コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 anslation initiation factor eIF2 (eukaryotic initiation factor 2).
2 erine 51 on the alpha subunit of translation initiation factor 2.
3 n of PKR and the alpha subunit of eukaryotic initiation factor 2.
4 orylation of the alpha-subunit of eukaryotic initiation factor 2.
5 es by phosphorylating eukaryotic translation initiation factor 2.
6 the alpha subunit of eukaryotic translation initiation factor 2.
7 orylation of the alpha subunit of eukaryotic initiation factor 2.
8 starved cells by phosphorylating translation initiation factor 2.
9 nding site overlaps with the binding site of initiation factor 2.
10 inding domain of the prokaryotic translation initiation factor 2.
11 phorylating the alpha-subunit of translation initiation factor 2.
12 r amino acids by phosphorylating translation initiation factor 2.
13 orylation of the alpha-subunit of eukaryotic initiation factor 2.
14 sphorylating the alpha subunit of eukaryotic initiation factor-2.
15 quitin-conjugating enzyme (15%); translation-initiation factor 2 (6%); and GTP-binding protein, Rab38
16 alysis of the flexible bacterial translation initiation factor 2 (91 kDa) using fsPTCR reduced overch
20 ic heme-regulated inhibitor (HRI)-eukaryotic initiation factor 2 alpha (eIF2 alpha) kinase is activat
21 ) that phosphorylates eukaryotic translation initiation factor 2 alpha (eIF2a), which orchestrates th
23 g at serine-51 phosphorylation on eukaryotic initiation factor 2 alpha (eIF2alpha) and activate the i
24 tional control by the eukaryotic translation initiation factor 2 alpha (eIF2alpha) bidirectionally re
25 bitor kinase (HRI), a eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase, plays crit
26 llular stress by deactivating the eukaryotic initiation factor 2 alpha (eIF2alpha) or other signal tr
27 PKR's pro-apoptotic role through eukaryotic initiation factor 2 alpha (eIF2alpha) phosphorylation is
28 ating protein translation through eukaryotic initiation factor 2 alpha (eIF2alpha) phosphorylation.
29 hosphorylation of the eukaryotic translation initiation factor 2 alpha (eIF2alpha), an important comp
30 ith and can methylate eukaryotic translation initiation factor 2 alpha (eIF2alpha), in vitro and in b
31 ) that phosphorylates eukaryotic translation initiation factor 2 alpha (eIF2alpha), which orchestrate
36 capsid-induced phosphorylation of eukaryotic initiation factor 2 alpha and with capsid-mediated inhib
37 encode members of the eukaryotic translation initiation factor 2 alpha kinase (EIF2AK) family that in
38 , p.Gly130Arg, in the eukaryotic translation initiation factor 2 alpha kinase 2 (EIF2AK2) gene, segre
39 de variants (SNVs) of eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3) slightly in
40 (phosphorylation) of eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3, also called
41 cientists discovered mutations in eukaryotic initiation factor 2 alpha kinase 4 (EIF2AK4) that cause
42 elic mutations in the eukaryotic translation initiation factor 2 alpha kinase 4 gene (EIF2AK4) are de
43 polysomes likewise depends on the eukaryotic initiation factor 2 alpha kinase 4, which associates wit
44 ment protein C1qB and eukaryotic translation initiation factor 2 alpha kinase 4-an orchestrator of th
45 nd phosphorylates the eukaryotic translation initiation factor 2 alpha subunit (cIF-2 alpha) to inhib
46 ication of S. mansoni eukaryotic translation initiation factor 2 alpha subunit (eIF2 alpha), through
47 R, we observed a reduced level of eukaryotic initiation factor 2 alpha subunit (eIF2alpha) phosphoryl
48 tein loss led to the induction of eukaryotic initiation factor 2 alpha subunit (eIF2alpha) signaling
49 ct characterized by deficiency of eukaryotic initiation factor 2 alpha subunit phosphorylation, delay
51 ation (phosphorylated eukaryotic translation initiation factor 2 alpha), and cell death [terminal deo
54 that UV light-induced eukaryotic translation initiation factor 2 alpha-subunit phosphorylation transl
55 n site, Ser-51 in the eukaryotic translation initiation factor 2 alpha-subunit, is replaced with a no
56 aspase-12, and phosphorylation of eukaryotic initiation factor-2 alpha in a human dopaminergic neuron
57 (PKR), which then phosphorylates translation initiation factor 2-alpha (eIF-2alpha), and inhibits tra
58 protein synthesis by inactivating eukaryotic initiation factor 2-alpha (eIF2-alpha), to examine the m
60 s demonstrated phosphorylation of eukaryotic initiation factor 2-alpha (eIF2alpha), a 'collapsed' pol
61 dependent on the presence of the eukaryotic initiation factor 2-alpha homology region, mapping to th
62 ation mediated by the eukaryotic translation initiation factor 2-alpha kinase 2/eukaryotic translatio
63 hat activation of the eukaryotic translation initiation factor 2-alpha kinase 2/eukaryotic translatio
64 , small molecule inhibitor of the eukaryotic initiation factor 2-alpha kinase 3 (EIF2AK3) or PERK, on
65 ation of eIF2alpha (eukaryotic translational initiation factor 2-alpha) and ensuing activation of p38
66 se RNA-like ER kinase/eukaryotic translation initiation factor 2-alpha/activating transcription facto
