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1 SPM is applicable for analyses of longitudinal data in m
2 SPM single subject and group analysis compared to the co
3 SPM single-subject analysis, and a group analysis in com
4 SPM's alternative pre-whitening method, FAST, performed
5 SPMs actively promote resolution of inflammation by cont
6 SPMs are also decreased in advanced plaques of fat-fed L
7 SPMs have potential to serve as targeted therapeutic age
8 SPMs, which include lipoxins, demonstrate comprehensive
11 ate that the (R,R)-diastereomer of 1,12-Me(2)SPM represents a promising lead compound in developing a
12 PM administration to mice revealed that Me(2)SPM significantly decreases spermidine levels in multipl
14 e mimetic, (R,R)-1,12-dimethylspermine (Me(2)SPM), to reduce the intracellular spermidine pools of SR
15 blasts from SRS patients can accumulate Me(2)SPM, resulting in significantly decreased spermidine lev
16 tent of dissemination of MBLs such as VIM-2, SPM-1 and NDM among Gram-negative pathogens cannot be ex
18 In this paper, the result of integrating a SPM module into a ToF-SIMS system is presented illustrat
22 few studies have compared survival after an SPM to survival of the same cancer occurring as first pr
24 Administration of resolvin D4 (RvD4), an SPM that was enriched at the natural onset of thrombus r
26 ess cost explains the exclusion of VIM-2 and SPM-1 from Escherichia coli and Acinetobacter baumannii,
29 of residual autocorrelated noise in FSL and SPM leads to heavily confounded first level results, par
30 ging (fMRI) analysis packages: AFNI, FSL and SPM, with regard to temporal autocorrelation modeling.
33 ed from n-3 PUFAs, including epoxy-PUFAs and SPM-precursors, increase linearly with elevated intake o
36 and time-period, the risk of developing any SPM or any haematological malignancy was significantly r
39 trospective information (when using archived SPM) for fish monitoring, complementing the currently us
40 gered specialized proresolving mediators (AT-SPMs), such as aspirin-triggered resolvins (AT-RvDs) and
44 (ToF) SIMS) with means to alternate between SPM and SIMS measurements, is one approach to meet that
47 oil leads to an increase in peripheral blood SPM concentrations and reprograms peripheral blood cells
49 ine was PUT, followed by SPD, HIS, TYR, CAD, SPM, PHE, and SER, with the total BAs content decreasing
50 We conclude that highly phagocytic, CD138(+) SPM-like cells with an anti-inflammatory phenotype may p
55 15-lipoxygenase-1 expression and consequent SPM biosynthesis involving ERK-1/2 during M2 polarizatio
56 s administration of MaR1, a highly conserved SPM, propagated inflammatory resolution after SCI, as re
58 murine peritonitis accompanied by decreased SPM levels without affecting proinflammatory leukotriene
61 omes observed in longitudinal studies, i.e., SPM relates the stochastic dynamics of variables (e.g.,
64 ray scan patterns, only found on high-end EC-SPM setups such as hopping mode scan, were easily implem
66 f" parts to deliver a simple yet powerful EC-SPM equipment capable of performing simple space-resolve
70 0(5), 4.17 x 10(5) and 1.46 x 10(5)M(-1) for SPM, SPD and PUT, respectively, which correlated well wi
72 eripheral blood cells, indicating a role for SPM in mediating the immune-directed actions of this sup
73 APOE genotype interactions were observed for SPMs expressed as a ratio of their parent compound, high
74 between pediatric overweight/obesity and FPM/SPM emergence, adjusting for age, sex, and race/ethnicit
75 t US-representative data and affirm that FPM/SPM emergence varies by race/ethnicity and sex and is po
76 ssociation of body mass index (BMI) with FPM/SPM emergence in a representative sample of US children
77 ard fMRI analysis packages (e.g., AFNI, FSL, SPM) focus on preprocessing and univariate analyses, lea
78 or paracrine signaling via locally generated SPMs in the vasculature may represent a novel homeostati
79 we recorded significantly (p < 0.05) higher SPM in the Ajkwa Estuary compared to neighboring estuari
80 dings contribute to our understanding of how SPM synthesis is regulated during the inflammatory respo
83 ased metabololipidomics was used to identify SPMs from n-3 polyunsaturated fatty acids in human IBD c
85 ls, we tested whether n-3 fatty acids impact SPM profiles in patients with CAD and promote clot remod
