ライフサイエンスコーパス: mRNA translation

1 ion of the EIF3F gene, while promoting eIF3f mRNA translation.

2 ency with PRC2 overexpression via control of mRNA translation.

3 family of oncogenes are master regulators of mRNA translation.

4 tes, nor whether it can selectively regulate mRNA translation.

5 that internal m(7)G methylation could affect mRNA translation.

6 NA in the cytoplasm and negatively regulates mRNA translation.

7 e effects of prolonged IFNgamma treatment on mRNA translation.

8 tein PABPC1 for activation of Musashi target mRNA translation.

9 ding RNAs, a number of which are involved in mRNA translation.

10 led changes in poly(A) tail length influence mRNA translation.

11 HFV nucleocapsid protein (CCHFV-NP) augments mRNA translation.

12 ntial for maturation of functional tRNAs and mRNA translation.

13 s and relieves its inhibitory activity on RP mRNA translation.

14 y stage, ranging from chromatin packaging to mRNA translation.

15 ally involved in ribosomal RNA synthesis and mRNA translation.

16 inding that RNA hydroxymethylation can favor mRNA translation.

17 through reprogramming gene transcription and mRNA translation.

18 y induces an anti-viral response by limiting mRNA translation.

19 p53 activation and a resultant inhibition of mRNA translation.

20 2 from a repressor to an activator of target mRNA translation.

21 l protein O-GlcNAcylation and increased Cd40 mRNA translation.

22 hosphorylation of eIF2alpha, an inhibitor of mRNA translation.

23 vation of ERK and mTOR signaling upstream of mRNA translation.

24 a transient adaptive reprogramming of global mRNA translation.

25 P2), rendering it unable to repress ferritin mRNA translation.

26 ss116 with Pet309 but also do not allow COX1 mRNA translation.

27 nts (ribosome profiling) maps and quantifies mRNA translation.

28 rated by alternative splicing promote axonal mRNA translation.

29 nuanced ligand response observed during bulk mRNA translation.

30 ress responses and an important regulator of mRNA translation.

31 rough the modulation of apolipoproteinB/Apob mRNA translation.

32 ledge gap is the role of nuclear proteins in mRNA translation.

33 found that RNA hydroxymethylation can favor mRNA translation.

34 ancreatic cancer proliferation by regulating mRNA translation.

35 cellular processes, including cap-dependent mRNA translation.

36 or suppressor of 5'-terminal oligopyrimidine mRNA translation.

37 all, noncoding RNA that negatively regulates mRNA translation.

38 s with hnRNP-Q1 as a means to inhibit Gap-43 mRNA translation.

39 tely elevating Ccnd1 transcription and Ccnd1 mRNA translation.

40 n, Torin1, and amino acid deprivation on TOP mRNA translation.

41 messenger RNA (mRNA) degradation and repress mRNA translation.

42 tory events such as alternative splicing and mRNA translation.

43 several aspects of RNA regulation, including mRNA translation.

44 synthesis, including ribosome biogenesis and mRNA translation.

45 nscription initiation, mRNA degradation, and mRNA translation.

46 recent advances in mathematical modelling of mRNA translation.

47 positively or negatively with cognate sense mRNA translation.

48 h from a repressor to an activator of target mRNA translation.

49 ry few cases involve the regulation of sense mRNA translation.

50 iptional output with selective modulation of mRNA translation.

51 tions of tRNA fragments in the regulation of mRNA translation, a critical component of cellular stres

52 rting the role of ABCF1 in m(6)A-facilitated mRNA translation, ABCF1-sensitive transcripts largely ov

53 retardation protein (FMRP) causes increased mRNA translation and aberrant synaptic development.

54 n-17a-dependent manner, which reduced global mRNA translation and altered nascent proteome synthesis.

55 ly, two functional start codons initiate fis mRNA translation and both are repressed by RgsA.

56 of p21 in Ola1(-/-) MEFs is due to enhanced mRNA translation and can be prevented by either reconsti

57 the consequent degradation of tryptophan in mRNA translation and cancer progression.

58 T and mTOR pathways, which in turn regulates mRNA translation and collagen expression.

59 strategy used by viruses to repress cellular mRNA translation and concomitantly allow the efficient t

60 characterized by persistently elevated uORF mRNA translation and concurrent gene expression reprogra

61 demonstrated that hnRNP-Q1 represses Gap-43 mRNA translation and consequently GAP-43 function.

