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1 equivalent bioelectrode cells with dissolved mediator.
2 Hypertension was set as the mediator.
3 adjustment for TIBC-so iron is not likely a mediator.
4 eeds at rt in the absence of a base or metal mediator.
5 3,3',5,5'-Tetramethylbenzidine (TMB) as the mediator.
6 g that afferent inputs are critical upstream mediators.
7 ytometry and measurements of proinflammatory mediators.
8 and subsequent expression of proinflammatory mediators.
9 ted post-ischemic expression of inflammatory mediators.
10 ified eosinophils as a novel source of these mediators.
11 fferentiation, and production of profibrotic mediators.
12 nappropriate synthesis of proresolving lipid mediators.
13 lammatory cells, along with reduced cytokine mediators.
14 s by directly up-regulating its key cellular mediators.
15 y primed to respond robustly to inflammatory mediators.
16 ) were increased in response to inflammatory mediators.
17 ein upregulated in asthma by type 2 immunity mediators.
18 ssortment of biologically relevant signaling mediators.
20 dase) with ferrocyanide as electron-transfer mediator, achieving a linear range from 0.05 to 1mM.
21 iation between SBP and mitral regurgitation (mediator-adjusted HR 1.22; CI 1.20, 1.25; p < 0.001).
22 AV-NT mice, the signaling pathways of the CR mediators, AMP-activated protein kinase (AMPK) and sirtu
23 EC expulsion that was coordinated with lipid mediator and cytokine production and lytic IEC death.
25 lexes revealed specific interactions between Mediator and the RSC, Arp2/Arp3, CPF, CF 1A and Lsm comp
26 cell subsets by flow cytometry, and soluble mediators and antibodies by ELISA; the percentage of mig
27 by phagosomal cargo, as well as inflammatory mediators and cellular activation affect many aspects of
28 ponse coincides with raised levels of immune mediators and infiltration of immune cells into infected
29 viewed, indicating that SPMs are physiologic mediators and pharmacologic agonists that stimulate reso
32 ell-type-specific regulation of inflammation mediators and shedding new light on the role of fibrobla
33 acid epoxides as new mast cell-derived lipid mediators and show that they are produced by PAF-AH2, an
36 s neurotoxin, gliotoxin, and proinflammatory mediator, and it alters the integrity and cohesion of th
37 ar lavage (BAL) fluid leukocytes, cytokines, mediators, and epithelial cell function for these asthma
38 complement, leukocyte CD11b and inflammatory mediators, and in Wistar rats increased fibrotic overgro
39 xpression of profibrotic and proinflammatory mediators, and increased TRPC6, PKC-alpha, and PKC-beta
40 lar morphology, surface phenotype, secretory mediators, and proliferative responses (referred to as a
41 sponses in clinical parameters, inflammatory mediators, and proportions of individual microbial taxa
42 ging biosupercapacitor based on an optimised mediator- and membrane-free enzymatic glucose/oxygen bio
44 tions when repeated measures of exposure and mediator are available and an exposure-mediator interact
45 sed skin expression of the anti-inflammatory mediator arginase-1 (P = 0.005), and a sustained reducti
46 ory/secretory products but few related lipid mediators as established by metabololipidomic analysis.
47 nflammation, RVX-297 reduced proinflammatory mediators assessed in splenic gene expression and serum
48 tive function at age 7-14 years (i.e., joint mediators beta = -0.07, 95% confidence interval: -0.12,
49 lack compared to the white RH, acting as the mediator between implicit prejudice and magnitude of the
52 eptors LGR4, LGR5 and LGR6 are Wnt signaling mediators, but their functions in squamous cell carcinom
54 olded protein response and the pro-apoptotic mediators CamkII and Stat1 was impaired in Trpc3-deficie
56 This finding provides a novel context for mediator-catalyzed RPA exchanges during the multistep pr
60 ein-coding gene SLC3A2 in cis by binding the Mediator complex to facilitate the establishment of enha
61 o subunits of the transcriptional regulatory Mediator complex, MED5a and MED5b, results in an increas
62 rometry of proteins in immunoprecipitates of mediator complexes revealed specific interactions betwee
66 cribed is particularly suitable for studying mediator-dependent microbial electron transfer processes
67 -A; however, exposure of SCs to inflammatory mediators derived from ZIKV-infected macrophages led to
68 elucidated the metabolic role of JAK2, a key mediator downstream of various cytokines and growth fact
69 nce that versican is a critical inflammatory mediator during poly(I:C)-induced acute lung injury and,
73 ulate unmeasured confounding of the exposure-mediator, exposure-outcome, and mediator-outcome relatio
74 a constituent of the eicosanoid inflammatory mediator family of molecules that promote both physiolog
75 es it enhanced the expression of the pro-Th1 mediators Fizz-1 and arginase 1, indicating that it coul
76 identified Prmt1 as a key common downstream mediator for beta-catenin/Hoxa9 functions in LSK-derived
77 i-inflammatory cytokine IL-10 was a critical mediator for PGRN-mediated anti-inflammation in collagen
78 antification (by the peak of current) of the mediators for individual species as well as in an aqueou
79 nd TRIB1 for triglycerides) that were causal mediators for the corresponding traits, as well as examp
80 ed with reduced secretion of proinflammatory mediators from microglia cells, ultimately rescuing neur
81 Our interpretation of these results is that Mediator functions as an assembly factor that facilitate
83 c approaches targeting an individual hormone/mediator have yielded somewhat disappointing body weight
84 the electrochemical properties of different mediators (hexacyanoferrate, HCF, riboflavin, RF) were c
85 rol an entire process by acting on a crucial mediator; however, this is a quite exceptional mechanism
86 cing increases expression of proinflammatory mediators; however, the observed response was modest.