87 iated with heightened inflammation, impaired SPM:LT ratio, defective efferocytosis, and a decrease in
92 esponders are maintained, with a decrease in SPM concentrations in patients resistant to DMARD therap
94 over, gene expression of enzymes involved in SPM biosynthesis were altered in submandibular glands (S
96 ion toward the M2 phenotype, but its role in SPM production and lipid mediator biosynthesis in genera
98 trum of the current Carba-R assay to include SPM, GES, and expanded IMP variants, increasing the glob
99 synthesis, whereas FLAP inhibition increases SPM levels, and 4) that the 15-LOX-1 inhibitor 3887 supp
100 es, 3) zileuton blocks resolution-initiating SPM biosynthesis, whereas FLAP inhibition increases SPM
101 he groundwork for further investigation into SPMs as alternatives to immunosuppressive therapies like
103 sion and subcellular localization of the key SPM biosynthetic enzyme 5-lipoxygenase (LOX) in vascular
106 soft tissues may result from dysregulated LM-SPM production, and that inhibition of 15-PGDH activity
108 increased AT-RvD3, RvD6, AT-PD1, and AT-LXB4 SPMs identified in Lovaza-treated patients with CAD enha
111 We used statistical parametric mapping (SPM V.12) software to compare groups and investigate vox
113 We used Statistical Parametric Mapping (SPM) to analyze time-series contributions of body segmen
116 diment, and suspended particulate materials, SPMs) from Miankaleh Wildlife/Gorgan Bay, (Caspian Sea,
117 aeal lipids in suspended particulate matter (SPM) and sediments mainly focused on a small class of fu
118 d primarily to suspended particulate matter (SPM) at sites in areas with a high land-cover fraction o
120 from archived suspended particulate matter (SPM) for identifying fish species using metabarcoding, w
122 TMPP sorbed to suspended particulate matter (SPM) was 56.4% of the total mass in wastewater, which wa
123 inal effluent, suspended particulate matter (SPM), and sludge collected from two WWTPs (denoted as WW
124 to study the dynamics of the Sao Paulo MBL (SPM-1) from beta-lactam-resistant Pseudomonas aeruginosa
126 o induced specialized proresolving mediator (SPM) biosynthetic enzymes arachidonate lipoxygenase (ALO
127 conserved specialized proresolving mediator (SPM) hosting potent anti-inflammatory and proresolving p
128 al of the specialized proresolving mediator (SPM) resolvin D1 (RvD1) to actively promote the resoluti
129 al blood specialized pro-resolving mediator (SPM) concentrations are linked with both DMARD responsiv
130 that the specialized pro-resolving mediator (SPM) Resolvin D1 (RvD1) promotes resolution of inflammat
131 y specialized pro-resolving lipid mediators (SPM) in histologically-defined stable and vulnerable reg
132 by specialized proresolving lipid mediators (SPM) that limit the host response within the affected ti
133 rolac or specialized proresolving mediators (SPM) called resolvins increases disease-free survival ra
134 ecently, specialized proresolving mediators (SPM) have been found to exert profound beneficial effect
135 produce specialized proresolving mediators (SPM; i.e., resolvins, protectins, and maresins) that pla
137 am specialized proresolving lipid mediators (SPMs) 14-hydroxydocosahexaenoic acid, 17-hydroxydocosahe
138 of specialized proresolving lipid mediators (SPMs) derived from eicosapentaenoic acid (EPA) and docos
139 at specialized proresolving lipid mediators (SPMs) generated from docosahexaenoic acid (DHA) can modu
141 of specialized proresolving lipid mediators (SPMs), generation of specific growth factors contributin
142 Specialized pro-resolving lipid mediators (SPMs)-resolvins (Rv), protectins (PD) and maresins (MaR)
143 se specialized proresolving lipid mediators (SPMs; lipoxins, resolvins, and protectins) stimulate res
144 thesized specialized proresolving mediators (SPMs) and proinflammatory and prothrombotic lipid mediat
146 -derived specialized proresolving mediators (SPMs) in 2-, 9-, and 18-mo-old APOE3 and APOE4 male and
147 -derived specialized proresolving mediators (SPMs) play a critical role in the active resolution of i
148 ed to as specialized proresolving mediators (SPMs) play an important role in the restorative response
149 oids and specialized proresolving mediators (SPMs) regulate leukocyte function and inflammation.
