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1 homologous protein), and phospho-eIF2alpha (eukaryotic initiation factor 2alpha).
2 (dsRNA) and block phosphorylation of PKR and eukaryotic initiation factor 2alpha.
3 synthesis caused by hyperphosphorylation of eukaryotic initiation factor 2alpha.
4 ptional factors through dephosphorylation of eukaryotic initiation factor-2alpha.
5 protein synthesis through phosphorylation of eukaryotic initiation factor-2alpha.
7 ess marker proteins including phosphorylated eukaryotic initiation factor-2alpha, activating transcri
8 eficiency, HRI is activated to phosphorylate eukaryotic initiation factor 2alpha and halt production
9 lity of Gcn2p to phosphorylate its substrate eukaryotic initiation factor-2alpha and induce GCN4 tran
10 hPNPase(old-35) precedes phosphorylation of eukaryotic initiation factor-2alpha and induction of gro
11 the translation initiation factor eIF2alpha (eukaryotic initiation factor 2alpha), and, through subse
12 ulate translation via phosphorylation of the eukaryotic initiation factor 2alpha, and transcription v
13 dings in this investigation was that PKR and eukaryotic initiation factor 2alpha are phosphorylated u
14 ebrospinal fluid of OPG-bearing mice was the eukaryotic initiation factor-2alpha binding protein, met
15 uces phosphorylation of the alpha subunit of eukaryotic initiation factor 2alpha by Gcn2 protein kina
16 n a manner dependent upon phosphorylation of eukaryotic initiation factor 2alpha by the transmembrane
17 lation of the translation initiation factor, eukaryotic initiation factor 2alpha, by the GCN2 kinase.
18 However, Abeta-induced inactivation of the eukaryotic initiation factor 2alpha decreases the synapt
19 mal inhibitors enhanced GADD34 stability and eukaryotic initiation factor 2alpha (eIF-2alpha) dephosp
22 ctivation of heme-regulated alpha-subunit of eukaryotic initiation factor-2alpha (eIF-2alpha) kinase
24 NASH (n = 21) were associated with increased eukaryotic initiation factor-2alpha (eIF-2alpha) phospho
25 anded RNA-dependent protein kinase (PKR) and eukaryotic initiation factor-2alpha (eIF-2alpha) was det
26 to amino acid deficiency, phosphorylation of eukaryotic initiation factor 2alpha (eIF2 approximately
27 ent of its canonical induction downstream of eukaryotic initiation factor 2alpha eIF2alpha phosphoryl
28 kinase 1/2 (ERK1/2 Tyr202/204; +65% +/- 9%), eukaryotic initiation factor 2alpha (eIF2alpha Ser51; -2
29 be mediated by increased phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) and is h
30 ed through the translation initiation factor eukaryotic initiation factor 2alpha (eIF2alpha) and the
31 ynthesis in cells through phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) by eIF2a
33 phosphorylation of the alpha-subunit of the eukaryotic initiation factor 2alpha (eIF2alpha) has been
34 associated with increased phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha) in the l
35 und in solid tumours, activated the upstream eukaryotic initiation factor 2alpha (eIF2alpha) kinase G
36 activate the ER stress-responsive pancreatic eukaryotic initiation factor 2alpha (eIF2alpha) kinase o
37 R kinase (EIF2AK3)], the ER stress-activated eukaryotic initiation factor 2alpha (eIF2alpha) kinase.
38 s of P58(IPK), the cellular inhibitor of the eukaryotic initiation factor 2alpha (eIF2alpha) kinases
40 mbryonic fibroblasts depleted for individual eukaryotic initiation factor 2alpha (eIF2alpha) kinases,
42 Mbf1 is required for optimal stress-induced eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
43 nt study, we investigated whether increasing eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
44 dd34 (damage-inducible protein 34) prolonged eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
45 endoplasmic reticulum (ER) kinase-dependent eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
46 ein induction, PKR-like ER kinase (PERK) and eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
47 S6 (rpS6) phosphorylation and a decrease in eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
48 Finally, CMV blocked both the induction of eukaryotic initiation factor 2alpha (eIF2alpha) phosphor
50 IFN)-induced, double-stranded RNA-activated, eukaryotic initiation factor 2alpha (eIF2alpha) protein
51 e previously reported that activation of the eukaryotic initiation factor 2alpha (eIF2alpha) stress p
52 a rudimentary amino acid starvation-sensing eukaryotic initiation factor 2alpha (eIF2alpha) stress r
53 asmic reticulum kinase (PERK) phosphorylates eukaryotic initiation factor 2alpha (eIF2alpha) to atten
54 e of several kinases that phosphorylates the eukaryotic initiation factor 2alpha (eIF2alpha) to inhib
55 SNCEE, we found the translational regulator eukaryotic initiation factor 2alpha (eIF2alpha) was hype