87 uggests, the host receptor herpesvirus entry mediator (HVEM) facilitates herpes simplex virus (HSV) e
88 rode in three different charges of the redox mediators (i.e., neutral FcCH2OH, cationic Ru(NH3)6(3+),
89 ated the expression of numerous inflammatory mediators implicated in the TSS-associated cytokine stor
90 as a previously unrecognized chemoresistance mediator in colorectal cancer, thereby establishing the
92 ify the CXCL2/MIF-CXCR2 axis as an important mediator in MDSC recruitment and as predictors and poten
93 weight changes, often leading to the hormone/mediator in question being dismissed as a potential obes
95 Here we demonstrate that the choice of redox mediator in these solar cells has a profound influence o
98 (EVs) have been recently reported as crucial mediators in cell-to-cell communication in development a
99 ut their crucial participation, likely being mediators in electron transfer, was indicated by specifi
100 to produce cytokines, chemokines, and lipid mediators in response to subsequent TLR stimulation.
102 Pancreatic stellate cells (PSCs) are key mediators in the production of this fibrotic stroma, upo
103 he expression of vasoactive and inflammatory mediators in the vitreous of patients with idiopathic ER
106 formation of the most relevant inflammation mediators including proteins and lipids in human fibrobl
107 t-TKA joint, expresses multiple inflammatory mediators, including the monocyte chemoattractant, chemo
108 itated by the Mediator, then acts to relieve Mediator-induced repression to generate an active form o
110 could be considered an essential regulatory mediator involved in modulation of neutrophil migration
112 ely to benefit patients in whom the targeted mediator is not only expressed but demonstrably driving
113 Interestingly, key autophagic markers and mediators LC3-II, Atg7 and Beclin1 were reduced in Delta
117 , reduced serum immunoglobulins and allergic mediators, lower mast cells and eosinophil counts, lower
119 ory response by targeting microbiota-derived mediators might be a promising therapy against I/R injur
120 moter GATA1 site eliminated LDB1 complex and mediator occupancy and resulted in loss of LCR/beta-glob
121 ls a new biological function for uPA-uPAR as mediator of a neuron-astrocyte cross talk that promotes
122 e identify cytohesin 1 (CYTH1) as a critical mediator of adhesive properties in primary human cord bl
123 tal posterior mesenchyme, where it acts as a mediator of anterior to posterior (AP) patterning, where
124 r and tumor suppressor FOXO3 is an important mediator of apoptosis, but the mechanisms that control i
126 intact angiotensin-(1-7) is not the primary mediator of beneficial effects ascribed to the ACE2/angi
127 ical models of sediment bioturbation - a key mediator of biogeochemical cycling - to determine whethe
128 early B-cell factor 2 (EBF2) is an essential mediator of brown adipocyte commitment and terminal diff
129 b as a significant (P=1.3x10(-21)) candidate mediator of CDC-induced Mvarphi polarization, and PKCdel
133 o the p19ARF-MDM2-p53 pathway, is a critical mediator of colorectal tumorigenesis following APC loss.
134 NF-kappaB has recently gained attention as a mediator of complex psychiatric phenomena such as stress
135 dings provide evidence that poly GA is a key mediator of cytotoxicity and that cross-talk between DPR
137 me maintenance complex components (MCMs) and mediator of DNA damage checkpoint 1 (MDC1) expression.
