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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
9 , (13)C-(13)C, and (1)H-(15)N 2D, 3D, and 4D MAS spectra, all of which show cross-peak doubling.
10 bility to mediate fast diffusion of VX and a MAS centrifugation effect.
11 , but their absence did not otherwise affect MAS manifestations.
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:
14                                   We used an MAS model established in mice transgenic for human IL-6
15 ion met 44% and 81% of modified HLH-2004 and MAS criteria, respectively.
16  isometric maximum voluntary contraction and MAS of the knee flexors using submaximal loads relative
17 N-H dipolar fields under (1)H decoupling and MAS.
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
20 enorca (Spain), BAMSE (Sweden), LISAplus and MAS (Germany), and PIAMA-NHS (the Netherlands).
21 arameters, and the combination of static and MAS analyses, can aid investigations of mixed carbonates
22                               Here, we apply MAS NMR to directly probe the dynamic histone protein re
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
30  of protein assemblies and organic solids by MAS NMR spectroscopy.
31 decalin has been studied using in situ (13)C MAS NMR spectroscopy.
32  individual's maximum voluntary contraction (MAS%MVC) and a single absolute load (MASABS).
33 A pronounced ligand effect was found, and CP MAS NMR experiments enabled us to probe important differ
34 rared Fourier transform (DRIFT) and (13)C CP MAS NMR measurements.
35 ques such as porosity measurements, (13)C CP MAS NMR spectroscopy, and fluorescence spectroscopy stro
36 ipitates is unequivocally proven by (13)C CP MAS NMR spectroscopy.
37  obtain natural abundance (13)C and (15)N CP MAS NMR spectra of microporous organic polymers with exc
38  cross polarization magic angle spinning (CP MAS) NMR spectroscopy.
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
41                 The observed (19)F-->(1)H CP-MAS spectra and dynamics are compared to those produced
42                  FTIR and (13)C and (15)N CP-MAS NMR of fresh and SO2 adsorbed modified G3 on PME con
43 ngle spinning nuclear magnetic resonance (CP-MAS NMR) spectroscopy, and atom probe tomography (APT).
44  cross-polarization magic-angle-spinning (CP-MAS) NMR.
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
47                                     (13)C CP/MAS NMR spectra show that the Fe(CO)3 moiety in polycrys
48  from spectral deconvolution of the (13)C CP/MAS spectra and the results has shown that all the extra
49                                     (13)C-CP/MAS NMR measurements of humic acids revealed an increasi
50                        Noninvasive ((13)C-CP/MAS NMR) and invasive methods (sequential chemical degra
51  (e.g., humic matter fractionation, (13)C-CP/MAS NMR, sequential chemical degradation) it was possibl
52  cross-polarization/magic angle spinning (CP/MAS).
53 g complementary spectroscopic techniques (CP/MAS (13)C NMR, Raman, FT-IR, and XPS) and high-resolutio
54                                        HR-CS MAS investigations revealed that the complexes were high
55                         Analysis using HR-CS MAS was accomplished by monitoring the CaF molecule, whi
56 rce molecular absorption spectrometry (HR-CS MAS) for F determination and electrothermal vaporization
57                              Coupled HPLC-CS-MAS/ESI-MS is the first analytical methodology capable o
58 source molecular absorption spectrometry (CS-MAS) using a commercial CS-AAS.
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
61                              Here, we detail MAS NMR experiments and sample labeling schemes designed
62 in, we make use of advances in (1)H-detected MAS NMR to describe the dynamics of the membrane domain
63 nuclear polarization (DNP) and (1)H-detected MAS techniques.
64 0(6) s(-1), as determined from the deuterium MAS line shapes.
65 er, in two-dimensional and three-dimensional MAS NMR spectra the CL-bound cyt-c displays a spectral r
66                          Two-dimensional DNP MAS NMR of the silica-bound peptide and solution NMR of
67 ernative sample preparation strategy for DNP MAS ssNMR studies of lipid membranes and integral membra
68                            Specifically, DNP MAS ssNMR experiments at 600 MHz/395 GHz on KL4 reconsti
69                                     This DNP MAS NMR approach allows efficient, high-throughput chara
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
72                      In this study we employ MAS (1)H NMR to probe the phase transitions of both solv
73                                 The employed MAS NMR sample conditions cause a previously noted subst
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
77      In this MFI zeolite, two distinct (19)F MAS NMR resonances with about equal intensity were obser
78           In unprecedented solid-state (19)F MAS NMR studies, the templating anions, engaged in anion
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
82 n, Clinical Modification diagnosis codes for MAS and either SLE or JIA.