67 orylation of the alpha subunit of eukaryotic initiation factor 2 and NF-kappaB activity at 72 h posti
68 epressible 2), phosphorylation of eukaryotic initiation factor 2, and increased synthesis of activati
71 at phosphorylation of eukaryotic translation initiation factor 2 at Ser-51 on the alpha subunit was n
72 ident kinase)/eIF2a (a subunit of eukaryotic initiation factor 2) axis of the ISR is strongly induced
74 orylation of the alpha subunit of eukaryotic initiation factor 2 causes translating mRNAs to accumula
75 ns, OmpA and OmpB, we identified translation initiation factor 2, cell division protein FtsZ, and cys
76 complex (30SIC(Cy3)) containing Cy3-labeled initiation factor 2 complexed with GTP leads to rapid de
77 nase)-eIF2alpha (alpha subunit of eukaryotic initiation factor 2)-dependent pathway by SubAB-mediated
78 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2 alpha), the primary physiolog
79 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2) and total shutoff of protein
83 hosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) and inhibit translation
84 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha) and the induction of ap
85 alpha-subunit of the eukaryotic translation initiation factor 2 (eIF-2alpha) and to apoptotic cell d
86 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) by activated PKR, and,
87 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) is a well-characterized
88 ated increase in alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha) phosphorylation and ini
90 R and the alpha subunit of protein synthesis initiation factor 2 (eIF-2alpha) was elevated severalfol
91 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha) was enhanced approximat
92 the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha), a process that prevent
93 e (PERK) and the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha), as well as induce robu
94 rate of PKR, the alpha subunit of eukaryotic initiation factor 2 (eIF-2alpha), was equally phosphoryl
99 tion mutations in the eukaryotic translation initiation factor 2D (eif-2D/eIF2D) reduce poly-GA and p
101 orylation of the alpha subunit of eukaryotic initiation factor-2 (eIF-2) is a well characterized mech
104 orylation of the alpha subunit of eukaryotic initiation factor-2 (eIF-2alpha) and inhibition of prote
108 ss the role of phosphorylation of eukaryotic initiation factor 2 (eIF2) and attendant gene expression
109 the translation initiation factor eukaryotic initiation factor 2 (eIF2) and thereby inhibits protein
112 e to phosphorylation of the alpha-subunit of initiation factor 2 (eIF2) by its specific kinase, GCN2,
114 Phosphorylation of the alpha-subunit of initiation factor 2 (eIF2) controls protein synthesis by
115 During translation initiation the eukaryotic initiation factor 2 (eIF2) forms a ternary complex (TC)
116 hange factor that converts protein synthesis initiation factor 2 (eIF2) from a GDP-bound form to the
117 cell; therefore, the eukaryotic translation initiation factor 2 (eIF2) gene family is a likely candi
119 rotein kinases that phosphorylate eukaryotic initiation factor 2 (eIF2) in coordinating stress gene r
120 tRNA(Met) binding to eukaryotic translation initiation factor 2 (eIF2) in response to eIF2 phosphory
130 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2) is fundamental to the process
135 rnary complex (TC) with GTP-bound eukaryotic initiation factor 2 (eIF2) to the small (40S) ribosomal
136 se R (PKR), which inactivates the eukaryotic initiation factor 2 (eIF2) translation initiation factor
137 er RNA induces phosphorylation of eukaryotic initiation factor 2 (eIF2) via the GC nonderepressing 2
138 that can regulate the activity of eukaryotic initiation factor 2 (eIF2), a critical translation initi
139 Activated GCN2 phosphorylates eukaryotic initiation factor 2 (eIF2), altering gene-specific trans
141 al complexes on the IRES requires eukaryotic initiation factor 2 (eIF2), eIF3, eIF4A, and the central
142 rly initiation complex containing eukaryotic initiation factor 2 (eIF2), GTP, and methionine-charged
143 he translation initiation complex eukaryotic initiation factor 2 (eIF2), have a profound impact on is
145 specific ternary complex between eukaryotic initiation factor 2 (eIF2), the initiator methionyl-tRNA
146 osphorylates the alpha subunit of eukaryotic initiation factor 2 (eIF2), thus rendering eIF2 inactive
147 Recruitment of the eukaryotic translation initiation factor 2 (eIF2)-GTP-Met-tRNAiMet ternary comp
148 ly GTPase, has been implicated in eukaryotic initiation factor 2 (eIF2)-mediated translational contro
156 1A stimulates 40S-binding of the eukaryotic initiation factor 2 (eIF2)/GTP/Met-tRNA(iMet) ternary co
157 s regulated by phosphorylation of eukaryotic initiation factor 2 (eIF2-P) that causes decreased globa
158 activate Gcn2p phosphorylation of eukaryotic initiation factor-2 (eIF2) and the general amino acid co
160 ular stresses, phosphorylation of eukaryotic initiation factor-2 (eIF2) elicits gene expression desig
