ライフサイエンスコーパス: mRNA

1 mRNA expression of PAX9, MSX1, AXIN2, and RUNX2 (known t

2 mRNA levels are determined by the balance between mRNA s

3 mRNA translation represents the last step of genetic flo

4 19b and a concomitant decrease in syndecan-1 mRNA.

5 ficant difference in the expression of IL-17 mRNA between OVA-treated skin of VAN and VAD mice.

6 ction between these miRNAs and TOP2alpha/170 mRNA.

7 ld increase in primiR-199a1 and primiR-199a2 mRNA levels in mouse islets cultured in 10 mm glucose co

8 nfected infants showed elevated pro-IL-1beta mRNA and protein.

9 ll as increased VEGFR1 and interleukin-1beta mRNA expression in females, and reduced brain derived ne

10 3) and increased (P = 0.037) placental IGF-2 mRNA expression.

11 High levels of Kv3.1 and Kv3.3 mRNA and protein were measured, with no evidence of comp

12 ted regions (UTRs) of E2F1 and E2F3 (E2F1/3) mRNAs.

13 ophyllide a oxygenase (CAO) gene having a 5' mRNA extension encoding a Nab1 translational repressor b

14 Moreover, ALKBH5 affects mRNA stability of receptor tyrosine kinase AXL in an m(6

15 e transcriptome and observed that it affects mRNA levels of hundreds of genes that are significantly

16 ecay (NMD) pathway degrades some but not all mRNAs bearing premature termination codons (PTCs).

17 o-transcriptionally by the precursors of all mRNAs.

18 on when cultured on bone slices, and altered mRNA expression of related chemokine receptors and ligan

19 to suppress p21(Cip1) promoter activity and mRNA and protein level.

20 by the vaccine was detected both in DNA and mRNA extracted from each tumor biopsy.

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

22 t on mitochondrial respiration/function, and mRNA export occurs in the absence of Fzo1, which is requ

23 showed long-range chromatin interactions and mRNA abundance associations with target genes, and were

24 of cell-free RNAs, efficient cell lysis and mRNA capture, achieving highest mRNA detection accuracy

25 nclusions: This study of sputum microRNA and mRNA expression from patients with asthma demonstrates t

26 We measured microRNA and mRNA expression using quantitative RT-PCR.

27 electron microscopy, ribosome profiling, and mRNA stability assays to examine the recruitment of Ccr4

28 yed higher discrepancies between protein and mRNA expression in paired primary/metastatic melanoma or

29 wed that in epimastigotes, TcHTE protein and mRNA levels decrease in response to increments in heme c

30 recognised by ZNF598 to initiate protein and mRNA quality control pathways.

31 y and reduced levels of occludin protein and mRNA without affecting the expression of other transmemb

32 Consequently, RNA-binding proteins and mRNA-encoded sequence elements serve as primary determin

33 RNA immunoprecipitation (RIP) and mRNA-decay assays reveal that QKI-7 binds and promotes m

34 periment, RNA immunoprecipitation (RIP), and mRNA stability analysis, we evaluated the potential bind

35 analysis of transcriptome-wide m(6)A-seq and mRNA-seq analysis identified the glutamine transporter S

36 bserved, including alternative splicing, and mRNA expression levels of proto-oncogenes and tumor supp

37 read premature transcription termination and mRNA shortening.

38 ediated posttranscriptional regulation of AR mRNA (messenger RNA) in CRPC.

39 gradation of mRNA during ribosome-associated mRNA surveillance pathways.

40 We confirmed that EPRS was induced at mRNA and protein levels (~1.5-2.5-fold increase) in fail

41 that these inclusions are decorated with ATI mRNA.

42 By analyzing Atoh7 mRNA and protein levels, RGC development and survival, a

43 intracellular Ca(2+) uptake and Na, K-ATPase mRNA were determined in the cultured epithelial cells fr

44 classes lies in the mechanisms that balance mRNA synthesis with mRNA decay.

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

46 levels are determined by the balance between mRNA synthesis and decay.

47 aine-homocysteine S-methyltransferase (Bhmt) mRNA and protein levels following repeated treatments we

48 Both mRNA and protein analyses show that PRL increased mother

49 aling pathways governing development at both mRNA and protein levels.

50 nes were detected in the circulation by both mRNA-based and genomic DNA-based sequencing.

