ライフサイエンスコーパス: mRNA transcript

1 roduction of multiple proteins from a single mRNA transcript.

2 of two or more somatic variants on the same mRNA transcript.

3 equence-specific recognition of the targeted mRNA transcript.

4 ne target, IFIT1/ISG56, by destabilizing its mRNA transcript.

5 all copies of miR-200c bound the immobilized mRNA transcript.

6 oRNAs and alternative polyadenylation of the mRNA transcript.

7 trin mRNA splicing and creating an elongated mRNA transcript.

8 thway leading to destabilization of the NOXA mRNA transcript.

9 ed nonsense-mediated decay of the respective mRNA transcript.

10 e with a sequence complementary to the Smad7 mRNA transcript.

11 the predicted effects on splicing of the pre-mRNA transcript.

12 tive splicing of its single gene-encoded pre-mRNA transcript.

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

14 However, they tended to have much longer pre-mRNA transcripts.

15 ibosomes are not uniformly distributed along mRNA transcripts.

16 hundreds to thousands of both noncoding and mRNA transcripts.

17 able change in the relative amounts of viral mRNA transcripts.

18 native polyadenylation to produce at least 8 mRNA transcripts.

19 ative polyadenylation to generate at least 8 mRNA transcripts.

20 resolution method for analysis of 5' ends of mRNA transcripts.

21 with fast translation initiation on nascent mRNA transcripts.

22 maintenance of normal levels of overlapping mRNA transcripts.

23 es simultaneously via the abundance of their mRNA transcripts.

24 ed a global survey of the decay rates of MTB mRNA transcripts.

25 rescued upon overexpression of human C9orf72 mRNA transcripts.

26 use recombinant sclerostin decreased cyp27B1 mRNA transcripts.

27 al capping of RNA polymerase II (Pol II) pre-mRNA transcripts.

28 in the relative abundance of DLL1 and LRIG1 mRNA transcripts.

29 essing small RNAs derived from processing of mRNA transcripts.

30 amounts of IFNgamma, T-bet, and IL-15Ralpha mRNA transcripts.

31 ncing (RNA-Seq) were used to identify CYP3A4 mRNA transcripts.

32 Polyadenylation sites mark the ends of mRNA transcripts.

33 ites allows a single gene to encode multiple mRNA transcripts.

34 ted novel approach for targeted reduction of mRNA transcripts.

35 ted KSPGs (lumican and keratocan), and their mRNA transcripts.

36 iptionally regulate the expression of target mRNA transcripts.

37 ed human immunodeficiency virus type 1 viral mRNA transcripts.

38 tors interact at cis regulatory sites on pre-mRNA transcripts.

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

40 he regulation, initiation, and processing of mRNA transcripts.

41 2 and RARA by reducing m(6)A levels in these mRNA transcripts.

42 nnotated, and now includes the major spliced mRNA transcripts.

43 n to include 10 374 novel lncRNAs and 58 640 mRNA transcripts.

44 rgeting nirK, typical nosZ and atypical nosZ mRNA transcripts.

45 gene expression up to 2-fold at the level of mRNA transcripts.

46 ignaling pathways, proteolysis products, and mRNA transcripts.

47 untranslated regions (UTR) of messenger RNA (mRNA) transcripts.

48 ukin-2(IL-2), IL-4, and IL-10 messenger RNA (mRNA) transcripts.

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

50 ociated with alterations in DNA copy number, mRNA transcript abundance and splicing, and both inter-

51 roviding absolute measurement of single-cell mRNA transcript abundance.

52 ranscripts, which is known to correlate with mRNA transcript abundance.

53 d bead-enhanced detection of three different mRNA transcripts, achieving a dynamic range spanning ove

54 as carried out combining proteomics, qRT-PCR mRNA transcripts analysis, and enzyme activities assessm

55 ike particles (VLPs) package the recombinant mRNA transcript and can be disassembled and reassembled

56 lineage tracing studies, spatially specific mRNA transcript and protein expression, and single-cell

57 expression through stabilisation of the vacA mRNA transcript and that the stabilising effect is of pa

58 li: the number of protein molecules made per mRNA transcript and the number of ribosomes required per

59 2 and CLN3 lead to a significant decrease in mRNA transcripts and a corresponding decrease in protein

60 uplex RNAs recruit argonaute 2 (AGO2) to pre-mRNA transcripts and altered splicing requires AGO2 expr

61 nvironmental variation on correlations among mRNA transcripts and among NMR metabolites.

