ライフサイエンスコーパス: eukaryotic translation initiation factor

1 Remarkably, Sui(-) mutations in eukaryotic translation initiation factor 1 (eIF1), eIF1A

2 Phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 (eIF-2alpha)

3 Eukaryotic translation initiation factor 2 (eIF2) is a h

4 The eukaryotic translation initiation factor 2 (eIF2) is cen

5 Recruitment of the eukaryotic translation initiation factor 2 (eIF2)-GTP-Me

6 ated phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) b

7 nt with salubrinal, a selective inhibitor of eukaryotic translation initiation factor 2 (eIF2alpha) d

8 RI, PKR, and PERK specifically phosphorylate eukaryotic translation initiation factor 2 (eIF2alpha) o

9 stances, ph-PKR targets the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) p

10 H2S transiently increases phosphorylation of eukaryotic translation initiation factor 2 (eIF2alpha) r

11 g kinases phosphorylate the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) t

12 GCN2 phosphorylates the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha),

13 ), which phosphorylates the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha),

14 duce phosphorylation of the alpha-subunit of eukaryotic translation initiation factor 2 (eIF2alpha),

15 d by phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha),

16 ISR) by phosphorylating the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha).

17 formation of phosphorylated alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha-P)

18 Heme-regulated inhibitor kinase (HRI), a eukaryotic translation initiation factor 2 alpha (eIF2al

19 displaying PI-induced phosphorylation of the eukaryotic translation initiation factor 2 alpha (eIF2al

20 of protein kinase R (PKR) and its substrate eukaryotic translation initiation factor 2 alpha (eIF2al

21 we found that, translational control by the eukaryotic translation initiation factor 2 alpha (eIF2al

22 e of PAH, whereas biallelic mutations in the eukaryotic translation initiation factor 2 alpha kinase

23 nd sustained activation (phosphorylation) of eukaryotic translation initiation factor 2 alpha kinase

24 ature, including complement protein C1qB and eukaryotic translation initiation factor 2 alpha kinase

25 These results suggest that UV light-induced eukaryotic translation initiation factor 2 alpha-subunit

26 hich the phosphorylation site, Ser-51 in the eukaryotic translation initiation factor 2 alpha-subunit

27 ism, we demonstrated that phosphorylation of eukaryotic translation initiation factor 2 at Ser-51 on

28 r of cellular complexes that dephosphorylate eukaryotic translation initiation factor 2 subunit alpha

29 ng pathways result in phosphorylation of the eukaryotic translation initiation factor 2 subunit alpha

30 Phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 was defective

31 guanine nucleotide exchange factor (GEF) for eukaryotic translation initiation factor 2, which stimul

32 vels of amino acid stores by phosphorylating eukaryotic translation initiation factor 2.

33 orylates its substrate, the alpha-subunit of eukaryotic translation initiation factor-2 (eIF2alpha) l

34 Dephosphorylation of eukaryotic translation initiation factor 2a (eIF2a) rest

35 and phosphorylate cellular targets, such as eukaryotic translation initiation factor 2alpha (eIF-2al

36 hosphorylate the regulatory serine 51 of the eukaryotic translation initiation factor 2alpha (eIF2alp

37 The integrated stress response mediated by eukaryotic translation initiation factor 2alpha (eIF2alp

38 Phosphorylation of eukaryotic translation initiation factor 2alpha (eiF2alp

39 at ECM detachment activates a canonical PERK-eukaryotic translation initiation factor 2alpha (eIF2alp

40 As phosphorylation of eukaryotic translation initiation factor 2alpha (eIF2alp

41 he genus Ranavirus encode a homologue of the eukaryotic translation initiation factor 2alpha (eIF2alp

42 inase knockout (PERK-KO) or phosphodeficient eukaryotic translation initiation factor 2alpha (eIF2alp

43 The eukaryotic translation initiation factor 2alpha (eIF2alp

44 additionally induces the phosphorylation of eukaryotic translation initiation factor 2alpha (eIF2alp

45 iral infection by actively dephosphorylating eukaryotic translation initiation factor 2alpha (eIF2alp

46 ein kinase/endoribonuclease, and ER-resident eukaryotic translation initiation factor 2alpha (eIF2alp

