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1 lear factor erythroid 2-related factor 2 and transcription factor 4.
2 ogen species and regulated by the activating-transcription factor-4.
3 eracting RNA clusters (3.6-fold) and curated transcription factors (4.1-fold), including zinc-finger
4 factor of activated T cells (NFAT) family of transcription factors [4, 5], we have quantified protein
7 acid deprivation did not require activating transcription factor 4, a critical component of the conv
8 These effects were mediated by activating transcription factor 4, a driver of exercise-induced ang
9 iolized cells stained with antibody to helix transcription factor 4, a factor associated with the cil
10 sitol-requiring enzyme 1alpha and activating transcription factor 4 abrogates autophagosome formation
11 nes (C/EBP homologous protein and activating transcription factor 4), accumulation of ceramide, loss
12 itol requiring kinase 1alpha, and activating transcription factor 4, all of which are featured change
13 factor 2alpha phosphorylation and activating transcription factor 4 and C/EBP homologous protein up-r
14 pha (eiF2alpha) and expression of activating transcription factor 4 and tribbles 3 were elevated in H
15 ted genes, including Phytochrome-Interacting Transcription Factors 4 and 5 (PIF4 and PIF5) and repres
17 d increased recruitment of TEAD4 (TEA domain transcription factor 4) and its coactivator YAP1 (Yes-as
18 B, high mobility group AT-hook 2, spalt-like transcription factor 4, and alpha-fetoprotein expression
20 expression levels of NANOG, octamer-binding transcription factor 4, and sex-determining region Y-box
21 pseudokinase tribbles homolog 3, activating transcription factor 4, and transcription factor CCAAT/-
22 log 1) was regulated by the ATF4 (activating transcription factor 4) arm of the unfolded protein resp
23 iched for components of the ATF4 (activating transcription factor 4) arm of the unfolded protein resp
24 ite the increased recognition of TBX4 (T-BOX transcription factor 4)-associated pulmonary arterial hy
26 stress/UPR genes, including BiP, activating transcription factor 4 (ATF-4), ATF-6, and a spliced for
28 by demonstrating the induction of activating transcription factor-4 (ATF-4) and growth arrest DNA dam
29 stent eif2-alpha phosphorylation (activating transcription factor 4 [ATF-4], C/EBP homologous transcr
30 In this work, we found that the activating transcription factor 4 (ATF4) activates a mitochondrial
31 rd increasing downstream signals, activating transcription factor 4 (ATF4) and ATF6 indicating potent
32 ial translation of mRNAs, such as activating transcription factor 4 (ATF4) and C/EBP-homologous prote
33 ivated, as the expression of both activating transcription factor 4 (ATF4) and CHOP (DDIT3), critical
34 ed stress response (ISR) effector activating transcription factor 4 (Atf4) and induction of the ISR t
35 hesis but enhances translation of activating transcription factor 4 (ATF4) and is a crucial evolution
36 CM phenotypes was mediated by the activating transcription factor 4 (ATF4) and its downstream effecto
37 associated transcription factors: activating transcription factor 4 (ATF4) and nuclear factor of acti
38 from siRNA-mediated knockdown of activating transcription factor 4 (ATF4) and overexpression of exog
39 indicated by decreased levels of activating transcription factor 4 (ATF4) and phosphorylated eukaryo
41 lood, Huang et al have identified activating transcription factor 4 (ATF4) as a novel regulator of fe
42 In silico analysis identified activating transcription factor 4 (ATF4) as a potential transcripti
44 ochondrial stressors, we identify activating transcription factor 4 (ATF4) as the main regulator of t
45 ranscription was conferred by two activating transcription factor 4 (ATF4) binding sites in the FGF21
46 es during EAE are not mediated by activating transcription factor 4 (ATF4) but are accompanied by act
47 production of the stress response activating transcription factor 4 (ATF4) by ineffective bypass of t
50 s pathway, linked functionally to activating transcription factor 4 (ATF4) following treatment with o
51 response (UPR) and an increase in activating transcription factor 4 (ATF4) has been previously report
52 nvestigate the protective role of activating transcription factor 4 (ATF4) in controlling the hepatic
53 We evaluate a potential role of activating transcription factor 4 (Atf4) in invertebrate and mammal
54 ated protein stability by binding activating transcription factor 4 (ATF4) in nuclear speckles and pr
55 muscle atrophy via expression of activating transcription factor 4 (ATF4) in skeletal muscle fibers.
