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1 n greatly enhances eEF2K activity and may be cytoprotective.
2 atocyte-derived Gal-9 is both diagnostic and cytoprotective.
3 nt to oxidative modification, C73A-KCNB1, is cytoprotective.
4 The iPLA(2)gamma pathway is cytoprotective.
5 ng, while in normal cells CD40 signalling is cytoprotective.
7 peptide-1 is an incretin hormone capable of cytoprotective actions that reduces inflammation and end
10 ding is necessary for lacritin mitogenic and cytoprotective activities, TGM2 cross-linking negatively
11 s controlling intracellular localization and cytoprotective activity are incompletely understood.
12 extract of M. pajang and quercetin displayed cytoprotective activity in HepG2 cells, with EC(50) valu
13 e that innate immune pathways have important cytoprotective activity in neurons and contribute to lim
14 t, again suggesting their involvement in the cytoprotective activity of bambangan kernel extract.
16 indings highlight the strong antioxidant and cytoprotective activity of the extract components, and i
18 e PPF were potent antioxidants and displayed cytoprotective activity through the activation of nuclea
20 meta-position of the B-ring exhibit improved cytoprotective activity, which is believed to result fro
25 endent phospholipase A2gamma (iPLA2gamma) is cytoprotective against complement-mediated GEC injury.
26 endent phospholipase A2gamma (iPLA2gamma) is cytoprotective against complement-mediated glomerular ep
28 NO) produced by bacterial NOS functions as a cytoprotective agent against oxidative stress in Staphyl
30 AAP-induced toxicity and may be considered a cytoprotective agent in this in vitro model of drug indu
31 ritransplant administration of an epithelial cytoprotective agent, fibroblast growth factor-7, mainta
33 human activated protein C (rhAPC) has shown cytoprotective and anti-inflammatory functions in some c
35 CXCR3-B down-regulated the expression of the cytoprotective and antiapoptotic molecule heme oxygenase
38 isms that allow rapid switch on/off of their cytoprotective and apoptosis-inducing signaling pathways
39 ein C (APC) and thrombin elicits paradoxical cytoprotective and cytotoxic signaling responses in vasc
40 Glutathione S-transferase P1 is a Phase II cytoprotective and detoxifying enzyme that is widely exp
44 identify the role of NF-kappaB in mediating cytoprotective and proinflammatory responses to inflamma
47 o examine expression levels of inflammatory, cytoprotective, and injury genes at different time point
50 endothelial growth factor (VEGF)-B activates cytoprotective/antiapoptotic and minimally angiogenic me
53 nt with simple ion channel block, were fully cytoprotective at concentrations that gave submaximal in
55 ent, ATF4 activated a coordinated program of cytoprotective autophagy and antioxidant responses, incl
56 ement for functional p53 in the promotion of cytoprotective autophagy by radiation was confirmed by t
58 ying a critical role for HSF1 in controlling cytoprotective autophagy through regulation of ATG7, whi
59 required for chemotherapeutic agent-induced cytoprotective autophagy through transcriptional up-regu
60 tosis, wherein targeting SQSTM1/p62 converts cytoprotective autophagy to an inefficient form due to c
61 lines, BRAFi or BRAF/MEK inhibition induced cytoprotective autophagy, and autophagy inhibition enhan
64 s are the first to define an Hsp70-TLR4-Trif cytoprotective axis in the lung and endothelial cells.
65 amined the calcium-induced expression of the cytoprotective beta cell transcription factor Npas4.
67 FBSH-III retained antioxidant activity and cytoprotective capacity after in vitro simulated gastroi
68 mitochondria-associated peptide that offers cytoprotective, cardioprotective, and neuroprotective ef
70 Prestwick drug library to identify putative cytoprotective compounds against light-induced, syntheti
71 , C. album (poly)phenols appear as promising cytoprotective compounds, modulating central events in t
72 trials is that therapy-induced autophagy is cytoprotective; consequently, inhibition of autophagy is
73 s), furan compounds (HMF and furfural F) and cytoprotective/cytotoxic effects upon Caco-2 cells (MTT,
74 iates activated nuclear translocation of the cytoprotective DAF-16/FOXO transcription factor and prot
76 ith the microwave system showed an increased cytoprotective effect against H2O2 induced oxidation in
78 Activation of IRE-1 RNase function exerts a cytoprotective effect and has been implicated in the pro
79 however Ulva compressa presented the highest cytoprotective effect by blunting the apoptosis process.