47 to activation of PKR-like ER kinase (PERK), eukaryotic translation initiation factor 2alpha (eIF2alp

48 nases, including GCN2 and PKR, phosphorylate eukaryotic translation initiation factor 2alpha (eIF2alp

49 nhanced protein levels in the heme-regulated eukaryotic translation initiation factor 2alpha (eIF2alp

50 NA of CReP/Ppp1r15b, a regulatory subunit of eukaryotic translation initiation factor 2alpha (eIF2alp

51 smic reticulum stress and phosphorylation of eukaryotic translation initiation factor 2alpha (eIF2alp

52 a the 5' UTRalpha and phosphorylation of the eukaryotic translation initiation factor 2alpha (eIF2alp

53 served markedly increased phosphorylation of eukaryotic translation initiation factor 2alpha (p-eIF2a

54 e ER kinase-dependent phosphorylation of the eukaryotic translation initiation factor 2alpha and enha

55 stress-inducible kinase that phosphorylates eukaryotic translation initiation factor 2alpha and spec

56 pore complex interacting protein (NPIP) and eukaryotic translation initiation factor 2alpha kinase (

57 ously showed that the PKR-like, ER-localized eukaryotic translation initiation factor 2alpha kinase b

58 This increase in eukaryotic translation initiation factor 2alpha phosphor

59 ing by GCN1.GCN20 and a stronger decrease in eukaryotic translation initiation factor 2alpha phosphor

60 sis, through activating pancreatic ER kinase/eukaryotic translation initiation factor 2alpha signalin

61 asGAP SH3-binding protein and phosphorylated eukaryotic translation initiation factor 2alpha unchange

62 ylation of protein kinase-like ER kinase and eukaryotic translation initiation factor 2alpha, and the

63 logous protein as well as phosphorylation of eukaryotic translation initiation factor 2alpha, indicat

64 g arsenite stress-induced phosphorylation of eukaryotic translation initiation factor 2alpha, inhibit

65 increased the levels of Bip, phosphorylated eukaryotic translation initiation factor 2alpha, inosito

66 four protein kinases known to phosphorylate eukaryotic translation initiation factor 2alpha, only th

67 ss-induced RNAs; tiRNAs) induces the phospho-eukaryotic translation initiation factor 2alpha-independ

68 amino acid-starved cells by phosphorylating eukaryotic translation initiation factor 2alpha.

69 EIF2AK3), the latter of which phosphorylates eukaryotic translation initiation factor-2alpha (eIF2alp

70 visiae translation initiation factor complex eukaryotic translation initiation factor 2B (eIF2B) and

71 Eukaryotic translation initiation factor 2B (eIF2B) is a

72 Eukaryotic translation initiation factor 2B (eIF2B) is t

73 The eukaryotic translation initiation factor 2B (eIF2B) prov

74 d by mutations in genes encoding subunits of eukaryotic translation initiation factor 2B (eIF2B).

75 pomyelinating disease caused by mutations in eukaryotic translation initiation factor 2B (eIF2B).

76 nous GSK-3beta, inhibited phosphorylation of eukaryotic translation initiation factor 2B epsilon, and

77 uMV resistance 03 (retr03), an allele of the eukaryotic translation initiation factor 2B-beta (eIF2Bb

78 siRNA against eukaryotic translation initiation factor 2Bepsilon (eIF2

79 the antihypertrophic effect of GSK-3beta is eukaryotic translation initiation factor 2Bepsilon (eIF2

80 Eukaryotic translation initiation factor 3 (eIF3) consis

81 er of the initiation pathway, the 13-subunit eukaryotic translation initiation factor 3 (eIF3) contro

82 CTD) of the a/Tif32 subunit of budding yeast eukaryotic translation initiation factor 3 (eIF3) intera

83 Eukaryotic translation initiation factor 3 (eIF3) is a c

84 Eukaryotic translation initiation factor 3 (eIF3) plays

85 Altered expression of the eukaryotic translation initiation factor 3 (eIF3) subuni

86 ments: the proteasome, COP9 signalosome, and eukaryotic translation initiation factor 3 (eIF3).