161 in kinases that phosphorylate the eukaryotic initiation factor-2 (eIF2) function in translational con
163 ntal stresses, phosphorylation of eukaryotic initiation factor-2 (eIF2) rapidly reduces protein synth
165 sphorylation of the alpha-subunit eukaryotic initiation factor-2 (eIF2), and its attendant regulation
170 he activation of the a subunit of eukaryotic initiation factor 2 (eIF2a) kinase GCN2 during MNV infec
171 f pSer51 of the alpha subunit of translation initiation factor 2 (eIF2alpha(P)) terminates signaling
172 ation of the alpha subunit of the eukaryotic initiation factor 2 (eIF2alpha) and inhibits global prot
173 orylates the alpha-subunit of the eukaryotic initiation factor 2 (eIF2alpha) and inhibits translation
174 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) and the consequent shuto
175 hosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) are activated in stresse
176 orylation of the alpha-subunit of eukaryotic initiation factor 2 (eIF2alpha) at a conserved serine re
178 R) kinase (PERK)-alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) branch of the unfolded p
179 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) by the endoplasmic retic
180 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) by the interferon-induce
182 tion of the alpha subunit of the translation initiation factor 2 (eIF2alpha) in an AR-dependent manne
183 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) in MEFs in an IFN-depend
184 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) in response to different
185 hosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) in response to stress.
187 lation through phosphorylation of eukaryotic initiation factor 2 (eIF2alpha) is essential to preserve
188 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) is known to be an import
189 nitiation factor alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) is known to occur in res
191 tivation of the alpha subunit of translation initiation factor 2 (eIF2alpha) kinase GCN2 and conseque
192 fically phosphorylate eukaryotic translation initiation factor 2 (eIF2alpha) on Ser51 to regulate glo
193 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) on serine 51 integrates
194 iver, including alpha subunit of translation initiation factor 2 (eIF2alpha) phosphorylation, activat
195 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) protein via phosphorylat
196 rylation of the alpha-subunit of translation initiation factor 2 (eIF2alpha) represses translation an
197 rylation of the alpha-subunit of translation initiation factor 2 (eIF2alpha) represses translation in
198 es phosphorylation of eukaryotic translation initiation factor 2 (eIF2alpha) resulting in inhibition
200 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) to activate the integrat
201 orylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) translation initiation f
202 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) was decreased, and host
203 kinase Gcn2, which phosphorylates eukaryotic initiation factor 2 (eIF2alpha) with attendant inhibitio
204 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), attenuating translation
205 alpha-subunit of the eukaryotic translation initiation factor 2 (eIF2alpha), increased levels of ATF
206 osphorylates the alpha-subunit of eukaryotic initiation factor 2 (eIF2alpha), inhibiting the function
207 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), is an important protect
208 -subunit of wild-type eukaryotic translation initiation factor 2 (eIF2alpha), one of the known substr
209 the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in decreased
210 the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in inhibition
211 the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha), resulting in the inhibi
212 ation of the alpha subunit of the eukaryotic initiation factor 2 (eIF2alpha), the cellular substrate
213 osphorylate the alpha subunit of translation initiation factor 2 (eIF2alpha), thus attenuating mRNA t
228 ated alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha-P), a regulator of genera
229 the alpha-subunit of eukaryotic translation initiation factor-2 (eIF2alpha) leading to inhibition of
230 e the beta subunit of eukaryotic translation initiation factor 2 (eIF2beta) and the N-terminal domain
232 eukaryotic translation initiation factor 5B/initiation factor 2 (eIF5B/IF2) impair yeast cell growth
233 actor eIF2alpha (alpha subunit of eukaryotic initiation factor 2), ensuring viral protein synthesis.
235 ed" translation despite inhibited eukaryotic initiation factor 2-guanosine triphosphate-initiator met
236 ed kinase of the alpha subunit of eukaryotic initiation factor 2 (HRI) is activated in rabbit reticul
237 ationships among the components of bacterial initiation factor 2 (IF-2) and eukaryotic IF-2 (eIF-2)/e
240 S ribosomes in the presence of mitochondrial initiation factor 2 (IF2(mt)), [(35)S]fMet-tRNA, and eit
242 lation factors in prokaryotes and eukaryotes-initiation factor 2 (IF2) and eukaryotic initiation fact
243 llosteric activation of the essential GTPase Initiation Factor 2 (IF2) during translation initiation.