80 ely deregulated in cancer cells, mediating a cytoprotective effect during blood-borne metastasis.
81 oneal administration of PC-S195A conferred a cytoprotective effect for thrombin in an in vivo inflamm
82 tivation by IGF-I is crucial to preserve its cytoprotective effect in astrocytes and may form part of
85 Here, we explore mechanisms underlying the cytoprotective effect of ferritin in endothelial cells e
86 culum (ER), this study addressed whether the cytoprotective effect of iPLA2gamma involves the ER stre
89 data support a model in which H2S exerts its cytoprotective effect on ISR signaling by inducing a tra
90 hage migration inhibitory factor (MIF) has a cytoprotective effect on lung endothelial cells; however
91 e stress after DETA-NO preconditioning; this cytoprotective effect was abolished by the NO scavenger.
95 showed the highest antioxidant activity and cytoprotective effects against tert-butyl hydroperoxide
96 le heat shock protein 70, Hsp72, has broadly cytoprotective effects and improves outcome following st
97 hat RBC-targeted scFv/TM exerts multifaceted cytoprotective effects and may find utility in systemic
98 ion of heme oxygenase 1 (HO-1), which exerts cytoprotective effects and modulates the renal response
100 hough adiponectin has been reported to exert cytoprotective effects in acute cardiac diseases, its ef
101 exerts anti-inflammatory, antiapoptotic, and cytoprotective effects in addition to its hematopoietic
102 17-mer, 17-mer[H105A], and 44-mer exhibited cytoprotective effects in cultured retina R28 cells.
104 r concentrations, STS-E412 provided EPO-like cytoprotective effects in primary neuronal cells and ren
105 n protease activated protein C (aPC) confers cytoprotective effects in various in vitro and in vivo d
107 d ARE-containing mRNAs may contribute to the cytoprotective effects of Hsp70 following cellular stres
109 mplete or partial loss, respectively, of the cytoprotective effects of partial beclin-1 knockdown, in
112 ed blood cell production and exert important cytoprotective effects on select vascular, immune, and c
114 ndicate that similar to APC, thrombin exerts cytoprotective effects via beta-arrestin-2 biased PAR1 s
116 HGF), a healing factor with regenerative and cytoprotective effects, are associated with inflammatory
117 mediating activated protein C (APC)-induced cytoprotective effects, including antiapoptotic, anti-in
123 e propose that polySia in semen represents a cytoprotective element to increase the number of vital s
124 s a stress-inducible, anti-inflammatory, and cytoprotective enzyme expressed in most cell types in th
126 osine kinase c-Met and overexpression of the cytoprotective enzyme heme oxygenase-1 (HO-1) play a cri
127 KEY POINTS: Haem oxygenase 1 (Hmox1) is a cytoprotective enzyme with anti-inflammatory and anti-ox
129 d cancers, where increased expression of the cytoprotective enzyme, heme oxygenase-1 (HO-1) is often
130 ession of heme oxygenase-1 (HO-1), a pivotal cytoprotective enzyme, postinfection and that overexpres
132 Nrf2, which regulates the expression of many cytoprotective enzymes including heme oxygenase-1 (HO-1)
135 ure assays, DAR did not stimulate release of cytoprotective factors, such as vascular endothelial gro
136 st marked changes, we found up-regulation of cytoprotective factors; a shift from oxidative phosphory
137 se optimum, the same domain is mitogenic and cytoprotective for epithelia via a syndecan-1 targeting
138 ther the drugs or radiation used promote the cytoprotective form of autophagy in the tumor cells as w
140 tial for mitochondrial turnover and serves a cytoprotective function in dopaminergic neurons in vivo.
