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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.
6           Attenuated reactivity unmasked the cytoprotective actions of NO in contrast to the cytotoxi
7  peptide-1 is an incretin hormone capable of cytoprotective actions that reduces inflammation and end
8 2S produced by the endogenous enzymes exerts cytoprotective actions.
9                                   The direct cytoprotective activities of activated protein C (APC) o
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.
15 ercetin, suggesting their involvement in the cytoprotective activity of quercetin.
16 indings highlight the strong antioxidant and cytoprotective activity of the extract components, and i
17                       The same was found for cytoprotective activity on lymphocytes, lipid peroxidati
18 e PPF were potent antioxidants and displayed cytoprotective activity through the activation of nuclea
19                                A significant cytoprotective activity was observed when AGS cells were
20 meta-position of the B-ring exhibit improved cytoprotective activity, which is believed to result fro
21  the highest GluN2B affinity and the highest cytoprotective activity.
22 nsights into TMBIM-mediated calcium leak and cytoprotective activity.
23 ydroxyl radicals, low cytotoxicity, and high cytoprotective activity.
24  phenolic composition, antioxidant power and cytoprotective activity.
25 endent phospholipase A2gamma (iPLA2gamma) is cytoprotective against complement-mediated GEC injury.
26 endent phospholipase A2gamma (iPLA2gamma) is cytoprotective against complement-mediated glomerular ep
27  anion channel antagonist that is putatively cytoprotective against ischemic insult.
28 NO) produced by bacterial NOS functions as a cytoprotective agent against oxidative stress in Staphyl
29                                          The cytoprotective agent amifostine protected rats from long
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
32 ry compound worth further investigation as a cytoprotective agent.
33  human activated protein C (rhAPC) has shown cytoprotective and anti-inflammatory functions in some c
34  to the discovery of its role in vasoactive, cytoprotective and anti-inflammatory responses.
35 CXCR3-B down-regulated the expression of the cytoprotective and antiapoptotic molecule heme oxygenase
36 end-organ protective properties mediated via cytoprotective and antiinflammatory mechanisms.
37 tion by activated protein C (APC) stimulates cytoprotective and antiinflammatory signaling.
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
41 gulates the expression of a large network of cytoprotective and metabolic enzymes and proteins.
42 cytoplasmic ribonucleoprotein complexes with cytoprotective and pro-survival properties.
43  present evidence that PINK1-Parkin has both cytoprotective and proapoptotic functions.
44  identify the role of NF-kappaB in mediating cytoprotective and proinflammatory responses to inflamma
45 ral well-established and recently discovered cytoprotective and RNA-based Hsp70 functions.
46 nctional serine protease with anticoagulant, cytoprotective, and anti-inflammatory activities.
47 o examine expression levels of inflammatory, cytoprotective, and injury genes at different time point
48 in appears to play a prominent prosecretory, cytoprotective, and mitogenic role.
49                      Possibly underlying its cytoprotective, anti-apoptotic, anti-oxidative effects,
50 endothelial growth factor (VEGF)-B activates cytoprotective/antiapoptotic and minimally angiogenic me
51                                          The cytoprotective antioxidant N-acetylcysteine inhibited Dp
52 rates the plasticity and cell-specificity of cytoprotective aPC signaling.
53 nt with simple ion channel block, were fully cytoprotective at concentrations that gave submaximal in
54 c apoptotic pathway which could overcome the cytoprotective autophagic mechanism.
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
57                Because SFN treatment induces cytoprotective autophagy in cultured human prostate canc
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
62  stress response that subsequently activated cytoprotective autophagy.
63 increased cell survival via the induction of cytoprotective autophagy.
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.
66                          On the basis of the cytoprotective capabilities of antifreeze proteins (AFPs
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
69 ozyme, was identified as a novel and leading cytoprotective compound.
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
75                               Since eEF2K is cytoprotective during hypoxia and other conditions of nu
76 ith the microwave system showed an increased cytoprotective effect against H2O2 induced oxidation in
77                 The coffee samples exerted a cytoprotective effect against oxidative stress, with imp
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
83 s identify a unique mechanism underlying the cytoprotective effect of aPC.
84          This study aimed to investigate the cytoprotective effect of chemical agonist-mediated M3R a
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
87                                          The cytoprotective effect of tPA required its receptor, LDL
88                                          The cytoprotective effect of tucuma was evaluated in lymphoc
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.
92                                         This cytoprotective effect was associated with enterocyte-med
93  hypoxia/reoxygenation (H/R) stages to exert cytoprotective effects against H/R injury.
94                        Moreover, H2S elicits cytoprotective effects against stressors in various cell
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
99             Shh coacervate also demonstrates cytoprotective effects for cardiomyocytes in a hydrogen
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.