87 e can be isolated from cells in complex with eukaryotic translation initiation factor 3 and ribosomal

88 protein metabolism were upregulated, such as eukaryotic translation initiation factor 3 and ribosome

89 -beta3 translation, a process that involved eukaryotic translation initiation factor 3 subunit b as

90 Two mutations were identified in eukaryotic translation initiation factor 3 subunit C (Ei

91 In addition, mTOR co-localised with Eukaryotic translation initiation factor 3 subunit F (eI

92 Eukaryotic translation initiation factor 3 subunit I (eI

93 OP9 signalosome, the proteasome lid, and the eukaryotic translation initiation factor 3, are revealin

94 report that the protein translation factor, eukaryotic translation initiation factor 3, subunit a (e

95 hat HIV protease cleaves eIF3d, a subunit of eukaryotic translation initiation factor 3.

96 eIF3a (eukaryotic translation initiation factor 3a), one of the

97 Complex assembly of the mRNA cap protein, eukaryotic translation initiation factor 4 (eIF4)E, with

98 is largely exerted at initiation through the eukaryotic translation initiation factor 4 F (eIF4F).

99 arboxypeptidase E (CPE) by inhibition of the eukaryotic translation initiation factor 4 gamma 1 trans

100 ro8 mutation is in the Eif4g3 gene, encoding eukaryotic translation initiation factor 4, gamma 3.

101 This process facilitates IFN-induced eukaryotic translation initiation factor 4A (eIF4A) acti

102 DEAD-box RNA helicases eukaryotic translation initiation factor 4A (eIF4A) and

103 phila Dpp pathway is negatively regulated by eukaryotic translation initiation factor 4A (eIF4A), whi

104 ollagen alpha2(I) mRNAs, by interacting with eukaryotic translation initiation factor 4A (eIF4A).

105 of the Su(dpp) mutations as an allele of the eukaryotic translation initiation factor 4A (eIF4A).

106 ) 1B (alpha-, beta-, and gamma-subunits) and eukaryotic translation initiation factor 4A (three isofo

107 Eukaryotic translation initiation factor 4A is an essent

108 4 directly inhibits the helicase activity of eukaryotic translation initiation factor 4A, a component

109 The eukaryotic translation initiation factors 4A (eIF4A) and

110 In cells depleted of CDK12 or eukaryotic translation initiation factor 4A3 (eIF4A3) fr

111 , using antibodies to EJC components Y14 and eukaryotic translation initiation factor 4aIII (eIF4AIII

112 peptide library profiling, we identified the eukaryotic translation initiation factor 4B (eIF4B) as a

113 We confirmed that Asp(563) in eukaryotic translation initiation factor 4B (eIF4B) is a

114 Eukaryotic translation initiation factor 4B (eIF4B) is a

115 Here, we found that the protein level of eukaryotic translation initiation factor 4B (eIF4B), an

116 found that ORF45 induced phosphorylation of eukaryotic translation initiation factor 4B (eIF4B), inc

117 of IFNs on the phosphorylation/activation of eukaryotic translation initiation factor 4B (eIF4B).

118 gh the phosphorylation of the S6K1-dependent eukaryotic translation initiation factor 4B.

119 tion initiation factor 4E-binding protein 1/ eukaryotic translation initiation factor 4E (4EBP1/eIF4E

120 f acute myeloid leukemia (AML) by regulating eukaryotic translation initiation factor 4E (eIF4E) acti

121 ERK activation stimulated phosphorylation of eukaryotic translation initiation factor 4E (eIF4E) and

122 s been found to be based on mutations in the eukaryotic translation initiation factor 4E (eIF4E) and

123 of translation engage mRNA that is bound by eukaryotic translation initiation factor 4E (eIF4E) at t

124 se interacting serine/threonine kinase (MNK)-eukaryotic translation initiation factor 4E (eIF4E) axis

125 The eukaryotic translation initiation factor 4E (eIF4E) bind

126 EITC caused an increase in expression of the eukaryotic translation initiation factor 4E (eIF4E) bind

127 Here, we show that eukaryotic translation initiation factor 4E (eIF4E) bind

128 hrough simultaneous activation of mTORC1 and eukaryotic translation initiation factor 4E (eIF4E) by N

