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1 ognized by GroEL, and it displays additional accessibility of tryptophans to acrylamide quenching.
2 t m(6)A controls the RNA-structure-dependent accessibility of RBMs to affect RNA-protein interactions
3 cular targeting mechanisms that regulate the accessibility of DNA to AID and differentially regulate
6 -25 immunofluorescence, reflecting increased accessibility of antibodies to antigenic sites rather th
7 t that later disruption of cell polarity and accessibility of EPEC to BL membrane proteins, such as b
10 e influence of Gb3 glycolipid binding on the accessibility of Trp34 to different quenching agents in
11 A at position -11 has no major effect on the accessibility of DNA to DNase I or KMnO(4) in the presen
12 de-out and inside-out membrane vesicles, the accessibility of Cys148 to either NEM or impermeant meth
13 ionic lipids) and DNA unbinding (measured as accessibility of DNA to ethidium bromide by electrophore
14 and far-UV CD, limited proteolysis, and the accessibility of tryptophans to fluorescence quenchers.
15 lance biosensor revealing an increase in the accessibility of HER2 to Herceptin following deglycosyla
16 helps open the major groove to increase the accessibility of G26 to hydrogen bond donors from the gu
18 00 intracellular localization, affecting the accessibility of p300 to its substrates, p53 and ATG7.
21 e effects, its main disadvantage is the poor accessibility of light to more deeply lying malignancies
22 rm a permeability barrier that regulates the accessibility of prohemocytes to niche derived signals.
23 onto a fused-silica optical fiber lowers the accessibility of Ac to O2, whereas covalent attachment o
24 After 42 days of storage, the accessibility of phosphatidylethanolamine to phospholipa
25 of oligopeptides either through altering the accessibility of His to photochemically produced oxidant
30 substrate binding loop, and (3) blocking the accessibility of Asp189 to the positive1y charged P1 res
31 is thought to be regulated by changes in the accessibility of chromatin to the recombinase machinery,
33 using oxidative cysteine cross-linking, and accessibility of cysteines to the lipid phase was determ
34 chain-length sensor, possibly explaining how accessibility of Dsk2 to the proteasome is limited unles
35 Removal of the CP47 subunit, which increases accessibility of FtsH to the D2 subunit, induced dark de
36 ortal region of FABP4 markedly increased the accessibility of ligands to the cavity while having only
38 mational change that alters the affinity and accessibility of NO to the distal heme pocket of the enz
40 ts of these experiments demonstrate that the accessibility of substrate to the peripheral anionic sit
42 by maintaining an appropriate plasticity and accessibility of sybII to the binding of its cognate SNA
43 utant protein was explained by the increased accessibility of water to the heme binding site, as obse
45 timulation of transcription neither improves accessibility of psoTFOs to their targets nor enhances r
46 ivities of XyG endotransglucosylases and the accessibility of XyG to their action, indicating a role
47 ions may be due to steric constraints on the accessibility of AID to these sites as the displaced str
48 regulation and DNA repair by influencing the accessibility of chromatin to transcription factors and
49 n strand plays a critical role in regulating accessibility of DNA to transcription factors and chroma
50 ioning plays a major role in controlling the accessibility of DNA to transcription factors and other
52 e architecture of DNA, thereby enhancing the accessibility of promoters to transcription factors.
53 loss of DNA methylation has little effect on accessibility of SINEs to transcription machinery or the
54 hat KIR phosphorylation is controlled by the accessibility of ITIM to tyrosine phosphatases and that
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