83 of solid materials and that are designed for MAS frequencies of 20 kHz and below, fail above 30 kHz.
84                   Low and constant loads for MAS assessment, which are particularly relevant in the c
85 he development of effective therapeutics for MAS.
86 d on 8bp deletion in BADH2 as unsuitable for MAS in rice cultivars under study.
87                                    Fulminant MAS was characterized by dramatic elevations in IFNgamma
88   These data demonstrate that both fulminant MAS and hemophagocytosis can arise independently of IFNg
89 ll-like receptor 9 (TLR-9)-induced fulminant MAS.
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
93 derate AS (AVA >1.0 cm(2) and MG <40 mm Hg) (MAS group).
94 repeated stimulation of TLR9 produced an HLH/MAS-like syndrome on a normal genetic background, withou
95         Detailed (17)O 1D and 2D MQ and HMQC MAS NMR studies demonstrate that signals in the Si-OH, S
96                                           HR-MAS (1)H NMR and neutron scattering experiments reveal t
97                                           HR-MAS NMR profiling demonstrates cancer-specific metabolic
98                                           HR-MAS NMR proved to be a very suitable technique for detec
99                                           HR-MAS NMR was also used to derive the molar percentage of
100 evelopment of these molecular agents, and HR-MAS NMR spectroscopy appears to be a very interesting to
101 onents in different formulations applying HR-MAS diffusion-ordered NMR spectroscopy are shown.
102 volume tissue biopsies using a commercial HR-MAS probe for the first time.
103 gal forces experienced under conventional HR-MAS frequencies of several kilohertz.
104  features limit the usefulness of current HR-MAS approaches for fragile samples.
105          In addition, the possibility for HR-MAS-based quantifications and the analysis of dynamic pr
106    This study shows the potential of (1)H HR-MAS as a rapid method for probing metabolomic profiles a
107                                      (1)H HR-MAS NMR metabolite profiling was achieved from a small s
108                                      (1)H HR-MAS NMR spectroscopy was used to track the metabolic cha
109 ations in chemical composition using (1)H HR-MAS NMR.
110 igh-resolution magic angle spinning ((1)H HR-MAS) nuclear magnetic resonance (NMR) spectroscopy in co
111 n magic angle spinning spectroscopy ((1)H HR-MAS).
112 ration of the sample, measurement time in HR-MAS NMR is very short.
113 rd disposable inserts classically used in HR-MAS NMR-based metabolomics.
114 pand the applicability and reliability of HR-MAS NMR spectroscopy.
115  full protocol for acquiring high-quality HR-MAS NMR spectra of biological tissues at low spinning ra
116               The performance of the slow HR-MAS NMR procedure is demonstrated on conventional (liver
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
125 -MACS), a simple conversion of a standard HR-MAS probe to muHR-MAS.
126 so points out the simplicity of using the HR-MAS NMR technique for food analyses.
127  of lemon and citron were studied through HR-MAS NMR spectroscopy, which was used directly on intact
128                 Samples were subjected to HR-MAS NMR spectroscopic profiling and acquired spectral da
129 cterize metabolic properties in CRC using HR-MAS NMR spectroscopy.
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
132 onist, but the utility of other biologics in MAS is not clear.
133                               Mean change in MAS score from baseline at week 4 in the PTMG was -0.3 (
134                   The recent developments in MAS NMR instrumentation and methodologies opened new vis
135 igmentation is an underrecognized finding in MAS and presents later in development compared with the
136 riants in other genes previously observed in MAS.
137               While intensive C recycling in MAS considerably improves the energy balance, we show th
138 autoinflammatory disease spectrum to include MAS and suggests new targets for therapy.
139 atment of hemophagocytic syndromes including MAS.
140                As assessment load increased, MAS%MVC (coefficient of variation (CV) = 8.1-12.1%; stan
141 t cause of anemia in fulminant TLR-9-induced MAS.
