ライフサイエンスコーパス: mRNA transcript

1 equence-specific recognition of the targeted mRNA transcript.

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

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

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

5 oRNAs and alternative polyadenylation of the mRNA transcript.

6 xon (IE) incorporated in the major erythroid mRNA transcript.

7 on any substrate, despite the presence of an mRNA transcript.

8 tumors, correlating with a reduction in p27 mRNA transcript.

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

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

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

12 2 and RARA by reducing m(6)A levels in these mRNA transcripts.

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

14 with fast translation initiation on nascent mRNA transcripts.

15 maintenance of normal levels of overlapping mRNA transcripts.

16 es simultaneously via the abundance of their mRNA transcripts.

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

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

19 rescued upon overexpression of human C9orf72 mRNA transcripts.

20 use recombinant sclerostin decreased cyp27B1 mRNA transcripts.

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

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

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

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

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

26 Polyadenylation sites mark the ends of mRNA transcripts.

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

28 ted novel approach for targeted reduction of mRNA transcripts.

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

30 iptionally regulate the expression of target mRNA transcripts.

31 ed human immunodeficiency virus type 1 viral mRNA transcripts.

32 argeted block to late synthesis of antiviral mRNA transcripts.

33 els of expression of nociceptor-specific pre-mRNA transcripts.

34 of translation when present in the 5'-UTR of mRNA transcripts.

35 ipts, diverging transcripts, and overlapping mRNA transcripts.

36 events made from constitutively spliced pre-mRNA transcripts.

37 S axons, and identified the presence of >300 mRNA transcripts.

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

39 o be complete and functional and to generate mRNA transcripts.

40 indicated normal pre-mRNA splicing producing mRNA transcripts.

41 ignaling pathways, proteolysis products, and mRNA transcripts.

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

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

44 ibosomes are not uniformly distributed along mRNA transcripts.

45 hundreds to thousands of both noncoding and mRNA transcripts.

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

47 native polyadenylation to produce at least 8 mRNA transcripts.

48 ative polyadenylation to generate at least 8 mRNA transcripts.

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

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

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

52 elongatus PCC 7942 exhibits oscillations in mRNA transcript abundance with 24-h periodicity under co

53 ents of RNA polymerase binding locations and mRNA transcript abundance, 5' sequences and translation

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

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

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

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

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

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

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

61 2 and CLN3 lead to a significant decrease in mRNA transcripts and a corresponding decrease in protein

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

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

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

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

66 wed strong upregulation of c-Met protein and mRNA transcripts and hepatocyte growth factor-stimulated

67 acid receptor-related orphan receptor-gammat mRNA transcripts and increased IL-17A protein and number

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

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

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

71 3H14 modulates pre-mRNA processing of select mRNA transcripts and plays a critical role in regulating

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

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

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

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

76 Piezo1 mRNA transcripts and protein were detected with quantita

77 ning revealed elevated levels of Wnt pathway mRNA transcripts and proteins within MS lesions, indicat

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

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

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

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

82 te for the first time that the 5'UTR of MRP2 mRNA transcripts and the uORF at -105 markedly influence

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

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

85 ntry site (IRES)-dependent, cap-independent, mRNA transcript, and its overexpression was sufficient t

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

87 genes, noncoding RNAs, prevalent leaderless mRNA transcripts, and antisense transcripts.

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

89 Some mRNA transcripts are also attenuated through premature t

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

91 Sema3A mRNA transcripts are expressed at significantly higher l

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

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

94 Many mRNA transcripts are known to reside in developing axons

95 The mRNA transcripts are then reverse-transcribed, physicall

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

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

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 observed that SF2 associates with cyclin D1b mRNA (transcript-b) in minigene analyses and with endoge

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

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

103 Likewise, ablation of PDE8B mRNA transcripts by an shRNA construct potentiates stero

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 Proteins bound to the poly(A) tail of mRNA transcripts, called poly(A)-binding proteins (Pabs)

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 flagellin-deficient strain stimulated fewer mRNA transcripts coding for proinflammatory cytokines in

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

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

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

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

121 By contrast, nociceptor-associated mRNA transcripts (e.g., Nav1.8, P2xr3, and Runx-1) were

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

123 iple promoter sequences resulting in various mRNA transcripts encoding a common protein but differing

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 the unspliced and incompletely spliced viral mRNA transcripts encoding the structural and enzymatic p