51 mediated mRNA decay (NMD) degrades EJC-bound mRNA, but the lack of suitable methodology has prevented

52 le in the adult mouse heart at baseline, but mRNA and protein are induced after ischemia-reperfusion

53 nthesis and were differentially regulated by mRNA decay pathways, raising the possibility that one di

54 ensor that is activated to splice the bZIP60 mRNA that produces a truncated transcription factor that

55 certain viruses that possess "nonself" cap0-mRNAs.

56 on of viral transcription by cleaving capped mRNA bound to PB2.

57 ism was higher in embryos injected with Cas9 mRNA (100%) compared to those injected with Cas9 protein

58 Single-cell mRNA sequencing revealed that systemic Akt1 deletion mai

59 g growth factor pharmacotherapy show that cf-mRNA reflects dynamic functional changes over time assoc

60 ty purification and qPCR was used to compare mRNA expression of nrg1,2,3,4 and erbB1,2,3,4 in PV and

61 Conversely, mRNA levels of pro-inflammatory markers (IL-6, IL-1beta,

62 y and cis-regulatory elements uncover a core mRNA-ncRNA transcriptional signature shared by IgG(+) an

63 As cotranslational mRNA decay is interconnected with translation, we also a

64 2A13, CYP2A6, and CYP2A7 (and higher CYP1A2) mRNA.

65 to one inflammatory disease may not deliver mRNA to another.

66 nerally, this suggests an LNP which delivers mRNA to one inflammatory disease may not deliver mRNA to

67 eshift-inducing stem-loops from E. coli dnaX mRNA and the gag-pol transcript of Human Immunodeficienc

68 to the dosage of maternally-expressed dorsal mRNA.

69 In patient fibroblasts, dual mRNAs encoded proteins localize in mitochondria and prod

70 In a hypomorphic murine model of PA, dual mRNAs normalize ammonia similarly to carglumic acid, a d

71 ndent post-transcriptional regulation of Dux mRNA.

72 7 regulated the translation of E2F1 and E2F3 mRNAs through the 5' untranslated regions (UTRs) of E2F1

73 We observed that C/ebpalpha and C/ebpbeta mRNA and protein were markedly reduced in Src-1/-2 doubl

74 hemical modifications of adenine base editor mRNA and guide RNA expand the applicability of CRISPR-as

75 This interaction may enable mRNA circularization, an apparently critical element of

76 hese RBPs identifies thousands of endogenous mRNA targets that respond to changes in RBP level, recap

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

78 ational repression but is required to enrich mRNAs in the germ lineage for robust germline developmen

79 ICH3 gene functionally and identified ERICH3 mRNA transcripts and protein isoforms that are highly ex

80 sion of the hypoxia-inducible erythropoietin mRNA.

81 Cap structures are ubiquitous on eukaryotic mRNAs, essential for post-transcriptional processing, tr

82 We examined mRNA levels of Gremlin 1 in key target tissues for insul

83 nd reduced brain derived neurotrophic factor mRNA in males.

84 the MTX infusion time (P = 1.5 x 10-3), FPGS mRNA expression (P = 2.1 x 10-3), and MTX systemic clear

85 remodelers that titrate protein output from mRNA populations.

86 genomic locations of SRTs are recovered from mRNA, and SRTs deposited by exogenous, TF-transposase fu

87 ered cell G6P but not ATP and decreased G6pc mRNA at high glucose.

88 g wheel in their home cage increased galanin mRNA in the LC of mice, which was correlated with and co

89 es to transcriptome complexity by generating mRNA isoforms with varying 3' UTR lengths.

90 ncreased the hypothalamic expression of Ghrh mRNA, although very few GHRH neurons were found to coexp

91 Recently, sequencing of salivary-gland mRNA libraries revealed increasingly complex and complet

92 alpha-cells did not express Glp1r mRNA and delta-cells expressed Glp1r mRNA but not protei

93 s Glp1r mRNA and delta-cells expressed Glp1r mRNA but not protein.

94 non-responders, display an increase of GPR56 mRNA in the blood.

95 e mice silences miR-370-3p and restores HCN4 mRNA and protein and I(f) in the sinus node and blunts t

96 IFN-stimulated genes (ISGs) on hepadnaviral mRNAs transcribed from cccDNA, we found that downregulat

97 Lower reaction volume and higher mRNA capture and barcoding efficiency significantly redu

98 ovirus LOXL2 -treated implants showed higher mRNA levels of LOXL2, ACAN, and other anabolic genes com

99 ll lysis and mRNA capture, achieving highest mRNA detection accuracy (R = 0.955) and comparable sensi

100 the transcription and processing of histone mRNAs.

