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1 MAS has the advantage of eliminating fat before LC-GC an
2 MAS is used to oxidize cytosolic NADH in mitochondria, a
3 MAS NMR and Fourier transform infrared measurements show
4 MAS spectra reveal a well-structured VDAC1 in 2D crystal
5 MAS spectra yield isotropic chemical shifts for each cry
6 MAS-ER doses were titrated over 2 weeks to a maximum dos
7 9 T and above, outstanding quality 2D and 3D MAS NMR spectra were obtained for tubular CA and CA-SP1
8 dipolar tensors and peak intensities from 3D MAS NMR spectra of wild-type and the A92E and G94D CypA
12 n fine structure (EXAFS) analysis and (27)Al MAS NMR spectroscopy supported by DFT-based molecular dy
13 ldren of the Multizentrische Allergiestudie (MAS) and 766 children of the Protection against allergy:
16 isometric maximum voluntary contraction and MAS of the knee flexors using submaximal loads relative
18 ncluding gastrin-releasing peptide (GRP) and MAS-related GPCR member A3 (MRGPRA3), in nociceptors exp
19 e gained through treatment trials of HLH and MAS in childhood may inform study design for therapy of
21 arameters, and the combination of static and MAS analyses, can aid investigations of mixed carbonates
23 The results suggest a requirement for ARALAR-MAS in priming pyruvate entry in mitochondria as a step
24 y condition tested Ca2+ activation of ARALAR-MAS was required to fully stimulate coupled respiration
25 ry and oxidation of L-lactate through ARALAR-MAS pathway is required for its neuroprotective function
26 There are several reports of SJIA-associated MAS dramatically benefiting from anakinra, a recombinant
27 of the dipolar couplings can be attained at MAS frequencies of 40 kHz and higher with appropriate de
28 ldren with rheumatic diseases complicated by MAS, and more organ system support is required in childr
29 omonuclear (13)C/(13)C dipolar couplings, by MAS of the sample, enables the use of uniformly (13)C/(1
33 A pronounced ligand effect was found, and CP MAS NMR experiments enabled us to probe important differ
35 ques such as porosity measurements, (13)C CP MAS NMR spectroscopy, and fluorescence spectroscopy stro
37 obtain natural abundance (13)C and (15)N CP MAS NMR spectra of microporous organic polymers with exc
39 etween transformations, solid-state (13)C CP-MAS NMR can be employed to directly monitor phenyl rotat
40 complete, as assessed by FT-IR and (13)C CP-MAS NMR spectroscopy and demonstrates (a) the first chem
43 ngle spinning nuclear magnetic resonance (CP-MAS NMR) spectroscopy, and atom probe tomography (APT).
45 cross-polarization magic angle spinning (CP-MAS) nuclear magnetic resonance (NMR) spectroscopy, the
46 ization magic angle spinning solid-state (CP-MAS) NMR spectroscopy, powder and single-crystal X-ray d
48 from spectral deconvolution of the (13)C CP/MAS spectra and the results has shown that all the extra
51 (e.g., humic matter fractionation, (13)C-CP/MAS NMR, sequential chemical degradation) it was possibl
53 g complementary spectroscopic techniques (CP/MAS (13)C NMR, Raman, FT-IR, and XPS) and high-resolutio
56 rce molecular absorption spectrometry (HR-CS MAS) for F determination and electrothermal vaporization
59 FBA and FICA showed a similar response to CS-MAS detection, potentially enabling the quantification o
60 atography (RP-HPLC) coupled off-line with CS-MAS for the identification of single organofluorines in
62 in, we make use of advances in (1)H-detected MAS NMR to describe the dynamics of the membrane domain
65 er, in two-dimensional and three-dimensional MAS NMR spectra the CL-bound cyt-c displays a spectral r
67 ernative sample preparation strategy for DNP MAS ssNMR studies of lipid membranes and integral membra
70 ization/magic angle spinning (DP/MAS) and DP/MAS with recoupled dipolar dephasing, (13)C cross-polari
71 direct polarization/magic angle spinning (DP/MAS) and DP/MAS with recoupled dipolar dephasing, (13)C
74 ta obtained from high-field and DNP-enhanced MAS NMR spectroscopy together with time-resolved optical
75 simultaneous microwave-assisted extraction (MAS) and unsaponifiable extraction, followed by on-line
76 MFI were also obtained, and again two (19)F MAS NMR resonances now with largely dissimilar intensiti
79 ant sensitivity gains, therefore making fast MAS conditions advantageous across the board compared wi
80 Optimal sensitivity attained due to the fast MAS probe technologies enabled the assignment of the loc
81 symmetry-based dipolar recoupling under fast MAS is expected to find numerous applications in studies
83 of solid materials and that are designed for MAS frequencies of 20 kHz and below, fail above 30 kHz.
