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1 (dsRNA) and block phosphorylation of PKR and eukaryotic initiation factor 2alpha.
2 synthesis caused by hyperphosphorylation of eukaryotic initiation factor 2alpha.
3 ptional factors through dephosphorylation of eukaryotic initiation factor-2alpha.
4 protein synthesis through phosphorylation of eukaryotic initiation factor-2alpha.
6 ess marker proteins including phosphorylated eukaryotic initiation factor-2alpha, activating transcri
7 lity of Gcn2p to phosphorylate its substrate eukaryotic initiation factor-2alpha and induce GCN4 tran
8 hPNPase(old-35) precedes phosphorylation of eukaryotic initiation factor-2alpha and induction of gro
9 the translation initiation factor eIF2alpha (eukaryotic initiation factor 2alpha), and, through subse
10 ulate translation via phosphorylation of the eukaryotic initiation factor 2alpha, and transcription v
11 dings in this investigation was that PKR and eukaryotic initiation factor 2alpha are phosphorylated u
12 ebrospinal fluid of OPG-bearing mice was the eukaryotic initiation factor-2alpha binding protein, met
13 uces phosphorylation of the alpha subunit of eukaryotic initiation factor 2alpha by Gcn2 protein kina
14 n a manner dependent upon phosphorylation of eukaryotic initiation factor 2alpha by the transmembrane
15 lation of the translation initiation factor, eukaryotic initiation factor 2alpha, by the GCN2 kinase.
16 mal inhibitors enhanced GADD34 stability and eukaryotic initiation factor 2alpha (eIF-2alpha) dephosp
19 ctivation of heme-regulated alpha-subunit of eukaryotic initiation factor-2alpha (eIF-2alpha) kinase
20 NASH (n = 21) were associated with increased eukaryotic initiation factor-2alpha (eIF-2alpha) phospho
22 anded RNA-dependent protein kinase (PKR) and eukaryotic initiation factor-2alpha (eIF-2alpha) was det
23 to amino acid deficiency, phosphorylation of eukaryotic initiation factor 2alpha (eIF2 approximately
24 ent of its canonical induction downstream of eukaryotic initiation factor 2alpha eIF2alpha phosphoryl
25 kinase 1/2 (ERK1/2 Tyr202/204; +65% +/- 9%), eukaryotic initiation factor 2alpha (eIF2alpha Ser51; -2
26 be mediated by increased phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) and is h
27 ed through the translation initiation factor eukaryotic initiation factor 2alpha (eIF2alpha) and the
28 ynthesis in cells through phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) by eIF2a
30 phosphorylation of the alpha-subunit of the eukaryotic initiation factor 2alpha (eIF2alpha) has been
31 associated with increased phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) in the l
32 und in solid tumours, activated the upstream eukaryotic initiation factor 2alpha (eIF2alpha) kinase G
33 activate the ER stress-responsive pancreatic eukaryotic initiation factor 2alpha (eIF2alpha) kinase o
