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1 e call MAntel-GLM to Infer Clinal Selection (MAGICS).
2 entists have shown an increasing interest in magic.
6 ent the modulated gene/gene set interaction (MAGIC) analysis to systematically identify genome-wide m
7 genome-wide association studies (DIAGRAM and MAGIC), and a proxy for the PFKM eQTL (rs11168327; r(2)
9 lved absorbance studies was polarized at the magic angle (54.7 degrees) relative to the excitation la
10 ein particles by circular dichroism (CD) and magic angle solid-state nuclear magnetic resonance (MAS
11 ments (17.6, 20.0, and 23.5 T) and ultrafast magic angle spinning (>60 kHz), high-quality spectra wer
13 SpSEEKFLRRIGRFG) are studied using deuterium magic angle spinning ((2)H MAS) line shape and spin-latt
18 various methods, such as cross-polarization magic angle spinning (CPMAS) (13)C NMR and single crysta
19 ontact times were used in cross-polarization magic angle spinning (CPMAS) NMR, CP rotational-echo dou
20 luded quantitative (13)C direct polarization/magic angle spinning (DP/MAS) and DP/MAS with recoupled
22 changes during storage, (1)H high resolution-magic angle spinning (HR-MAS) NMR spectroscopy of apple
25 nd subsequent application of high-resolution magic angle spinning (HRMAS) (1)H nuclear magnetic reson
26 his paper describes a proton high resolution magic angle spinning (HRMAS) nuclear magnetic resonance
27 or all three compounds under both static and magic angle spinning (MAS) conditions at 21.1 T, allowin
28 designed 3D (2)H-(13)C-(13)C solid-state NMR magic angle spinning (MAS) experiment is presented and d
30 dard addition of water is combined with (1)H magic angle spinning (MAS) NMR detection, absolute quant
31 st demonstration of natural-abundance (43)Ca magic angle spinning (MAS) NMR experiments on bone, usin
32 e we report atomic-level characterization by magic angle spinning (MAS) NMR of the muscle isoform of
41 the fibril formation process in vitro, and a magic angle spinning (MAS) NMR study of the fibrils form
42 pic labeling strategies and multidimensional magic angle spinning (MAS) NMR techniques at high magnet
47 absorption fine structure (EXAFS) and (27)Al magic angle spinning (MAS) nuclear magnetic resonance (N
48 ce-specific backbone resonance assignment of magic angle spinning (MAS) nuclear magnetic resonance (N
49 cy driven dipolar recoupling (RFDR) and (1)H magic angle spinning (MAS) nuclear Overhauser effect spe
53 of oriented sample (OS) solid-state NMR and magic angle spinning (MAS) solid-state NMR techniques to
55 vity on natural abundance samples using fast magic angle spinning (MAS), indirect detection of low-ga
57 field of dynamic nuclear polarization under magic angle spinning (MAS-DNP) could be used to dramatic
58 lysis of the (77)Se{(1)H} cross-polarization magic angle spinning and (77)Se spin-echo solid-state NM
59 R1rho rates, which were measured under fast magic angle spinning conditions, vary by an order of mag
60 ing sPREs in practically the entire range of magic angle spinning frequencies used for biomolecular s
61 The impact of the sample temperature and magic angle spinning frequency on epsilon is investigate
63 al, immunohistochemistry and high resolution magic angle spinning magnetic resonance spectroscopy (MR
65 ound to end-binding protein EB1 and free, by magic angle spinning NMR and molecular dynamics simulati
67 th solid-state wide-line and high resolution magic angle spinning NMR as well as with fluorescence co
69 version by solid state (13)C cross-polarized magic angle spinning NMR reveals that solid heptacene ha
73 NMR crystallography approach based on (51)V magic angle spinning NMR spectroscopy and Density Functi
78 ol) in monounsaturated model membranes using magic angle spinning NMR to measure these interactions t
80 eled agonist CP-55,940-d(6) measured by (2)H magic angle spinning NMR, as well as by activation of G
81 an array of approaches (limited proteolysis, magic angle spinning NMR, Fourier transform infrared spe
82 tion of solid-state (13)C-cross-polarization magic angle spinning nuclear magnetic resonance ((13)C-C