88 These data demonstrate that both fulminant MAS and hemophagocytosis can arise independently of IFNg
90 molecular absorption spectrometry (HR-CS GF MAS) via molecular absorption of phosphorus monoxide.
91 d using deuterium magic angle spinning ((2)H MAS) line shape and spin-lattice relaxation measurements
92 xagonal packing is also consistent with (1)H-MAS NMR spectra of the L(o) phase, NMR diffusion experim
94 repeated stimulation of TLR9 produced an HLH/MAS-like syndrome on a normal genetic background, withou
100 evelopment of these molecular agents, and HR-MAS NMR spectroscopy appears to be a very interesting to
106 This study shows the potential of (1)H HR-MAS as a rapid method for probing metabolomic profiles a
110 igh-resolution magic angle spinning ((1)H HR-MAS) nuclear magnetic resonance (NMR) spectroscopy in co
115 full protocol for acquiring high-quality HR-MAS NMR spectra of biological tissues at low spinning ra
117 00 MHz and suggest that high-quality slow HR-MAS spectra can be expected at higher magnetic fields us
118 h-resolution magic-angle sample spinning (HR-MAS) (1)H NMR spectroscopy of tissue biopsies combined w
119 High Resolution Magic Angle Spinning (HR-MAS) is an NMR technique that can be applied to semi-sol
120 1)H high resolution-magic angle spinning (HR-MAS) NMR spectroscopy of apple pulp was performed before
121 High-resolution magic-angle spinning (HR-MAS) nuclear magnetic resonance (NMR) is an essential to
122 1)H-High Resolution-Magic Angle Spinning (HR-MAS) nuclear magnetic resonance (NMR) spectroscopy for t
123 1)H high-resolution magic-angle spinning (HR-MAS) nuclear magnetic resonance (NMR) spectroscopy have
124 y a high-resolution magic angle spinning (HR-MAS) proton ((1)H) NMR spectroscopic examination of inta
127 of lemon and citron were studied through HR-MAS NMR spectroscopy, which was used directly on intact
130 ralar/AGC1 knockout neurons reflect impaired MAS activity and limited mitochondrial pyruvate supply.
131 s-effect DNP enhancements can be achieved in MAS experiments on frozen solutions by simply incorporat
135 igmentation is an underrecognized finding in MAS and presents later in development compared with the
144 de a strong incentive for WWTPs to integrate MAS, but it is crucial that WWTPs maintain their barrier
145 emission balances of a WWTP with integrated MAS, based on a substance flow analysis of the elements
147 o fully protonated proteins that, at 100-kHz MAS and above, spectral resolution is high enough to det
149 and R1rho relaxation rates at fast (60 kHz) MAS and high magnetic field (1 GHz), we were able to des
155 ction as well as the use of multidimensional MAS solid-state NMR methods for resolving and assigning
156 ion based 2D and 3D (13)C-(13)C, (13)C-(15)N MAS NMR experiments for rigid residues along with J-base
159 tion of respiration occurs in the absence of MAS through Ca(2+) influx through the mitochondrial calc
160 nd ligands, in which case the application of MAS NMR dipolar recoupling requires the low temperatures
162 ngs provide evidence that the combination of MAS-ER and topiramate is efficacious in promoting abstin
163 orted our hypothesis that the combination of MAS-ER and topiramate would be superior to placebo in ac
164 ible primarily because of the development of MAS rotors that spin at frequencies of 40 to 60 kHz or h
168 atients had other characteristic findings of MAS including hyperfunctioning endocrinopathies, polyost
172 y play a central role in the pathogenesis of MAS, the role of other cytokines is still not clear.
185 ld (B0 = 3 T) (13)C{(1)H} cross-polarization MAS NMR, carbamate is confirmed through splitting of the
186 ically induced dynamic nuclear polarization) MAS (magic angle spinning) NMR demonstrates that indeed
187 /(13)C labeling and with deuterated protein, MAS at omegar/2pi = 60 kHz, omega0H/2pi = 1000 MHz, and
188 r polarization-enhanced (13)C-double quantum MAS-NMR has been used to probe directly the retinylidene
189 let GP1balpha and G-protein-coupled receptor MAS effectively bound Ig21 by displacing Ig20 from autoi
191 c-angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy and first-principles density funct
192 c angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy, XRD, FT-IR spectroscopy, and N2 p
193 ngle solid-state nuclear magnetic resonance (MAS SS-NMR) spectroscopy establish that alpha-Syn adopts
194 ning solid-state nuclear magnetic resonance (MAS SSNMR) have experienced a remarkable development in
195 ning solid-state nuclear magnetic resonance (MAS ssNMR) spectroscopy are used to gain insight into th
196 Angle Spinning Nuclear Magnetic Resonsance (MAS-NMR) spectroscopy, demonstrated increased abundance
197 of extended-release mixed amphetamine salts (MAS-ER) and topiramate or placebo for 12 weeks under dou
198 assessed using the modified Ashworth Scale (MAS), Myotonometry and repeated passive stretch techniqu
201 l be valuable for marker-assisted selection (MAS) programs to rapidly introgress G. barbadense phytoc
202 n order to employ marker assisted selection (MAS) to select a high oleic disease resistant peanut and
204 a component of the malate-aspartate shuttle (MAS), is stimulated by modest increases in cytosolic Ca(
208 ied molecular sieves was monitored by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffra
211 ) achieves highest Mean Average Specificity (MAS), a scalar measure for ROC curve, of 0.97 (0.96).