56 e we reveal an essential role for activating transcription factor 4 (ATF4) in survival following MYC
57 ling pathway of ER stress-induced activating transcription factor 4 (ATF4) in the regulation of Mulle
65 HRI also activates the eIF2alphaP-activating transcription factor 4 (ATF4) ISR in primary erythroid p
67 ively enhances the translation of activating transcription factor 4 (ATF4) mRNA to induce stress resp
68 ively enhances the translation of activating transcription factor 4 (ATF4) mRNA to induce stress resp
71 trast, obese mice lacking hepatic activating transcription factor 4 (Atf4) showed an exaggerated ISR
73 nase RNA-like ER kinase (PERK) or activating transcription factor 4 (ATF4) significantly reduced the
75 f AP20187 significantly increased activating transcription factor 4 (ATF4) translation and concomitan
76 are transcriptionally induced by activating transcription factor 4 (Atf4) via C/ebp-Atf-Response-Ele
77 of the bZip transcription factor activating transcription factor 4 (ATF4) was induced by glutathione
78 eIF2alpha phosphorylation induces activating transcription factor 4 (ATF4), a basic leucine zipper tr
80 by using targeted deletion of the activating transcription factor 4 (ATF4), a key downstream effector
81 ed cells stimulated expression of activating transcription factor 4 (ATF4), a master transcription fa
83 of triglyceride metabolism by the activating transcription factor 4 (ATF4), a member of the basic leu
84 important effector of the ISR is activating transcription factor 4 (ATF4), a transcription factor th
85 element binding protein 2 (CREB2)/activating transcription factor 4 (ATF4), a transcriptional repress
86 eases translation of the metazoan activating transcription factor 4 (ATF4), activating the integrated
87 rsenite, in a manner dependent on activating transcription factor 4 (ATF4), an important mediator of
88 ing protein-1 mRNA, expression of activating transcription factor 4 (ATF4), and cleavage of ATF6 were
89 rt-term cold exposure induces the activating transcription factor 4 (ATF4), and its downstream target
90 ulator of amino acid homeostasis, activating transcription factor 4 (ATF4), is dysfunctional in HD be
91 transcriptional effectors of UPR, activating transcription factor 4 (ATF4), is essential for prostate
92 ch changes DISC1 interaction with activating transcription factor 4 (ATF4), modifies gene expression
93 rove the selective translation of activating transcription factor 4 (ATF4), potentiating YAP expressi
94 lectively increase translation of Activating Transcription Factor 4 (ATF4), resulting in the inductio
95 l that these compounds upregulate activating transcription factor 4 (ATF4), sensitizing cells to stre
96 We examined the contribution of activating transcription factor 4 (ATF4), the central node of the i
97 ions, increased the production of activating transcription factor 4 (ATF4), the transcriptional maste
98 PERK and its downstream factor, activating transcription factor 4 (ATF4), were crucial for this ind
99 mologous protein (Chop/Ddit3) and activating transcription factor 4 (Atf4), were upregulated in the c
100 ter system to detect induction of activating transcription factor 4 (ATF4), which controls expression
102 cts with the transcription factor Activating Transcription Factor 4 (ATF4), which is involved in the
103 ue (BAT) display induction of the activating transcription factor 4 (ATF4), which promotes fibroblast
104 rine synthesis were stimulated by activating transcription factor 4 (ATF4), which was activated by mT
105 rKO islets revealed activation of activating transcription factor 4 (ATF4), which was mediated by mam
106 rKO islets revealed activation of activating transcription factor 4 (ATF4), which was mediated by mam
108 as increased in coordination with activating transcription factor 4 (ATF4)-dependent REDD1 expression
109 e histone demethylase JMJD3 is an activating transcription factor 4 (ATF4)-dependent target gene.
121 leucine zipper (bZIP) domains of activating transcription factor-4 (ATF4) and CCAAT box/enhancer-bin
122 addition, the CREB-related factor activating transcription factor-4 (ATF4) has been shown to interact
123 or 2 (eIF2alpha) phosphorylation, activating transcription factor-4 (ATF4) induction, and increased e
127 of the transcriptional activators activating transcription factor 4, C/EBPalpha, Runx1, and Runx2.