62 educed expression of Bdnf exon IV-containing mRNA transcripts and BDNF protein in the cerebral cortex

63 CRACM1, -2, and -3 mRNA transcripts and CRACM1 and -2 proteins were detecta

64 ed miR-146a to its multiple predicted target mRNA transcripts and found that miR-146a was predicted t

65 ene regulation, where they act by binding to mRNA transcripts and inhibiting their translation (i.e.

66 When standardized to reference targets, mRNA transcripts and microRNAs can be reliably quantifie

67 RNA surveillance system is active on all pre-mRNA transcripts and modulated by nutrient availability.

68 vels of TGF-beta1, IL-6, IL-23, and IL-1beta mRNA transcripts and of TGF-beta1, IL-6, and IL-1beta pr

69 3H14 modulates pre-mRNA processing of select mRNA transcripts and plays a critical role in regulating

70 elative to B cells, but hnRNPLL binds Ighg2b mRNA transcripts and promotes an increase in levels of t

71 usly that human endogenous retroviral (HERV) mRNA transcripts and protein are found in cells of HIV-1

72 moral artery significantly upregulates mDia1 mRNA transcripts and protein in the injured vessel, part

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

74 tin, leptin receptor (long isoform), and PTH mRNA transcripts and protein were detected in an overlap

75 Piezo1 mRNA transcripts and protein were detected with quantita

76 stimulation leads to destabilization of TNF mRNA transcripts and subsequent failure to produce TNF p

77 -beta1, TGF-beta2, IL-6, IL-23, and IL-1beta mRNA transcripts and TGF-beta1, IL-6, and IL-1beta prote

78 duces transition from short to fully spliced mRNA transcripts and that this transition is blocked by

79 the 3'-untranslated region (UTR) of several mRNA transcripts and the eukaryotic initiation factor 4G

80 AtpA and AtpD, are translated from the same mRNA transcript, and both contain a PPG motif; however,

81 n within the coding region of the associated mRNA transcript, and enhances its translation by relievi

82 tion was observed among DNA copy number, the mRNA transcript, and protein expression of the HER-2 gen

83 IL-1beta, TNF-alpha, and cathepsin S (Ctss) mRNA transcripts, and greater nitrotyrosine and 4-hydrox

84 me sequencing can be used to determine which mRNA transcripts are actively being translated.

85 Some mRNA transcripts are also attenuated through premature t

86 Most human pre-mRNA transcripts are alternatively spliced, but the sign

87 Sema3A mRNA transcripts are expressed at significantly higher l

88 Various non-5-HT(3) receptor mRNA transcripts are expressed in mouse urothelium and e

89 Overall, these results suggest that sperm mRNA transcripts are indicators of low dose toxicant-ind

90 Many of these target mRNA transcripts are involved in regulating processes co

91 Many mRNA transcripts are known to reside in developing axons

92 ies to date have explored whether particular mRNA transcripts are more critical than others in facili

93 Interactions between certain RBPs and mRNA transcripts are notoriously difficult to predict, a

94 The mRNA transcripts are then reverse-transcribed, physicall

95 A) in a surface RNA polymerase reaction; the mRNA transcripts are then translated into proteins by ce

96 icular injury can be detected in sperm using mRNA transcripts as indicators of insult.

97 cused on developing RNA flow cytometry using mRNA transcripts as proxies distinguishing NKG2C from NK

98 antification of both high- and low-abundance mRNA transcripts, as well as micro-RNAs that are not eas

99 polyadenylation to generate full-length B19V mRNA transcripts at levels sufficient to support product

100 ved RNA surveillance mechanism through which mRNA transcripts bearing premature termination codons (P

101 l and can also alter the reading frame in an mRNA transcript because 1,N (6)-erA is incompletely inci

102 precursors encoded in open-reading frames of mRNA transcripts but also cryptic peptides encoded in ap

103 Intron splicing of a nascent mRNA transcript by spliceosome (SPL) is a hallmark of ge

104 t the absolute quantification of single-cell mRNA transcripts by digital, one-step reverse transcript

105 ound to both enhance the binding kinetics of mRNA transcripts by disrupting complex secondary structu

106 esting instability and degradation of mutant mRNA transcripts by the cellular machinery.

107 transglutaminase 1 enzyme (Tg-1) and Muc5AC mRNA transcripts by the ocular surface epithelia.