129 Here, we show that mice in which eukaryotic translation initiation factor 4E (eIF4E) cann

130 Elevated eukaryotic translation initiation factor 4E (eIF4E) func

131 Naturally existing variation in the eukaryotic translation initiation factor 4E (eIF4E) homo

132 Here we show that a functional reduction of eukaryotic translation initiation factor 4E (eIF4E) in D

133 ow that genetically increasing the levels of eukaryotic translation initiation factor 4E (eIF4E) in m

134 Expression of eukaryotic translation initiation factor 4E (eIF4E) is c

135 The eukaryotic translation initiation factor 4E (eIF4E) is f

136 Eukaryotic translation initiation factor 4E (eIF4E) is o

137 Eukaryotic translation initiation factor 4E (eIF4E) is t

138 The initiation factor eukaryotic translation initiation factor 4E (eIF4E) play

139 Translation initiation factor eukaryotic translation initiation factor 4E (eIF4E) play

140 Eukaryotic translation initiation factor 4E (eIF4E) prom

141 clear retention of PCBP1, recruitment to the eukaryotic translation initiation factor 4E (eIF4E) prom

142 hibitor of kappaB alpha (IkappaB-alpha) S32, eukaryotic translation initiation factor 4E (eIF4E) S209

143 down-regulated by JNK2alpha2APF, among which eukaryotic translation initiation factor 4E (eIF4E) show

144 Importantly, either MYC or eukaryotic translation initiation factor 4E (eIF4E) was

145 tion-dissociation of the cap-binding protein eukaryotic translation initiation factor 4E (eIF4E) with

146 Structural complexes of the eukaryotic translation initiation factor 4E (eIF4E) with

147 Association of eukaryotic translation initiation factor 4E (eIF4E) with

148 Here, we focus on eukaryotic translation initiation factor 4E (eIF4E), a p

149 In oocytes, Maskin also binds eukaryotic translation initiation factor 4E (eIF4E), an

150 nclude ribosomal protein S6 kinase 1 (S6K1), eukaryotic translation initiation factor 4E (eIF4E), and

151 Phosphorylation and activation of eukaryotic translation initiation factor 4E (eIF4E), eIF

152 rs often overexpress the cap binding protein eukaryotic translation initiation factor 4E (eIF4E), lea

153 K signals to Mnk1 lead to phosphorylation of eukaryotic translation initiation factor 4E (eIF4E), whi

154 mRNA translation by promoting sumoylation of eukaryotic translation initiation factor 4E (eIF4E), whi

155 The rate-limiting factor for translation is eukaryotic translation initiation factor 4E (eIF4E), whi

156 The analogues were bound tightly to eukaryotic translation initiation factor 4E (eIF4E), wit

157 ing means to target a specific oncogene, the eukaryotic translation initiation factor 4E (eIF4E), wit

158 rgistically inhibited phosphorylation of the eukaryotic translation initiation factor 4E (eIF4E)-bind

159 bserved that Eap1p, which is a member of the eukaryotic translation initiation factor 4E (eIF4E)-bind

160 tioning in mice, we investigated the role of eukaryotic translation initiation factor 4E (eIF4E)-eIF4

161 K and AKT signaling are required to activate eukaryotic translation initiation factor 4E (eIF4E)-init

162 Notably, ON 01910.Na suppressed eukaryotic translation initiation factor 4E (eIF4E)-medi

163 A translation is dependent on mTORC1 and the eukaryotic translation initiation factor 4E (eIF4E).

164 erminal domain, which displays similarity to eukaryotic translation initiation factor 4E (eIF4E).

165 ition or blockade of its downstream effector eukaryotic translation initiation factor 4E activity equ

166 ransition machinery, decreases expression of eukaryotic translation initiation factor 4E and cyclin D

167 in HuR and the posttranscriptional regulator eukaryotic translation initiation factor 4E as two possi

168 ts demonstrate the importance of the p38-MNK-eukaryotic translation initiation factor 4E axis in TNF

169 apamycin (mTOR)-dependent phosphorylation of eukaryotic translation initiation factor 4E binding prot

170 ibosomal protein S6, S6 kinase 1 (S6K1), and eukaryotic translation initiation factor 4E binding prot

171 The translational repressor 4E-BP, the eukaryotic translation initiation factor 4E binding prot

172 t, mammalian target of Rapamycin (mTOR), and eukaryotic translation initiation factor 4E binding prot

173 Discovery of oocyte-specific eukaryotic translation initiation factor 4E distinguishe

174 reased sensitivity to dominant inhibition of eukaryotic translation initiation factor 4E function.

