ライフサイエンスコーパス: mRNA abundance

1 ether accounted for the observed increase in mRNA abundance.

2 ale spatial-temporal profiling of whole-body mRNA abundance.

3 ngth are largely independent from changes in mRNA abundance.

4 y with consequent effects on decay rates and mRNA abundance.

5 in polysome assembly that was independent of mRNA abundance.

6 rrelated with reduced transferrin receptor 1 mRNA abundance.

7 granzyme C protein levels were regulated by mRNA abundance.

8 A, leading to a net increase in steady-state mRNA abundance.

9 ation and down-regulated tumor PRL and Pttg1 mRNA abundance.

10 d possibly responsible for the difference in mRNA abundance.

11 e up-regulation in expression and % relative mRNA abundance.

12 ultiple upstream open reading frames and low mRNA abundance.

13 n levels mirror alterations in corresponding mRNA abundance.

14 0.05), which correlated with increased CHIP mRNA abundance.

15 A levels and coordinately altered amelogenin mRNA abundance.

16 ion and expression levels but not HIF-1alpha mRNA abundance.

17 in OMP-GFP mice had no detectable effect on mRNA abundance.

18 ignals could post-transcriptionally regulate mRNA abundance.

19 s are maintained constant despite changes in mRNA abundance.

20 a one-color or a two-color design to measure mRNA abundance.

21 for the arachidonic acid inhibition of G6PD mRNA abundance.

22 so significantly reduced VEGFR-2 protein and mRNA abundance.

23 uctions in both translational efficiency and mRNA abundance.

24 a regulatory mechanism beyond the control of mRNA abundance.

25 e, but negatively correlated with 11betaHSD1 mRNA abundance.

26 ler changes in protein abundance compared to mRNA abundance.

27 redict functional GVs that alter splicing or mRNA abundance.

28 per mRNA molecule correlates positively with mRNA abundance.

29 acteria, driving genome-wide oscillations in mRNA abundance.

30 al mechanism of A-to-I editing in regulating mRNA abundance.

31 ur earlier, but had no significant effect on mRNA abundance.

32 mechanism of editing-dependent regulation of mRNA abundance.

33 ription termination site) was independent of mRNA abundance.

34 to changes in binding levels as measured by mRNA abundance.

35 e bodies irrespective of their corresponding mRNA abundance.

36 ciated with MYCN gene amplification and MYCN mRNA abundance.

37 ent evolutionary conservation of protein and mRNA abundances.

38 8), and used microarray analysis to quantify mRNA abundances.

39 tes has been hindered by their extremely low mRNA abundance(14-16), lack of mRNA polyadenylation and

40 und to closely match the temporal changes in mRNA abundance; 22% of genes that increased expression d

41 Differences in global mRNA abundance across this developmental window were est

42 This genome-wide single-cell map of mRNA abundance, alongside the well-studied life history

43 DNA replication from histone messenger RNA (mRNA) abundance, altering the efficiency of replication

44 a significant positive correlation with AQP2 mRNA abundance among mpkCCD subclones (Ets1), and 2 show

45 hment yielded a 3-fold increase in Wolbachia mRNA abundance and a concomitant 3.3-fold increase in th

46 hibition by fructose is specific because the mRNA abundance and activity of the fructose transporter

47 PTBP1 controls mRNA abundance and alternative splicing of important cel

48 d "m(6)A-switch", affects transcriptome-wide mRNA abundance and alternative splicing.

49 vels using standard conditions regardless of mRNA abundance and assay type, thereby increasing throug

50 c-Jun increased c-Src mRNA abundance and c-Src promoter activity involving an

51 ve trait loci (eQTL) regulating variation in mRNA abundance and determined the mode of gene action an

52 liced beta-globin construct has no effect on mRNA abundance and does not affect localization.

53 es of genic H3K79 methylation correlate with mRNA abundance and dynamically respond to changes in gen

54 Testosterone increased AT1aR mRNA abundance and hydrogen peroxide generation in cultu

55 We studied the correlation structure of mRNA abundance and identified 105 co-expression gene mod

56 To more accurately represent gradations in mRNA abundance and identify all genes expressed in each

57 Similarly, increased CCK-2 receptor mRNA abundance and increased 125I-gastrin binding was de

58 terleukin-6 (IL-6) increases PHB protein and mRNA abundance and induces PHB promoter activation.