108 nderstand gene function, the encoding DNA or mRNA transcript can be manipulated and the consequences

109 In this process, different mRNA transcripts can be produced through altered excisio

110 Larger RNAs, such as mRNA transcripts, can be site-specifically labeled if th

111 oduction of noncanonical and cancer-specific mRNA transcripts, can lead to loss-of-function in tumor

112 man patients with ARDS, inflammasome-related mRNA transcripts (CASP1, IL1B, and IL18) were increased

113 Remarkably, the mRNA transcripts commonly reduced by toxic LNA ASOs were

114 ase in IL-1beta, IFN-gamma, MHC II, and Ctss mRNA transcripts compared with young wild-type mice and

115 NAs (ceRNAs) sequester microRNAs to regulate mRNA transcripts containing common microRNA recognition

116 decay is involved in the degradation of CLN1 mRNA transcripts containing the p.R151X mutation in huma

117 cluding endorepellin, were present; however, mRNA transcripts corresponding to regions of domain III

118 re identified with retained introns in their mRNA transcripts, corresponding with a significant reduc

119 gions of interest containing combinations of mRNA transcripts, CpG sites, and SNPs by jointly testing

120 ing to full-length and alternatively spliced mRNA transcripts, decreasing mRNA levels across the life

121 ed Cx43 protein levels due to decreased GJA1 mRNA transcripts dependent upon beta-catenin transcripti

122 report the alternative splicing of the TRPC3 mRNA transcript (designated TRPC3c), resulting in omissi

123 tial expression of a Y-chromosome associated mRNA transcript, Eif2s3y, and the X-linked, X-inactivati

124 -splicing events, resulting in at least nine mRNA transcripts encoding at least 12 functionally diffe

125 cal to generating appropriate levels of B19V mRNA transcripts encoding capsid proteins and small nons

126 Here, we report that alternate mRNA transcripts encoding human ether-a-go-go-related ge

127 Here, we show that mRNA transcripts encoding I(Na) and I(Kr) channels (SCN5

128 Analysis of mRNA transcripts enriched through immunoprecipitation of

129 a more than 10(3)-fold increase in exosomal mRNA transcripts, even from cells with low basal levels

130 nd analyzed the lineage derivation from TFF2 mRNA transcript-expressing (TTE) cells.

131 Microarray analyses of mRNA transcript expression identified a limited number o

132 CagA contributes to the DNA copy change and mRNA transcript expression of the HER-2 gene and, conseq

133 vance of SPAG5 gene copy number aberrations, mRNA transcript expression, and protein expression and a

134 of granzyme B protein but not the levels of mRNA transcript expression.

135 , with global upregulation of immune-related mRNA transcripts following infection and comparatively m

136 the gene fused to a 3' tag that targets the mRNA transcript for degradation by the host nonsense-med

137 ained more intensely and exhibited increased mRNA transcripts for both proteins compared to those in

138 Real-time polymerase chain reaction detected mRNA transcripts for Dra and Slc26a6 in mouse incisor en

139 hown that Type I-III BNSTALG neurons express mRNA transcripts for each of the Kv4 alpha subunits.

140 cription factor, and RORgammat and increased mRNA transcripts for IL-23 receptor (IL-23R) and IL-26,

141 in reaction (scRT-PCR) studies revealed that mRNA transcripts for Kv4.2, Kv4.3, and all four KChIPs w

142 s from psoriasis patients revealed increased mRNA transcripts for several members of this RTK family

143 r lung, as determined by increased levels of mRNA transcripts for the keratinocyte-derived chemokine,

144 CA2 pyramidal neurons express mRNA transcripts for the major PNN component aggrecan, i

145 Additionally, mRNA transcripts for these genes, including a homolog bi

146 We confirmed the presence of mRNA transcripts for two missense alterations, four muta

147 The mRNA transcript from this allele missed the exon 16 and

148 cess that creates translatable mitochondrial mRNA transcripts from cryptogene encoded RNAs and is uni

149 lates the expression of numerous alternative mRNA transcripts from genes involved in synaptic plastic

150 ASXL3 mRNA transcripts from the mutated allele are prone to no

151 injury while simultaneously evaluating sperm mRNA transcripts from the same animals.