83 spectroscopy (XAS), (13)C Cross polarization-magic angle spinning nuclear magnetic resonance (CP-MAS
84 mography, complemented with (27)Al and (31)P magic angle spinning nuclear magnetic resonance (MAS NMR
85 e matrix were investigated using solid-state magic angle spinning nuclear magnetic resonance spectros
86 ders of magnitude in length scale--including magic angle spinning nuclear magnetic resonance spectros
87 ructure of Nafion 211 using calibrated (19)F magic angle spinning nuclear magnetic resonance spectros
90 lies that are stable and are not affected by magic angle spinning of the samples at frequencies betwe
91 inescent scaffolds, (13)C cross-polarization magic angle spinning solid-state (CP-MAS) NMR spectrosco
93 shift data and interhelical cross peaks from magic angle spinning solid-state NMR of a liposomal prep
97 t with dynamic nuclear polarization enhanced magic angle spinning solid-state NMR to study this chall
101 y induced dynamic nuclear polarization) MAS (magic angle spinning) NMR demonstrates that indeed the p
102 at low temperature and high viscosity) MAS (magic angle spinning) NMR that both populations are pres
105 rstitial oxygen, can be resolved by advanced magic angle turning and phase-adjusted sideband separati
106 pin-locking the (1)H magnetization along the magic angle, the (1)H spin diffusion is suppressed such
107 ility, and present a refined high-resolution magic-angle coil spinning (HR-MACS) resonator that impro
108 1)H NMR microprobe featuring high-resolution magic-angle coil spinning (HR-MACS), a simple conversion
113 diffraction, solid-state cross-polarization/magic-angle spinning (13)C NMR, and Bloch-decay (13)C NM
115 of C. elegans based on (1)H high-resolution magic-angle spinning (HR-MAS) nuclear magnetic resonance
116 )C dynamic nuclear polarization at 5 T under magic-angle spinning (MAS) at 82 K using a mixture of mo
119 peptides or proteins by measuring RDCs using magic-angle spinning (MAS) in combination with dipolar r
120 blies in the escape from CypA dependence, by magic-angle spinning (MAS) NMR and molecular dynamics (M
121 powder XRD, (1)H double-quantum solid-state magic-angle spinning (MAS) NMR and small-angle neutron s
123 n structure determination by proton-detected magic-angle spinning (MAS) NMR has focused on highly deu
124 ic reaction centers (RCs) as modification of magic-angle spinning (MAS) NMR signal intensity under il
128 y depends on their dynamics, and solid-state magic-angle spinning (MAS) nuclear magnetic resonance (N
132 I3-SH3 in amyloid fibril form as revealed by magic-angle spinning (MAS) solid-state nuclear magnetic
135 gh-quality membrane protein samples for both magic-angle spinning and oriented-sample solid-state NMR
136 ratio for solid-state NMR experiments under magic-angle spinning and static conditions, respectively
137 ta yielded orientational restraints, whereas magic-angle spinning data yielded interhelical distance
138 amically hyperpolarized (1)H to (13)C during magic-angle spinning dynamic nuclear polarization (DNP)
140 application of (1)H-detected experiments at magic-angle spinning frequencies of >50 kHz enables the
141 , based on a series of temperature-dependent magic-angle spinning multinuclear nuclear-magnetic-reson
142 ng this protocol, proteoliposome samples for magic-angle spinning NMR and uniformly aligned samples (
143 mensional (2D) solid-state (29)Si and (27)Al magic-angle spinning NMR methodologies, including T(1)-r
145 This approach combining oriented-sample and magic-angle spinning NMR spectroscopy in native-like lip
147 study provides, to our knowledge, the first magic-angle spinning NMR structure of an intact filament
149 we utilized state-of-the-art high-resolution magic-angle spinning nuclear magnetic resonance (HRMAS N
150 )3 NASICON series has been analyzed by (31)P magic-angle spinning nuclear magnetic resonance (MAS NMR
152 tate NMR measurements at very fast (100 kHz) magic-angle spinning rates and at high (23.5 T) magnetic
153 guided by structure restraints obtained from magic-angle spinning solid-state NMR experimental data.
