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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
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
10 propose a mechanism for PM inhibition of AGE/ALE formation involving cleavage of alpha-dicarbonyl int
13 O and GLA and inhibited formation of the AGE/ALE N(epsilon)-(carboxymethyl)lysine during reaction of
18 PM, as a potent inhibitor of both AGE and ALE formation, may prove useful for limiting the increas
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
26 have developed the Boulder ALignment Editor (ALE), which is a web-based RNA alignment editor, designe
29 conducted activation likelihood estimation (ALE) meta-analyses directly comparing the voxelwise conv
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
36 forms, incorporating alternative last exons (ALEs) that are more proximal to the transcription start
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
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
55 e false clusters better than the widely used ALE method by performing numerical experiments, and that
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