62 mRNA translation and decay appear often intimately linke

63 he mRNA 5'-cap are useful tools for studying mRNA translation and degradation, with emerging potentia

64 ic WNT3 further regulates the specificity of mRNA translation and development of neurons and oligoden

65 ase activity links development with maternal mRNA translation and ensures irreversibility of the oocy

66 g protein 1 (JAKMIP1) in regulating neuronal mRNA translation and establish JAKMIP1 knockout mice as

67 t mice did not exhibit enhanced retinal Cd40 mRNA translation and failed to up-regulate expression of

68 NA repair, apoptosis, metabolism, autophagy, mRNA translation and feedback mechanisms.

69 des an important resource for studying local mRNA translation and has the potential to reveal both co

70 play an important role in the regulation of mRNA translation and have therapeutic potential in cance

71 which cells sense and restore dysfunctional mRNA translation and how this is linked to cell prolifer

72 Neurons lacking FMRP show aberrant mRNA translation and intracellular signalling.

73 of PPR proteins and the mechanisms governing mRNA translation and intron splicing in plant mitochondr

74 negatively regulates the elongation stage of mRNA translation and is activated under different stress

75 mRNA translation and its regulation shape the human prot

76 mRNA fate, in terms of P-body localization, mRNA translation and mRNA stability: P-bodies contain mo

77 G4DNA in the cytoplasm are known to modulate mRNA translation and participate in stress granule forma

78 (mTORC1) has an essential role in dendritic mRNA translation and participates in mechanisms underlyi

79 displayed antiviral activity: inhibitors of mRNA translation and predicted regulators of the sigma-1

80 cially proteins involved in DNA replication, mRNA translation and proteasome function.

81 caused alterations in proteins required for mRNA translation and protein secretion, reduced producti

82 athways which lead to adaptive regulation of mRNA translation and protein synthesis.

83 of cis-NATs known to regulate cognate sense mRNA translation and provide a foundation for future stu

84 , which invert the programmed local speed of mRNA translation and provide direct evidence for the cen

85 They regulate gene expression by suppressing mRNA translation and reducing mRNA stability.

86 these uS12 variants impaired the accuracy of mRNA translation and rendered cells highly sensitive to

87 transcriptional program leading to enhanced mRNA translation and resulting in an increased PD-1 amou

88 iting that is enriched for genes involved in mRNA translation and ribosome function.

89 nit alpha (eIF2alpha), causing inhibition of mRNA translation and shutdown of viral protein productio

90 ve molecular switch for turning off or on RP mRNA translation and subsequent ribosome biogenesis.

91 isoforms through APA in coding sequence and mRNA translation and that the p63-PABPN1 loop modulates

92 ote carcinogenesis by effects on both global mRNA translation and upregulated expression of specific

93 tomic modifications, can positively regulate mRNA translation and/or stability, and both DNA and RNA

94 nger RNAs (mRNAs), leading to alterations of mRNA translation and/or stability.

95 3 (eIF3) acts as a distinct repressor of FTL mRNA translation, and eIF3-mediated FTL repression is di

96 the stage for discussion on mTOR signaling, mRNA translation, and metabolic adaptation in T cells.

97 d by the balance between gene transcription, mRNA translation, and protein degradation, among other f

98 ibution by the timing of gene transcription, mRNA translation, and protein transport.

99 recognized role of Pdcd4 in controlling BDNF mRNA translation, and provided a new method that boostin

100 atypical brain amino acid profile, abnormal mRNA translation, and severe neurological abnormalities.

101 NP L, synergizes with miR-297, reduces VEGFA mRNA translation, and triggers apoptosis, thereby suppre

102 rimentally defined, we systematically probed mRNA, translation, and protein signatures that were eith

103 T The elongation and/or termination steps of mRNA translation are emerging as important control point

104 global protein synthesis and increased uORF mRNA translation are followed by normalization of protei

105 n transcriptional factors, genes involved in mRNA translation are highly represented in our interacto

106 Autophagy and cap-dependent mRNA translation are tightly regulated by the mechanisti

107 protein 1) and enhanced cap-independent Cd40 mRNA translation as assessed by a bicistronic reporter t

108 omains of DNA-based life, where they mediate mRNA translation as part of polyribosomes in animals.