150 dogenous specialized proresolving mediators (SPMs) that actively stimulate resolution of inflammation
151 zed that specialized proresolving mediators (SPMs), a class of immune regulators promoting resolution
153 , termed specialized proresolving mediators (SPMs), in the cerebrospinal fluid (CSF) of adults with T
156 ther two specialized proresolving mediators (SPMs), lipoxin B4 (LXB4) and resolvin E1 (RvE1), modulat
159 between specialized pro-resolving mediators (SPMs) like resolvin D1 (RvD1) and pro-inflammatory facto
164 f the following secondary plant metabolites (SPMs): glucosinolate breakdown products, carotenoids, ch
165 Incorporating a Scanning Probe Microscope (SPM) unit which provides topography measurements with hi
168 (HAADF-STEM) and scanning probe microscopy (SPM) suggests that piezoelectric BaTiO(3) NPs display a
169 g high resolution scanning probe microscopy (SPM), and specifically using the subset of SPM known as
170 overview of using Scanning Probe Microscopy (SPM), in particular Scanning Tunneling Microscopy (STM),
173 t molars (FPMs) and second permanent molars (SPMs) is an important developmental milestone influencin
174 cytic MPhi resembling small peritoneal MPhi (SPM) that expressed CD138(+) and the scavenger receptor
175 microfluidic sample preparation multiplexer (SPM) and assay procedure is developed to improve amplifi
176 microfluidic sample preparation multiplexer (SPM) has been developed and evaluated for Ebola virus de
177 rognostic ability of somatic point mutation (SPM) and copy number variation (CNV) data, gene-level an
178 erparamagnetic multiwalled carbon nanotubes (SPM-MWCNTs) in an aqueous system containing Lake Tai sed
180 penemases such as KPC, NMC-A, IMI, SME, NDM, SPM, IMP, VIM, and OXA-23, 40, 48, 58, 72, 181, and 232
181 dence of second primary malignant neoplasms (SPMs) is a well-known late effect after cancer, few stud
183 Environmental DNA was extracted from nine SPM samples differing in location, organic content, and
185 However, when normalized to the amount of SPM, concentrations were on average >20 times higher at
187 nduced inflammation, providing a new area of SPM activity to investigate in this major area of therap
188 on and prevented the related biosynthesis of SPM in response to pathogenic Escherichia coli, assessed
189 dence that the inappropriate biosynthesis of SPM in the lesioned spinal cord hampers the resolution o
190 ry in adult female mice, the biosynthesis of SPM is not induced in the lesion site up to 2 weeks afte
191 cids are precursors in the biosynthesises of SPM, the aim of the present study was to establish the r
198 se activity is required for the induction of SPM-biosynthetic pathways in human M2-like monocyte-deri
200 administration of intermediate precursors of SPM biosynthesis (e.g., 17-HDHA) could be more efficient
203 rospective cohort study assessed the risk of SPM in MM using the Taiwan National Cancer Registry and
206 (SPM), and specifically using the subset of SPM known as noncontact atomic force microscopy (ncAFM).
207 The package estimates several versions of SPM currently available in the literature including disc
208 stimulating local endogenous biosynthesis of SPMs and the generation of specific growth factors.