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

60 th PDE3i pre-cardiac transplantation, PDE3A1 mRNA abundance and microsomal PDE3 enzyme activity were

61 en aged 18-89 yr demonstrated that mtDNA and mRNA abundance and mitochondrial ATP production all decl

62 miR153/miR27a/miR142-5p/miR144 affected Nrf2 mRNA abundance and nucleo-cytoplasmic concentration of N

63 m that Caprin-2 over-expression enhances AVP mRNA abundance and poly(A) tail length.

64 ed with neuronal maturation, correlated with mRNA abundance and potentially influenced miRNA binding

65 inistration increased abdominal aortic AT1aR mRNA abundance and promoted a striking increase in AngII

66 imulus increased GluR2 (also known as Gria2) mRNA abundance and promoted synaptic incorporation of Gl

67 sed the repressive effect of IL-17 on CXCL10 mRNA abundance and promoter activity and also reversed t

68 In this study, we evaluated APOBEC2 mRNA abundance and protein expression and the results in

69 phosphoenolpyruvate carboxykinase and G6Pase mRNA abundance and raised the blood glucose level.

70 -/-) mice showed a <2-fold increase in Cox-2 mRNA abundance and reduced prostaglandin E(2) content co

71 infection causes significant changes in host mRNA abundance and regulation of several cellular biolog

72 lin-41), we observed only modest changes in mRNA abundance and ribosome loading.

73 as associated with decreases in both overall mRNA abundance and ribosome loading; however, these chan

74 fferential translation efficiency using both mRNA abundance and ribosome occupancy.

75 ontrast, we observed that bone marrow CXCL12 mRNA abundance and specific CXCL12 levels are sharply re

76 s between CELFs and MBNLs in control of both mRNA abundance and splicing appear to have evolved to en

77 For the major IGF components, we assessed mRNA abundance and total protein levels.

78 Measuring IL-10 mRNA abundance and transfection with an IL-10 promoter-l

79 ulatory divergence to species differences in mRNA abundance and translation efficiency.

80 eraction with TTP to changes at the level of mRNA abundance and translation in a transcriptome-wide m

81 Global analysis of cellular mRNA abundance and translation indicates that this is an

82 ta with previous measurements of protein and mRNA abundance and translation rate, we provide evidence

83 ess the relative contributions of changes in mRNA abundance and translation to regulatory evolution.

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

85 , termed the eIF5A regulon, at the levels of mRNA abundance and translation.

86 The mRNA abundance and up-regulation in expression of ABCG2

87 samples were removed for estimation of host mRNA abundance and viral load.

88 stress and that photon flux correlated with mRNA abundance and, therefore, bioluminescence provided

89 nal gels, as well as known correlations with mRNA abundances and codon bias, providing absolute prote

90 We measured messenger RNA (mRNA) abundance and protein production through the yeast

91 nted CYP17A1 and CYP11A1 gene transcription, mRNA abundance, and androgen biosynthesis.

92 pletion by siRNA resulted in decreased INTS6 mRNA abundance, and decreased association of CPSF and Cs

93 AhR and IRS2 (insulin receptor substrate 2) mRNA abundance, and PCB-77 concentrations were quantifie

94 Associations between DNA polymorphisms and mRNA abundance are a natural target of genetic investiga

95 yclohexamide suggest that MGP, OPN, and VCAF mRNA abundance are controlled at different and multiple

96 In contrast, few changes in mRNA abundance are observed, indicating that regulation

97 We show that TC and TAC mRNA abundances are divergently associated with clinical

98 correlation (P = 0.0006) between reduced ATM mRNA abundance, as measured by real-time RT-PCR, and abe

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

100 eight, but increased UCP2, GR and 11betaHSD1 mRNA abundance at every sampling age.

101 a general process that maintains appropriate mRNA abundance at the posttranscriptional level.

102 Differences in mRNA abundance between exponentially growing and station

103 sumption of gene expression analysis is that mRNA abundances broadly correlate with protein abundance

104 sults from tethering assays: the decrease in mRNA abundance brought about by tethering siRNA-resistan

105 on in M3 GAS restored the regulation of grab mRNA abundance but did not alter capsule mRNA levels.

106 erred gene-dose-dependent increases in SCN5A mRNA abundance but reduced sodium channel protein abunda

107 vely correlated with UCP2, GR and 11betaHSD2 mRNA abundance, but negatively correlated with 11betaHSD

108 miR-519 did not alter HuR mRNA abundance, but reduced HuR biosynthesis, as determi

109 Allergen challenge reduced lung cav1 mRNA abundance by 40%, cav1 protein by 30%, and the numb

110 promoter the deletion of which reduced rivR mRNA abundance by 70%.