141 intermediate filament protein that exerts a cytoprotective function in mature sensory and motor neur
152 that might have significant implications for cytoprotective functions and therapeutic targeting of th
154 he integrated stress response (ISR) that has cytoprotective functions as well as apoptotic signals th
155 nism of the signaling pathways mediating the cytoprotective functions of H2S is not well understood.
156 2 transcription factor is well known for its cytoprotective functions through regulation of genes inv
157 s a transcription factor that is crucial for cytoprotective gene expression and is generally thought
158 nstressed adult mouse hepatocytes produces a cytoprotective gene expression profile and induces lipog
160 ession of injury markers Kim-1, p21, and the cytoprotective gene heme oxygenase-1 accompanied this.
161 n as NF-E2-related factor 2 (Nrf2), is a key cytoprotective gene that regulates critical antioxidant
162 In summary, fish-derived omega-3s increase cytoprotective genes and decrease proapoptotic genes, im
163 ro-oxidant, tBHQ regulates the expression of cytoprotective genes by activation of redox-sensing tran
164 , presumably to ensure maximum activation of cytoprotective genes during potentially fatal conditions
165 This compound induced the expression of cytoprotective genes in keratinocytes isolated from wild
166 regulator that promotes the transcription of cytoprotective genes in response to oxidative/electrophi
167 SKN-1/Nrf transcription factors activate cytoprotective genes in response to reactive small molec
168 species (ROS) that lead to the induction of cytoprotective genes such as the UDP-glucuronosyltransfe
169 ttractive possibility is the exploitation of cytoprotective genes that exist solely for self-preserva
170 er cells provokes NRF2-mediated induction of cytoprotective genes, because it logjams the ubiquitin l
171 lated factor 2 (Nrf2), a master regulator of cytoprotective genes, is controlled by dimeric Kelch-lik
172 Instead, ATF4 activates the expression of cytoprotective genes, which reprogram cellular metabolis
181 tional responses, controls the expression of cytoprotective heat shock proteins (HSPs), molecular cha
184 enoprotection corresponded with increases in cytoprotective heme oxygenase 1 and IL-10 mRNAs, selecti
185 unction is a consequence of induction of the cytoprotective, heme-degrading enzyme heme oxygenase-1 (
186 t, whereas low-concentration thrombin may be cytoprotective, higher thrombin concentrations may contr
187 it was associated with the overexpression of cytoprotective HO-1 and anti-apoptotic Bcl-2/Bcl-xL.
188 oxide (NO), a gaseous messenger known to be cytoprotective; however, the underlying mechanism remain
189 , this is caused by compromised secretion of cytoprotective IL-18 from IKKalpha-mutant intestinal epi
192 trongly suggests that chaperone proteins are cytoprotective in neurodegenerative proteinopathies invo
194 is lethal when exposure is extreme but also cytoprotective in that sublethal exposure leads to the s
195 2 p45-related factor 2 (Nrf2) orchestrates a cytoprotective inducible program, which counteracts the
196 ce, suppresses toxic inflammation, increases cytoprotective insulin-like growth factor 1 (IGF1) signa
197 sented here show that the anti-inflammatory, cytoprotective intracellular and extracellular chaperone
198 urodegeneration and that the balance between cytoprotective JNK and cytotoxic p38 signaling dictates
200 ugh binding to the 3'UTR constitutes a novel cytoprotective mechanism of Hsp27 during stress in neuro
201 ulation of iNOS levels may remove a critical cytoprotective mechanism of importance in tumour angioge
202 dings suggest a novel role of autophagy as a cytoprotective mechanism to negatively regulate and prev
203 Proteins which might be involved in the cytoprotective mechanism were investigated using western
205 of antioxidant, anti-inflammatory, and other cytoprotective mechanisms important in protection from k
206 e transfer is sufficient to recapitulate the cytoprotective mechanisms in CD31(-) pancreatic beta cel
207 nt for bladder cancer therapy, but inducible cytoprotective mechanisms may limit its potential effica
211 on monoxide (CO), one of the products of the cytoprotective molecule heme oxygenase-1 (HO-1) in cance
212 gulates the transcription of several hundred cytoprotective molecules, including antioxidants, detoxi
214 These data demonstrate that MP4CO induces cytoprotective Nrf2 and HO-1 and decreases NF-kB activat