175 and also reduce the level of phosphorylated eukaryotic translation initiation factor 4E in the tumor

176 s HuR) regulates the alternative splicing of eukaryotic translation initiation factor 4E nuclear impo

177 A trend for an increase of eukaryotic translation initiation factor 4E phosphorylat

178 s of Akt, mammalian target of rapamycin, and eukaryotic translation initiation factor 4E phosphorylat

179 mport factor 1 (Eif4enif1), which encodes an eukaryotic translation initiation factor 4E transporter

180 ammalian target of rapamycin, phosphorylated eukaryotic translation initiation factor 4E, phosphoryla

181 p38 MAPK, MAPK-interacting kinase (MNK), and eukaryotic translation initiation factor 4E, which is a

182 hosphorylates and inactivates members of the eukaryotic translation initiation factor 4E-binding (eIF

183 rough an RNA-RNA interaction and an adjacent eukaryotic translation initiation factor 4E-binding 3'CI

184 kissing-loop T-shaped structure (kl-TSS) and eukaryotic translation initiation factor 4E-binding Pani

185 omplex 1, ribosomal protein S6 kinase 1, and eukaryotic translation initiation factor 4E-binding prot

186 ulation of the translation repressor, 4E-BP (eukaryotic translation initiation factor 4E-binding prot

187 tion of mammalian target of rapamycin (mTOR)/eukaryotic translation initiation factor 4E-binding prot

188 ncoding cell-cycle regulators via the mTORC1/eukaryotic translation initiation factor 4E-binding prot

189 pamycin (mTOR) signaling pathway to preserve eukaryotic translation initiation factor 4E-binding prot

190 ase (Chk) 1 serine 345 (S345), Chk 2 S33/35, eukaryotic translation initiation factor 4E-binding prot

191 anslation at a different level by inhibiting eukaryotic translation initiation factor 4E-binding prot

192 mitochondrial structure, and accumulation of eukaryotic translation initiation factor 4E-binding prot

193 Ser 79, tuberous sclerosis 2 at Thr 1462 and eukaryotic translation initiation factor 4E-binding prot

194 a constitutively active alternate substrate, eukaryotic translation initiation factor 4E-binding prot

195 tion of the 40S ribosomal protein S6 and the eukaryotic translation initiation factor 4E-binding prot

196 ammalian target of rapamycin (mTOR)-directed eukaryotic translation initiation factor 4E-binding prot

197 ribosomal protein S6 kinases (S6Ks) and the eukaryotic translation initiation factor 4E-binding prot

198 Using mice with deletion of eukaryotic translation initiation factor 4E-binding prot

199 ing studies revealed hyperphosphorylation of eukaryotic translation initiation factor 4E-binding prot

200 properties: first, it preferentially targets eukaryotic translation initiation factor 4E-binding prot

201 Eukaryotic translation initiation factor 4E-binding prot

202 ating p70S6K/ribosomal protein S6 (RPS6) and eukaryotic translation initiation factor 4E-binding prot

203 mTORC1 activation inhibits eukaryotic translation initiation factor 4E-binding prot

204 , or introduction of the Akt and mTOR target eukaryotic translation initiation factor 4E.