109 l cues by regulating ribosome biogenesis and mRNA translation at multiple levels to sustain prolifera

110 in 2 (CYFIP2) has been suggested to regulate mRNA translation at synapses and this may include local

111 MRP), an mRNA binding protein that regulates mRNA translation at synapses.

112 rites that provide a local energy supply for mRNA translation at synapses.

113 The net result is an increase in mRNA translation at the single-cell level.

114 Toolkit will greatly facilitate the study of mRNA translation based on ribosome profiling.

115 essing) inhibitory neurons increased general mRNA translation, bolstered synaptic plasticity and enha

116 striking upregulation of pathways linked to mRNA translation both in CLL cells derived from lymph no

117 epleting PCIF1 does not substantially affect mRNA translation but is associated with reduced stabilit

118 Evidence also exists for clock control of mRNA translation, but the extent and mechanisms for this

119 (N) with this conserved sequence facilitates mRNA translation by a unique N-mediated translation stra

120 For example, localized mRNA translation by chloroplastic ribosomes occurs in th

121 tion of the protein, but rather to decreased mRNA translation by nonsense-mediated decay regulation o

122 termines the reading frame of messenger RNA (mRNA) translation by the ribosome.

123 Post-transcriptional regulation of COX-2 mRNAs translation by SGs indicates a role in IL-1beta-me

124 n-independent and that mechanisms regulating mRNA translation, cell cycle progression, and gene expre

125 out eukaryotic evolution and plays a role in mRNA translation, cellular proliferation, cellular diffe

126 analysis reveals a global switch in maternal mRNA translation coinciding with oocyte re-entry into th

127 ediating mGluR-LTD through the regulation of mRNA translation complexes stalled at the level of elong

128 scent peptide-mediated anchoring of ribosome-mRNA translation complexes to the inclusions is suggeste

129 Thus, eIF2alpha-dependent mRNA translation controls memory consolidation via auton

130 mRNA translation decodes nucleotide into amino acid sequ

131 sed Ccnb1 and Moloney sarcoma oncogene (Mos) mRNA translation, delayed spindle assembly and increased

132 c molecular pathway lies alongside the known mRNA translation-dependent processes necessary for long-

133 Inhibition of axonal beta-actin mRNA translation disrupts arbor dynamics primarily by re

134 Excessive mRNA translation downstream of group I metabotropic glut

135 Exacerbated mRNA translation during brain development has been linke

136 ere we performed genome-wide measurements of mRNA translation during histidine starvation in fission

137 tress granule formation is known to regulate mRNA translation during oxidative stress.

138 is regulated at the level of messenger RNA (mRNA) translation during human hematopoietic development

139 HA-tagged histones in U2OS cells and single mRNA translation dynamics in both U2OS cells and neurons

140 Here, we profiled global mRNA translation dynamics in the mouse primary macrophag

141 ulate protein expression levels by affecting mRNA translation efficiency, but the underlying mechanis

142 sh a mechanism for how codon usage regulates mRNA translation efficiency.

143 usage plays an important role in regulating mRNA translation efficiency. We found that the rare codo

144 he retina of diabetic mice, the repressor of mRNA translation, eIF4E-binding protein 1 (4E-BP1), is O

145 n system to directly compare the velocity of mRNA translation elongation.

146 to catalyze the hypusine modification of the mRNA translation factor eIF5A and promotes oncogenesis t

147 showed AD-associated hyperphosphorylation of mRNA translation factor eukaryotic elongation factor 2 (

148 ighlight the potential power of manipulating mRNA translation for crop improvement.

149 nscription factors, regulators of chromatin, mRNA translation, GTPases, vesicle trafficking, and the

150 convallatoxin as a novel antiviral, limiting mRNA translation has a dramatic impact on CMV infection

151 The finding that Rbfox proteins regulate mRNA translation has implications for Rbfox-related dise

152 itochondrial outer membrane (MOM)-associated mRNA translation, how this process is sensitive to mitoc

153 by anchor the complex for multiple rounds of mRNA translation.IMPORTANCE Poxvirus genome replication,

154 effector that has been shown to repress TOP mRNA translation in a few specific cases.

155 thways that regulate protein homeostasis and mRNA translation in a manner that was both rapamycin-sen

156 ome heterogeneity playing a role in specific mRNA translation in a multicellular eukaryote.

