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1 the mutated protein to be non-functional by crystal structure analysis.
2 racterized via UV/vis spectroscopy and X-ray crystal structure analysis.
3 was also accomplished and confirmed by X-ray crystal structure analysis.
4 ed by means of DFT calculations and an X-ray crystal structure analysis.
5 mutant that lacks HAUSP binding based on the crystal structure analysis.
6 he solid state have been determined by X-ray crystal structure analysis.
7 ntact surfaces on both proteins according to crystal structure analysis.
8 ehavior in the solid state as shown by X-ray crystal structure analysis.
9 microanalysis, mass spectrometry, and X-ray crystal structure analysis.
10 53 with DNA that complements and extends the crystal structure analysis.
11 via multinuclear NMR spectroscopy and X-ray crystal structure analysis.
12 iterative medicinal chemistry aided by X-ray crystal structure analysis, a new series of inhibitors h
14 ino-6-chloro-benzimidazole) was subjected to crystal structure analysis and a high resolution crystal
16 conformational aspects were studied by X-ray crystal structure analysis and molecular mechanics calcu
19 ative process of synthesis, crystallography, crystal structure analysis, and computational methods.
20 crocycles were characterized by X-ray single-crystal structure analysis, and, in all cases, NMR spect
28 hich is similar to a motif recently shown by crystal structure analysis in BtuC and previously shown
34 tes peptide conformational data derived from crystal structure analysis of an MN-isolate peptide (RP1
36 importance of these waters directly by X-ray crystal structure analysis of complexes with four mutant
40 eocontrol in complex settings allowing X-ray crystal structure analysis of natural and unnatural dias
43 number of biophysical techniques, including crystal structure analysis of receptor-stapled peptide c
45 ylbutyric acid was established as R by X-ray crystal structure analysis of the (R)-(+)-alpha-methylbe
48 ransferase activity, we have carried out the crystal structure analysis of the Gal-T1.LA complex with
52 e correlated with contacts implicated by the crystal structure analysis of the trp repressor-operator
56 e ORAI1 gene, modeling of mutations on ORAI1 crystal structure, analysis of ORAI1 mRNA and protein ex
59 nts (by stopped-flow IR spectroscopy), X-ray crystal structure analysis, quantum chemical calculation
67 product is deep blue in color, and an X-ray crystal structure analysis reveals it to be the S4 symme
75 hese results, combined with a computer-aided crystal structure analysis, suggest a model in which p53
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