ライフサイエンスコーパス: mRNA

1 mRNA accumulation in stress granules correlates with lon

2 mRNA and miRNA expression profile frequently performed t

3 mRNA profiling by microarray analysis revealed that the

4 Claudin-18.1 mRNA levels were measured in airway epithelial brushings

5 Programmed cell death-1 mRNA expression was increased in tissue homogenates from

6 Using an ex vivo assay for HIV-1 mRNA, we demonstrated that despite this immunomodulatory

7 risk cytogenetics (p = 0.002), higher IDO-1 mRNA (p = 0.005), higher composite IDO-1 score (p < 0.00

8 guidance protein, either by targeting slit-1 mRNA or, potentially, by modulating the canonical Notch

9 itro studies confirmed an increase in IL-17C mRNA and protein levels in cells infected with cagA-posi

10 osting the ability of LPS to induce IL-1beta mRNA and pro-IL-1beta while inhibiting the production of

11 In the process of identifying 248 mRNAs and 15 microRNAs as differentially expressed, we a

12 reased collagen deposition, collagen 1 and 3 mRNA expression, TGF-beta production, and activation of

13 necrosis factor receptor-associated factor 6 mRNAs, whereas concentrations of the T-cell co-activator

14 was a late marker of cell-cycle entry; Ki-67 mRNA oscillated with highest levels in G2 while protein

15 al clinical and biological function of IL-6R mRNA expression in ovarian cancer.

16 ative cleavage and polyadenylation of NaV1.8 mRNA.

17 nto the N-terminal coding region and, when a mRNA structure overlaps or partially overlaps with the r

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

19 ibe for the first time the presence of ACSL6 mRNA in human skeletal muscle and the role that ACSL6 pl

20 ACTB mRNA expression levels in lymphoblastic lines and fibrob

21 We show that PHA-4 directly activates mRNA expression of a broad cohort of epithelial genes, i

22 components functionally interact, affecting mRNA export and splicing as well as plant development.

23 s(2) modification in yeast tRNA(Lys) affects mRNA decoding and tRNA-mRNA translocation.

24 We find that transcription of nearly all mRNAs is strongly dependent on TFIID function.

25 A accelerated the rate of recruitment of all mRNAs tested, regardless of their degree of structural c

26 In trypanosomes, all mRNAs, and non-coding RNAs such as small nucleolar RNAs

27 otein renders it constitutively active as an mRNA-destabilizing factor.

28 e intriguing notion that transcription of an mRNA, despite carrying a canonical coding sequence, can

29 erformed genome-wide sequencing and analyzed mRNA and miRNA expression, DNA copy number, and DNA meth

30 pendent reporter gene (SRE-LUC) activity and mRNA expression of pro-proliferative and pro-migratory M

31 ires identifying the protein composition and mRNA cargos of the ribonucleoprotein particles (RNPs) th

32 re-assembly, transcriptional elongation, and mRNA processing.

33 red from plasma, and both DNA genotyping and mRNA expression levels in peripheral blood mononuclear c

34 ing cytoplasmic transit, nuclear import, and mRNA synthesis.IMPORTANCE The fates of HIV-1 reverse tra

35 Protein and mRNA expression analyses revealed that kidney proximal t

36 served that SIRT1 repressed LEF1 protein and mRNA expression, ultimately reducing LEF1 transcriptiona

37 tions of these enhanced sgRNAs (e-sgRNA) and mRNA encoding Cas9, we show that a single intravenous in

38 PARylation, nucleocytoplasmic shuttling and mRNA binding.

39 iated mRNAs results in ribosome stalling and mRNA degradation.

40 Conserved among animal mRNAs, IRE-RNA structures are noncoding and bind Fe(2+)

41 in the mature cyst, potentially preserved as mRNA in preparation for excystation.

42 ion of DNA for shorter nucleic acids such as mRNA or siRNA.

43 includes a shift from a protein-coding ASCC3 mRNA to a shorter ALE isoform of which the RNA, rather t

44 that Ire1-mediated cleavage of ER-associated mRNAs results in ribosome stalling and mRNA degradation.

45 in GC cells significantly decreased ATP6V1A mRNA and protein expression, while YY1 overexpression in

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

47 The apolipoprotein B mRNA editing enzyme catalytic polypeptide-like APOBEC3A

48 Apolipoprotein B mRNA-editing catalytic polypeptide (APOBEC) 3 proteins h

49 gether, we demonstrate that apolipoprotein B mRNA-editing catalytic polypeptide 3 expression and edit

50 study, we demonstrated that apolipoprotein B mRNA-editing catalytic polypeptide 3A (A3A) and A3G expr

51 show here that a single marker, Neuromedin B mRNA (Nmb), identifies RTN neurons in rodents.