205 We show that the nematode eukaryotic translation initiation factor 4E/G (eIF4E/G)

206 in CD4 T cells through the activation of the eukaryotic translation initiation factor 4E/MAPK-interac

207 regulators, including p70-S6 kinase and the eukaryotic translation initiation factor, 4E binding pro

208 Eukaryotic translation initiation factor-4E (eIF4E) reco

209 Disrupting the eukaryotic translation initiation factor 4F (eIF4F) comp

210 mes, poxviruses must commandeer the critical eukaryotic translation initiation factor 4F (eIF4F) to r

211 Eukaryotic translation initiation factor 4F (eIF4F), com

212 n factor 4G (eIF4G), the scaffold subunit of eukaryotic translation initiation factor 4F (eIF4F), pre

213 tional control by constitutive activation of eukaryotic translation initiation factor 4F (eIF4F), the

214 ese events are required for formation of the eukaryotic translation initiation factor 4F complex (eIF

215 an Arg- and Ser-rich segment (RS1 domain) of eukaryotic translation initiation factor 4G (eIF4G) and

216 nslation initiation factors, including human eukaryotic translation initiation factor 4G (eIF4G) and

217 MNK binds eukaryotic translation initiation factor 4G (eIF4G) and

218 Eukaryotic translation initiation factor 4G (eIF4G) func

219 Eukaryotic translation initiation factor 4G (eIF4G) play

220 Remarkably, depleting eukaryotic translation initiation factor 4G (eIF4G), the

221 n translation initiation by interaction with eukaryotic translation initiation factor 4G (eIF4G), we

222 ed with both protein synthesis and levels of eukaryotic (translation) initiation factor 4G1 (eIF4G1).

223 Cleavage of eukaryotic translation initiation factor 4GI (eIF4GI) by

224 Eukaryotic translation initiation factor 4GI (eIF4GI) is

225 This is accompanied by the cleavage of the eukaryotic translation initiation factor 4GI (eIF4GI).

226 Eukaryotic translation initiation factor 4h (Eif4h) enco

227 Eukaryotic translation initiation factor 5A (eIF5A) is a

228 Eukaryotic translation initiation factor 5A (eIF5A), the

229 denosylmethionine decarboxylase 1 (AMD1) and eukaryotic translation initiation factor 5A (eIF5A), two

230 The ubiquitous eukaryotic translation initiation factor 5A (eIF5A), whi

231 e in the biosynthesis of hypusine containing eukaryotic translation initiation factor 5A (eIF5A), whi

232 silon-(4-amino-2-hydroxybutyl)lysine) in the eukaryotic translation initiation factor 5A (eIF5A).

233 thione and for deoxyhypusine modification of eukaryotic translation initiation factor 5A (eIF5A).

234 he only currently known hypusinated protein, eukaryotic translation initiation factor 5A.

235 Two of these proteins, are eukaryotic translation initiation factor 5A1 (eIF5A1) th

236 The translation initiation GTPase eukaryotic translation initiation factor 5B (eIF5B) bind

237 of this Gly in the Switch II element of the eukaryotic translation initiation factor 5B (eIF5B) from

238 Our data reveal a transient increase of eukaryotic translation initiation factor 5B (eIF5B), the

239 bunit joining is controlled by the G-protein eukaryotic translation initiation factor 5B (eIF5B).

240 Mutations that impair GTP hydrolysis by eukaryotic translation initiation factor 5B/initiation f

241 RKR-like endoplasmic reticulum kinase (PERK)-eukaryotic translation initiation factor alpha (eIF2alph

242 on mutant induced protein kinase R (PKR) and eukaryotic translation initiation factor alpha (eIF2alph

243 i, global translation was fully restored and eukaryotic translation initiation factor alpha was depho

244 culum stress pathway proteins phosphorylated eukaryotic translation initiation factor alpha, phosphor

245 ) and its downstream targets, phosphorylated eukaryotic translation initiation factor and p70 S6 kina

246 tein kinase R (PKR) and the alpha subunit of eukaryotic translation initiation factor are not phospho

247 Eukaryotic translation initiation factor (eIF) 1 is a ce

248 In protein synthesis initiation, the eukaryotic translation initiation factor (eIF) 2 (a G pr

249 SG formation is triggered by both eukaryotic translation initiation factor (eIF) 2alpha ph

250 numerous functions of individual subunits of eukaryotic translation initiation factor (eIF) 3, little

251 The eukaryotic translation initiation factor (eIF) 4B promot

252 The eukaryotic translation initiation factor (eIF) 4B promot

253 H(2)O(2) also induced phosphorylation of eukaryotic translation initiation factor (eIF) 4E and eI

254 the 40S ribosomal protein S6 (rpS6) and the eukaryotic translation initiation factor (eIF) 4E-bindin

255 The wheat germ eukaryotic translation initiation factor (eIF) 4F binds

256 These pathways convergently signal to the eukaryotic translation initiation factor (eIF) 4F comple

257 The eukaryotic translation initiation factor (eIF) 4G is a s

258 The eukaryotic translation initiation factor (eIF) 4G is req

259 Eukaryotic translation initiation factor (eIF) 5 is cruc

260 s, one factor remained putative for decades: eukaryotic translation initiation factor (eIF) 5A.