154 or dual data acquisition of multidimensional magic-angle spinning solid-state NMR experiments is pres
155 eled octasaccharide heparin analogue enabled magic-angle spinning solid-state NMR of the GAG bound to
156 ntroduce an iterative approach that combines magic-angle spinning solid-state NMR spectroscopy and at
158 rotein structure determination methods using magic-angle spinning solid-state nuclear magnetic resona
159 itates rapid acquisition of multidimensional magic-angle spinning solid-state nuclear magnetic resona
160 n function (PDF) analysis and ex situ (23)Na magic-angle spinning solid-state nuclear magnetic resona
165 l (2D) and three-dimensional high-resolution magic-angle-spinning (13)C solid-state nuclear magnetic
167 t tissue samples by means of high-resolution magic-angle-spinning (HR-MAS) NMR spectroscopy and we pr
169 S31N mutant of M2(18-60) determined using 3D magic-angle-spinning (MAS) NMR spectra acquired with a (
173 shift anisotropy (CSA) tensors, recorded in magic-angle-spinning NMR experiments, provide direct res
176 microscopy and circular dichroism and (11)B magic-angle-spinning NMR spectroscopy, is stable in wate
179 bility of dynamic nuclear polarization (DNP) magic-angle-spinning NMR techniques, along with a judici
180 esicles were studied using (31)P solid-state magic-angle-spinning nuclear magnetic resonance spectros
185 we demonstrate through (13)C high-resolution magic-angle-spinning that (13)C acetate from fermentatio
187 sed on these experimental findings, a novel "magic boron" counting rule is proposed to estimate the n
189 a decade, RNAi has ruled the lab, offering a magic bullet to disrupt gene expression in many organism
193 w-molecular-weight, synthetic BH3 mimetics ("magic bullets") to disrupt the protein-protein interacti
194 can help us understand how the experience of magic can be aesthetically pleasurable, not despite, rat
195 of film growth, from the nucleation of h-BN magic clusters and their sintering to form compact trian
198 During the growth of the shell over the magic core, the core/shell nanocrystals change from type
200 ucose and Insulin-related Traits Consortium (MAGIC) data sets revealed no association with glucometab
202 ing and building it is referred to as "black magic dust" though the staining is often film-like in na
204 transformations of correlation coefficients, MAGIC features fast computation and adaption to variatio
205 ification by common database search engines, MAGIC generates in silico spectra by overwriting the ori
206 ional studies in A. thaliana, especially the MAGIC genetic reference population descended from these
209 hough magnesium was found to be ineffective, MAGiC illustrates an effective strategy for rapid and ef
213 ulated data, we show that the performance of MAGIC is comparable to that of PSMC' even on single dipl
228 of the radio galaxy IC 310 obtained with the MAGIC (Major Atmospheric Gamma-ray Imaging Cherenkov) te
229 r insulin secretion and sensitivity from the MAGIC (Meta-Analyses of Glucose and Insulin-related trai
231 mitochondria-mediated proteostasis mechanism MAGIC (mitochondria as guardian in cytosol) and provide
233 d psilocybin, a classic psychedelic found in magic mushrooms, and a task-free functional MRI (fMRI) p
234 huasca, lysergic acid diethylamide (LSD) and magic mushrooms; demographics, current well-being and pa
240 te ligands, {Pd84 }(Gly) , and the next in a magic number series for this cluster family-a new {Pd72
241 f Au279 follows the mathematical formula for magic number shells: Au@Au12@Au42@Au92@Au54, which is fu
242 Our modeling predicts the existence of a "magic number" effect associated with special, highly sta
246 stems to be decoded from the overall cluster magic-number nuclearity, to the symmetry and building bl
248 scribe the thermodynamic stability of these 'magic-number' colloidal nanoclusters as a function of th
251 nced stability corresponding to the expected magic numbers of 20 and 40 electrons, respectively; whil
253 ounts from 11 to 46 are studied to probe the magic numbers predicted by the spherical jellium model,
255 have a shell structure in which nuclei with 'magic numbers' of neutrons and protons are analogous to
259 py (40 Gy, 5-FU, cisplatin) or chemotherapy (MAGIC or FLOT) for cT3, Nx, M0 esophageal adenocarcinoma
260 ticentre Asthma Genetics in Childhood Study (MAGICS)/Phase II International Study of Asthma and Aller
261 me-wide association studies (GWAS) using the MAGIC population suggests that omega-6 desaturation is l
262 d a subset of 380 SSD lines of the resulting MAGIC population were phenotyped for earliness and genot
263 ucasian children (651 asthmatics) (ISAAC II/ MAGICS population); genotypes of two SNPs were imputed.
265 multiparent advanced generation intercross (MAGIC) population showed that significant natural variat
268 density functional theory demonstrate a new magic ratio rule (MRR) that captures the contribution of
269 ort calculations and also agree with recent "magic ratio rules", which capture the role of connectivi
276 nt the structure of ultra-stable Au144(SR)60 magic-sized nanoclusters obtained from atomic pair distr
278 The global regulatory nucleotide ppGpp ("magic spot") regulates transcription from a large subset
279 In bacteria, a modified nucleotide ppGpp ('magic spot') is a pleiotropic second messenger that medi
280 of the issues is the efficient placement of magic state distillation sub circuits, so-called distill
281 The leading proposals for doing so, such as magic-state distillation and colour-code techniques, hav
285 Assumption Genomic Inference of Coalescence (MAGIC), that reconstructs key features of the evolutiona
286 en concepts that have long been discussed in magic theory, particularly misdirection, and those that
289 omated glycopeptide identification platform (MAGIC) to identify peptide sequences and glycan composit
290 as mating cues, leading to the appearance of magic traits (i.e. phenotypic traits involved in both lo
296 il Adjuvant Gastric Infusional Chemotherapy (MAGIC) trial established perioperative epirubicin, cispl
298 tification for this growing interest is that magic tricks offer novel experimental approaches to cogn
300 Multiparent Advanced Generation Inter-Cross (MAGIC) winter wheat population to explore Bayesian netwo
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