142       Like previous HLH models, TLR9-induced MAS was IFN-gamma dependent; however, unlike other model
143                            We have initiated MAS and large-scale planting of elite dura and pisifera
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
146                Our data provide insight into MAS-like syndromes in patients with inflammatory disease
147 o fully protonated proteins that, at 100-kHz MAS and above, spectral resolution is high enough to det
148 enylallyl dissolved in o-terphenyl at 40 kHz MAS.
149  and R1rho relaxation rates at fast (60 kHz) MAS and high magnetic field (1 GHz), we were able to des
150 uman IL-6 (IL-6TG mice) challenged with LPS (MAS mice).
151 red with the conventional slow- and moderate-MAS approaches.
152                        More specifically, MQ MAS and HMQC sequences were used to probe the (17)O loca
153 onversion of a standard HR-MAS probe to muHR-MAS.
154                             Multidimensional MAS-NMR reveals mutation-induced chemical shift changes
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
157                                       (23)Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveal
158                                     (2)H NMR MAS spectra and T1 relaxation times obtained from the de
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
161 y factor for energy and emission balances of MAS at WWTP.
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
165                             The diagnosis of MAS is most commonly a clinical diagnosis because mutati
166 n some cases may aid in earlier diagnosis of MAS.
167 hould be recognized as a clinical feature of MAS.
168 atients had other characteristic findings of MAS including hyperfunctioning endocrinopathies, polyost
169 N-gamma neutralization in an animal model of MAS.
170                             Murine models of MAS and HLH illustrate that interferon-gamma (IFNgamma)
171 ibody and a TLR-9 agonist, and parameters of MAS were evaluated.
172 y play a central role in the pathogenesis of MAS, the role of other cytokines is still not clear.
173                    The clinical phenotype of MAS is variable because of mosaicism, but oral pigmentat
174 thogenic role of IFN-gamma in the setting of MAS.
175 AS (1-year: 96 +/- 1%; 5-year: 82 +/- 3%) or MAS (1-year: 96 +/- 1%; 5-year: 81 +/- 3%).
176 ents with MAS, and some patients with HLH or MAS lack defects in cytotoxic T cell killing.
177 y (CV = 4.8-7.0%) contributed to the overall MAS%MVC variability.
178                               However, (31)P MAS NMR spectra of analyzed series display a higher numb
179 d P(OGe)4 environments are expected in (31)P MAS NMR spectra of R3c NASICON samples.
180 electron spectroscopy and confirmed by (31)P MAS NMR spectroscopy.
181 -glycero-3-phosphocholine liposomes by (31)P MAS NMR.
182 eous solvent in the small and densely packed MAS NMR samples.
183               Clinically and pathologically, MAS bears strong similarity to hemophagocytic lymphohist
184               Current treatment of pediatric MAS varies based on the underlying rheumatic disease.
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
190 uter bacterial membrane with high-resolution MAS NMR spectroscopy.
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
199 nge in muscle tone (Modified Ashworth Scale [MAS]) in the PTMG from baseline to 4 weeks.
200 lerance genes and marker assisted selection (MAS) can accelerate wheat breeding for this trait.
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
203 fish (ESC) and motile aeromonad septicaemia (MAS), respectively.
204 a component of the malate-aspartate shuttle (MAS), is stimulated by modest increases in cytosolic Ca(
205  depends on ARALAR-malate aspartate shuttle (MAS), with a 46% drop in aralar KO neurons.
206 y step in the malate-aspartate NADH shuttle, MAS.
207 nd in the gel as can be seen from the (29)Si MAS NMR spectra.
208 ied molecular sieves was monitored by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffra
209          Spider major ampullate gland silks (MAS) vary greatly in material properties among species b
210                 A multiplex allele-specific (MAS) assay has been developed for the detection of HIV-1
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
216 luding both static and magic-angle spinning (MAS) experiments.
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
219 om CypA dependence, by magic-angle spinning (MAS) NMR and molecular dynamics (MD).
220 le-quantum solid-state magic-angle spinning (MAS) NMR and small-angle neutron scattering (SANS) were
221        Utilizing (17)O magic-angle spinning (MAS) NMR at multiple magnetic fields (17.6-35.2 T/750-15
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)
225 Cs) as modification of magic-angle spinning (MAS) NMR signal intensity under illumination.
226 -(13)C and (13)C-(15)N magic angle spinning (MAS) NMR spectra.
227  signal intensities in magic-angle spinning (MAS) NMR spectra.