216 tion of clotting factors Va and VIIIa; (2) a cytoprotective on the basis of endothelial barrier stabi
217 at radiation-induced autophagy can be either cytoprotective or nonprotective, a functional difference
218 The unfolded protein response (UPR) is a cytoprotective pathway that relieves endoplasmic reticul
219 hat CDK20 positively modulate the KEAP1-NRF2 cytoprotective pathway to regulate tumor progression and
224 ghest antioxidant activity were screened for cytoprotective potential in MCF-7 cells, including the m
226 nfolded protein response (UPR), an important cytoprotective program induced by hypoxia, affects the b
227 n elicit differentiation, proliferation, and cytoprotective programs, underscoring the rising recogni
229 rate) was shown to have antiinflammatory and cytoprotective properties in preclinical experiments and
231 polyphenols, and to evaluate antioxidant and cytoprotective properties of the partridgeberry polyphen
233 roadly used antibiotic also known to possess cytoprotective properties, enhances survival of grafted
234 GRP78, a multifunctional protein with potent cytoprotective properties, is an emerging therapeutic ta
239 nstrate a corresponding up-regulation of the cytoprotective protein heme oxygenase-1 (HO-1) which is
241 eded to investigate the involvement of other cytoprotective proteins in the cytoprotection mechanism.
242 ated factor (Nrf2) induces the expression of cytoprotective proteins that maintain and restore redox
244 e subpopulations can be modulated to mediate cytoprotective, reparative, and even regenerative functi
247 Previously, we had shown that this conserved cytoprotective response is regulated by the thermosensor
248 of bixin derived from induction of the NRF2 cytoprotective response since it was only observed in Nr
249 sion in the liver produces a Notch-dependent cytoprotective response through direct transcriptional a
251 ponents within the lysosome, is an essential cytoprotective response to pathologic stresses that occu
252 P1 is the key regulator of the NRF2-mediated cytoprotective response, and increasingly recognized as
255 unexpected interaction between two important cytoprotective responses that are likely to have signifi
257 tophagy are engaged as primary and secondary cytoprotective responses, respectively, to Sigma1 ligand
258 f TCF7 in human and mouse islets impairs the cytoprotective responsiveness to GIP and enhances the ma
259 induced hepatic lipophagy plays an important cytoprotective role against liver injury, but its mechan
260 e cellular prion protein (PrP) often plays a cytoprotective role by regulating autophagy in response
267 n the kidney during endotoxemia and served a cytoprotective role in mitigating acute kidney injury.
268 bound transcription factor ATF6alpha plays a cytoprotective role in the unfolded protein response (UP
271 (TRAF2), an E3 ubiquitin ligase, coordinates cytoprotective signaling downstream of both TNF receptor
272 otential of novel APC variants with superior cytoprotective signaling function as enhanced therapeuti
275 helial cells and suggest that SGK1-dependent cytoprotective signaling involves effects on maintaining
282 by crosstalking with c-Met to potentiate its cytoprotective signals in airway epithelial cells during
283 ponse to influenza infection by facilitating cytoprotective signals through c-Met signaling to limit
287 cies (ROS) production and the ability of the cytoprotective system to detoxify the reactive intermedi
289 target for a first-in-class mechanism-based, cytoprotective therapy in the unmet high medical need in
290 Here we show that ER-localized THBS1 is cytoprotective to rat, mouse, and human beta-cells expos
291 lated factor 1 (Nrf1, also called NFE2L1), a cytoprotective transcription factor critical for the exp
294 eic acid and is coupled to activation of the cytoprotective transcription factor SKN-1 in both labora
295 e demonstrate genetic ablation of the master cytoprotective transcription factor, nuclear factor (ery
296 its splicing target, bZIP60, govern the two cytoprotective UPR signaling pathways known to date.
297 cetin) and quercetin have shown antioxidant, cytoprotective, vasoprotective, antiproliferative and an
298 ts help explain the differentiation of APC's cytoprotective versus thrombin's proinflammatory effects
300 of ubiquitin-tagged damaged mitochondria is cytoprotective, we tested the hypothesis that TRAF2 medi
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