157 his rapid growth generates a high demand for mRNA translation in a timing-dependent manner, but its u

158 TLR4 activation blocks mRNA translation in all tested cell types, without reduc

159 cell type (neutrophils) directly regulating mRNA translation in another (macrophages).

160 earch for cis-NATs influencing cognate sense mRNA translation in Arabidopsis (Arabidopsis thaliana).

161 oping brain and further confirms the role of mRNA translation in autism pathogenesis.

162 vale algae species and is essential for atpI mRNA translation in Chlamydomonas.

163 genesis, but the mechanisms that modulate RP-mRNA translation in coordination with other cellular pro

164 ation of endoplasmic reticulum (ER)-targeted mRNA translation in DIS3L2-deficient cells.

165 Local mRNA translation in growing axons allows for rapid and p

166 gnaling and the spatiotemporal regulation of mRNA translation in highly complex developing systems.

167 intricate regulation of compartment-specific mRNA translation in mammalian CNS axons supports the for

168 Here we demonstrate that the timing of Ccnb1 mRNA translation in mouse oocytes is dependent on the pr

169 uced O-GlcNAcylation of 4E-BP1 promotes Cd40 mRNA translation in Muller glia.

170 iRNAs) are important regulators of localized mRNA translation in neuronal dendrites.

171 Anti-IgM also increased mRNA translation in normal blood B cells, but without cl

172 n impaired cap-dependent and cap-independent mRNA translation in pancreatic cancer cells.

173 Anti-IgM significantly increased mRNA translation in primary CLL cells, measured using bu

174 q approach to explore the timing of maternal mRNA translation in quiescent oocytes as well as in oocy

175 female mice to comprehensively characterize mRNA translation in Scn10a-positive nociceptors in chemo

176 to comprehensively characterize and compare mRNA translation in Scn10a-positive nociceptors in the T

177 lpha) controls transcriptome-wide changes in mRNA translation in stressed cells.

178 ntal role of mRNA localization and dendritic mRNA translation in synaptic maintenance and plasticity

179 its secretion is dependent on activation of mRNA translation in synchrony with the cell cycle and th

180 own as a mechanism for controlling mammalian mRNA translation in the cytoplasm, but what would be the

181 n of 4E-BP1/2 prevented the increase in Cd40 mRNA translation in TMG-exposed cells, and expression of

182 embly and ribosome profiling to study global mRNA translation in tomato (Solanum lycopersicum) roots.

183 ow that GADD34 drives substantial changes in mRNA translation in unstressed cells, particularly targe

184 Overexpression of W73V suppressed reporter mRNA translation in vitro and in vivo and reduced the le

185 on is functionally coupled to messenger RNA (mRNA) translation in bacteria, but how this is achieved

186 ), ribonucleoprotein complexes that regulate mRNA translation, in the delayed translation of COX-2 mR

187 ed when myoblasts were also treated with the mRNA translation inhibitor cycloheximide.

188 Dynamic regulation of mRNA translation initiation and elongation is essential

189 nally, Mss116 is required for efficient COX1 mRNA translation initiation and elongation.

190 plex 1 (mTORC1) that represses cap-dependent mRNA translation initiation by sequestering the translat

191 educed activity of mTORC1 and its downstream mRNA translation initiation factors eIF4B and 4EBP1, as

192 nternal ribosome entry site (IRES)-dependent mRNA translation initiation pathway results in continued

193 ive ribosome profiling to gain insights into mRNA translation initiation, highlighting distinctions b

194 e protein synthesis is largely controlled by mRNA translation initiation, whether cellular translatio

195 behavioral alterations caused by exacerbated mRNA translation initiation.

196 tends to autism models involving exacerbated mRNA translation initiation.

197 DEAD/DEAH box RNA helicase, DHX33, promotes mRNA translation initiation.

198 Among the three phases of mRNA translation-initiation, elongation, and termination

199 hat MYC alters the efficiency and quality of mRNA translation into functional proteins.

200 us, DMD is required to safeguard ER-targeted mRNA translation, intracellular calcium homeostasis, and

201 mRNA translation is a key step in decoding genetic infor

202 Regulation of mRNA translation is a major control point for gene expre

203 ation, but it remains unclear whether Gap-43 mRNA translation is also regulated.