213 droxy-DHA (HDHA) and unbalanced formation of SPMs (in particular D-series Rvs) accompanied by enhance
215 clusion and Relevance: The adverse impact of SPMs on survival is substantial for AYAs and may partial
218 ese, the morbidly obese had higher levels of SPMs-RvD3, RvD4 and PD1-and white blood cells (WBC) and
220 with decreased cortical DHA and a number of SPMs, which together may contribute to the development o
223 At the same time, a distinct pattern of SPMs was profiled, with an increase for D-series resolvi
224 ysis, we identified unbalanced production of SPMs (i.e., D- and E-series resolvins, protectin D1, mar
225 tical factor for the deficient production of SPMs by obese leukocytes because the formation of D-seri
226 stinal inflammation and to study profiles of SPMs, we generated a novel animal model of lymphatic obs
227 cularly resolvin D1 (RvD1), and the ratio of SPMs to pro-inflammatory leukotriene B4 (LTB4), are sign
228 s research highlights the beneficial role of SPMs in pulmonary bacterial infections and provides the
229 ssolved organic matter (DOM) and sediment on SPM-MWCNTs under various conditions and the interaction
235 e error rates for the fMRI software packages SPM, FSL, and AFNI, as well as a nonparametric permutati
238 d the relationship between changes in plasma SPM concentrations and peripheral blood platelet and leu
239 gs elucidate the potential utility of plasma SPM concentrations as biomarkers of DMARD responsiveness
241 fy subsets of large PMs (LPM) and small PMs (SPM), which differed in granularity and maturation marke
242 lated vascular cells and tissues can produce SPMs and assessed expression and subcellular localizatio
243 and in sterile inflammation in vivo promotes SPM biosynthesis by a mechanism involving an increase in
244 ors that are active in AT and AR and propose SPMs, including 15-epi-LXA(4) or MaR1, as a potential st
248 have lower levels and/or absence of specific SPMs that were restored with Lovaza; these SPMs promote
249 thways, producing epimeric forms of specific SPMs, whereas other drugs can disrupt timely resolution.
250 olyamines, norspermidine (NSP) and spermine (SPM), also inhibit amphibian lymphocyte proliferation, b
252 ost important biogenic polyamines; spermine (SPM), spermidine (SPD) and putrescine (PUT), or electroc
253 The results showed that DOM can stabilize SPM-MWCNTs by providing sterically and electrostatically
262 Here we demonstrated for the first time that SPM is a promising source of eDNA for metabarcoding anal
263 animal studies is reviewed, indicating that SPMs are physiologic mediators and pharmacologic agonist
265 2 representing 20 million children), and the SPM analysis included ages 9 to 13 y ( n = 2,774 represe
267 ing an on-chip concentration protocol in the SPM and the single molecule detection capability of the
270 LXB4 or RvE1 also induced expression of the SPM biosynthetic enzymes 12-lipoxygenase and 15-lipoxyge
271 te this dysregulation, the abundances of the SPM products of these enzymes (ie, RvD1 and RvD2) were u
272 ent the first software implementation of the SPM-methodology by providing an R package stpm, which wa
277 c SPMs that were restored with Lovaza; these SPMs promote macrophage phagocytosis of blood clots.
279 g actions of MaR1 in SCI, we found that this SPM facilitated several hallmarks of resolution of infla
283 th muscle cells (VSMCs) converted 17-HDHA to SPMs, including resolvin D1 (RvD1) and other D-series re
284 increases acetylated COX2 and N-AS-triggered SPMs in microglia of AD mice, leading to resolution of n
285 er, these studies suggest that an underlying SPM dysregulation could be contributing to SS progressio
288 ity together with promoting resolution using SPM represents a novel therapeutic strategy to resolve c
289 Together, they suggest that low vascular SPMs may enable progression of chronic vascular inflamma
292 hat were differentially regulated in LPMs vs SPMs, including those that regulate the cycle, metabolis
295 rognosis, and a unique cohort LGG, for which SPM data was more predictive than CNV data and the predi