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1  the plasmid DNA molecule indirectly via two noncovalent bonds.
2 bunits of approximately 15 kDa associated by noncovalent bonds.
3  ions only if these are not held together by noncovalent bonds.
4  two identical 28-kDa subunits associated by noncovalent bonds.
5  12-kDa subunits (alpha(2)beta(2)) linked by noncovalent bonds.
6 s with axial ligands is a sensitive test for noncovalent bonding.
7 e 5+ ions completely destroys their tertiary noncovalent bonding.
8 ons are one of the most important classes of noncovalent bonding, and are seen throughout biology, ch
9  of positively cooperative binding, in which noncovalent bonds are reduced in length and thereby incr
10                  The basis for unprecedented noncovalent bonding between anions and the aryl centroid
11 therwise been realized from the formation of noncovalent bonds between the ligand and repressor monom
12 , are stabilized by longitudinal and lateral noncovalent bonds between the tubulin subunits.
13 nzyme katanin uses ATP hydrolysis to disrupt noncovalent bonds between tubulin dimers within the micr
14  was consistent with the formation of weaker noncovalent bonds between uranium and the carbonyl oxyge
15 we simulate the weakening or dilution of the noncovalent bonds during protein unfolding, and identify
16 less inclined to donate their electrons into noncovalent bonds, e.g., (CDCl2)2, and when relatively b
17 adily donate their nonbonding electrons into noncovalent bonds, e.g., DMF, and when spacer units that
18 The second wheel of Cy3R can form additional noncovalent bonds, e.g., salt bridges, cation-pi interac
19             Some recently studied biological noncovalent bonds have shown increased lifetime when str
20 nding affinity is described as the strongest noncovalent bond in nature, and is ~10(6) - 10(8) times
21                        Finally, we show that noncovalent bonding in a DNA duplex can be preserved fol
22                 However, the ECD data on the noncovalent bonding in the 5+ to 13+ ions, determined ov
23 ent bonds in aptazyme ligases (as opposed to noncovalent bonds in antibodies) potentiated stringent w
24 directed protocols--which rely on the use of noncovalent bonding interactions between molecular build
25 halogen substituents and the strength of the noncovalent bonding interactions between the analyte and
26 ting their formation using various different noncovalent bonding interactions have been introduced an
27 ents that can be tuned through the extensive noncovalent bonding interactions in these interfaces.
28                                              Noncovalent bonding interactions of nitric oxide (NO) wi
29 ycol chain length has on the strength of the noncovalent bonding interactions taking place between cy
30 y using redox energy and precisely organized noncovalent bonding interactions to pump positively char
31 yzed by other antibodies or proteins through noncovalent bonding interactions with the substrates.
32 ding and unfolding, investigate covalent and noncovalent bonding interactions, and probe enzyme kinet
33 iffusion pathways, effected entirely through noncovalent bonding interactions, has inspired chemists
34 g affinities as a result of a combination of noncovalent bonding interactions, including face-to-face
35                      The subtle interplay of noncovalent bonding interactions, resulting from the tin
36 ted by threadlike precursors, as a result of noncovalent bonding interactions, to produce [2]pseudoro
37 tem relies solely on reversible, yet stable, noncovalent bonding interactions.
38 r than fragile supermolecules resulting from noncovalent bonding interactions.
39 t with one another by means of programmable, noncovalent bonding interactions.
40 single crystals as a consequence of multiple noncovalent-bonding interactions between each of the inc
41 e solid state, it has been demonstrated that noncovalent-bonding interactions with a variety of molec
42 ike materials through the utilization of the noncovalent bond, is a developing area of research.
43 lts with the P378L carboxylase indicate that noncovalent bonds maintain the two-chain structure even
44  product ions and by denaturing the tertiary noncovalent bonding of the molecular ions under a variet
45 ly this ion activation breaks intramolecular noncovalent bonds of the ion's secondary and tertiary st
46       In model A, the proton involved in the noncovalent bond suffers a smaller downfield shift becau
47       In model B, the proton involved in the noncovalent bond suffers a smaller downfield shift becau
48 itive-strand genomic RNAs linked together by noncovalent bonds that can be dissociated under mild con
49 by the strengths as well as lifetimes of the noncovalent bonds that lead to the formation of the stru
50  efficient capture, dissociation of tertiary noncovalent bonds that prevent product separation, and m
51 o 9+, not the 10+ to 13+ ions, have tertiary noncovalent bonding; this is indicated as hydrogen bondi
52 lating a metal center by way of covalent and noncovalent bonding, thus preserving its unsaturated val
53 bone bond, but with negligible excitation of noncovalent bonds; thus ECD of a linear protein ion prod
54 and possibly CO) result from anesthetic-like noncovalent bonding to sites within protein or other tis
55        The second is the presence of CN...Se noncovalent bonds which show similarities to the more co
56 n swapping, a domain of a protein breaks its noncovalent bonds with the protein core and its place is
57 nd induce extension by reversibly disrupting noncovalent bonds within this polymeric network.

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