152 Drop-seq analyzes mRNA transcripts from thousands of individual cells simu

153 cing generates a diversity of messenger RNA (mRNA) transcripts from a single mRNA precursor and contr

154 FST mRNA transcripts FST 317/344 were also significantly ele

155 We identify the cell cycle-regulated mRNA transcripts genome-wide in the osteosarcoma-derived

156 n of the main open reading frame (ORF) in an mRNA transcript has been reported to be regulated by ups

157 tion of full-length capsid proteins encoding mRNA transcripts, has been suggested as a step that bloc

158 genome-wide studies of alternatively spliced mRNA transcripts have become increasingly important in c

159 Importantly, increased LTC4 S mRNA transcripts identified a subpopulation of EoE patie

160 be associated with reduced expression of BLK mRNA transcript in human B cell lines; however, little i

161 hic factor (BDNF) gene generates a truncated mRNA transcript in naive brain that is suppressed upon c

162 apid, global degradation of host (and viral) mRNA transcripts in a process termed host shutoff.

163 gonaute proteins, and the ability to repress mRNA transcripts in a sequence-specific manner.

164 viously focused on the detection of aberrant mRNA transcripts in a subset of disorders for which RNA

165 idization technique to visualize HIV gag-pol mRNA transcripts in cerebellum and lymph node tissues fr

166 Most pre-mRNA transcripts in eukaryotic cells must undergo splici

167 to examine expression of alternative CYP3A4 mRNA transcripts in hepatocytes in response to developme

168 /= 0.27), negatively correlated with HIV gag mRNA transcripts in HIV-infected NSG-huPBMC brain.

169 Alternative splicing diversifies mRNA transcripts in human cells.

170 sequences mark the intron boundaries of pre-mRNA transcripts in multicellular eukaryotes.

171 dium channel alpha subunits revealed NaV 1.7 mRNA transcripts in nearly all retrogradely labelled col

172 r-1a, -1b, -2a, -2b, -2f, and -2g; and Tg1-1 mRNA transcripts in ocular surface tissues increased in

173 We identify ZC3H14 mRNA transcripts in the human central nervous system, an

174 ry factor (IRF)-7 among the most upregulated mRNA transcripts in the lung.

175 constructs designed to induce expression of mRNA transcripts in trans with respect to the SSA system

176 One approach is to label newly synthesized mRNA transcripts in vivo through the incorporation of mo

177 LTC4 S mRNA transcripts in whole blood and urinary excretion of

178 ctive and precise system to deplete specific mRNA transcripts in zebrafish embryos.

179 criptomics, measures the expression level of mRNAs (transcripts) in a given cell population at a spec

180 a role for MRB1590 in editing mitochondrial mRNA transcripts, in particular the transcript encoding

181 the targeted degradation of stored maternal mRNA transcripts including sirtuin 1 and ubiquitin prote

182 d proinflammatory mediators as well as viral mRNA transcripts, including Tax, HBZ, and Env.

183 s and is required for translation of complex mRNA transcripts, including those encoding key cell-cycl

184 recently described assay, aberrantly spliced mRNA transcripts initiated in the vector A2UCOE sequence

185 ember of the LARP1 interactome is mTOR whose mRNA transcript is stabilized by LARP1.

186 Surprisingly, the pattern of mRNA transcripts is similar to neurons.

187 is processed from the ubiquitous hnRNP K pre-mRNA transcript, is achieved by inhibition of its biogen

188 are potent regulatory elements located in 5' mRNA transcript leaders.

189 bsequent allosteric conformational switch on mRNA transcript length has not yet been investigated.

190 of thermoregulation resulting in lower eftM mRNA transcript level at 37 degrees C compared to 25 deg

191 lation of NnCYP76B6 resulted in reduction of mRNA transcript levels as well as CPT content in compari

192 nCYP76B6 showed a significant enhancement in mRNA transcript levels coincident with enhanced CPT accu

193 hannel, as whole-DRG-protein and single-cell mRNA transcript levels did not change.

194 Quantitative PCR (Q-PCR) measured mRNA transcript levels for several quiescent and fibroti

195 Analyses of mRNA transcript levels from the NAc of mice that self-ad

196 ta1 and FOXM1 expression at both protein and mRNA transcript levels in ERalpha-positive breast cancer

197 mokine receptor 1 [duffy blood group]) whose mRNA transcript levels in plasma exosomes significantly

198 The mRNA transcript levels of each gene were calculated.

199 overexpressions mediated distinct effects on mRNA transcript levels of fibrillar procollagens, their

200 The mRNA transcript levels of five gene targets, including a

201 Indeed, mRNA transcript levels of HOIL-1L were elevated in tumor

202 wild type mice, which coincided with altered mRNA transcript levels of MCP-1, Cx43 and TGFbeta.