138 results illustrate that SIX1 is the central mediator of dorsal mandibular arch identity, thus ensuri
140 ent SUMOylation of FOXP1 may be an important mediator of early cortical development and neuronal netw
141 e adaptor protein p130Cas/BCAR1 is a crucial mediator of ErbB2 transformation and that its overexpres
144 of organismal metabolism.HDAC3 is a critical mediator of hepatic lipid metabolism and its loss leads
145 tion, cells were incubated with NRG1-beta, a mediator of HER2-HER3 signaling, or A83-01, an inhibitor
146 the extracellular matrix may be an important mediator of HIV-1 interaction with alpha4beta7-expressin
147 enosine monophosphate (cAMP) is an important mediator of hormonal stimulation of cell growth and diff
150 TEMENT: Toll-like receptor 4 (TLR4) is a key mediator of innate immune signaling and has been implica
151 te that adipose Dnmt3a is a novel epigenetic mediator of insulin resistance in vitro and in vivo.
152 ription 3 (STAT3) is a pleiotropic signaling mediator of many cytokines, including interleukin-6 (IL-
155 MFN2 encodes mitofusin 2, a membrane-bound mediator of mitochondrial membrane fusion and inter-orga
156 yostatin/activin type I receptor (ALK4) as a mediator of muscle atrophy and muscle regeneration.
158 actor acetylhydrolase 1B1 (LIS1), a critical mediator of neuronal migration in developing brain, is e
159 ell as how BDNF may function as a downstream mediator of newer pharmacological agents currently under
162 the protein phosphatase Shp2 is an important mediator of oligodendrocyte differentiation and myelinat
164 onents of axon infrastructure is a potential mediator of pathophysiological damage after demyelinatio
165 ) is a clinically and functionally important mediator of PCa bone and visceral metastases, activating
166 transcription factor CREB3L1 as an essential mediator of PERK's pro-metastatic functions in breast ca
167 and provide evidence of IL-1 signaling as a mediator of post-traumatic astrogliosis and seizure susc
168 togen-inducible gene 6 (Mig-6) is a critical mediator of progesterone receptor (PGR) action in the ut
169 memory B cell responses.IgE is an important mediator of protective immunity as well as allergic reac
174 ibition of protein translation as a critical mediator of the antileukemic effects of withaferin A and
175 f cFGF23 fragments, probably is an important mediator of the association between ID and mortality.
178 particular, thrombin was identified as a key mediator of the effects induced by SW620Exos in target c
179 ish peroxidase and potassium ferrocyanide as mediator of the electron transfer) was adsorbed on the s
180 ats, suggesting that serotonin is a critical mediator of the energy balance impact of GLP-1 receptor
183 hese results indicate that miR-146a is a key mediator of the renal tubular response to IRI that limit
185 oskeleton is a key phosphorylation-dependent mediator of the toxicity of wild-type tau and of all the
186 (IRE1alpha) endoribonuclease (RNase), a key mediator of the UPR, cleaves Xbp1 mRNA to generate a pot
190 cells identified nitric oxide (NO) as major mediator of this phenotype in PDX and in patient-derived
194 ociated death domain (TRADD) is an essential mediator of TNF receptor signaling, and serves as an ada
195 ctor beta-activated kinase 1 (TAK1) is a key mediator of toll-like receptors and pro-inflammatory cyt
196 , we demonstrate that GA101 is a more potent mediator of trogocytosis than RTX in vitro in both norma
199 osomes in postshock mesenteric lymph are key mediators of acute lung injury triggering the macrophage
200 actone-exposed DCs showed that expression of mediators of antigen presentation, including MHC class I
203 e I interferons (IFNalpha/beta) are critical mediators of any anti-viral immune response and IFNbeta
209 also be useful in utilizing the RPE cells as mediators of drug delivery to intracellular targets and
212 sion of TK receptors, the phosphorylation of mediators of ERK1/2 and p38 pathways and STAT3 (S727) we
213 esults show that CD36 and PAFR are important mediators of HDM allergy development and that inhibiting
215 rging evidence that specialized proresolving mediators of inflammation accelerate wound healing by pr
216 pancreatic stellate cells (PSC) as prominent mediators of inflammatory and fibrotic processes during
218 es for TNF and, to a lesser extent, IL-17 as mediators of liver inflammation and fibrosis induced by
220 s arising from cancer mutations are the main mediators of many effective cancer immunotherapies in hu
223 sdermin (GSDM) family, which are emerging as mediators of programmed cell death in a variety of proce
224 n of genes encoding neoantigens as potential mediators of resistance to immune checkpoint therapy.