111 he Ras effector Akt is known to regulate p27 mRNA abundance by phosphorylating and inactivating the F

112 Changes in NaPi-2b mRNA abundance by sugars were accompanied by similar cha

113 Zinc supplementation increased MT mRNA abundance by up to 2-fold in RNA from leukocyte sub

114 together, our results support a concept that mRNA abundance can be modulated through altering ratios

115 together, our results support a concept that mRNA abundance can be modulated through altering ratios

116 etected based on relevant predictors such as mRNA abundance, cellular role, molecular weight, sequenc

117 Globally, mRNA abundance changes explain only ~10% of protein abun

118 tein production is reflected in commensurate mRNA abundance, comparable synergy in IL-1beta protein p

119 adenosine methylation, and increased ghrelin mRNA abundance compared with TT subjects.

120 profiling technologies can generally produce mRNA abundance data for all genes in a genome.

121 integrating barley genotypic, phenotypic and mRNA abundance data sets directly within GeneNetwork's a

122 Within 4 days, bacterial mRNA abundance declined >98%, indicating rapid killing.

123 reases upon Pseudomonas infection, the SINA3 mRNA abundance decreases in response to Pseudomonas infe

124 Global mRNA abundance depends on the balance of synthesis and d

125 te exhaustively informing about steady-state mRNA abundance, DNA microarrays have been used with limi

126 Marked up-regulation and/or % relative mRNA abundance during lactation were observed for genes

127 educes to identifying biological quantities (mRNA abundance, enzyme concentrations, etc.) which are d

128 Such approaches rely on the assumption that mRNA abundance estimates from RNA-seq are reliable estim

129 erences contribute to overall uncertainty in mRNA abundance estimates.

130 it the same experimental data on single-cell mRNA abundance even though they have qualitatively diffe

131 ular combined treatments greatly compromised mRNA abundance fidelity.

132 mRNA abundance for 20 of the 21 genes in the interval wa

133 PCR was used to quantify changes in relative mRNA abundance for 333 genes that responded to ABA, NaCl

134 hypothalamus (HYP) were dissected; relative mRNA abundance for 5-HT(B), 5-HT(A), 5-HT(B), and D rece

135 R3-dependent increases in human keratinocyte mRNA abundance for ABCA12 (ATP-binding cassette, sub-fam

136 weaned animals, a significant suppression of mRNA abundance for carboxypeptidase E, 14-3-3 protein an

137 Altered mRNA abundance for genes associated with glucose and lip

138 nes, increased rRNA abundance, and decreased mRNA abundance for genes of methanogenesis.

139 onstrates hepatocyte-specific differences in mRNA abundance for numerous genes between BALB/cByJ and

140 eucine limitation also resulted in increased mRNA abundance for ribosomal protein genes, increased rR

141 In this study, we compared levels of mRNA abundance for several cluster designation (CD) gene

142 Quantitative RT-PCR demonstrated reduced mRNA abundance for the antiapoptotic factors BCL-2, IAP2

143 B and perforin, but only minimal changes in mRNA abundance for these genes.

144 Increases in RNA polymerase II binding and mRNA abundances for Aqp2 far outstripped corresponding m

145 at cells at the top of the biofilms had high mRNA abundances for genes involved in general metabolic

146 antitative reverse transcription-PCR data on mRNA abundance from 171 genes were collected and analyze

147 High-throughput measurements of mRNA abundances from microarrays involve several stages

148 e primarily responsible for the shape of the mRNA abundance gradient in parainfluenza virus 3, wherea

149 We found that the mRNA abundance gradients differed significantly between

150 Measurements of mRNA abundance have given evidence that ES cells express

151 orter NKCC2/BSC1 protein abundances or UT-A1 mRNA abundance in any of the groups.

152 ted trait that correlates strongly with CMG2 mRNA abundance in cells of each ethnic/geographical grou

153 nals are major determinants of overall Kv1.4 mRNA abundance in cells.

154 fluorescence is directly proportional to GFP mRNA abundance in cells.

155 Here we quantify genome-wide mRNA abundance in each cell of the Caenorhabditis elegan

156 those genes that show increased or decreased mRNA abundance in females following a blood meal, and th

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

158 uvant therapy, we examined global changes in mRNA abundance in HeLa cells after CPT treatment using A

159 how that TNF-alpha decreased PHB protein and mRNA abundance in intestinal epithelial cells in vitro a

160 eotide delivery system capable of regulating mRNA abundance in live human cells.