203 and SMART-seq, can reveal simultaneously the mRNA transcript levels of thousands of genes in thousand

204 mutase, catalase, and heat shock protein 30) mRNA transcript levels were examined.

205 SERCA2A mRNA transcript levels were reduced in HCM regardless of

206 of WsMYC2 showed significant enhancement of mRNA transcript levels which corroborated well with the

207 urements such as various epigenetic marks or mRNA transcript levels.

208 ion of these glucagon-induced messenger RNA (mRNA) transcript levels.

209 understanding of an important enzyme in the mRNA transcript life cycle and allow functional analogie

210 ncertainties about the complete structure of mRNA transcripts limit the progress of research in this

211 ges to DJ-1 were concomitant with changes in mRNA transcripts mainly involved in catecholamine metabo

212 Different mRNA transcripts may encode functionally distinct protei

213 re, while the C-terminal half encoding viral mRNA transcript modifications consists of a flexible app

214 ls (669 U/mL vs. 106 U/mL, P = 0.01), higher mRNA transcript numbers of thymic stromal lymphopoietin

215 Alternative mRNA transcripts occur in more than 90% of human genes a

216 hine-Dalgarno sequence, but still within the mRNA transcript of gene II.

217 G methylation sites and cis-eQTLs for 302 3'-mRNA transcripts of 288 genes.

218 of predicting the risk for AMR by measuring mRNA transcripts of AMR-associated genes in plasma exoso

219 Sequencing revealed two mRNA transcripts of FAM136A in lymphoblasts from patient

220 Consistent with our in vitro results, mRNA transcripts of IL-4 correlated with CCL17, but not

221 mRNA transcripts of muscle proteolytic (ubiquitin protea

222 mRNA transcripts of subfamily I.2.C catechol 2,3-dioxyge

223 that RNAi reagents designed to suppress the mRNA transcripts of the same gene often produce a spectr

224 idization to examine the distribution of the mRNA transcripts of these genes in the apteronotid telen

225 y score for EoE, p(EoE), based on esophageal mRNA transcript patterns from biopsies of patients with

226 NCAM and ST8SiaII mRNA transcripts peaked by embryonic day (E)9, remained

227 Less than one rpoS mRNA transcript per cell was observed in the middle or b

228 Post-transcriptional processing of mRNA transcripts plays a critical role in establishing t

229 ino antisense oligonucleotide prevented B19V mRNA transcripts polyadenylated at the (pA)d site during

230 he generation of a sufficient number of B19V mRNA transcripts polyadenylated at the distal polyadenyl

231 149 synthetic genetic interactions, and 225 mRNA transcripts (primarily consisting of stress- and nu

232 Post-transcriptional control of mRNA transcript processing by RNA binding proteins (RBPs

233 le, as well as monitoring the number of lacI mRNA transcripts produced in the presence and absence of

234 mRNA transcript profiles based on gp130, SH2D1B, TNFalph

235 mRNA transcript profiles in liver were consistent with d

236 th CTDs and subsequently analyzed esophageal mRNA transcript profiles in patients with EoE with or wi

237 ication and simultaneous host messenger RNA (mRNA) transcript profiling.

238 Assays of mRNA transcripts, protein expression, and subcellular lo

239 se to hypoxic stress and stabilizes the PIM1 mRNA transcript, resulting in PIM1 protein overexpressio

240 ession of gene products via hybridization to mRNA transcripts, resulting in suppression of translatio

241 Using whole genome sequencing of mRNA transcripts (RNA-Seq) and immunoprecipitation-enric

242 allow for counting of the absolute number of mRNA transcripts samples taken from single cells.

243 dicts splice junctions from an arbitrary pre-mRNA transcript sequence, enabling precise prediction of

244 appear to decrease the half-life of the tra mRNA transcript, suggesting that RteR does not bind to t

245 High throughput deep sequencing of mRNA transcripts (termed RNAseq) has been used to study

246 al (NS) gene of influenza A virus encodes an mRNA transcript that is alternatively spliced to express

247 8 (NS) of the influenza virus genome encode mRNA transcripts that are alternatively spliced to expre

248 n by RNA Polymerase II and completion of pre-mRNA transcripts that are dependent on hormone signaling

249 eavage and polyadenylation (ApA) to generate mRNA transcripts that differ in the lengths of their 3'

250 t in E. coli most translation occurs on free mRNA transcripts that have diffused into the ribosome-ri

251 to be RAG-mediated, and are associated with mRNA transcripts that initiate from 3' regions of Notch1