128 on, particularly up-regulation of activating transcription factor-4, CHOP (C/EBP homologous protein),
129 The ER-stress element and the activating transcription factor 4 element in the CHOP promoter were
130 ound that a well-known oncogene, ETS variant transcription factor 4 (ETV4), serves as a molecular tra
132 control nonderepressible 2 kinase-activating transcription factor 4 (GCN2-ATF4) pathway activation an
137 t in BioTapestry, includes 22 genes encoding transcription factors, 4 genes encoding known signaling
138 ose-regulated protein-78 (GRP78), activating transcription factor 4, growth arrest and DNA damage-ind
139 alian vascular factor Kruppel-like family of transcription factor 4 has a conserved role in augmentin
141 ion of WNT-dependent inhibitory Kruppel-like transcription factor 4 in miR-199a-5p-overexpressing cel
144 e inhibitor bortezomib, levels of activating transcription factor-4 increase dramatically early in dr
145 aryotic initiation factor-2alpha, activating transcription factor 4, inositol requiring kinase 1, and
147 The transcription factor ATF4 (activating transcription factor 4) is induced by multiple PD-releva
148 nduced nuclear translocation of Kruppel-like transcription factor 4 (KLF4), a known repressor of SMC
149 r transcription factors, GR and Kruppel-like transcription factor 4 (KLF4), cooperatively transactiva
150 nscriptionally regulated by the Kruppel-like transcription factor 4 (KLF4), we determined the spatial
151 ap mesenchyme progenitors induced activating transcription factor 4-mediated nutritional stress respo
152 poorly translated mRNAs, notably activating transcription factor 4 mRNA, for reprogramming of gene e
153 with enhanced expression of octomer-binding transcription factor 4 (OCT-4) and several other genes c
154 s well as down-regulation of octamer-binding transcription factor 4 (Oct-4) expression and matrix met
156 ve for alkaline phosphatase, octamer-binding transcription factor 4 (Oct-4), stage-specific embryonic
158 are within binding sites of octamer-binding transcription factor 4 (OCT4) and signal transducer and
159 ed stem cell markers such as octamer binding transcription factor 4 (Oct4) and stage-specific embryon
160 ation of pluripotency marker Octamer-binding transcription factor 4 (OCT4) by at least 10% and increa
162 ly transcription factors and octamer-binding transcription factor 4 (OCT4), respectively, illuminatin
163 rt-term cyclic expression of octamer-binding transcription factor 4 (Oct4), sex-determining region Y-
165 nd POU5F1, the gene encoding octamer-binding transcription factor 4 (Oct4; also known as POU domain,
166 d eIF2alpha (p-eIF2alpha) but not activating transcription factor 4 or C/EBP homologous protein that
167 ivation of the PKR-like ER kinase/activating transcription factor 4 (PERK/ATF4) ER stress pathway, in
168 tral thermoregulator PHYTOCHROME INTERACTING transcription FACTOR 4 (PIF4), whose degradation is othe
169 y transcription factor Oct4 (octamer-binding transcription factor 4) plays an unappreciated role in t
171 gnalling by activating mTORC2 via activating transcription factor 4/sestrin 2 activation whilst promo
172 e treatment and is independent of activating transcription factor 4 signaling and protein translation
173 ndoplasmic reticulum kinase)-ATF (activating transcription factor) 4 signaling axis in atherogenic ma
175 Here, we investigated the role of SRY-box transcription factor 4 (SOX4) in regulating TEC dediffer
176 lular reactive oxygen species and activating transcription factor 4 target gene expression precede ce
179 could physically interact with beta-catenin/transcription factor 4 (TCF4) and disrupt their complex
186 basic helix-loop-helix transcription factor transcription factor 4 (TCF4) in the nervous system is u
191 ain-of-function of the psychiatric risk gene transcription factor 4 (TCF4) severely disrupts the colu
192 ted as inhibitors of the beta-catenin/T cell transcription factor 4 (Tcf4) signaling pathway using a
193 ereas we observed early dysregulation of the transcription factor 4 (Tcf4) that may drive cortical ch
194 schizophrenia, SNPs in or in the vicinity of transcription factor 4 (TCF4), neurogranin (NRGN) and an
195 c chondrocytes showed that HIF1alpha lowered transcription factor 4 (TCF4)-beta-catenin transcription
200 1.39 (1.24-1.55)] and at 18q21 [rs1452787 at transcription factor 4 (TCF4); P = 2.61 x 10(-8) , OR (9
204 on factor AP-2 gamma (Tfap2c) and TEA domain transcription factor 4 (Tead4) expression in the presenc
205 hepatocytes and tumor cells, YAP/TEA domain transcription factor 4 (TEAD4)-dependent transcriptional
207 lity of the CFTR Y-box for sequence-specific transcription factors; 4) that trichostatin A, an inhibi
208 the HD-ZIP III proteins, well-known polarity transcription factors(4)-the expression of which is conc
209 h the transcription factor TEAD4 (TEA domain transcription factor 4) to regulate chromatin accessibil
212 in Stat4 (Signal Transducer and Activator of Transcription Factor 4) was the causative mutation.
213 protein kinase RNA-like ER kinase, activator transcription factor 4) were assessed in transgenic mice