGpp (guanosine penta- or tetraphosphate), a pleiotropic regulator of th
65 ons involving the expansion of tri-, tetra-, penta-, or hexanucleotide repeats cause more than 40 dif
66  zinc bioavailability is inositol hexa- (and penta-) phosphate or phytate.
67 prehensive study of the planar tetra- (ptC), penta- (ppC), and hexacoordinate carbon (phC) by coverin
68  this element, which promotes binding of the penta- rather than that of the dipeptide.
69 ries an unmodified aromatic chromophore, the penta- through decaketides have undergone oxidative cycl
70       Half-lives of 1.5-3 min were found for penta- to mono-acetylation of H3, dynamically acetylated
71 s enzyme is active as a monomer, prefers the penta- to the monoglutamyl form of 5-CHO-H(4)PteGlu(n),
72 ors having different glycine branch lengths (penta-, tri-, or monoglycine), while PBP2a can only cros
73 of underacylated endotoxins (i.e., tetra- or penta- vs hexa-acylated) is determined by post-CD14 inte