52 Endurance training increased the basal mRNA level of hexokinase-2, hormone sensitive lipase, gl

53 Identification of genes whose basal mRNA expression predicts the sensitivity of tumor cells

54 BDNF mRNA levels, assessed by quantitative PCR and in situ hy

55 tion factors, and overexpression of IFN-beta mRNA and protein were similar in MSK1/2 and DUSP1 knocko

56 which we show is able to target the IFN-beta mRNA.

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

58 ped and validated a multivariate whole-blood mRNA-based predictor of melatonin phase which requires f

59 axonal compartments of the neuron, for both mRNA and microRNA (miRNA).

60 We benchmark Structure-seq2 on both mRNA and rRNA structure in rice (Oryza sativa).

61 Export of both mRNAs is dependent on the cellular NXF1/TAP pathway, but

62 kinase ERK2 over what would be predicted by mRNA levels.

63 pig embryos via zygotic co-delivery of Cas9 mRNA and dual sgRNAs targeting the PDX1 gene, which when

64 F-alpha, IFN-gamma, IL-1beta, IL-6, and CCL2 mRNAs), and attenuated the wasting syndrome and severity

65 allele (AA) showed significantly lower CD28 mRNA expression ex-vivo than either GG or AG (p < 0.001)

66 this splicing factor alters splicing of cell mRNAs involved in the maturation of many other cell mRNA

67 nvolved in the maturation of many other cell mRNAs.

68 eals that under favourable growth conditions mRNAs coding for proteins involved in the translation ma

69 ntry channel of the 40S subunit and contacts mRNA via conserved residues whose functional importance

70 represses translation of aptamer-containing mRNAs.

71 7 predicted "noncoding RNAs" to conventional mRNAs coded by protein-coding genes.

72 tability, but instead to a decrease in Cxcl1 mRNA stability.

73 1,25(OH)2D3 increased CYP27B1 mRNA levels in HCEC, but had no effect on CYP27B1 protei

74 ttranscriptional mechanism to degrade Cyp7a1 mRNA.

75 ation or demethylation occurs in cytoplasmic mRNA.

76 Transfer RNA (tRNA) decodes mRNA codons when aminoacylated (charged) with an amino a

77 Creating a cDNA library for deep mRNA sequencing (mRNAseq) is generally done by random pr

78 miR171 destabilizes mRNAs encoding the root-specific family of SCARECROW-Lik

79 bunit, consistent with its role in directing mRNAs onto the ribosome.

80 Consistent with in vivo findings, DUSP5 mRNA expression increased in adipocytes in response to T

81 We tagged endogenous mRNA or protein products of the gene miranda that is req

82 xpression of adhesion-associated endothelial mRNA targets.

83 98 annotated) and 27 (15 annotated) enriched mRNAs at the vegetal and animal pole, respectively.

84 the latter of which exhibited increased Erk5 mRNA expression.

85 oc5 mutant zebrafish rescue with human EXOC5 mRNA completely reversed the mutant phenotype.

86 ion, with Star-PAP impacting lowly expressed mRNAs and long-noncoding RNAs to the greatest extent.

87 Interaction between the exsA mRNA and Sr0161 leads to a block in the synthesis of a c

88 Thus, expression of a 5' extended mRNA isoform causes transcriptional interference at the

89 -vivo tissue sections, which will facilitate mRNA trafficking studies in pre-clinical models.

90 ast growth factor 21 (FGF21), elevated Fgf21 mRNA and protein solely in the heart, and upregulation o

91 In addition, we found that Fkh mRNA was undetectable in Drosophila S2 cells, and M. sex

92 driver of clinical symptoms, placental Flt1 mRNA levels strongly correlate with maternal blood press

93 al electrical resistance, paracellular flux, mRNA expression, Western blotting, and immunofluorescenc

94 Biopsies were analysed for mRNA levels of selected genes, and GLUT4 and Akt protein

95 that Top3beta is the major topoisomerase for mRNAs, and requires both RNA binding and catalytic activ

96 against estimating protein fold-changes from mRNA fold-changes between different cell-types, and high

97 a T7 phage display cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells an

98 ontrol the supply of full-length, functional mRNAs coding for a variety of proteins essential to cell

99 ed whether kidney tissue expression of GDF15 mRNA correlates with circulating levels of GDF-15 and wh

100 cleavage and polyadenylation (APA) generates mRNA isoforms with different 3' untranslated regions (3'

101 Whole genome mRNA expression profiling identified nicotinamide N-meth

102 We show using the gfp mRNA (encoding green fluorescent protein) that non-sRNAs

103 models is that faster translation of a given mRNA is unlikely to generate more of the encoded protein

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

105 ce, followed by a delayed reduction in GluA2 mRNA expression.