103                Whether TNF-alpha also exerts cytoprotective effects in heart failure is not known.
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
106                           In addition to the cytoprotective effects of APC on endothelial cells, podo
107 d ARE-containing mRNAs may contribute to the cytoprotective effects of Hsp70 following cellular stres
108                     These findings imply the cytoprotective effects of NF-kappaB activation on oligod
109 mplete or partial loss, respectively, of the cytoprotective effects of partial beclin-1 knockdown, in
110                                          The cytoprotective effects of pigment epithelium-derived fac
111            Here, we investigated whether the cytoprotective effects of Tbeta4 can increase the effect
112 ed blood cell production and exert important cytoprotective effects on select vascular, immune, and c
113           Understanding how EPCR-APC induces cytoprotective effects through activation of PAR1, whose
114 ndicate that similar to APC, thrombin exerts cytoprotective effects via beta-arrestin-2 biased PAR1 s
115                                      Similar cytoprotective effects were observed after transient shR
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
118 on substrate translocation and abolishes the cytoprotective effects.
119 ectedly high GluN2B affinity but do not show cytoprotective effects.
120 AR1, but its effects on cells contrast APC's cytoprotective effects.
121 C at Arg41 can initiate distinctive APC-like cytoprotective effects.
122 AR3 in the complex mechanisms underlying APC cytoprotective effects.
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
125                            Expression of the cytoprotective enzyme heme oxygenase-1 (HO-1) is signifi
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
128           Heme oxygenase-1 (HO-1), a pivotal cytoprotective enzyme, has antiviral activity for a numb
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
131 sion of heme oxygenase-1, an antioxidant and cytoprotective enzyme.
132 Nrf2, which regulates the expression of many cytoprotective enzymes including heme oxygenase-1 (HO-1)
133 ependent on STAT3 signaling and induction of cytoprotective factors in epithelial cells.
134                   The benefits resulted from cytoprotective factors including vascular endothelial gr
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
139 53 null H1299 cells but was converted to the cytoprotective form with induction of p53.
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
142                                         This cytoprotective function of ATG16L1 was associated with t
143          The study further characterizes the cytoprotective function of DJ-1 and PD-mutated variants
144                The importance of Trx1 in the cytoprotective function of DJ-1 is confirmed using a pha
145 mic mRNA complexes and is sufficient for the cytoprotective function of TSN during stress.
146           Furthermore, our work connects the cytoprotective function of TSN with its positive role in
147                                   One is the cytoprotective function that can in theory be inhibited
148 pe digestive epithelia and provide important cytoprotective function.
149 th Ly294002 resulted in loss of MOR-mediated cytoprotective function.
150           Holo-RBP4 is recognized to possess cytoprotective function.
151 ion factor well known for its cell-intrinsic cytoprotective function.
152 that might have significant implications for cytoprotective functions and therapeutic targeting of th
153                                          MDP cytoprotective functions are generally attributed to ant
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
159 vated activation of Nrf2 and upregulation of cytoprotective gene expression.
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
173  responds by activating the transcription of cytoprotective genes.
174 idative stress by the regulation of multiple cytoprotective genes.
175 nvolved in the activation of antioxidant and cytoprotective genes.
176  by increasing the expression of a number of cytoprotective genes.
177  constitutive NRF2-mediated transcription of cytoprotective genes.
178 by inducing the transcription of an array of cytoprotective genes.
179 n expression and increased the expression of cytoprotective H-ferritin.
180 ich also led to suppressed expression of the cytoprotective heat shock protein 72.
181 tional responses, controls the expression of cytoprotective heat shock proteins (HSPs), molecular cha
182 es (2-37) and compared their cytotoxicity to cytoprotective heat-shock-inducing activity (HSA).
183        The master regulator of the classical cytoprotective "heat shock" response, heat shock factor
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
190 nt tumors, the autophagy is not of necessity cytoprotective in function.
191 ducible factor-1alpha (HIF-1alpha), which is cytoprotective in ischemia.
192 trongly suggests that chaperone proteins are cytoprotective in neurodegenerative proteinopathies invo
193              We conclude that eIF2alpha-P is cytoprotective in response to UVB by a mechanism featuri
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
199 ation, and also enhanced the accumulation of cytoprotective markers.
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
204 erated by pathological stress, possibly as a cytoprotective mechanism.
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
208 ls, which can promote cardiac repair through cytoprotective mechanisms.
209 o potentiate TKI anti-leukemia activity in a cytoprotective microenvironment.
210  suggest that we have discovered a conserved cytoprotective modifier of amyloidogenic processes.