161 Furthermore, MNK controlled TNF mRNA abundance in MDDC and MDM upon NOD1 triggering.

162 Examination of mRNA abundance in methanol-grown Delta hdrA1C1B1 strains

163 d detained introns in OGT and OGA to control mRNA abundance in order to buffer O-GlcNAc changes.

164 DGAT1 and DGTT1 also show increased mRNA abundance in other TAG-accumulating conditions (min

165 Expression studies revealed Eap1 mRNA abundance in peri-pubertal mouse hypothalamus.

166 nous miRNA by detecting shifts in individual mRNA abundance in polyribosome profiles following miRNA

167 We present here a global study of changes in mRNA abundance in response to hydrogen availability for

168 taneously measure biochemical activities and mRNA abundance in single cells to understand the heterog

169 f nonmyeloid lineage, TcdB increased SLC11A1 mRNA abundance in such cells through the actions of the

170 an essential step in gene expression to set mRNA abundance in the cytoplasm.

171 icroarrays were used to examine variation in mRNA abundance in the differentiating xylem of a E. gran

172 nd increased pyruvate dehydrogenase kinase 4 mRNA abundance in the heart, EDL and soleus.

173 mber of T. cruzi mRNAs that is important for mRNA abundance in the intracellular amastigote stage of

174 n has long-term consequences for UCP2 and GR mRNA abundance in the lung irrespective of its timing.

175 titative PCR demonstrated an increase in FAK mRNA abundance in the N-MYC-amplified IMR-32 compared wi

176 (Arda) transcripts, which showed reciprocal mRNA abundance in wild-type and mutant samples.

177 e used to quantify changes in their relative mRNA abundances in three specific tuber tissues (meriste

178 Accordingly, we quantified transcript (mRNA) abundance in seven silk gland types and three non-

179 E4, shows a dramatic increase in expression (mRNA abundance) in the hydEF-1 mutant during anaerobiosi

180 mic cap methylation was also associated with mRNA abundance increases for a number of transcription,

181 n contrast to our previous finding that NAC1 mRNA abundance increases upon Pseudomonas infection, the

182 B-RAF regulates p27(Kip1) mRNA abundance independently of cyclin D1.

183 ying T cell quiescence and suggests that low mRNA abundance is a crucial feature for maintaining quie

184 cteristic (ROC) analysis revealed that MACC1 mRNA abundance is a good indicator of metastatic recurre

185 ndicate that miR393j-3p regulation of ENOD93 mRNA abundance is a key control point for soybean nodule

186 MCAM mRNA abundance is also increased by ET-1 stimulation, th

187 or more modes of dosage compensation, where mRNA abundance is decreased in response to higher dosage

188 of Alzheimer's disease with age and gender."mRNA abundance is determined by the rates of transcripti

189 TTR mRNA abundance is greatly increased in cultured cortical

190 S1P1 mRNA abundance is higher in ASCs isolated from blood com

191 Much work has shown that mRNA abundance is highly variable between closely relate

192 Microarray profiling of mRNA abundance is often ill suited for temporal-spatial

193 ls of lignin-related genes showed that their mRNA abundance is regulated by two genetic loci, demonst

194 qRT-PCR analyses revealed that GPC1 mRNA abundance is regulated coordinately with PC biosynt

195 restriction also increased NKCC1 protein and mRNA abundance, it did not lead to its elevated activity

196 nd no significant changes in either of their mRNA abundance levels comparing conditional knock-out mi

197 SVD uncovers in the mRNA abundance levels data matrix of genes x arrays, i.e

198 els the measured data, where the profiles of mRNA abundance levels of most genes as well as the distr

199 In retrospect, however, steady-state mRNA abundance levels were a poor substitute for TF acti

200 fferentiation, single-UTR genes change their mRNA abundance levels, while multi-UTR genes mostly chan

201 expression, we observe wild-type amelogenin mRNA abundance levels.

202 xpression of the PTEN 3' UTR enhanced PTENP1 mRNA abundance limiting tumor cell proliferation, provid

203 After removing genes in the plateau region, mRNA abundance, main cellular functional categories and

204 potheses about how component traits, such as mRNA abundance, may interact to condition more complex b

205 nces from >2,000 human genes on steady-state mRNA abundance, mRNA stability and protein production.

