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1 ial rotation but are incapable of undergoing free rotation.
2 n forming long fiber networks that allow for free rotations.
5 ly tethered within a magnetic field allowing free rotation about the yaw axis actively seeks a narrow
6 render retinal less flexible by restricting free rotation around either the C10-C11 (9,11-bridged re
7 head-tail junction of myosin is provided by free rotation around the bonds of the polypeptide backbo
10 neither polycyclic, nor macrocyclic and have free rotation around the triple bond enabling conformati
11 the evaluation of the effect on rates of the free rotation available to the phenyl groups in 2,4-diph
12 lishes the loss on binding of the entropy of free rotation between the two rings of the biphenyl TCB.
13 ncy concentrations, whereas the stalling and free rotation experiments have multiple-site occupancy.
15 ectroscopy studies reveal varying degrees of free rotation in the flanking cyclopropenylidene groups
16 ough compounds 1-4 were not expected to have free rotation in the solid state, the rotational potenti
19 ream of the cleavage site, as opposed to the free rotation mechanism proposed for DNA relaxation; as
21 for a catalytic mechanism in which there is free rotation of a 4'-ketopyranose intermediate within t
22 This was attributed to the possibility that free rotation of dendrimer nullifies the distance betwee
25 pterin (AMT) and methotrexate (MTX) in which free rotation of the amide bond between the phenyl ring
27 elsewhere on the same duplex that restricts free rotation of the duplex and/or complex, I.e. the rea
28 ncy of the Fe-S bond lowering the barrier of free rotation of the exchangeable axial ligand, which is
30 lso, the absence of the methyl group and the free rotation of the methoxy group on the dihydronaphtha
33 model of GenK catalysis is proposed wherein free rotation of the radical-bearing carbon is prevented
34 ethylene bridge (4h-j) linkers that preclude free rotation of the substituted-benzene molecular fragm
35 la(93) to Glu(96) surface loop, which allows free rotation of the sugars into nonproductive binding m
36 two adjacent Pt-N bonds, followed by nearly free rotation of the terminal pyridine ring or rings and
38 onding to the largest moment of inertia, and free rotation was shown to be hindered in the bilayer in
39 mation, or (2) an uncoupled mechanism termed free rotation, where multiple supercoils are removed per
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