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1 -hybrid screen and confirmed its identity by peptide sequence analysis.
2 roscopy, electrospray mass spectrometry, and peptide sequence analysis.
3 ined from binding free energy estimation and peptide sequence analysis.
4 homogeneity and subjected to amino-terminal peptide sequence analysis.
5 ntified as Xenopus ARF by immunoblotting and peptide sequence analysis.
6 subsequent phosphorylation site mapping and peptide sequence analysis.
7 nformative fragment patterns in tandem MS/MS peptide sequencing analysis.
10 genes for the 58- and 55-kDa subunits using peptide sequence analysis and searching of the yeast gen
12 tor IIH (TFIIH) by affinity purification, by peptide sequence analysis, and by expression of the enti
13 were then characterized by SDS-PAGE, tryptic peptide sequence analysis, and Western blot analysis.
14 ) was identified, supported through in-depth peptide sequencing analysis, and found to carry mitochon
16 amino acid residue of HAV VP1, we performed peptide sequence analysis by protease-catalyzed [18O]H2O
18 arison of the deduced amino acid sequence to peptide sequence analysis data from purified acetyl xyla
32 onate inactivated the enzyme completely, and peptide sequence analysis revealed that tetranitromethan
34 factor to apparent homogeneity and found, by peptide sequence analysis, that it belongs to the NF1 pr
35 coelute with a PP2A enzyme complex, shown by peptide sequence analysis to contain a B' subunit, B56 e
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