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1                                     Abducens internuclear and ascending tract of Deiters (ATD) inputs
2                                 The abducens internuclear and ascending tract of Deiters (ATD) pathwa
3  and soma-dendritic distribution of abducens internuclear and ATD synaptic endings are correlated wit
4 synaptic membrane profile, both the abducens internuclear and ATD synaptic endings are labeled with g
5 as inferred from comparative analyses of the internuclear and intranuclear coherence between bipolar
6 interproton distance and the (13)C-(1)H-(1)H internuclear angle.
7 hat this clustering is due to a short-ranged internuclear attraction.
8 e alkylidene CHR fragment relative to the MC internuclear axis.
9 obules in chromatin and did not abrogate the internuclear bridges seen in the FA-G mutant cells.
10 ance of aneuploid cells and the formation of internuclear chromatin bridges, indicating that nuclear
11    Regarding the latter, the efficiencies of internuclear coherence transfers may be encoded in spect
12 GP was no longer apparent, despite increased internuclear coherence.
13 duced dosage of the gene product, failure of internuclear communication, and failure of transvection
14                                          The internuclear connectivity indicated by the NMR data sugg
15 ng NMR experiment that generates (15)N-(15)N internuclear contacts in protein systems using an optimi
16                             The measured H-C internuclear correlation times indicated differences in
17 gs that are necessary for the observation of internuclear correlations in 2-D experiments.
18 ainly chemical shifts, relaxation rates, and internuclear coupling constants.
19  electron correlation, the onset of electron-internuclear coupling, and quasi-particle formation.
20 EDOR) pulse sequence was used to measure the internuclear dipolar coupling, and the results demonstra
21                       In isotropic solution, internuclear dipolar couplings average to zero as a resu
22 ed on characteristic NMR chemical shifts and internuclear dipolar couplings.
23  train, the magnitude and orientation of the internuclear dipole vector, within the chemical shift an
24 field, Brownian diffusion no longer averages internuclear dipole-dipole interactions to zero.
25 the MCH plane and is perpendicular to the MC internuclear direction.
26 etermined using 3940 (1970 per VEGF monomer) internuclear distance and 476 (238 per VEGF monomer) dih
27     The structure is based on a total of 887 internuclear distance and dihedral restraints derived fr
28 active site loses its ability to restore the internuclear distance between substrate and Fe(IV)=O tha
29 -resonance (REDOR) NMR was used to probe the internuclear distance between the (19)F and the (31)P-la
30                                 Finally, the internuclear distance between the amino nitrogens and th
31 proportionally to the difference in a single internuclear distance between the ground and transition
32  The DRAWS technique was used to measure the internuclear distance between two 13C labels at the carb
33                                          The internuclear distance changes only slightly from the lig
34                                    A minimal internuclear distance is maintained in explants from con
35 3A is essential for nuclear distribution and internuclear distance maintenance in Drosophila.
36                                A (13)C-(13)C internuclear distance measurement from (13)CO(i) to (13)
37 (17)O HETCOR NMR spectra as well as accurate internuclear distance measurements at natural abundance.
38                                              Internuclear distance measurements on PLB using rotation
39 fied conformation (the AC conformer) with an internuclear distance of 4.4 A.
40 duced by molecular dynamics simulations with internuclear distance restraints determined by NMR.
41 uality allowed the correct identification of internuclear distance restraints encoded in 3D spectra w
42 gnetic tags, without the use of conventional internuclear distance restraints.
43         Profiles of cumulative energy versus internuclear distance show large fluctuations and provid
44 llows the NN bond polarization energy and NN internuclear distance to be correlated in three states o
45 ate the average electron position beyond the internuclear distance.
46 e the dependence of the wave function on the internuclear distance.
47                          We observed similar internuclear distances (4.5 +/- 0.2 A) in both Neu and N
48 turn, is employed in experiments to estimate internuclear distances and molecular torsion angles.
49 mics simulated-annealing scheme in which the internuclear distances and van der Waals repulsive terms
50                                          The internuclear distances are extracted by using a simple a
51 onal resonance NMR methods, we show that the internuclear distances between [1-(13)C]Leu7 and [3-(13)
52 loit nuclear Overhauser effects to determine internuclear distances between pairs of protons, without
53                                          The internuclear distances between the HFP 13CO groups and t
54 d explains the difference in the equilibrium internuclear distances for the two spin states.
55 ed to characterize the binding by estimating internuclear distances from (19)F of oritavancin to (13)
56                                              Internuclear distances from (19)F of the DFPBV to the (1
57             High-precision determinations of internuclear distances from NMR recoupling techniques, r
58 ional-echo double resonance NMR by measuring internuclear distances from the (19)F of FBV to (13)C an
59 l-echo double resonance (REDOR) NMR provided internuclear distances from the 19F of this glycopeptide
60 viations from calculated curves based on the internuclear distances from X-ray crystallography.