206 ned with time-course analysis to measure the mRNA-abundance, mRNA-translation rate and protein expres

207 as OGD stimulated robust increases in PGHS-2 mRNA abundance, neither oxygen nor glucose deprivation a

208 thogen invasion, we analyzed in parallel the mRNA abundance of 22,792 host genes throughout 36 (genot

209 While associations between the mRNA abundance of a gene and its proximal SNPs (cis-eQTL

210 ce protein abundance and loci that influence mRNA abundance of a given gene.

211 lanta expression of 10A06 or SPDS2 increased mRNA abundance of a set of antioxidant genes upon nemato

212 In addition, the mRNA abundance of all the AtDi19-related gene family mem

213 IL-8 increased the mRNA abundance of both mucin genes in two human respirat

214 DNA microarray hybridization to compare the mRNA abundance of C. elegans genes in wild-type animals

215 Our results suggest that instantaneous mRNA abundance of canonical markers is tenuously linked

216 In addition, high NaCl decreases mRNA abundance of GDPD5 via an increase of its degradati

217 effects of RAC, sex, and social rank on the mRNA abundance of genes encoding serotonin and dopamine

218 ve been used to study the difference between mRNA abundance of genes under different conditions.

219 of miR-22 showed significant effects on the mRNA abundance of Irf8, which encodes the transcription

220 of top single nucleotide polymorphisms with mRNA abundance of nearby genes.

221 ream region of the gene for their effects on mRNA abundance of NRG1 types I-IV in human postmortem hi

222 ith twice as much mitochondrial DNA, and the mRNA abundance of Pgc1alpha and Erralpha increased by 10

223 Suppressed mRNA abundance of phosphoenolpyruvate carboxykinase and

224 e to light signals in part by regulating the mRNA abundance of SbTB1.

225 ed salicylic acid levels, and changes in the mRNA abundance of senescence- and defense-associated gen

226 Protein and mRNA abundance of several angiogenic factors including C

227 There was significantly lower mRNA abundance of sonic hedgehog pathway elements at P0

228 mRNA abundance of the 14 NRPS identified in the A. fumig

229 to develop gold-standards for estimating the mRNA abundance of the discordant genes reported here.

230 c-Jun inhibits high NaCl-induced increase of mRNA abundance of the TonEBP/OREBP target genes AR and B

231 The mRNA abundance of the two ace genes was significantly re

232 esenchymal phenotypes function by regulating mRNA abundance of their respective genes.

233 mRNA synthesis from decay, cells control the mRNA abundance of those gene regulons that characterize

234 sol and triiodothyronine (T3) influenced the mRNA abundance of UCP2, glucocorticoid receptor (GR) and

235 0.045) were also observed between placental mRNA abundance of vitamin D metabolic components and cir

236 log plots between 1.5 and 280 mueeq/L-hr for mRNA abundances of 10(7) to 10(10) transcripts/mL (0.07-

237 itude of template concentration, and average mRNA abundances of approximately 0.01 molecule per cell

238 The mRNA abundances of genes coding for components involved

239 Comparison of the mRNA abundances of these genes in wild-type, Deltahns, D

240 n D metabolites and placental messenger RNA (mRNA) abundance of vitamin D metabolic pathway component

241 We evaluated the pattern of mRNA abundance over the first 48 h of spore development

242 (P < 0.0001); and reduced their expression (mRNA abundance) (P < 0.005).

243 The growth phenotypes and mRNA abundance patterns of the mutant strains contradict

244 Defensin mRNA abundance, peptide expression and processing are di

245 piratory deficiency caused increases in CHO1 mRNA abundance, phosphatidylserine synthase protein and

246 Changes in mRNA abundance play a dominant role in determining most

247 Peak induction of hepatic IL-6 mRNA abundance post PH was attenuated >80% in heterozygo

248 cancer cells and personalized patient cancer mRNA abundance profile from a mixed tumour profile.

249 ction of cancer cells and the patient cancer mRNA abundance profile from tumour samples in four cance

250 tion with RNA-Sequencing-based developmental mRNA-abundance profiles and neuropathy disease genes ill

251 recovery gene downregulation (RRGD), whereby mRNA abundance rapidly decreases promoting transcriptome

252 ions showed strong cis- and trans-effects on mRNA abundance, relatively few of these extend to the pr

253 Bidirectional regulation of dendritic mRNA abundance represents a potentially powerful means t

254 nisms likely make important contributions to mRNA abundance rhythms.