128 Analysis of mRNA transcripts enriched through immunoprecipitation of

129 Human IL-23Ralpha (HuIL23Ralpha)-chain mRNA transcripts exist that lack exon 9 ("Delta9"); thes

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

131 is associated with significant loss of ANXA7 mRNA transcript expression (P = 1 x 10(-15); linear regr

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

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

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

135 ANXA7 mRNA transcript expression, dichotomized at the median,

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 We also validated that mRNA transcripts for both VEGF and the gemcitabine metab

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

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

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

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

143 8R and CD69 correlated with severity, as did mRNA transcripts for perforin and granzyme B, but not Fa

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

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

146 ural retina resulted in the amplification of mRNA transcripts for the m1 to m5 mAChR subtypes.

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

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

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

150 ts induces the transcription of a novel HDMX mRNA transcript from the HDMX-P2 promoter.

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

152 and efficiently isolate ribosome-associated mRNA transcripts from any cell type in vivo.

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

154 tibody against HA yields ribosome-associated mRNA transcripts from specific cell types.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 o the upregulation of many broadly expressed mRNA transcripts in dorsal root ganglia.

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

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

174 /= 0.27), negatively correlated with HIV gag mRNA transcripts in HIV-infected NSG-huPBMC brain.

175 Alternative splicing diversifies mRNA transcripts in human cells.

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

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

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

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

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

181 of IL-1beta, IL-6, TNF-alpha, and TGF-beta1 mRNA transcripts in their conjunctival epithelia than di

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

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

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

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

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

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

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

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

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

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

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

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

194 rthern blotting demonstrated that the ebpABC mRNA transcript level was significantly decreased in the

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

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

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

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

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

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

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

202 Mechanical unloading significantly decreased mRNA transcript levels of Beclin-1, autophagy-related ge

203 The mRNA transcript levels of each gene were calculated.

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

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

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

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

208 SERCA2A mRNA transcript levels were reduced in HCM regardless of

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

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

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

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

213 Different mRNA transcripts may encode functionally distinct protei

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

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

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

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

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

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

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

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

222 mRNA transcripts of muscle proteolytic (ubiquitin protea

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

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

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

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

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

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

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

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

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

232 149 synthetic genetic interactions, and 225 mRNA transcripts (primarily consisting of stress- and nu

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

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

235 mRNA transcript profiles based on gp130, SH2D1B, TNFalph

236 mRNA transcript profiles in liver were consistent with d

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

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

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

240 quence, promoter methylation, messenger RNA (mRNA) transcript, protein data for ANXA7 (and EGFR), and

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

242 eutics inhibit mTOR-dependent translation of mRNA transcripts, resulting in blockade of Otub1 express

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

244 'target' gene products via hybridization to mRNA transcripts, resulting in translational blockade or

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

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

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

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

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

250 8 (NS) of the influenza virus genome encode mRNA transcripts that are alternatively spliced to expre

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

252 A search for YGCY motifs in 24 pre-mRNA transcripts that are mis-spliced in DM1 patients re

253 LF2 in a functional screen for B-ALL-derived mRNA transcripts that can substitute for IL3 signaling.

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

255 Measurements of mRNA transcripts that encode ion channel proteins within

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

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

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

259 characterized oligonucleotide substrates and mRNA transcripts, that RNase E can cleave certain RNAs r

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

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

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

263 system with known translationally regulated mRNA transcript thymidylate synthase (TS).

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

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

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

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

268 enerated gene expression profiles for 22 184 mRNA transcripts using RNA derived from peripheral blood

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

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

271 The mRNA transcript was not significantly reduced in affecte

272 ecently, a dataset of 3,404 miRNA-associated mRNA transcripts was identified by immunoprecipitation o

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

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

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

276 Cytokine and chemokine mRNA transcripts were assessed at lymph nodes (LN) and p

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

278 levels of MMP-9 and its regulating cytokine mRNA transcripts were evaluated by semiquantitative real

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

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

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

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

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

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

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

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

287 Sprouty-2 protein and mRNA transcripts were significantly upregulated in human

288 SPRY1 and SPRY2 mRNA transcripts were significantly upregulated in human

289 The alternative mRNA transcripts were validated by either rapid amplific

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

291 ruplex motif is present in the 5'-UTR of the mRNA transcript, where it modulates the efficiency of tr

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

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

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 old increase in the amount of eis leaderless mRNA transcript, with a corresponding increase in protei

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