106 at IL-34-Mphis possess significantly greater mRNA levels of select restriction factor genes than CSF-

107 HEC1 mRNA and protein are highly expressed in many malignanci

108 Histone mRNAs are rapidly degraded when DNA replication is inhib

109 18a-5p in the 3'-untranslated region of hPXR mRNA.

110 the 3'-end processing of thousands of human mRNAs by juxtaposing poly(A) signals (PASs) and cleavage

111 e serum (protein), spleen, and hypothalamus (mRNA).

112 t mice, as marked by decreased Arg1 and Il10 mRNA expression and decreased interleukin (IL)-4, IL10 a

113 signature and IL-1 receptor-like 1 (IL1RL1) mRNA expression.

114 We examined the global changes in mRNA abundance in healthy lung and lung lesions and in t

115 fferentiation without concomitant changes in mRNA levels, suggesting that BET proteins are regulated

116 ring macrophages, manifested by elevation in mRNA expression of Tnfalpha and Il1beta, increased intra

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

118 nction and biological significance of m5C in mRNA in mammals.

119 Modifications in mRNA constitute ancient mechanisms to regulate gene expr

120 methyladenosine (m(6)A) RNA modifications in mRNA requires an understanding of when and where in the

121 best characterized for its essential role in mRNA nuclear export, cofunctions with Los1 in tRNA nucle

122 cal CTD, which orchestrates various steps in mRNA synthesis.

123 onths of age revealed a dramatic increase in mRNAs encoding various chemokines, cytokines, growth fac

124 We measured significant increases in mRNAs associated with a type 2 immune response (interleu

125 bited slower mRNA decay and showed increased mRNAs and levels of protein expression in Mettl3-deficie

126 nism would provoke a never-ending increasing mRNA synthesis rate in smaller daughter cells.

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

128 and consequently reduced translation of Irs1 mRNA, the effects of a post-weaning obesogenic diet on I

129 s the action of a pertinent microRNA and its mRNA target in MNs.

130 t diet-induced obese (DIO) rats, the apoA-IV mRNA level is significantly reduced and that the estroge

131 mors than in non-TNBC tumors, and high c-Jun mRNA level was associated with shorter disease-free surv

132 is critical to the translation of HAdV late mRNA.

133 while expression of their associated linear mRNAs concomitantly decreased.

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

135 ist L165041 in mice increased hepatic LPCAT3 mRNA abundance and LPCAT enzymatic activity, which is as

136 r how the intron-containing but unspliced M1 mRNA bypasses the normal quality-control checkpoints.

137 ber gain at 3q resulted in increased MAP3K13 mRNA in HNSCC tumor samples and cell lines.

138 430 is crucial for the clearance of maternal mRNA during maternal zygotic transition in embryonic dev

139 lerates the decay of m(6)A-modified maternal mRNAs and impedes zygotic genome activation.

140 ction of the non-transposase-encoding mature mRNA isoform in Drosophila germ cells.

141 e dynein/dynactin complex in anterograde mbp mRNA transport.

142 result in failure to properly distribute mbp mRNA in oligodendrocytes, indicating a paradoxical role

143 encing multiple steps in AGO2-miRNA-mediated mRNA decay.

144 Expression of mERbeta2 mRNA was detected in mouse reproductive tissues (ovary,

145 In the analysis, 10,726 microRNA-mRNA interactions were identified to be associated with

146 rocess that creates functional mitochondrial mRNAs in Kinetoplastids.

147 rved a significant correlation between MMP13 mRNA levels and RUNX2 gene expression in human OA chondr

148 t the increased ribosome loading of modified mRNAs renders them more permissive for initiation by fav

149 ation N(6)-methyladenosine (m(6)A) modulates mRNA processing and activity.

150 rs and may act as gatekeepers of monoallelic mRNA expression.

