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1                                              ALE is released as open source software under the UoI/NC
2                                              ALE pinpoints synthetic errors in both single and metage
3                                              ALE-1, a homologue of lysostaphin, is a peptidoglycan hy
4                                              ALE-1-targeting domain binding studies employing various
5      Unlike AGEs, very little is known about ALE effects in vitro.
6 , and accumulation of the immunoreactive AGE/ALE N( epsilon )-(carboxymethyl)lysine (CML).
7 st in part, by trapping intermediates in AGE/ALE formation and propose a mechanism for PM inhibition
8  trap reactive carbonyl intermediates in AGE/ALE formation, thereby inhibiting the chemical modificat
9 rded evidence of the key role of heme in AGE/ALE formation.
10 propose a mechanism for PM inhibition of AGE/ALE formation involving cleavage of alpha-dicarbonyl int
11          These results indicate that the AGE/ALE inhibitor PM protected against a range of pathologic
12                Our data suggest that the AGE/ALE inhibitory activity and the therapeutic effects of P
13 O and GLA and inhibited formation of the AGE/ALE N(epsilon)-(carboxymethyl)lysine during reaction of
14 uch's membrane, which is associated with AGE/ALE formation.
15                                Levels of AGE/ALEs are increased in diseases like diabetes.
16 ced glycation/lipoxidation end products (AGE/ALEs).
17 ced glycation/lipoxidation endproducts (AGEs/ALEs) in 63 postmortem human donors.
18    PM, as a potent inhibitor of both AGE and ALE formation, may prove useful for limiting the increas
19 Raman spectra from a broad range of AGEs and ALEs, each with a characteristic fingerprint.
20                        Pooling of results by ALE meta-analyses was stratified for population (mood di
21 essfully fabricated after one- and two-cycle ALE of the trilayer graphene, respectively.
22         Using real Pacific Biosciences data, ALE identifies 12 of 12 synthetic errors in a Lambda Pha
23 At the single-base level with Illumina data, ALE recovers 215 of 222 (97%) single nucleotide variants
24    At the genome level with real-world data, ALE identifies three large misassemblies from the Spiroc
25                    Surprisingly, gene-distal ALE isoforms were four times more often localized to neu
26 have developed the Boulder ALignment Editor (ALE), which is a web-based RNA alignment editor, designe
27 ctive lead (antibacterial ligand efficiency (ALE)>0.4).
28 oci for an activation likelihood estimation (ALE) analysis.
29  conducted activation likelihood estimation (ALE) meta-analyses directly comparing the voxelwise conv
30 antitative Activation Likelihood Estimation (ALE) meta-analysis.
31            Activation likelihood estimation (ALE) was used to perform a quantitative meta-analysis of
32 f the graphene layers, atomic layer etching (ALE), a cyclic etching method achieved through chemical
33 e present an Assembly Likelihood Evaluation (ALE) framework that overcomes these limitations, systema
34     Following adaptive laboratory evolution (ALE), the knockouts increase their growth rate by up to
35 lines and found that alternative last exons (ALEs) often confer isoform-specific localization.
36 forms, incorporating alternative last exons (ALEs) that are more proximal to the transcription start
37                                   Binding of ALE-1 to S. aureus cells through its C-terminal 92 resid
38 d 50% identity with the N-terminal region of ALE-1 from Staphylococcus capitis EPK1.
39 hibited lysine modification and formation of ALEs during copper-catalyzed oxidation of low density li
40 hich the linkage between genomic position of ALEs and subcellular localization enables coordinated in
41 en BD-youths and BD-adults identified by our ALE meta-analyses are useful as brain-based diagnostic o
42 AGE) and advanced lipoxidation end products (ALE) in tissue proteins during aging and in chronic dise
43 otein by advanced lipoxidation end products (ALEs) during lipid peroxidation reactions in vitro.
44 n of the advanced lipoxidation end products (ALEs) N(epsilon)-(carboxymethyl)lysine, N(epsilon)-(carb
45 oducts (AGEs) and lipoxidation end products (ALEs), to protect against diabetes-induced retinal vascu
46 rom a protein-coding ASCC3 mRNA to a shorter ALE isoform of which the RNA, rather than an encoded pro
47                                    Synthetic ALE (malondialdehyde-lysine [MDA-Lys]) (50 micromol/l) c
48                        We also conclude that ALEs derived from polyunsaturated fatty acids are increa
49                         We hypothesized that ALEs can have proinflammatory effects in monocytes.
50               These new results suggest that ALEs can promote monocyte activation and vascular compli
51                                          The ALE-1-targeting domain belongs to the SH3b domain family
52           In this study, we demonstrated the ALE process of graphene layers without noticeably damagi
53                              In summary, the ALE framework provides a comprehensive, reference-indepe
54                          We believe that the ALE technique presented herein can be applicable to all
55 e false clusters better than the widely used ALE method by performing numerical experiments, and that

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