204 Deregulated global mRNA translation is an emerging feature of cancer cells.

205 ore transcriptional competency when maternal mRNA translation is blocked, whereas inhibition of histo

206 Our data suggest that efficient mRNA translation is determined by a triplet-of-triplet g

207 Taken together, dysregulation of mRNA translation is emerging as a unifying mechanism und

208 out neurons, type 1 adenylyl cyclase (Adcy1) mRNA translation is enhanced, leading to excessive produ

209 onto COX1 mRNA can occur, activation of COX1 mRNA translation is impaired.

210 mRNA translation is likely to be an important mediator o

211 y initiation is repressed, and cap-dependent mRNA translation is maintained during mitosis despite mT

212 The regulation of mRNA translation is of fundamental importance in biologi

213 PDCD4 mRNA translation is regulated by an interplay between th

214 Cap-dependent mRNA translation is regulated by two disordered proteins

215 During neuronal development, local mRNA translation is required for axon guidance and synap

216 Cytosolic mRNA translation is subject to global and mRNA-specific

217 Furthermore, we show that BCL11A mRNA translation is suppressed by LIN28B through direct

218 r viral infection), canonical, cap-dependent mRNA translation is suppressed in human cells.

219 Although messenger RNA (mRNA) translation is a fundamental biological process, i

220 make it a powerful new tool for quantifying mRNA translation kinetics.

221 tionships between immunity, endocytosis, and mRNA translation lead to hypothesize that toll-like rece

222 possesses RNA topoisomerase activity, binds mRNA translation machinery and interacts with an RNA-bin

223 , which suggests that mechanisms controlling mRNA translation may be exploitable for therapy.

224 Local mRNA translation mediates the adaptive responses of axon

225 nifested as alterations in the efficiency of mRNA translation modulating protein levels in the absenc

226 Quantitative and qualitative changes in mRNA translation occur in tumor cells and support cancer

227 Local mRNA translation occurs in growing axons enabling precis

228 Specifically, regulation of mRNA translation occurs pervasively during stress to act

229 cally, phosphorylation of eIF2alpha promotes mRNA translation of Atf4.

230 a focused RNAi approach that Nup155 controls mRNA translation of p21 (CDKN1A), a key mediator of the

231 Herein, we show that Aven stimulates the mRNA translation of the mixed lineage leukemia (MLL) pro

232 factor 4F complex (eIF4F) and initiation of mRNA translation of type II interferon-stimulated genes.

233 eaking down the targeted transcript, inhibit mRNA translation or alter the maturation of the pre-mRNA

234 -I editing are varied and include effects on mRNA translation, pre-mRNA splicing, and micro-RNA silen

235 not change global translation or individual mRNA translation profiles as measured by single-cell nas

236 reporter assay, we investigated how rates of mRNA translation, protein synthesis and degradation cont

237 efore hnRNP-Q1-mediated repression of Gap-43 mRNA translation provides an additional mechanism for re

238 well-documented attenuation of cap-dependent mRNA translation, rapamycin can augment NMD of certain t

239 Here we measured the host mRNA translation rate during a vaccinia virus-induced ho

240 normalizes stimulus-induced and constitutive mRNA translation rate, decreases lactate and key glycoly

241 urse analysis to measure the mRNA-abundance, mRNA-translation rate and protein expression during the

242 Given previous findings of high Ccnb2 mRNA translation rates in prophase-arrested oocytes, we

243 In-silico mRNA translation rates were compared for each mRNA in bo

244 We found that the mRNAs' translation rates were repressed, by up to 530-fo

245 ryo transition involves extensive changes in mRNA translation, regulated in Drosophila by the PNG kin

246 Emerging evidence demonstrates that mRNA translation regulation pathways are key factors in

247 ished roles as an inhibitor of cap-dependent mRNA translation, relatively little is known about its e

248 t is therefore important that the process of mRNA translation remains in excellent synchrony with cel

249 The diversity of MTOR-regulated mRNA translation remains unresolved.

250 mRNA translation represents the last step of genetic flo

251 Genome-wide analysis of mRNA translation revealed a great diversity in ES6S-medi

252 bations in cellular pathways associated with mRNA translation, ribosome biogenesis and stress signali

253 binding to the CARE and stimulation of VEGFA mRNA translation, simultaneously permitting miR-297-medi

254 ects post-transcriptional gene regulation in mRNA translation, stability, and localization, and exhib