101 HS2ST1 variants cause a reduction in HS2ST1 mRNA and decreased or absent heparan sulfate 2-O-sulfotr

102 s not linked to increased translation of IgG mRNA, but rather to impairment of autophagy.

103 conditions in vitro and analyzed changes in mRNA and protein levels to identify mechanisms of tumor

104 abidopsis thaliana and a mutant defective in mRNA methylation (m(6)A).

105 es responded differently to XRN1 deletion in mRNA synthesis and were differentially regulated by mRNA

106 We find that the rate-limiting step in mRNA cleavage frequently involves unmasking of target si

107 roughput methods to identify various RREs in mRNAs that FMRP may bind to in vivo.

108 icate that PQS in the non-template increases mRNA production rate and yield.

109 A detection feasible down to ~600 individual mRNA transcripts.

110 ates the IRE1alpha nuclease, which initiates mRNA splicing of X-box binding protein-1 (XBP1).

111 stension of satellites (SADS) and p16(Ink4a) mRNA expression were identified in alveolar bone osteocy

112 P-STRUCTURE-seq method to capture the intact mRNA structurome in Arabidopsis thaliana.

113 in components, including: the first internal mRNA m7G database containing 44 058 experimentally valid

114 ion, regulation and pathogenesis of internal mRNA m7G.

115 ing 44 058 experimentally validated internal mRNA m7G sites, a sequence-based high-accuracy predictor

116 Intriguingly, mRNAs encoding for antiviral factors bypass this transla

117 ility to block the expression of IFN and ISG mRNA.

118 ble to detect amplicons of 16S rRNA and katG mRNA generated from 0.1 pg and 10 pg total RNA taken for

119 (control-NM), in order to identify which key mRNA and microRNAs are regulating this complex process i

120 , localization, and local translation of key mRNAs in learning and memory and expand on the notion of

121 not only to a nonspecific depletion of KIF1A mRNA but also to an accelerated proteasomal degradation

122 e highly efficient at cis-cleaving mammalian mRNAs and showed that they can be tightly regulated by a

123 echanism of translational repression of manY mRNA by the sRNA SgrS through a binding interaction upst

124 Although induction of many mRNAs by budesonide plus formoterol was supra-additive,

125 orrespondingly, MKT1 is associated with many mRNAs, although not with those encoding ribosomal protei

126 In this report, MAP3K8 mRNA levels were found decreased in the lungs of IPF pat

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

128 , the DF paralogs act redundantly to mediate mRNA degradation and cellular differentiation.

129 NAs are natural products of RNase E-mediated mRNA decay and associate with major RNA-binding proteins

130 Nonsense-mediated mRNA decay (NMD) degrades EJC-bound mRNA, but the lack o

131 Nonsense-mediated mRNA decay (NMD) is a conserved translation-coupled qual

132 The nonsense-mediated mRNA decay (NMD) pathway degrades some but not all mRNAs

133 retained only 31 explanatory striatal miRNA-mRNA pairs that are precisely associated with the shape

134 apparently critical element of mitochondrial mRNA stability and quality control.

135 In cancer cell lines and xenograft models, mRNA and protein expressions of the type I IFN pathway w

136 ticle (LNP)-encapsulated nucleoside-modified mRNA encoding full-length gB.

137 ggest that the use of gB nucleoside-modified mRNA-LNP vaccines is a viable strategy for improving on

138 ructures of its functional complexes with mt-mRNA, mt-tRNAs, recycling factor and additional trans fa

139 IL-17 each suppressed Il25, Il33, and muc5ac mRNA expression in cultured airway epithelial cells.

140 icing defect, we tested wild-type and mutant mRNA substrates, containing 333 nt of the C8alpha intron

141 process requires factors involved in mutant mRNA decay, as in zebrafish and mouse.

142 rmore, we tested the effects of KIF3B mutant mRNA expression in the developing zebrafish retina.

143 Conversely, bFGF suppresses MYO18B mRNA irrespective of CEBPB, miR-520G overexpression or I

144 These NASAR mRNAs merit further development as alternative SARS-CoV-

145 berrantly counted along with a cell's native mRNA and result in cross-contamination of transcripts be

146 ocyte stress (Urinary pellet podocin:nephrin mRNA ratio), podocyte detachment (Urinary pellet podocin

147 SIRT6 protein, but not mRNA, expression was markedly reduced in VSMCs in human

148 to 3'-untranslated regions (3'-UTR) of NOX2 mRNA.