151 Assuming that most mRNA-chromatin interactions indicate the physical proxim

152 rall ribosome density, which affected mostly mRNAs encoding ribosomal proteins.

153 Instead, p62 delayed the degradation of MYC mRNA by repressing the expression of let-7a and let-7b,

154 ion of let-7a and let-7b, thus promoting MYC mRNA stabilization at the post-transcriptional level.

155 are: (i) sRNAs can potentially bind nascent mRNAs in the nucleoid, and (ii) localization patterns an

156 or inhibiting expression of the coding NDC80 mRNA isoform.

157 mporal gene expression changes in a neuronal mRNA pool during an olfactory long-term associative memo

158 Ninety were novel mRNAs over 4-fold enriched at the vegetal pole and six w

159 cell-to-cell variations in the abundance of mRNA and reporter protein in yeast.

160 h known roles in maintaining the accuracy of mRNA codon translation.

161 ctions as an enhancer-dependent activator of mRNA 3' processing.

162 oach can facilitate near-infrared imaging of mRNA localization in vivo and in ex-vivo tissue sections

163 ce of an active gene, ADH1, independently of mRNA-capping activity.

164 ds significant insight into our knowledge of mRNA-specific translational activation and the function

165 on is extensively regulated at the levels of mRNA stability, localization and translation.

166 trosome integrity do not result from loss of mRNA export.

167 dominantly in the 3' untranslated regions of mRNA, and destabilizes target mRNAs through direct recru

168 Regulation of mRNA splicing, processing and stability is increasingly

169 ctors act primarily to effect the release of mRNA and tRNA from the ribosome, with the splitting of t

170 NA biochemistry, we identified a core set of mRNA m(6) A writer proteins in Arabidopsis thaliana.

171 nd on the degradation of specific subsets of mRNA.

172 thway that requires extensive uridylation of mRNA decay intermediates.

173 l molecules binding to RG4s in the 5'-UTR of mRNA.

174 Changes in the 3'UTR composition of mRNAs can alter gene expression by regulating transcript

175 ce resulting in the selective degradation of mRNAs.

176 on the extensive changes in distribution of mRNAs in the cell body and axon compartments of peripher

177 synthesis, processing and nuclear export of mRNAs.

178 tant miRNAs that regulated a large number of mRNAs in the control group but not in the exposed groups

179 ceptor stimulation influenced recruitment of mRNAs to heavy polysomes and translation of subsets of g

180 ortex of mice, where we identify a subset of mRNAs that are translated in dendrites by neuronal ribos

181 F4E regulates the translation of a subset of mRNAs.

182 binding effects of the RNA helicase MOV10 on mRNA degradation, the potentially different ADAR1 bindin

183 ion and protein synthesis, certain oncogenic mRNAs are spared.

184 cinoma (PC), via either somatic mutations or mRNA downregulation, suggesting an important tumour supp

185 but not female, deletion animals overexpress mRNA for dopamine receptor 2 and adenosine receptor 2a i

186 suppresses IL-27 production by promoting p28 mRNA degradation.

187 Upon DNA damage, p53 mRNA is released from stress granules and associates wit

188 In parallel, mRNA expression of myosin heavy chain 7 and natriuretic

189 In adipose tissue, PER2 mRNA rhythms were delayed by 0.97 +/- 0.29 hr (p < 0.01)

190 the PFKFB3 gene and was required for PFKFB3 mRNA and protein expression.

191 these common gene variants on cardiac PITX2 mRNA is currently under study.

192 0.045) were also observed between placental mRNA abundance of vitamin D metabolic components and cir

193 Our data suggest that the decay of platelet mRNAs is slowed by the natural loss of the mRNA surveill

194 tified individual and shared defects in PLP1 mRNA expression and splicing, oligodendrocyte progenitor

195 full-length viral RNAs or surrogate gag-pol mRNAs competent for Gag synthesis to non-PM membranes or

196 ardless of diet, decreased fetal liver Pparg mRNA expression and increased placental androgen recepto

197 nding of when and where in the life of a pre-mRNA transcript the modifications are made.

198 Aberrant alternative pre-mRNA splicing (AS) events have been associated with seve

199 ferentiation is regulated by alternative pre-mRNA splicing.

200 er supported by genetic interactions and pre-mRNA splicing assays.

201 that inhibition or slowing of canonical pre-mRNA processing events shifts the steady-state output of

202 ate that H2A.Z is required for efficient pre-mRNA splicing and indicate a role for H2A.Z in coordinat

203 tilize sudemycin compounds that modulate pre-mRNA splicing.

