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1 3/H4 during their deposition on DNA by NAP1 (nucleosome assembly protein 1).
2 ion vehicle used for this analysis was NAP1, nucleosome assembly protein 1.
3 similar overall architecture with the yeast nucleosome assembly protein 1 and human SET/TAF-1beta/IN
4 helicase-interacting protein 1), along with nucleosome assembly protein 1, as novel ubiquitin-intera
5 cribe the cloning and analysis of Drosophila nucleosome assembly protein 1 (dNAP-1), a core histone-b
6 ompared the abilities of dNLP and Drosophila nucleosome assembly protein-1 (dNAP-1) to promote the de
7 emodeling factor (ACF), purified recombinant nucleosome assembly protein 1 (dNAP1), purified native c
11 mber of cellular proteins, in particular the nucleosome assembly protein 1-like protein 1 (NAP1L1), b
12 re we show that the acidic histone chaperone nucleosome assembly protein 1 (NAP-1) from yeast reversi
15 coactivator p300, we obtained cDNAs encoding nucleosome assembly protein 1 (NAP-1), a 60-kDa histone
17 found that the cytoplasmic histone chaperone nucleosome assembly protein 1 (Nap1) associates with the
19 d adding an excess of the histone chaperone, nucleosome assembly protein 1 (NAP1) to the H3/H4 prior
27 mbly and remodeling factor (ACF), Drosophila nucleosome assembly protein-1, plasmid DNA, and ATP.
28 The self-association properties of the yeast nucleosome assembly protein 1 (yNAP1) have been investig
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