225 retina, FZD4 and the ligand NDP are critical mediators of signalling and are mutated in familial exud
226 alarmins, have been recognized as signaling mediators of sterile inflammatory responses after trauma
227 n resistance, have been considered the major mediators of T2D risk; however, recent evidence shows th
228 Our study identifies TDPs as functional mediators of tardigrade desiccation tolerance, expanding
230 we modeled illness and medication beliefs as mediators of the relationship between health literacy an
236 her, our study identifies YAP/TAZ as central mediators of VEGF signaling and therefore as important r
237 udy's aim was to define the effects of these mediators on neutrophil functions and the underlying cel
241 the exposure-mediator, exposure-outcome, and mediator-outcome relationships in order to see how the r
242 dentified evidence networks for 70% of drug-mediator pairs where most mediators were not known direc
244 Additional analyses of immunoinflammatory mediator performance (T-helper Type 17 [Th17]/Th2 and Th
245 in and histamine, two important inflammatory mediators previously described in the periodontitis dise
246 Leukotriene B4 (LTB4), a proinflammatory mediator produced by the enzyme 5-lipoxygenase (5-LO), i
247 acteria-induced profibrotic and inflammatory mediator production by peritoneal leukocytes isolated fr
250 tween proinflammatory and proresolving lipid mediators provides a link between metabolic and cellular
251 structure of Med14 facilitate a large-scale Mediator rearrangement that is essential for holoenzyme
252 Adenosine, a key extracellular signaling mediator, regulates several aspects of metabolism by act
253 ocytosis (SM) may suffer from mast cell (MC) mediator-related symptoms insufficiently controlled by c
255 complemented by Skin Prick Testing (SPT) and mediator release assay to determine the IgE cross-linkin
258 d vessels to a multidimensional one in which mediators released from multiple cells engage distinct s
259 ne B4 and prostaglandin E2 and pro-resolving mediators resolvin D1, resolvin D2, and protectin D1.
260 ega-3s) in vitro and in vivo and the omega-3 mediator, resolvin D1, in vitro increase Abeta phagocyto
263 resolution cryo-electron microscopy map of a Mediator-RNA polymerase II holoenzyme reveals that chang
266 a highly conserved specialized proresolving mediator (SPM) hosting potent anti-inflammatory and pror
267 he downstream specialized proresolving lipid mediators (SPMs) 14-hydroxydocosahexaenoic acid, 17-hydr
269 e estrogen receptor (ER) coactivator protein Mediator subunit 1 (MED1) have revealed its specific rol
271 or from an electrode during MES rely on: (i) mediators such as H2; (ii) physical contact through elec
272 Elevated activation of key inflammatory mediators such as JNK and IkappaB kinase (IKK) occurs ra
273 and lactate dehydrogenase, and inflammatory mediators such as monocyte chemoattractant protein 1 (MC
275 tify and measure recently described chemical mediators, termed specialized pro-resolving mediators th
276 Indeed, protein levels of fibrosis signaling mediator TGF-beta remained the same and the second messe
277 as an endocrine and local anti-inflammatory mediator that antagonizes pro-inflammatory actions of FG
278 hosphate, an endogenous microglial signaling mediator that inhibits HDAC activity, enhances basal Rgs
279 mediators, termed specialized pro-resolving mediators that actively regulate the resolution of acute
281 proresolving mediators comprise a family of mediators that include arachidonic acid-derived lipoxins
282 , identified in recent years, are endogenous mediators that include the n-3-derived families resolvin
283 s triggers production of innate inflammatory mediators that stimulate the production of matrix metall
284 ion of compliance, and analyses of treatment mediators that will facilitate further therapeutic devel
285 D73 is a newly recognized "immune checkpoint mediator" that interferes with anti-tumor immune respons
286 to the PIC is known to be facilitated by the Mediator, then acts to relieve Mediator-induced repressi
287 erfere with IFN production or its downstream mediators, thereby allowing successful infection of the
288 y which IFN-alpha serves as a proatherogenic mediator through repression of eNOS-dependent pathways.
289 ve as shuttles to protect and deliver active mediators to locally modulate cellular function during i
290 Nociceptor sensory neurons detect immune mediators to produce pain, and release neuropeptides tha
291 flammatory cytokines, followed by regulatory mediators, to ensure that this potentially destructive p
293 ehensive analysis of multiple cell types and mediators was performed by using flow cytometry and a mu
294 tion, exudation levels and many inflammatory mediators, was therefore evaluated in an in vivo model.
295 o systematically identify novel Golgi stress mediators, we performed a transcriptomic analysis of cel
298 s for 70% of drug-mediator pairs where most mediators were not known direct targets for the drug.
299 suggested to involve an intracellular redox mediator, which is released during light irradiation.
300 cytokines, growth factors, and angiogenesis mediators, with CXCL12 among the most significantly upre
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