34 R kinase (EIF2AK3)], the ER stress-activated eukaryotic initiation factor 2alpha (eIF2alpha) kinase.
35 s of P58(IPK), the cellular inhibitor of the eukaryotic initiation factor 2alpha (eIF2alpha) kinases
36 mbryonic fibroblasts depleted for individual eukaryotic initiation factor 2alpha (eIF2alpha) kinases,
38 nt study, we investigated whether increasing eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
39 endoplasmic reticulum (ER) kinase-dependent eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
40 ein induction, PKR-like ER kinase (PERK) and eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
41 S6 (rpS6) phosphorylation and a decrease in eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
42 Finally, CMV blocked both the induction of eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
43 IFN)-induced, double-stranded RNA-activated, eukaryotic initiation factor 2alpha (eIF2alpha) protein
45 e previously reported that activation of the eukaryotic initiation factor 2alpha (eIF2alpha) stress p
46 a rudimentary amino acid starvation-sensing eukaryotic initiation factor 2alpha (eIF2alpha) stress r
47 e of several kinases that phosphorylates the eukaryotic initiation factor 2alpha (eIF2alpha) to inhib
48 SNCEE, we found the translational regulator eukaryotic initiation factor 2alpha (eIF2alpha) was hype
49 ER kinase and subsequent phosphorylation of eukaryotic initiation factor 2alpha (eif2alpha), both of
50 es translation initiation by phosphorylating eukaryotic initiation factor 2alpha (eIF2alpha), impedin
51 f the PERK arm stimulates phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha), resulti
52 nretinide and bortezomib are mediated by the eukaryotic initiation factor 2alpha (eIF2alpha)-ATF4 sig
53 KR)-like endoplasmic reticulum kinase (PERK)/eukaryotic initiation factor 2alpha (eIF2alpha)-dependen
54 nize SAMD9 to prevent granule formation in a eukaryotic initiation factor 2alpha (eIF2alpha)-independ
55 g the activity of the pancreatic eIF2 kinase/eukaryotic initiation factor 2alpha (eIF2alpha)-like ER
61 yzed the effects of NTZ on the regulation of eukaryotic initiation factor-2alpha (eIF2alpha) and its
62 that modulates the phosphorylation level of eukaryotic initiation factor-2alpha (eIF2alpha) in respo
63 latency is an active process controlled by a eukaryotic initiation factor-2alpha (eIF2alpha) kinase (
64 . cerevisiae with a partial loss-of-function eukaryotic initiation factor-2alpha (eIF2alpha) kinase (
65 t results in phosphorylation of the parasite eukaryotic initiation factor-2alpha (eIF2alpha), leading
67 t to phosphorylate its substrate, eIF2alpha (eukaryotic initiation factor 2alpha), halting cellular t
68 d with a defect in translation, constitutive eukaryotic initiation factor 2alpha hyperphosphorylation
69 ed ATF6 translocation and phosphorylation of eukaryotic initiation factor 2alpha in mouse cortical ne
71 h enables it to phosphorylate its substrate, eukaryotic initiation factor 2alpha, leading to translat
73 in the level of nuclear ATF6, phosphorylated eukaryotic initiation factor 2alpha, nuclear XBP1, and t
74 sident kinase (phospho-PERK), phosphorylated eukaryotic initiation factor-2alpha (phospho-eIF2alpha),
75 general control nonderepressible 2-dependent eukaryotic initiation factor 2alpha phosphorylation and
76 ng cells exhibited a significant increase in eukaryotic initiation factor 2alpha phosphorylation and
77 BP1 and G3BP2 cannot form SGs in response to eukaryotic initiation factor 2alpha phosphorylation or e
79 indicative of proliferation such as reduced eukaryotic initiation factor 2alpha phosphorylation, inc
80 A activity to amino acid starvation requires eukaryotic initiation factor 2alpha phosphorylation, inc
81 sponse to hypertonic stress does not involve eukaryotic initiation factor 2alpha phosphorylation, sug
82 ine A induced stress granules independent of eukaryotic initiation factor 2alpha phosphorylation, sug
83 ely depleted within a few days, resulting in eukaryotic initiation factor 2alpha phosphorylation, TCR
84 tol-requiring enzyme 1alpha (IRE1alpha), and eukaryotic initiation factor 2alpha phosphorylation.
85 acentas, providing a potential mechanism for eukaryotic initiation factor 2alpha phosphorylation.
86 A-activated protein kinase (PKR) via the PKR eukaryotic initiation factor-2alpha phosphorylation homo
87 Since ceramide potently promotes RAX and eukaryotic initiation factor-2alpha phosphorylation, a p
89 Protein kinase R phosphorylates and inhibits eukaryotic initiation factor 2alpha, resulting in inhibi
90 epresses PKR-mediated phosphorylation of the eukaryotic initiation factor 2alpha subunit (eIF-2alpha)
91 ylation of the translation initiation factor eukaryotic initiation factor 2alpha, suggesting a novel
93 sly shown that phosphorylation of Toxoplasma eukaryotic initiation factor-2alpha (TgIF2alpha) is a co
95 In addition, increased phosphorylation of eukaryotic initiation factor 2alpha, the translation fac
97 r protein kinase R, which phosphorylates the eukaryotic initiation factor 2alpha to inhibit global pr
98 cted with rQNestin34.5, the level of phospho-eukaryotic initiation factor 2alpha was lower than that
99 le stress pathways is the phosphorylation of eukaryotic initiation factor 2alpha, which is phosphoryl
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