245 The initiation of protein synthesis uses initiation factor 2 (IF2) in prokaryotes and a related p
246 ecycling factor (RRF) activity or increasing initiation factor 2 (IF2) levels enhanced initiation wit
248 ukaryotic initiation and elongation factors, initiation factor 2 (IF2), eukaryotic initiation factor
251 sence of the full-length form of Translation Initiation Factor 2 (IF2-1) or deficiency in helicase ac
252 cule tracking, the timing of initiator tRNA, initiation factor 2 (IF2; encoded by infB) and 50S subun
253 ent increased phosphorylation of translation initiation factor 2, IkappaBalpha, and JNK, indicating i
254 nase, and its downstream effector eukaryotic initiation factor 2 in human leukemia (HL60) and ovarian
256 n of PKR and the alpha subunit of eukaryotic initiation factor 2, indicating that K1L and C7L functio
257 the eIF-2alpha (alpha subunit of eukaryotic initiation factor 2) kinase PERK to transiently arrest p
258 The ZPR1 domain consists of an elongation initiation factor 2-like zinc finger and a double-strand
259 utathione, enhanced activation of eukaryotic initiation factor 2-mediated stress response, and enhanc
260 ifm1 mutants, lacking the mitochondrial initiation factor 2 (mIF2), are unable to respire, indic
261 factors that together with the mitochondrial initiation factor 2 (mt-IF-2) specifically interact with
262 in kinase R, which phosphorylates eukaryotic initiation factor 2, nor oligoadenylate synthetase, whic
263 orylation of the alpha subunit of eukaryotic initiation factor 2 on serine 51 was not detectably incr
264 es phosphorylation of eukaryotic translation initiation factor 2 on the alpha-subunit (eIF2alpha) and
265 f both protein kinase R (PKR) and eukaryotic initiation factor 2 on the alpha-subunit in skeletal mus
267 (AADR) such as phosphorylation of eukaryotic initiation factor 2 (p-eIF2) leading to increased mRNA l
268 ts of the APOL1-G1 variant on the eukaryotic initiation factor 2 pathway highlighted differences betw
269 s the ages, corroborating similar eukaryotic initiation factor 2 phosphorylation responses to asparag
270 ecrease in eIF2alpha (eukaryotic translation initiation factor 2) phosphorylation in astrocytes in th
271 orylation of the alpha subunit of eukaryotic initiation factor 2, requiring PKR-like endoplasmic reti
272 hosphorylate the alpha-subunit of eukaryotic initiation factor 2, revealing a new molecular mechanism
273 dent of source of infection, with eukaryotic initiation factor 2 signaling being the most enriched ca
274 ere downregulation of eukaryotic translation initiation factor 2 signaling in the HIC cohort (z score
275 R, phosphorylation of eukaryotic translation initiation factor 2 subunit 1 (eIF2alpha), the SG assemb
277 EIF2AKs phosphorylate eukaryotic translation initiation factor 2 subunit 1 (EIF2S1, also known as EIF
278 impaired autophosphorylation and eukaryotic initiation factor 2 subunit alpha (eIF2alpha) phosphoryl
279 ylates its substrate, eukaryotic translation initiation factor 2 subunit alpha (eIF2alpha), causing i
282 hosphorylation of the eukaryotic translation initiation factor 2 subunit alpha (EIF2S1 or EIF2A), whi
283 nae, increased phosphorylation of eukaryotic initiation factor 2 subunit alpha (P-eIF2alpha), reduced
284 ed phosphorylation of eukaryotic translation initiation factor 2 subunit alpha, increased expression
286 of phosphorylation of eukaryotic translation initiation factor 2 subunit-alpha (eIF2alpha, encoded by
287 osphorylates the alpha subunit of eukaryotic initiation factor 2, thereby inhibiting protein synthesi
288 osphorylates the alpha-subunit of eukaryotic initiation factor 2, thereby inhibiting protein synthesi
289 ate group on the alpha subunit of elongation initiation factor 2, thereby reversing the shutoff of pr
290 the alpha subunit of eukaryotic translation initiation factor 2 was defective after virus infection
291 ion of the alpha-subunit of eIF2 (eukaryotic initiation factor 2), which inhibits its guanine nucleot
292 al control via phosphorylation of eukaryotic initiation factor 2, which is implicated in learning and
293 ange factor (GEF) for eukaryotic translation initiation factor 2, which stimulates formation of the e
294 al localization of phosphorylated eukaryotic initiation factor 2, which we show is sufficient to indu