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
213 idated, Plin5 provides a basis for the novel cytoprotective nature of lipid droplets.
214    These data demonstrate that MP4CO induces cytoprotective Nrf2 and HO-1 and decreases NF-kB activat
215  of rapamycin (mTOR) signaling and activated cytoprotective Nrf2 signaling.
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
220                                         Both cytoprotective pathways have been well studied in isolat
221 rrier function and induces proliferative and cytoprotective pathways in the small bowel.
222  block pathologic signaling while preserving cytoprotective pathways.
223 tional factor that induces antioxidative and cytoprotective pathways.
224 ghest antioxidant activity were screened for cytoprotective potential in MCF-7 cells, including the m
225 tivity may not be directly related with high cytoprotective potential.
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
228                             Hsp70 has potent cytoprotective properties and has been described as a TL
229 rate) was shown to have antiinflammatory and cytoprotective properties in preclinical experiments and
230           Nitric oxide (NO) has demonstrated cytoprotective properties in various cells, but its bene
231 polyphenols, and to evaluate antioxidant and cytoprotective properties of the partridgeberry polyphen
232                      iPSC-derived EVs impart cytoprotective properties to cardiac cells in vitro and
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
235 , Lauraceae; BL) were examined for potential cytoprotective properties.
236 , Lauraceae; BL) were examined for potential cytoprotective properties.
237 n miRNAs and proteins with proangiogenic and cytoprotective properties.
238 ion of PERK signaling in oligodendrocytes is cytoprotective, protecting mice against EAE.
239 nstrate a corresponding up-regulation of the cytoprotective protein heme oxygenase-1 (HO-1) which is
240                             alphaKlotho is a cytoprotective protein, the expression of which is reduc
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
243                 Stress pathways coordinate a cytoprotective repair response, while simultaneously ini
244 e subpopulations can be modulated to mediate cytoprotective, reparative, and even regenerative functi
245 ches, we demonstrate that HIPK2 can elicit a cytoprotective response in cancer cells via NRF2.
246        Such a mechanism allows for a greater cytoprotective response in human AML cells and encourage
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
250                            SG formation is a cytoprotective response to environmental stress and resu
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
253 g oxidative stress and, as such, represent a cytoprotective response.
254 rf2) is a transcription factor that mediates cytoprotective responses against stress.
255 unexpected interaction between two important cytoprotective responses that are likely to have signifi
256  coordinately regulates basal metabolism and cytoprotective responses to radiation injury.
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
261                 Analogous to its established cytoprotective role during nutrient starvation, autophag
262  sorafenib/obatoclax lethality, indicating a cytoprotective role for autophagy in this setting.
263                            Here, we reveal a cytoprotective role for mitochondrial ROS (mtROS) in Cae
264                         These data suggest a cytoprotective role for Plin5 to promote lipid storage b
265       While UPF1 is best known for its basal cytoprotective role in degrading aberrant RNAs, UPF1 als
266                          MiR-150 conferred a cytoprotective role in lung epithelial cells after oxida
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
269  is induced in normoxic myofibers, playing a cytoprotective role.
270                                          The cytoprotective secretory form of clusterin, as evaluated
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
273 hat block proinflammatory pathways but spare cytoprotective signaling in endothelial cells.
274        Our results suggest that H2S-mediated cytoprotective signaling in the setting of I/R injury is
275 helial cells and suggest that SGK1-dependent cytoprotective signaling involves effects on maintaining
276 ter, we identified a novel aPC/PAR-dependent cytoprotective signaling mechanism.
277                This study elucidated a novel cytoprotective signaling pathway initiated by the APP tr
278 elopment and function and promotes cell-cell cytoprotective signaling responses.
279                                  APC elicits cytoprotective signaling through activation of protease
280 at a cleavage site that selectively mediates cytoprotective signaling.
281 effector, which contributes to TRAF2-induced cytoprotective signaling.
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
284 ession in beta-cells should be explored as a cytoprotective strategy in type 1 diabetes.
285 sis in the presence of stromal co-culture or cytoprotective survival signals.
286                                    FLT3 is a cytoprotective system in the heart and a potential thera
287 cies (ROS) production and the ability of the cytoprotective system to detoxify the reactive intermedi
288 aracterised by the upregulated expression of cytoprotective target genes.
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
292             Here we demonstrate that the key cytoprotective transcription factor NRF2 controls lncRNA
293 tified novel crosstalk between HIPK2 and the cytoprotective transcription factor NRF2.
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
299                     Whether DAR was directly cytoprotective was examined in cultured rat hepatocytes
300  of ubiquitin-tagged damaged mitochondria is cytoprotective, we tested the hypothesis that TRAF2 medi

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