149 Single-cell or single-nuclei mRNA sequencing of dissociated mouse kidneys and of diss

150 KO cells exhibited elevated levels of NUDT3 mRNA substrates and increased P-body abundance.

151 tified the nucleotide bases in the occluding mRNA 3'UTR that interact with MIR200C-3p.

152 Differential expression analysis of mRNA from chondrocytes harvested from knees of rats with

153 teins are important enzymes for catalysis of mRNA deadenylation in eukaryotes.

154 In the context of mRNA biomarker profiling, formalin fixed paraffin embedd

155 d facilitates 3'->5' exosomal degradation of mRNA during ribosome-associated mRNA surveillance pathwa

156 Thus, EDC4 not only serves as an enhancer of mRNA turnover that binds DCP2, but also as a repressor t

157 scriptome studies involve the examination of mRNA transcript abundance and gene expression patterns i

158 logical examination and by the expression of mRNA and protein markers of fibrosis.

159 The functional importance of mRNA localization to centrosomes is unclear.

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

161 Moreover, we found the intensity of mRNA expression in the liver correlated with the pKa of

162 ge of long reads spanning the full length of mRNA transcripts, we provide support for 23,865 splice i

163 Here, we integrate genome-wide measures of mRNA expression, miRNA expression, DNA methylation, and

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

165 ription factors assemble on the promoters of mRNA genes to form large macromolecular complexes that i

166 ed system for simultaneous quantification of mRNA and protein of a given gene via dual fluorescent re

167 Here, we describe regulation of mRNA stability and P-body dynamics by the inositol pyrop

168 ns and ER stress, leads to the regulation of mRNA stability and protein synthesis through posttranscr

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

170 its unique function in the stabilization of mRNA, which is associated with inflammatory autoimmune d

171 deadenylation, is the rate-limiting step of mRNA degradation in eukaryotic cells.

172 sense RNAs or untranslated regions (UTRs) of mRNA transcripts.

173 These include the nuclear accumulation of mRNAs encoding components of the negative limbs of the c

174 Integrative analyses of mRNAs, miRNAs, lncRNAs, chromatin accessibility and cis-

175 usly read through UAG and UGA stop codons of mRNAs.

176 NP granules differentially controls fates of mRNAs localized within the same cytoplasmic domain.

177 s full-length HIV-1 RNA from a large pool of mRNAs as virion genome during virus assembly.

178 vironmental changes, including regulation of mRNAs that require extensive uridine insertion/deletion

179 the SG assembly G3BP paralogs, or release of mRNAs from ribosomes via translation elongation.

180 ned within the first five codons of a set of mRNAs that are enriched for translational enhancer seque

181 pression of functionally coordinated sets of mRNAs and involves combinatorial and dynamic interaction

182 alization, stability, and translatability of mRNAs.

183 strength of stabilizing selection acting on mRNA levels in a species is strongly associated with tha

184 to assess the effects of those mutations on mRNA levels.

185 Importantly, the polarity of ribosomes on mRNAs encoding multiple TMDs was disproportionately affe

186 PC, alters core clock gene expression and/or mRNA accumulation in a way that favors bacterial growth

187 actin motor, myosin-V, are essential for osk mRNA posterior localization.

188 CC enzyme activity vs. single (PCCA or PCCB) mRNA alone.

189 ere found to bind cooperatively to the PDCD4 mRNA and mitigate miR-21-mediated translation repression

190 uR positively mediated the stability of Pfn1 mRNA and influenced actin polymerization.

191 temperatures decreased (P = 0.026) placental mRNA expression of a glucose transporter (GLUT-3) and in

192 podocyte detachment (Urinary pellet podocin mRNA:creatinine ratio: UPPod:CR) and a tubular marker (U

193 nuclear export of intronless and intron-poor mRNAs and lncRNAs.

194 s of piRNAs in humans is posttranscriptional mRNA silencing, their functions are similar to what we h

195 Pre-mRNA processing of these genes is critical and mediated

196 bryonic day 13-13.5 (E13-13.5) corrected pre-mRNA splicing in the juvenile Usher syndrome type 1c (Us

197 icroscopy and ability to support histone pre-mRNA processing in the presence of polyadenylation facto

198 The increase in pre-mRNA is delayed and due to enhanced transcription and li

199 ecific RNA-target sequences and modulate pre-mRNA splicing by sterically blocking the binding of spli

200 kinase for the parasite-specific mode of pre-mRNA processing.