228                Protein magic angle spinning (MAS) NMR spectroscopy has generated structural models of
229                        Magic Angle Spinning (MAS) NMR spectroscopy is a powerful method for analysis
230                   Fast magic angle spinning (MAS) NMR spectroscopy is becoming increasingly important
231          Subsequently, magic-angle spinning (MAS) NMR spectroscopy with sensitivity enhancement by dy
232 ion intermediate using magic angle spinning (MAS) NMR spectroscopy.
233            We report a magic angle spinning (MAS) NMR structure of the drug-resistant S31N mutation o
234                        Magic angle spinning (MAS) NMR studies of amyloid and membrane proteins and la
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
237 ing dipolar recoupling magic angle spinning (MAS) NMR.
238 y using (13)C and (1)H magic-angle spinning (MAS) NMR.
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
242                  (6)Li magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy is th
243      (13)C solid-state magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, supp
244 ionally, fast (25 kHz) magic-angle spinning (MAS) provides optimal sensitivity and resolution.
245 apidly with increasing magic angle spinning (MAS) rates.
246 ear polarization (DNP) magic-angle spinning (MAS) solid-state NMR (ssNMR) spectroscopy has the potent
247               Although magic angle spinning (MAS) solid-state NMR is a powerful technique to obtain a
248       Multidimensional magic angle spinning (MAS) solid-state NMR of uniformly (13)C,(15)N-labeled pr
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
251 esolution under sample magic-angle spinning (MAS).
252 ection under ultrafast magic angle spinning (MAS).
253 ear polarization under magic angle spinning (MAS-DNP) could be used to dramatically increase the sens
254 obtained in high-field magic-angle-spinning (MAS) NMR experiments.
255 0) determined using 3D magic-angle-spinning (MAS) NMR spectra acquired with a (15)N-(13)C ZF-TEDOR tr
256          Here we apply magic-angle-spinning (MAS) NMR to examine the structure and dynamics of these
257                        Magic-angle-spinning (MAS) solid-state NMR (ssNMR) spectroscopy allows for the
258                  Using magic-angle-spinning (MAS) solid-state NMR spectroscopy, we examined the proto
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-
262 ge in membrane-bound proteins in solid-state MAS NMR.
263  liquid-state, (27)Al and (29)Si solid-state MAS), and dynamic light scattering.
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
267 HLH-2004 and macrophage activation syndrome (MAS) criteria.
268              Macrophage activation syndrome (MAS) is a devastating cytokine storm syndrome complicati
269              Macrophage activation syndrome (MAS) is an acute episode of overwhelming inflammation ch
270 hogenesis of macrophage activation syndrome (MAS) is not clearly understood: a large body of evidence
271 r flares and macrophage activation syndrome (MAS).
272 is (HLH) and macrophage activation syndrome (MAS).
273  HLH-sibling macrophage activation syndrome (MAS).
274                    McCune-Albright syndrome (MAS), a mosaic condition associated with cafe au lait pi
275              Integrating microalgae systems (MAS) at municipal wastewater treatment plants (WWTPs) to
276                        Our results show that MAS can considerably improve energy balances of WWTPs wi
277                                          The MAS NMR approach reported here establishes the foundatio
278                                          The MAS spectra reveal two sets of resonances, indicating th
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
281 tion of the cytoskeletal organization at the MAS.
282 hazard ratio: 0.50; p = 0.04) but not in the MAS group.
283                        We have optimized the MAS assay to determine subtype B DRMs in dried blood spo
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
286 r recoupling) pulse sequence under ultrafast MAS.
287 uitably combines proton-detection, ultrafast-MAS and multiple frequency dimensions to overcome this l
288 e collected on unoriented samples undergoing MAS.
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
292 d applied and frequency of oscillation) when MAS is assessed.
293                            In agreement with MAS NMR data, proteolysis experiments performed on the f
294                       In addition, mice with MAS had a significant increase in numbers of liver CD68(
295                                    Mice with MAS showed a significant upregulation of the IFN-gamma p
296                                    Mice with MAS treated with an anti-IFN-gamma antibody showed a sig
297                                 In mice with MAS, treatment with the anti-IFN-gamma antibody signific
298 lso found in livers and spleens of mice with MAS.
299                   We present 4 patients with MAS who developed oral mucosal pigmentation during child
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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