204 S proteins via its role in governing MVC pre-mRNA splicing.IMPORTANCE The Parvovirinae are small none

205 site, and the branchsite (BS) of nascent pre-mRNA.

206 n in the regulation of premessenger RNA (pre-mRNA) splicing.

207 y bind to two distinct sites of the SMN2 pre-mRNA, thereby stabilizing a yet unidentified ribonucleop

208 f the hexanucleotide AAUAAA motif in the pre-mRNA polyadenylation signal by the cleavage and polyaden

209 o U1-70K to induce splicing of lipogenic pre-mRNAs.

210 litting reaction, which necessarily precedes mRNA and tRNA release.

211 RNA biogenesis components regulate precursor mRNA splicing of P-transposable element transcripts in v

212 t of novel therapies targeting the precursor mRNA splicing pathway.

213 Expression of multiple late viral protein mRNAs was lost in the presence of either drug, consisten

214 g, revealed different aspects of the protein-mRNA relationship.

215 ryotic cells; their cargo includes proteins, mRNA and microRNA (miR) that can be transferred to recip

216 otes the translation of c-MYC, BCL2 and PTEN mRNAs in the human acute myeloid leukemia MOLM-13 cell l

217 ks significantly (1.8-fold) up-regulated Pxr mRNA levels in WT mice.

218 normal tissues confirmed tissue-specific RD3 mRNA levels.

219 vity and hence expression of let-7-regulated mRNAs.

220 f the CCR4-Not deadenylase complex, restored mRNA levels for a class of downregulated, H3K36me3-rich

221 Messenger RNA (mRNA) modification provides an additional layer of gene

222 n 1 (SDC1), SMAD7, and SMAD6 messenger RNAs (mRNAs).

223 biofilms, which have potentially higher rRNA:mRNA ratios and higher rRNA carryover during RNA-seq ana

224 voring either ribosome recycling on the same mRNA or de novo ribosome recruitment.

225 dent with preferential translation of select mRNAs that participate in stress alleviation.

226 methylation activity that influences several mRNA processing events.

227 A third of the TRSs generated sg mRNAs with variant leader-body junction sequences.

228 We have found that the expression of SGLT2 mRNA and protein is increased in renal biopsies from hum

229 FXS disease model, we found FMRP binds shrub mRNA (human Chmp4) to repress Shrub expression, causing

230 xpressed significantly lower levels of SIRT1 mRNA than controls.

231 CISH were marked by m(6)A, exhibited slower mRNA decay and showed increased mRNAs and levels of prot

232 and controls showed no differences in SMCHD1 mRNA or protein abundance but revealed regulatory change

233 oli (APC) regulates the localization of some mRNAs at cellular protrusions but the underlying mechani

234 natal exposure to genistein on gene specific mRNA levels in vaginal tissue.

235 ogression through the regulation of specific mRNA targets, thus strengthening the possibility of a di

236 , some of which are potential stage-specific mRNA interactors that likely reflect the dynamics of RNA

237 ogram involves enhanced decoding of specific mRNAs that are depleted in terminally differentiating/en

238 Homodirectional changes in steady-state mRNA abundance and translation were observed for all but

239 XCL8 3'-UTRs unexpectedly led to substantial mRNA decreases.

240 time PCR measurements of SK channel subunits mRNA in supraoptic nucleus punches revealed a diminished

241 ctivation to asparaginase, yet surprisingly, mRNA levels of key ISR gene targets such as Atf5 and Tri

242 Molecular Beacon (MB) specific for survivin mRNA is available.

243 fragments that could tandemly bind to target mRNA.

244 ted regions of mRNA, and destabilizes target mRNAs through direct recruitment of the CCR4-NOT deadeny

245 However, target mRNAs recognized by both miRNA and AUF1 are less abundan

246 uency of cleavage sequences, putative target mRNAs for these VapCs were identified; these were closel

247 he translation and stability of their target mRNAs, and play key roles in development, homeostasis an

248 ished DGCR8 as a direct interactor of Tcf7l1 mRNA, a core component of the pluripotency network.

249 sed in gonadotrope-precursor cells, but Tet1 mRNA levels decrease markedly with completion of cell di

250 ng regions and introns were less stable than mRNAs that end at 3'-UTR poly(A) sites.