201 We discuss different levels of pre-mRNA splicing regulation such as post-translational modi

202 ell cycle and describe its dependence on pre-mRNA splicing and accurate alternative splicing.

203 One pre-mRNA that is alternatively spliced and linked to neurode

204 ns introduced by mis-splicing of PgABCA2 pre-mRNA were prevalent in field-selected larvae from India

205 s introns from messenger RNA precursors (pre-mRNA).

206 uridylation and decay thereby protecting pre-mRNA upon KPAF3 displacement by editing.

207 rescue disease-relevant splicing of tau pre-mRNA in a variety of cellular systems, including primary

208 mpounds are shown to directly target tau pre-mRNA in cells, via chemical cross-linking and isolation

209 g the binding of splicing factors to the pre-mRNA, are a promising therapeutic modality to treat a ra

210 Because the majority of genes undergo pre-mRNA splicing, most cellular processes depend on proper

211 Most pre-mRNAs proceed through 3' adenylation, uridine insertion/

212 ntial role in the selection of the precursor mRNA branch-site adenosine, the nucleophile for the firs

213 Some negative-sense RNA viruses prime mRNA transcription using host 5' cap sequences, usurping

214 We identified neuronal Prkag3 mRNA as a mechanistic substrate for NMD that contributes

215 assays reveal that QKI-7 binds and promotes mRNA degradation of downstream targets CD144, Neuroligin

216 nal mode of Gle1 regulation to ensure proper mRNA export and translation.

217 We show here that CP33B is bound to psbA mRNA in vivo, as was shown previously for CP33C and SRRP

218 in eukaryotes is RNA splicing, which readies mRNA for translation.

219 g the many cellular mechanisms that regulate mRNA fate, covalent nucleotide modification has emerged

220 with multiple mechanisms acting to regulate mRNA levels.

221 members and ADPRylation in gene regulation, mRNA processing, and protein abundance.

222 Moreover, in TPR-depleted cells reporter mRNAs generated from short transcripts accumulate in nuc

223 lysome assembly, and translation of reporter mRNAs with structured 5'UTRs.

224 (miRNA) target sites within a messenger RNA (mRNA) can act cooperatively, leading to more repression

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

226 We analyzed levels of messenger RNAs (mRNAs) encoding proteins involved in autophagy in coloni

227 We analyzed BE tissues for messenger RNAs (mRNAs) that associate with BE progression and identified

228 ng interactions with the 3' end of 16S rRNA, mRNA Shine-Dalgarno (SD) sequences positioned upstream o

229 Here, we show that low SASH1 mRNA expression is associated with poor survival in aden

230 egulators, while also destabilizing sentinel mRNAs that are primed to activate rescue pathways when m

231 r of target of Myb protein 1 (Stm1; SERPINE1 mRNA-binding protein 1 [SERBP1] in mammals), and recentl

232 Simplex mRNA Sequencing (RNA-Seq) based isoform quantification a

233 driver genes were concatenated into a single mRNA construct to vaccinate patients with metastatic gas

234 s whose genes are co-transcribed on a single mRNA molecule.

235 Sirtuin 1 (SIRT) mRNA levels were lower in PLAC when compared to DM+RSV,

236 tein levels by decreasing the amount of SNCA mRNA loaded into polysomes, mechanistically providing a

237 ollowed by SIRT3-dependent increases in SOD2 mRNA during sustained anchorage-independence.

238 necessary for RBM24-based elevation of Sox2 mRNA half-life.

239 by nsun-1 depletion, translation of specific mRNAs was remodeled leading to reduced production of col

240 ochemistry and live-cell imaging of specific mRNAs, we describe for the first time the subcellular lo

241 These SMN-specific mRNAs are associated with neurogenesis, lipid metabolism

242 , we found a global stabilization of spliced mRNAs upon T cell activation, although the stability of

243 the present study, we evaluated tissue SPP1 mRNA and OPN protein expression as markers of recurrence

244 As and their target mRNAs, facilitating sRNA-mRNA annealing, typically resulting in translation inhib

245 hin infected cells, EBOV downregulates STAT1 mRNA and interferon signaling, and it upregulates putati

246 the two processes that buffers steady-state mRNA levels.

247 nosine is the most abundant and best studied mRNA modification in flowering plants.

248 full-length SARS-CoV-2 genome and subgenomic mRNAs.