61 L-Leu-L-Phe we have determined a total of 16 internuclear distances in the 2.5-6 A range.
62 ble-resonance NMR has been used to determine internuclear distances in the complex of glutamine-bindi
63 cell-wall complexes that are consistent with internuclear distances obtained from (13)C{(19)F} and (1
64    NOESY-HSQC, an NMR approach that measures internuclear distances of 6 angstrom or less, and struct
65                                              Internuclear distances represent one of the main structu
66 ical shift resolution required for measuring internuclear distances to (13)C in the retinal chain (C8
67 ne bilayers by determining multiple critical internuclear distances using nuclear Overhauser enhancem
68                                              Internuclear distances were calculated from the initial
69  and ring-current rules, Si bonds at greater internuclear distances, a feature that allows easier des
70 ve a high degree of precision with regard to internuclear distances, geometries, and charges within t
71 o consistent with six other REDOR-determined internuclear distances, most of which agree with values
72  (REDOR) to determine intra- and interligand internuclear distances.
73 ng linear correlations with boron-phosphorus internuclear distances.
74 physiologic signals conveyed by the abducens internuclear (eye velocity and eye position) and ATD (he
75 dividual nRt neurons to the strength of this internuclear inhibition, we obtained whole-cell recordin
76  that the characteristic length scale of the internuclear interaction scales with the density, which
77  these latter measurements also resolve weak internuclear interactions that suggest the formation of
78 a direct bilateral projection of hypoglossal internuclear interneurons onto facial motoneurons.
79                                  Hypoglossal internuclear interneurons projecting to the facial nucle
80                                     Abducens internuclear neurons are responsible for conjugate gaze
81  were VEGF immunopositive, and that abducens internuclear neurons expressed the VEGF receptor Flk1.
82                                     Abducens internuclear neurons of host animals showed a complete r
83 stics and synaptology of axotomized abducens internuclear neurons, which mediate gaze conjugacy for h
84 ns receive two main pontine inputs: abducens internuclear neurons, whose axons course through the med
85 divided into broad categories: supranuclear, internuclear, nuclear, and gaze-holding systems.
86                             Cogan's anterior internuclear ophthalmoplegia (INO) is characterized by I
87                                Patients with internuclear ophthalmoplegia (INO) may have preserved ve
88 ld male presented with left Cogan's anterior internuclear ophthalmoplegia (INO), left appendicular at
89 ), autoimmune retinopathy (n = 1), bilateral internuclear ophthalmoplegia (n = 1), and headache (n =
90 motor deficits in multiple sclerosis include internuclear ophthalmoplegia and nystagmus, resulting in
91 disturbances, or brainstem syndromes such as internuclear ophthalmoplegia developing over several day
92  FINDINGS: Studies have supported the use of internuclear ophthalmoplegia, a model to study effects o
93                                              Internuclear ophthalmoplegia, a new finding, was present
94 ognised syndromes such as optic neuritis and internuclear ophthalmoplegia, respectively.
95 n comparison to those evoked by the abducens internuclear pathway as determined electrophysiologicall
96 genic compensatory mechanism of the abducens internuclear pathway that could lead to the observed fir
97                                 The abducens internuclear pathway through the medial longitudinal fas
98 orseradish peroxidase labeling, the abducens internuclear projection is predominantly, if not exclusi
99 ser effects (trnOe) experiments to determine internuclear proton distances.
100 ell as the detection of numerous unambiguous internuclear proximities defining both the structure of
101  the nuclear spreading is due to long-ranged internuclear repulsion.
102 sition rate depends strongly on both the N-O internuclear separation and the molecular orientation an
103        During mitosis, the rate of change of internuclear separation in Deltakif12 cells is reduced c
104 ated by one or two covalent bonds, where the internuclear separation is known and the measured dipola
105 d that autoionization cannot occur until the internuclear separation of the fragments is greater than
106 upling across hydrogen bonds: (1) the H...O' internuclear separation r(HO)('), (2) the H...O'=C' angl
107 lso contain binuclear complexes with a 4.4 A internuclear separation.
108 rajectories of chemical reactions (change of internuclear separations with time) on the femtosecond t
109  anions XS(-), the unusual shortening of the internuclear Si...N distance is always observed.
110 n Mo/ZSM-5 catalyst by direct observation of internuclear spatial interaction between Bronsted acid s
111                     The majority of abducens internuclear synaptic endings contact distal dendrites,
112                                     Abducens internuclear synaptic endings furthermore have a higher
113 atory neurotransmitters utilized by abducens internuclear synaptic endings whose burst-tonic physiolo
114     We identify two mechanisms for resolving internuclear tensions: nuclear deformation and dispersio
115 way (~20 degrees ) from the boron-phosphorus internuclear vector, leading to an improved understandin
116 direct information on the orientation of the internuclear vector.
117 n times of tumbling motion of the (13)C-(1)H internuclear vectors in the glucose-treated sample are l
118 each constraint restricts the orientation of internuclear vectors with respect to the laboratory fram

 
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