251 ntegrative omics analyses, and discover that mRNA levels of DTL, DCAF4, 12 and 13 are consistently el

252 mal motoneuron development and indicate that mRNA handling is a critical component of SMA.

253 Here, we investigate the possibility that mRNA structures facilitate the 3'-end processing of thou

254 The mRNA expression levels of some genes related to neurotra

255 We analyzed the mRNA levels for 36,778 transcript expression traits (pro

256 red with that of the wild type, however, the mRNA levels of the wild-type and mutant cells were compa

257 st ribosomal protein Rps3/uS3 resides in the mRNA entry channel of the 40S subunit and contacts mRNA

258 osis and necroinflammation and increased the mRNA and protein expression of cytokines and chemokines

259 It is a potent inhibitor of the mRNA decapping scavenger enzyme (DcpS), but the mechanis

260 dose-dependent, and durable silencing of the mRNA encoding glycolate oxidase and increased serum glyc

261 cerevisiae and S. pombe Although >80% of the mRNA genes in each species were found to display APA, S.

262 RNAs, leading to enhanced degradation of the mRNA or inhibition of translation.

263 t mRNAs is slowed by the natural loss of the mRNA surveillance and ribosome rescue factor Pelota.

264 and second, p38-mediated inactivation of the mRNA-destabilizing factor tristetraprolin, which we show

265 endent ALYREF binding near the 3' end of the mRNA.

266 ing complete sequence complementarity to the mRNA for the important viral gene activator ICP0, inhibi

267 Consistent with these observations, the mRNAs of SOCS family genes encoding the STAT signalling

268 oid cultures, elevated IFN-gamma reduced the mRNAs encoding for RANKL, TRAP, and Cathepsin K.

269 Here, we show that the mRNAs and proteins of these four chemotaxis pathways and

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

271 connectivity of VTA dopamine neurons, their mRNA translational profile, and basic electrophysiologic

272 2 and RARA by reducing m(6)A levels in these mRNA transcripts.

273 These mRNAs' 3'UTRs have enriched binding motifs for several R

274 Top canonical pathways represented by these mRNAs include Wnt/beta-catenin, TGF-beta, and stem cell

275 determine the spatial organization of these mRNAs and proteins, which can be modulated through postt

276 e production of new miRNAs that target these mRNAs at sites distal to the stop codon.

277 For Flt1, just three mRNA isoforms account for > 94% of all transcripts, with

278 High throughput mRNA expression profiling can be used to characterize th

279 whereas miR-30c targets the 3'-UTR of Tnrc6a mRNA to weaken its function.

280 Its binding to mRNA is regulated by tyrosine 396 phosphorylation, and t

281 hile changes in the coding sequences lead to mRNAs encoding distinct proteins.

282 ng that Top3beta is specifically targeted to mRNAs by its RNA binding domain.

283 mTORC1 to regulate the translation of 5'TOP mRNAs such as those encoding ribosome proteins (RP).

284 La-related protein 1 (LARP1) binds TOP mRNAs, regulating their stability and translation.

285 Total mRNA analysis identified a set of host genes that are up

286 these genomes increased from <0.3% of total mRNA from the oxic zone to a max of 22% under anoxia.

287 ast tRNA(Lys) affects mRNA decoding and tRNA-mRNA translocation.

288 as not elevated in serum, and FGF21 and UCP1 mRNAs were not induced in liver or brown adipose tissue

289 Unlike mRNAs, microRNAs were not asymmetrically distributed.

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

291 excessive glutamate transmission upregulated mRNA expression of Fgfrs and their ligands Fgfs Deleting

292 contrast, the translocation of longer 3' UTR mRNAs from RNPs to polysomes correlated with the product

293 ates were repressed, by up to 530-fold, when mRNA structures overlapped with the ribosome's footprint

294 ormed a subtractive screening approach where mRNA from PGE2-G response-positive and -negative cell li

295 ion of SREBP target gene expression, whereas mRNAs involved in glycolysis, gluconeogenesis, and T cel

296 induced by RBM3 and the mechanisms by which mRNAs encoding cold shock proteins escape cooling-induce

297 with downstream targets, transcriptome-wide mRNA 3' UTR interaction sites were experimentally determ

298 en implicated in coupling transcription with mRNA splicing and DNA damage response.

299 the amount of Top3beta that associates with mRNAs, indicating that Top3beta is specifically targeted

300 hrough interactions with target sites within mRNAs, leading to enhanced degradation of the mRNA or in