56 ER kinase and subsequent phosphorylation of eukaryotic initiation factor 2alpha (eif2alpha), both of
57 es translation initiation by phosphorylating eukaryotic initiation factor 2alpha (eIF2alpha), impedin
58 f the PERK arm stimulates phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha), resulti
59 g and activation through a process requiring eukaryotic initiation factor 2alpha (eIF2alpha), the tra
60 ses often involve chronic phosphorylation of eukaryotic initiation factor 2alpha (eIF2alpha), with de
61 nretinide and bortezomib are mediated by the eukaryotic initiation factor 2alpha (eIF2alpha)-ATF4 sig
62 KR)-like endoplasmic reticulum kinase (PERK)/eukaryotic initiation factor 2alpha (eIF2alpha)-dependen
63 nize SAMD9 to prevent granule formation in a eukaryotic initiation factor 2alpha (eIF2alpha)-independ
64 g the activity of the pancreatic eIF2 kinase/eukaryotic initiation factor 2alpha (eIF2alpha)-like ER
70 yzed the effects of NTZ on the regulation of eukaryotic initiation factor-2alpha (eIF2alpha) and its
71 that modulates the phosphorylation level of eukaryotic initiation factor-2alpha (eIF2alpha) in respo
72 latency is an active process controlled by a eukaryotic initiation factor-2alpha (eIF2alpha) kinase (
73 . cerevisiae with a partial loss-of-function eukaryotic initiation factor-2alpha (eIF2alpha) kinase (
74 t results in phosphorylation of the parasite eukaryotic initiation factor-2alpha (eIF2alpha), leading
76 t to phosphorylate its substrate, eIF2alpha (eukaryotic initiation factor 2alpha), halting cellular t
77 However, Abeta-induced inactivation of the eukaryotic initiation factor 2alpha halts the transcript
78 d with a defect in translation, constitutive eukaryotic initiation factor 2alpha hyperphosphorylation
79 ely, genetically reducing phosphorylation of eukaryotic initiation factor 2alpha in excitatory neuron
80 ed ATF6 translocation and phosphorylation of eukaryotic initiation factor 2alpha in mouse cortical ne
82 bles rapid and reversible phosphorylation of eukaryotic initiation factor 2alpha, leading to inhibiti
83 h enables it to phosphorylate its substrate, eukaryotic initiation factor 2alpha, leading to translat
85 in the level of nuclear ATF6, phosphorylated eukaryotic initiation factor 2alpha, nuclear XBP1, and t
86 n mice by stimulating the phosphorylation of eukaryotic initiation factor 2alpha (p-eIF2alpha) and su
88 slation, the protein kinase R-like ER kinase-eukaryotic initiation factor 2alpha (PERK/eIF2alpha) arm
89 sident kinase (phospho-PERK), phosphorylated eukaryotic initiation factor-2alpha (phospho-eIF2alpha),
90 ting translation of highly translated mRNAs, eukaryotic initiation factor 2alpha phosphorylation also
91 ng cells exhibited a significant increase in eukaryotic initiation factor 2alpha phosphorylation and
92 general control nonderepressible 2-dependent eukaryotic initiation factor 2alpha phosphorylation and
93 BP1 and G3BP2 cannot form SGs in response to eukaryotic initiation factor 2alpha phosphorylation or e
95 indicative of proliferation such as reduced eukaryotic initiation factor 2alpha phosphorylation, inc
96 A activity to amino acid starvation requires eukaryotic initiation factor 2alpha phosphorylation, inc
97 sponse to hypertonic stress does not involve eukaryotic initiation factor 2alpha phosphorylation, sug
98 ine A induced stress granules independent of eukaryotic initiation factor 2alpha phosphorylation, sug
99 ely depleted within a few days, resulting in eukaryotic initiation factor 2alpha phosphorylation, TCR
100 tol-requiring enzyme 1alpha (IRE1alpha), and eukaryotic initiation factor 2alpha phosphorylation.
101 acentas, providing a potential mechanism for eukaryotic initiation factor 2alpha phosphorylation.
102 A-activated protein kinase (PKR) via the PKR eukaryotic initiation factor-2alpha phosphorylation homo
103 Since ceramide potently promotes RAX and eukaryotic initiation factor-2alpha phosphorylation, a p
105 Protein kinase R phosphorylates and inhibits eukaryotic initiation factor 2alpha, resulting in inhibi
107 epresses PKR-mediated phosphorylation of the eukaryotic initiation factor 2alpha subunit (eIF-2alpha)
108 ylation of the translation initiation factor eukaryotic initiation factor 2alpha, suggesting a novel
110 sly shown that phosphorylation of Toxoplasma eukaryotic initiation factor-2alpha (TgIF2alpha) is a co
112 In addition, increased phosphorylation of eukaryotic initiation factor 2alpha, the translation fac
114 r protein kinase R, which phosphorylates the eukaryotic initiation factor 2alpha to inhibit global pr
115 cted with rQNestin34.5, the level of phospho-eukaryotic initiation factor 2alpha was lower than that
116 le stress pathways is the phosphorylation of eukaryotic initiation factor 2alpha, which is phosphoryl