255 results in a significant increase in target mRNA abundance, ribosome occupancy and protein output fr

256 ts expressing 10A06 exhibited elevated SPDS2 mRNA abundance, significantly higher spermidine content,

257 ergence often buffers species differences in mRNA abundance, such that ribosome occupancy is more con

258 ive correlation between m(6)A deposition and mRNA abundance, suggesting a regulatory role of m(6)A in

259 ion of DNA methyltransferases decreased BCL6 mRNA abundance, suggesting a role for these methylated C

260 ational divergence acts to buffer changes in mRNA abundance, suggesting a widespread role for stabili

261 s correlate positively with IL-2 protein and mRNA abundance, suggesting that CCR5 affects IL-2 gene r

262 e-induced increases in glucose-6-phosphatase mRNA abundance, suggesting that it did not prevent fruct

263 ory changes play a greater role in divergent mRNA abundance than in divergent translation efficiency.

264 uninvestigated genes exhibiting profiles of mRNA abundance that varied markedly under daily and cons

265 ethylated H3K4me3 for the regulation of OST1 mRNA abundance, thereby modulating the dehydration stres

266 enesis of microRNAs (miRNAs), which regulate mRNA abundance through posttranscriptional silencing, co

267 While trypanosomes regulate mRNA abundance to effect the major changes accompanying

268 ontent (and/or probably function) influences mRNA abundance, translation, and alternative splicing, w

269 First, genome-wide measurements of mRNA abundance, translation, and ribosome occupancy afte

270 cations in regulating transcription rate and mRNA abundance under stress is beginning to emerge.

271 exhibited only slight decreases in relative mRNA abundances under metal-reducing conditions.

272 polymorphism microarrays and quantified the mRNA abundance using genome-wide expression arrays and m

273 Protein and mRNA abundance was analyzed by means of immunoblotting,

274 s, H3K36me3, SETD2 copy number (CN) or SETD2 mRNA abundance was assessed in two independent cohorts:

275 IFN-gamma mRNA abundance was associated with lower furin mRNA leve

276 cells survive in, and exit from this state, mRNA abundance was examined using oligonucleotide-based

277 d to predict the timing of gene function, as mRNA abundance was found to correlate with the order in

278 Under all conditions, SOS1 mRNA abundance was higher in Thellungiella than in Arabi

279 ver linc-HOXA1 RNA abundance was high, Hoxa1 mRNA abundance was low and vice versa.

280 see text] females administered PCB-77, IRS2 mRNA abundance was lower in adipose tissue compared with

281 Increased AT1aR mRNA abundance was maintained during progressive passagi

282 dinal two-class microarray analysis in which mRNA abundance was measured as a function of time in cel

283 ted to the heart, because no increase in TRH mRNA abundance was observed in the hypothalamus, kidney,

284 In vivo, COX2 mRNA abundance was reduced in the liver and spleen of Ma

285 ptimized Rs-rbcLS operon, the messenger RNA (mRNA) abundance was ~25% of rbcL transcript and RsRubisc

286 Using DNA microarrays to estimate mRNA abundance, we found a number of distinguishable pat

287 By quantifying metabolic fluxes and global mRNA abundance, we investigated the genetic and metaboli

288 though effects on translation initiation and mRNA abundance were also observed.

289 s suggested more than half of the changes in mRNA abundance were due to RNA stability, we found a sma

290 DNA methylation and mRNA abundance were quantified for genes encoding compon

291 UCP2 and GR mRNA abundance were significantly lower in AX fetuses co

292 ssion in LY6D(+) CLPs severely affects FOXO1 mRNA abundance, whereas depletion of FOXO1 activity in L

293 rnative splicing but also markedly increased mRNA abundance, which we show resulted from sharply elev

294 n due to a global increase in messenger RNA (mRNA) abundance, which reduces the threshold to activati

295 , two of which (T1 and T2) can explain flp-1 mRNA abundance, while the third (T3) is at the end of th

296 g for protein quantification and RNA-seq for mRNA abundance will provide a template for future mRNA-p

297 RAGE, which rapidly provides measurements of mRNA abundance with extremely high sensitivity using flu

298 n abundance (47% in E. coli) is explained by mRNA abundance, with the number of proteins per mRNA log

299 ctivity and a significant decrease in PIP2;7 mRNA abundance within 2 h.

300 sised that inter-individual variation in Sry mRNA-abundance would result in a spectrum of phenotypes