ライフサイエンスコーパス: mRNA abundance

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

2 in polysome assembly that was independent of mRNA abundance.

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

4 rrelated with reduced transferrin receptor 1 mRNA abundance.

5 granzyme C protein levels were regulated by mRNA abundance.

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

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

8 d possibly responsible for the difference in mRNA abundance.

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

10 ultiple upstream open reading frames and low mRNA abundance.

11 n levels mirror alterations in corresponding mRNA abundance.

12 0.05), which correlated with increased CHIP mRNA abundance.

13 A levels and coordinately altered amelogenin mRNA abundance.

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

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

16 ignals could post-transcriptionally regulate mRNA abundance.

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

18 for the arachidonic acid inhibition of G6PD mRNA abundance.

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

20 uctions in both translational efficiency and mRNA abundance.

21 a regulatory mechanism beyond the control of mRNA abundance.

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

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

24 ination of genetic variation at the level of mRNA abundance.

25 onmethylated cytosines had no effect on IGF2 mRNA abundance.

26 wever, neither HDL nor apoA-I increased eNOS mRNA abundance.

27 regulation based on analysis of steady-state mRNA abundance.

28 type PAP in yeast leads to a decrease in PAP mRNA abundance.

29 ription termination site) was independent of mRNA abundance.

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

31 e bodies irrespective of their corresponding mRNA abundance.

32 ciated with MYCN gene amplification and MYCN mRNA abundance.

33 ether accounted for the observed increase in mRNA abundance.

34 per mRNA molecule correlates positively with mRNA abundance.

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

36 ngth are largely independent from changes in mRNA abundance.

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

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

39 imensions for mapping phenotypes composed of mRNA abundances.

40 ent evolutionary conservation of protein and mRNA abundances.

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

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

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

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

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

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

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

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 by inositol is not mediated at the level of mRNA abundance and does not require the INO2-INO4-OPI1 r

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

55 stimated at the genome scale by using global mRNA abundance and half-life data, revealing genes subje

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 barley lines we generated novel phenotypic, mRNA abundance and SNP-based genotyping data sets, added

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 ngle genome-wide set of absolute or relative mRNA abundances and (ii) the DNA sequence of the regulat

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

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

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

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

96 In contrast, Rubisco small subunit mRNA abundance appears to be transcriptionally up-regula

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

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

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

100 We mapped Pdi mRNA abundance as a quantitative trait in 108 (B6 x BTBR

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

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

103 Differences in mRNA abundance between exponentially growing and station

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

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

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

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

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

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

110 T-1 concentration and ET-1, ET(A), and ET(B) mRNA abundance, but the differences with untreated diabe

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

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

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

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

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

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

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

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

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

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

121 s, this increase was not due to elevated p53 mRNA abundance, cytoplasmic export of p53 mRNA, or UVC-t

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

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

124 From the analysis of the mRNA abundance data, our method does not bias towards pr

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

126 Muscle IGF-I, but not GHR, mRNA abundance decreased with increasing gestational age

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

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

129 Furthermore, analyses of mRNA abundance distributions indicate limitations in the

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

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

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

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

134 ular combined treatments greatly compromised mRNA abundance fidelity.

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

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

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

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

139 Altered mRNA abundance for genes associated with glucose and lip

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

141 echanism involves a coordinated reduction in mRNA abundance for key enzymes involved in the biochemic

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

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

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

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

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

147 ection assays showed that ischemia increased mRNA abundance for TNF-alpha and inducible nitric oxide

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

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

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

151 aise variation in taurine transporter (TauT) mRNA abundance from cells maintained in hyperosmotic med

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

167 cluded in the cohort of genes with increased mRNA abundance in PCOS theca cells were aldehyde dehydro

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

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

170 criptional silencing of the PG gene, with PG mRNA abundance in ripe fruit reduced by 98% or more.

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

172 t a quantitative description of variation in mRNA abundance in terms of GCA (general combining abilit

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

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

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

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

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

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

179 ightened in VHL(+) cells, given that (i) p53 mRNA abundance in VHL(+) and VHL(-) cells was comparable

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

181 iciency and supplementation altered specific mRNA abundances in a manner detectable by differential d

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

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

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

185 We found that IRF-1 mRNA abundance increased far more than transcription rat

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

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

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

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

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

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

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

193 TTR mRNA abundance is greatly increased in cultured cortical

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

195 In the first experiment, we found that AVT mRNA abundance is higher in sex-changing females that at

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

197 Although the reduction in FLC mRNA abundance is likely to contribute to the esd4 pheno

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

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

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

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

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

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

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

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

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

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

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

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

210 The pattern of the 2.0-kb promoter transgene mRNA abundance most closely mimicked that of the endogen

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

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

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

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

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

216 ave shown that the circadian clock regulates mRNA abundance of about 10% of the transcriptome in plan

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

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

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

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

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

222 Changes in mRNA abundance of genes characteristic of oxidative stre

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

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

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

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

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

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

229 Suppressed mRNA abundance of phosphoenolpyruvate carboxykinase and

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

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

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

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

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

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

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

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

238 0.045) were also observed between placental mRNA abundance of vitamin D metabolic components and cir

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

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

241 The mRNA abundances of genes coding for components involved

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

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

244 nt terminal-phase males had no effect on AVT mRNA abundance or any behavior we measured but did incre

245 ctomized females had no effect on either AVT mRNA abundance or AVT-IR soma size compared with control

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

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

248 cin-induced diabetes cause decreases in PDP2 mRNA abundance, PDP2 protein amount, and PDP activity in

249 Defensin mRNA abundance, peptide expression and processing are di

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

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

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

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

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

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

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

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

258 were also organized relative to time of day mRNA abundance, revealing groups accumulating peak mRNA

259 nisms likely make important contributions to mRNA abundance rhythms.

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

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

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

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

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

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

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

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

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

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

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

271 y analysis has provided opportunities to map mRNA abundance to quantitative trait loci (QTL) througho

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

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

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

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

276 and found a dose-dependent decrease in NK3r-mRNA abundance via Northern blotting.

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

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

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

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

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

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

283 Increased AT1aR mRNA abundance was maintained during progressive passagi

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

285 PGS1 mRNA abundance was not decreased in ino2 or ino4 mutants

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

287 c increase in IRF-1 transcription, yet IRF-1 mRNA abundance was similar in uninfected and infected ce

288 The eNOS messenger ribonucleic acid (mRNA) abundance was measured using real-time quantitativ

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

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

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

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

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

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

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

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

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

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

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

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