252 region (UTR) truncation of growth-promoting mRNA transcripts that relieves intrinsic microRNA- and A

253 gene expression profiling failed to identify mRNA transcripts that were differentially regulated by t

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

255 proach does not require amplification of the mRNA transcript, thereby allowing for simplified analyse

256 partially complementary sequences on target mRNA transcripts, thereby causing their degradation, dea

257 en microRNAs (miRNAs) and the messenger RNA (mRNA) transcripts they regulate, and thereby often fail

258 s RNA binding proteins are deposited onto an mRNA transcript to modulate post-transcriptional process

259 to recognize active Polymerase II-derived TE mRNA transcripts to both trigger and correctively reesta

260 ition with caffeine was shown to restore CHM mRNA transcripts to near wild-type levels.

261 odons (PTCs) and are predicted to predispose mRNA transcripts to nonsense-mediated decay (NMD).

262 ent strategy for the analysis of full length mRNA transcripts using arrays of silicon photonic micror

263 The expression of multiple IGF1 or Igf1 mRNA transcript variants in human and mouse skeletal mus

264 mRNA transcript variants of the AR gene are expressed in

265 yed higher levels of Abca1, Abcg1, and Pparg mRNA transcripts versus Ager-expressing Ldlr(-/-) mice i

266 Nrf2 was markedly enhanced, the level of its mRNA transcript was barely changed in the fat-1 transgen

267 The mRNA transcript was not significantly reduced in affecte

268 The abundance of viral and cellular mRNA transcripts was profiled using RNASeq and different

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

270 Two types of OsCAF1B mRNA transcript were detected in an inverse expression p

271 Overall 1479 lncRNA transcripts and 1109 mRNA transcripts were aberrantly expressed in 6- and 20-

272 escue assay, and demonstrated that all three mRNA transcripts were able to rescue abcc6a morpholino-i

273 cells, where a 5,000-fold increase in IGFBP5 mRNA transcripts were documented.

274 Although several mRNA transcripts were highly upregulated, an increase at

275 In contrast to GrB, PRF mRNA transcripts were little changed over 5 days of stim

276 a CMV promoter to drive expression of IL-37, mRNA transcripts were not present in colons at the resti

277 ression of COL I and lower expression of OCN mRNA transcripts were noted in the PDL-MSCs compared to

278 Truncated mRNA transcripts were observed in CYP2B11-H2 and CYP2B11

279 ) subsets by using immunohistochemistry, and mRNA transcripts were quantified by using a microarray.

280 of paraffin-embedded tissue was isolated and mRNA transcripts were quantified with real-time polymera

281 In contrast, HPV16 and HPV18 mRNA transcripts were readily identified in primary cerv

282 LncRNA and mRNA transcripts were remarkably different in 20-week-ol

283 Only a few hundred mRNA transcripts were selectively expressed by macrophag

284 the resolution reaction, approximately 1,500 mRNA transcripts were significantly different from place

285 SPRY1 and SPRY2 mRNA transcripts were significantly upregulated in human

286 The alternative mRNA transcripts were validated by either rapid amplific

287 ischer 344 rats identified 128 altered sperm mRNA transcripts when compared to control using linear m

288 ar reprogramming, including the induction of mRNA transcripts which encode anti-inflammatory cytokine

289 on by inhibiting polyadenylation of selected mRNA transcripts, which prevents binding of the ribosome

290 sed the expression of IL-1beta and TNF-alpha mRNA transcripts, while decreasing the frequency of CD45

291 ear the 3' end of a pre-mRNA create multiple mRNA transcripts with different 3' untranslated regions

292 rom two promoters, P1 and P2, to produce two mRNA transcripts with long 5' UTR.

293 ssion, by promoting efficient translation of mRNA transcripts with low 5'UTR GC content.

294 r, flavopiridol, decreases uaRNA and nascent mRNA transcripts with similar kinetics.

295 For example, therapies targeting specific mRNA transcripts with splice-site-directed oligonucleoti

296 ternative polyadenylation (APA) and generate mRNA transcripts with varying lengths, typically of the

297 nse showed modulation of approximately 7,500 mRNA transcripts, with high expression of cytokines that

298 first time, the presence of RSV proteins and mRNA transcripts within BAL and blood neutrophils from i

299 al = 13.7 mug/L) altered the abundance of 26 mRNA transcripts within the liver of exposed pre-metamor

300 RNA targets from three different full length mRNA transcripts yielded a approximately 10 pM LOD with