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1 en and nitrogen species and regulated by the activating-transcription factor-4.
2 on by amino acid deprivation did not require activating transcription factor 4, a critical component
3 down of inositol-requiring enzyme 1alpha and activating transcription factor 4 abrogates autophagosom
4 response genes (C/EBP homologous protein and activating transcription factor 4), accumulation of cera
5 alpha, inositol requiring kinase 1alpha, and activating transcription factor 4, all of which are feat
6 initiation factor 2alpha phosphorylation and activating transcription factor 4 and C/EBP homologous p
7 factor 2alpha (eiF2alpha) and expression of activating transcription factor 4 and tribbles 3 were el
9 such as the pseudokinase tribbles homolog 3, activating transcription factor 4, and transcription fac
10 ulator homolog 1) was regulated by the ATF4 (activating transcription factor 4) arm of the unfolded p
11 f genes enriched for components of the ATF4 (activating transcription factor 4) arm of the unfolded p
12 Several ER stress/UPR genes, including BiP, activating transcription factor 4 (ATF-4), ATF-6, and a
14 and anoxia by demonstrating the induction of activating transcription factor-4 (ATF-4) and growth arr
15 ed to persistent eif2-alpha phosphorylation (activating transcription factor 4 [ATF-4], C/EBP homolog
16 trends toward increasing downstream signals, activating transcription factor 4 (ATF4) and ATF6 indica
17 h preferential translation of mRNAs, such as activating transcription factor 4 (ATF4) and C/EBP-homol
18 UPR was activated, as the expression of both activating transcription factor 4 (ATF4) and CHOP (DDIT3
19 rotein synthesis but enhances translation of activating transcription factor 4 (ATF4) and is a crucia
22 ypes of mitochondrial stressors, we identify activating transcription factor 4 (ATF4) as the main reg
23 of FGF21 transcription was conferred by two activating transcription factor 4 (ATF4) binding sites i
24 sphorylation of eIF2alpha, which upregulates activating transcription factor 4 (ATF4) expression.
25 culum stress pathway, linked functionally to activating transcription factor 4 (ATF4) following treat
26 ed protein response (UPR) and an increase in activating transcription factor 4 (ATF4) has been previo
27 ve was to investigate the protective role of activating transcription factor 4 (ATF4) in controlling
29 d the signaling pathway of ER stress-induced activating transcription factor 4 (ATF4) in the regulati
36 ently that HRI also activates the eIF2alphaP-activating transcription factor 4 (ATF4) ISR in primary
38 and selectively enhances the translation of activating transcription factor 4 (ATF4) mRNA to induce
40 a heme-regulated inhibitor kinase/eIF2alpha/activating transcription factor 4 (ATF4) signaling modul
41 protein kinase RNA-like ER kinase (PERK) or activating transcription factor 4 (ATF4) significantly r
42 istration of AP20187 significantly increased activating transcription factor 4 (ATF4) translation and
43 zed enzymes are transcriptionally induced by activating transcription factor 4 (Atf4) via C/ebp-Atf-R
44 expression of the bZip transcription factor activating transcription factor 4 (ATF4) was induced by
47 ancer-derived cells stimulated expression of activating transcription factor 4 (ATF4), a master trans
48 regulation of triglyceride metabolism by the activating transcription factor 4 (ATF4), a member of th
50 P response element binding protein 2 (CREB2)/activating transcription factor 4 (ATF4), a transcriptio
51 ically increases translation of the metazoan activating transcription factor 4 (ATF4), activating the
52 ulated by arsenite, in a manner dependent on activating transcription factor 4 (ATF4), an important m
53 X-box-binding protein-1 mRNA, expression of activating transcription factor 4 (ATF4), and cleavage o
54 master regulator of amino acid homeostasis, activating transcription factor 4 (ATF4), is dysfunction
55 RNAs but selectively increase translation of Activating Transcription Factor 4 (ATF4), resulting in t
57 ISC1 interacts with the transcription factor Activating Transcription Factor 4 (ATF4), which is invol
58 sion and purine synthesis were stimulated by activating transcription factor 4 (ATF4), which was acti
59 nts that the histone demethylase JMJD3 is an activating transcription factor 4 (ATF4)-dependent targe
69 y the basic leucine zipper (bZIP) domains of activating transcription factor-4 (ATF4) and CCAAT box/e
71 iation factor 2 (eIF2alpha) phosphorylation, activating transcription factor-4 (ATF4) induction, and
73 er binding of the transcriptional activators activating transcription factor 4, C/EBPalpha, Runx1, an
74 UPR induction, particularly up-regulation of activating transcription factor-4, CHOP (C/EBP homologou
76 on general control nonderepressible 2 kinase-activating transcription factor 4 (GCN2-ATF4) pathway ac
77 luding glucose-regulated protein-78 (GRP78), activating transcription factor 4, growth arrest and DNA
81 e proteasome inhibitor bortezomib, levels of activating transcription factor-4 increase dramatically
82 rylated eukaryotic initiation factor-2alpha, activating transcription factor 4, inositol requiring ki
85 d early activation of the PKR-like ER kinase/activating transcription factor 4 (PERK/ATF4) ER stress
86 ugh arsenite treatment and is independent of activating transcription factor 4 signaling and protein
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