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1 ial rotation but are incapable of undergoing free rotation.
2 ree translation and linear displacement with free rotation.
3 n forming long fiber networks that allow for free rotations.
4 ues are not fluorescent primarily because of free rotation about an aryl-alkene bond (Figure 1b).
5 only an entropic contribution by suppressing free rotation about the biaryl bond.
6 ere tested to understand the implications of free rotation about the CDC ligand carbon-carbon bonds.
7 ly tethered within a magnetic field allowing free rotation about the yaw axis actively seeks a narrow
8 n contrast to the Felkin-Anh model, in which free rotation around a bond is required to achieve the t
9  render retinal less flexible by restricting free rotation around either the C10-C11 (9,11-bridged re
10  head-tail junction of myosin is provided by free rotation around the bonds of the polypeptide backbo
11       In solution, the NMR spectra show that free rotation around the C-C bonds connecting the ferroc
12 lations to determine the both complexes have free rotation around the CPh-B1 bond.
13 neither polycyclic, nor macrocyclic and have free rotation around the triple bond enabling conformati
14 the beam's boundary conditions allowing only free rotations around its nodal axes.
15 the evaluation of the effect on rates of the free rotation available to the phenyl groups in 2,4-diph
16 lishes the loss on binding of the entropy of free rotation between the two rings of the biphenyl TCB.
17 ncy concentrations, whereas the stalling and free rotation experiments have multiple-site occupancy.
18                                              Free rotation implies that NLs act as swivels.
19 ectroscopy studies reveal varying degrees of free rotation in the flanking cyclopropenylidene groups
20 ough compounds 1-4 were not expected to have free rotation in the solid state, the rotational potenti
21                                         This free rotation is inconsistent with the prevailing model
22                                         This free rotation mechanism for a type I topoisomerase diffe
23 ream of the cleavage site, as opposed to the free rotation mechanism proposed for DNA relaxation; as
24 gation and supercoil release, establishing a free rotation mechanism.
25  for a catalytic mechanism in which there is free rotation of a 4'-ketopyranose intermediate within t
26  This was attributed to the possibility that free rotation of dendrimer nullifies the distance betwee
27                         Release, detected as free rotation of DNA in the presence of an intercalating
28 lar interactions increase significantly, the free rotation of H(2) molecules is increasingly hindered
29 pH 4 in the deoxyMb structure, allowing more free rotation of His64.
30 pterin (AMT) and methotrexate (MTX) in which free rotation of the amide bond between the phenyl ring
31                           In addition, while free rotation of the beta-methyl group results in a sing
32  elsewhere on the same duplex that restricts free rotation of the duplex and/or complex, I.e. the rea
33 ncy of the Fe-S bond lowering the barrier of free rotation of the exchangeable axial ligand, which is
34                                          The free rotation of the fluorescent molecular rotor, only o
35 ic framework in which the linker hinders the free rotation of the fluorophores and excludes certain c
36 lso, the absence of the methyl group and the free rotation of the methoxy group on the dihydronaphtha
37  show these high conductivities are aided by free rotation of the NH(4) (+) units and significant gyr
38                  Additionally, we found that free rotation of the phenyl ring is necessary for high a
39                                       Due to free rotation of the phenylene rings, TPS-DEVD is nonemi
40  model of GenK catalysis is proposed wherein free rotation of the radical-bearing carbon is prevented
41 ethylene bridge (4h-j) linkers that preclude free rotation of the substituted-benzene molecular fragm
42 la(93) to Glu(96) surface loop, which allows free rotation of the sugars into nonproductive binding m
43  two adjacent Pt-N bonds, followed by nearly free rotation of the terminal pyridine ring or rings and
44 rization of these molecules in solution, the free rotations of the triphenylene units around the C-C
45                                              Free rotation, pi-flips and ionic diffusion are ruled ou
46 tum rotation tunneling rather than the quasi-free rotation process.
47 onding to the largest moment of inertia, and free rotation was shown to be hindered in the bilayer in
48 mation, or (2) an uncoupled mechanism termed free rotation, where multiple supercoils are removed per