249 d in the coding region and reduce the target mRNA by RNase H1 while the mRNA resides in the ribosomes

250 ly, leading to more repression of the target mRNA than expected by independent action at each site.

251 itate base-pairing with trans-encoded target mRNAs.

252 s MARF1 to prevent the decay of MARF1 target mRNAs.

253 s) efficiently inhibit translation of target mRNAs by forming a duplex that sequesters the Shine-Dalg

254 nd that it accelerates degradation of target mRNAs, mediated by three N-terminal Repression Domains (

255 ore, a total of four miRNAs and their target mRNAs were predicted to involve in synthesis of melanin,

256 nally by binding small RNAs and their target mRNAs, facilitating sRNA-mRNA annealing, typically resul

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

258 definitive functions for endogenous targeted mRNAs and their relevance to modulation of in vivo tissu

259 is fundamental to ensuring delivery of Task3 mRNA to distal primary cortical neurites.

260 native lengthening of telomeres (ALT)], TERT mRNA expression by RNA-sequencing, whole-genome/exome se

261 Here we show that mRNA-1273 induces potent neutralizing antibody responses

262 The mRNA and protein expression levels in blood, brain, hear

263 The mRNA expression levels of ST6GAL-I and SOX9 in human gas

264 The mRNA levels of mouse PL genes were robustly decreased in

265 The mRNA-1273 vaccine induced anti-SARS-CoV-2 immune respons

266 ules, and PD-1 expression was studied at the mRNA and protein levels.

267 IKZF3 was unable to upregulate IL-10 at the mRNA or protein level in CD4(+) T cells and did not driv

268 s modulated across the stripe to control the mRNA production rate.

269 n content associated with loss of eIF4E, the mRNA 5'-cap binding protein of the initiation complex an

270 NSP1 binds to 18S ribosomal RNA in the mRNA entry channel of the ribosome and leads to global i

271 elicase Ski2 binds to 80S ribosomes near the mRNA entrance and facilitates 3'->5' exosomal degradatio

272 tions causing nonsense-mediated decay of the mRNA leads to a wide spectrum of clinical phenotypes inc

273 id self-cleavage and subsequent decay of the mRNA.

274 he nucleus where it selectively binds to the mRNA processing protein, heterogeneous nuclear ribonucle

275 Unexpectedly, the mRNA for GATA3 and IL-5 correlated better with mRNA for

276 reduce the target mRNA by RNase H1 while the mRNA resides in the ribosomes.

277 ng cell states during development from their mRNA profiles provides insight into their gene regulator

278 a few hours after inoculation and that their mRNAs are also detectable in roots and pods, which clear

279 ffinity but also the selectivity among these mRNAs.

280 Translation of these mRNAs occurs during early seed germination, even before

281 y, tissue hydroxyproline content, and tissue mRNA expression of fibrosis-associated genes (Ccl11, Il1

282 use of poly-dT primers to reverse transcribe mRNA, followed by linear amplification through in vitro

283 cose, to proteins involved in transcription, mRNA processing, and signaling.

284 ful control of the amounts of transcription, mRNA, and proteins made by key brain genes-stoichiometry

285 c assemblies of proteins and non-translating mRNAs.

286 ation apparatus (composed of ribosome, tRNA, mRNA, and translation factors) and regulates crucial ste

287 find that WIN preexposure blunts the typical mRNA response to cocaine and instead results in alternat

288 Unexpectedly, mRNA and protein expression of the epithelial marker E-c

289 l of inhibiting let-7c interaction with UTRN mRNA and thus upregulating utrophin.

290 validated by in situ hybridization for Vgat mRNA.

291 as key regulators of both cellular and viral mRNA function.

292 for its function in the modulation of viral mRNA processing and viral DNA replication.IMPORTANCE Hum

293 nscripts could generate chimeric human-viral mRNAs with coding potential.

294 n regions, both of which are associated with mRNA expression QTLs.

295 NA for GATA3 and IL-5 correlated better with mRNA for CD30, TNFR2, ICOS, CCR4, and CD200R1 than for C

296 DNAm levels at 39 DMPs were correlated with mRNA expression.

297 mechanisms that balance mRNA synthesis with mRNA decay.

298 ed is influenced by molecular factors within mRNA and protein sequences.

299 ize, the latter phenotype complemented by WT mRNA but not by SSBP1 mutant transcripts.

300 irmed that miR-466o-3p directly targeted WT1 mRNA.