212 arization at 5 T under magic-angle spinning (MAS) at 82 K using a mixture of monoradicals with narrow
213 under both static and magic angle spinning (MAS) conditions at 21.1 T, allowing the complete set of
214 sed static in situ and magic-angle spinning (MAS) ex situ (13)C nuclear magnetic resonance (NMR) to e
215 -(13)C solid-state NMR magic angle spinning (MAS) experiment is presented and demonstrated on the mic
217 y measuring RDCs using magic-angle spinning (MAS) in combination with dipolar recoupling methods.
218 ination of (13)C/(15)N magic angle spinning (MAS) NMR and (2)H NMR to study the structural and functi
220 le-quantum solid-state magic-angle spinning (MAS) NMR and small-angle neutron scattering (SANS) were
222 is combined with (1)H magic angle spinning (MAS) NMR detection, absolute quantification of water in
223 ion by proton-detected magic-angle spinning (MAS) NMR has focused on highly deuterated samples, in wh
224 el characterization by magic angle spinning (MAS) NMR of the muscle isoform of human cofilin 2 (CFL2)
235 s and multidimensional magic angle spinning (MAS) NMR techniques at high magnetic fields, providing v
236 recent developments in magic angle spinning (MAS) NMR technology have made it possible to spin solid
239 amics, and solid-state magic-angle spinning (MAS) nuclear magnetic resonance (NMR) is a unique method
240 esonance assignment of magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectra of 5-30 kD
241 ure (EXAFS) and (27)Al magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopies in
243 (13)C solid-state magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, supp
246 ear polarization (DNP) magic-angle spinning (MAS) solid-state NMR (ssNMR) spectroscopy has the potent
249 S) solid-state NMR and magic angle spinning (MAS) solid-state NMR techniques to measure orientation r
250 a labeling scheme for magic angle spinning (MAS) solid-state NMR that is based on deuteration in com
253 ear polarization under magic angle spinning (MAS-DNP) could be used to dramatically increase the sens
255 0) determined using 3D magic-angle-spinning (MAS) NMR spectra acquired with a (15)N-(13)C ZF-TEDOR tr
259 lography, (1)H NMR, solution and solid-state MAS (19)F NMR spectroscopies, CV and MS studies that the
260 use (14)N, (2)H, (13)C, and (1)H solid-state MAS NMR to elucidate cation reorientation dynamics, micr
261 (87)Rb, (39)K, (13)C, and (14)N solid-state MAS NMR to probe microscopic composition of Cs-, Rb-, K-
264 ization to PBDA, demonstrated by solid-state MAS-NMR, Raman, and optical absorption spectroscopy.
265 e assessment of musculo-articular stiffness (MAS) with the free-oscillation technique is a popular me
266 is (HLH) and macrophage activation syndrome (MAS) are 2 similar diseases characterized by a cytokine
270 hogenesis of macrophage activation syndrome (MAS) is not clearly understood: a large body of evidence
279 his approach facilitates and accelerates the MAS NMR assignment process, shortening the spectral acqu
280 e various RN(n)(v)-symmetry sequences at the MAS frequency of 40 kHz experimentally and by numerical
284 ising potential of proton-detected ultrafast MAS NMR for monitoring structural and dynamic changes ca
285 ted NMR measurements on bone under ultrafast MAS conditions to provide atomistic-level elucidation of
287 uitably combines proton-detection, ultrafast-MAS and multiple frequency dimensions to overcome this l
289 ds for protein structure determination using MAS SSNMR, as well as its application to the study of am
290 t only demonstrates the possibility of using MAS-DNP to greatly facilitate the acquisition of 2D (29)
291 tions at low temperature and high viscosity) MAS (magic angle spinning) NMR that both populations are
300 rs are often not identified in patients with MAS, and some patients with HLH or MAS lack defects in c
301 ding to the gradient, with 187 patients with MAS; and 2) according to the AVA, with 187 patients with
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