255 We here show that mRNA translation stress in cis triggered by the gly-ala

256 These data illustrate an mRNA translation stress-response pathway for E2F1 activa

257 F277 recognizes nascent uS5 in the course of mRNA translation, suggesting cotranslational assembly of

258 bitors undergoes a reversible remodelling of mRNA translation that evolves in parallel with drug sens

259 hat N(6)-methyladenosine (m(6)A) facilitates mRNA translation that is resistant to eIF4F inactivation

260 Regulation of mRNA translation, the process by which ribosomes decode

261 the scope and mechanism of eIF4F-independent mRNA translation, these findings reshape our current per

262 Besides enforcing viral mRNA translation, these processes profoundly impact host

263 te no evidence of a reduction in the rate of mRNA translation, these uS12 variants impaired the accur

264 Mechanistically, METTL3 enhances mRNA translation through an interaction with the transla

265 processes is the repression of initiation of mRNA translation through GCN2 phosphorylation of eIF2alp

266 Inhibiting activity-dependent mRNA translation through mechanistic target of rapamycin

267 In most cases, RISC inhibits mRNA translation through the 3'-untranslated region (UTR

268 forming CTORC2, and controls messenger RNA (mRNA) translation through phosphorylation of LARP1 and r

269 city switches from injury-associated protein mRNA translation to CK2alpha translation with endoplasmi

270 for DHPS in beta cells to link polyamines to mRNA translation to effect facultative cellular prolifer

271 the neuronal soma and make use of localized mRNA translation to rapidly respond to different extrace

272 ereas zinc-finger disruption decreases viral mRNA translation, tubule formation and virus replication

273 tiation, providing a mechanism for selective mRNA translation under heat shock stress.

274 sms of beta-cell dysfunction at the level of mRNA translation under such conditions.

275 e ribosome and leads to global inhibition of mRNA translation upon infection.

276 Models of mRNA translation usually presume that transcripts are li

277 ate that Rictor is regulated at the level of mRNA translation via heat-shock transcription factor 1 (

278 icularly through cap-dependent initiation of mRNA translation via the phosphorylation and inactivatio

279 We demonstrate that GLD-1 represses ced-3 mRNA translation via two binding sites in its 3' untrans

280 Anti-IgM-induced mRNA translation was associated with increased expressio

281 oplasts, the impact of cis-NAT expression on mRNA translation was confirmed for 4 out of 5 tested cis

282 tection of MTOR-dependent changes in non-TOP mRNA translation was obscured by low sensitivity and met

283 Surprisingly, we found that p53 mRNA translation was suppressed by FDXR deficiency via I

284 tress granule protein G3BP1, known to arrest mRNA translation, was identified as a regulator of RIG-I

285 s the effects of phosphorylated eIF2alpha on mRNA translation, was sufficient to reverse the social d

286 Similar effects on O-GlcNAcylation and Cd40 mRNA translation were also observed in the retina of a m

287 During cell culture, changes in recombinant mRNA translation were consistent with changes in transcr

288 Inhibition of SGs clearance blocked COX-2 mRNA translation whereas blocking the assembly of SGs by

289 ciate with polyribosomes, which are units of mRNA translation, whereas the Top3 homologs from E. coli

290 hat the NS1 non-tubular form upregulates BTV mRNA translation, whereas zinc-finger disruption decreas

291 ulated by distinct oncogenes at the level of mRNA translation, which can be exploited for new immunot

292 ng as a negative regulator of p21(Waf1/Cip1) mRNA translation, which promotes exit of the Bmi1-Cre(ER

293 f BCR stimulation to increase messenger RNA (mRNA) translation, which can promote carcinogenesis by e

294 HAdVs) shut down host cellular cap-dependent mRNA translation while initiating the translation of vir

295 bited both cap-dependent and cap-independent mRNA translation while maintaining mRNA polysomal associ

296 led clear trends toward global reductions in mRNA translation with a significant reduction in the pol

297 Therefore, LNP uptake, endosomal escape, and mRNA translation with and without TLR4 activation are qu

298 lts in PI3Kdelta-dependent induction of E2F1 mRNA translation with the consequent activation of c-Myc

299 d rates of cell population growth and global mRNA translation, with peak rates occurring at normal ph

300 that FASTKD3 is required for efficient COX1 mRNA translation without altering mRNA levels, which res