261 The integrity of eukaryotic translation initiation factor (eIF) interacti

262 site (IRES) with 40S ribosomal subunits and eukaryotic translation initiation factor (eIF)3 enable 4

263 argets both cap-binding complex (Cbc)1p- and eukaryotic translation initiation factor (eIF)4E-bound m

264 The GTP-binding eukaryotic translation initiation factor eIF2 delivers i

265 GCN2 phosphorylates the alpha subunit of the eukaryotic translation initiation factor eIF2, leading t

266 ough phosphorylation of the alpha-subunit of eukaryotic translation initiation factor, eIF2.

267 -stimulated gene product, phosphorylates the eukaryotic translation initiation factor eIF2alpha and c

268 n interferon-induced kinase that targets the eukaryotic translation initiation factor eIF2alpha.

269 -PP1 phosphatase activity, dephosphorylating eukaryotic translation initiation factor (eIF2alpha), an

270 ic labeling, we show that the mRNAs encoding eukaryotic translation initiation factors eIF2B2 and eIF

271 by regulating the local protein synthesis of eukaryotic translation initiation factors eIF2B2 and eIF

272 the EJC, interacts directly with the pivotal eukaryotic translation initiation factor eIF3.

273 However, a comparison of the growth of eukaryotic translation initiation factor eIF4A and pixie

274 ic PAS usage regulates the expression of the eukaryotic translation initiation factor EIF4A1, the tum

275 Eukaryotic translation initiation factor eIF4AI, the fou

276 translation through the phosphorylation of a eukaryotic translation initiation factor, eIF4B.

277 The eukaryotic translation initiation factor eIF4E is deregu

278 The eukaryotic translation initiation factor eIF4E recognize

279 The interaction of the eukaryotic translation initiation factor eIF4E with the

280 Eukaryotic translation initiation factor eIF4E, an essen

281 We show that the eukaryotic translation initiation factor eIF4E, an oncop

282 nteraction between the cap structure and the eukaryotic translation initiation factor eIF4E.

283 The eukaryotic translation-initiation factor eIF4E is a rate

284 o improve outcomes and include targeting the eukaryotic translation initiation factor (eIF4E) with it

285 quire resistance to asTORi by downregulating eukaryotic translation initiation factor (eIF4E)-binding

286 n of fluorophosphate mRNA cap analogues with eukaryotic translation initiation factor (eIF4E).

287 ce gene, sbm1, in pea we have identified the eukaryotic translation initiation factor, eIF4E, as a su

288 found to be based on mutations in the plant eukaryotic translation initiation factors, eIF4E and eIF

289 in was associated with the 4F subunit of the eukaryotic translation initiation factor (eIF4F) complex

290 Ofs is homologous to eukaryotic translation initiation factor eIF4G.

291 ovel approach to investigate the role of the eukaryotic translation initiation factor eIF5A in human

292 Eukaryotic translation initiation factor eIF5A promotes

293 droxylase (DOHH) catalyzes the activation of eukaryotic translation initiation factor (eIF5A), a prot

294 Eukaryotic translation initiation factor eIF5B is a ribo

295 Eukaryotic translation initiation factor eIF5B is a ribo

296 en VPg of turnip mosaic virus and wheat germ eukaryotic translation initiation factors eIFiso4E and e

297 aliana knockout lines for the plant-specific eukaryotic translation initiation factors eIFiso4G1 (i4g

298 The process is mediated by eukaryotic translation initiation factors (eIFs) in conj

299 now present a novel study of rate control by eukaryotic translation initiation factors (eIFs) using y

300 unctions as an essential subunit of the eIF3 eukaryotic translation initiation factor in animals, yea