ライフサイエンスコーパス: transcript level

1 CSF3, LOC100152038, and LOC100736831 at the transcript level.

2 that was not proportional to the cAMP sponge transcript level.

3 ulted in a substantial reduction in reporter transcript level.

4 gulated at the protein level, but not at the transcript level.

5 l gene expression analysis at the individual transcript level.

6 nocytes start to resemble Kupffer cells on a transcript level.

7 h m(6)A methylation extent compared to their transcript level.

8 d most commonly in ecDNA, thereby increasing transcript level.

9 els of H2A.Z in the gene body correlate with transcript levels.

10 duplicated segments exhibit dosage-dependent transcript levels.

11 in Kinase 1 (SnRK1) despite unaffected SnRK1 transcript levels.

12 n, which culminate in changes in accumulated transcript levels.

13 -mediated decay factor, UPF1, rescues ATP5G1 transcript levels.

14 ein biogenesis to increase relative to their transcript levels.

15 l embryos showed reduced Smad1 but not Smad5 transcript levels.

16 ans is higher than that showing differential transcript levels.

17 FOXK1 protein levels and a reduction of p21 transcript levels.

18 resence of a peptide substrate increase gene transcript levels.

19 hormone profiles, and RARbeta2 and RARgamma2 transcript levels.

20 hip between peak translation states and peak transcript levels.

21 the gene borders are the main regulators of transcript levels.

22 interact with the MOR promoter and modulate transcript levels.

23 nts such as various epigenetic marks or mRNA transcript levels.

24 1282X cells despite the presence of adequate transcript levels.

25 largely regulated at the translation but not transcript levels.

26 ential mechanisms for age-related changes in transcript levels.

27 istically with drl1 mutants and reduced drl2 transcript levels.

28 Small interfering RNA was used to decrease transcript levels.

29 genotypes were associated with high IL22RA2 transcripts levels.

30 Whereas BRCA1 is downregulated at transcripts levels, 53BP1 loss is caused by activation o

31 Many methods for transcript-level abundance estimation reduce the computa

32 P2A19 and CYP2C36) genes displayed different transcript levels across treated versus UNT.

33 s lacking Ulp2 display a twofold increase in transcript levels across two particular chromosomes: chr

34 udied in terms of their in vitro and in vivo transcript levels after different treatments and their b

35 that regulate display of sLe(X) reveal high transcript levels among circulating monocytes and low le

36 Transcript level analysis and overexpression studies dem

37 Transcript level and activity labelling of cathepsin B w

38 ined a fragmented form with a relatively low transcript level and high m(6)A methylation in the cells

39 a variety of RNAs, the relationship between transcript level and m(6)A methylation extent, and diffe

40 this impairment occurred at the proIL-1beta transcript level and was independent of the RTA, the vir

41 n rhythms of PPC phosphorylation, PPC kinase transcript levels and activity, and the classic circadia

42 nscriptional regulatory processes may change transcript levels and affect cell-to-cell variability or

43 as documented through increased beta-amylase transcript levels and associated starch hydrolysis metab

44 By quantifying the transcript levels and by analyzing the sequence of the r

45 unoFISH to simultaneous quantify protein and transcript levels and distribution in cultured HER2 posi

46 t, the T-DNA insertion caused a 40 % rise in transcript levels and enzyme activity in Arabidopsis see

47 gions surrounding the gene borders influence transcript levels and govern polymerase behavior during

48 insights into the relationship between gene transcript levels and HLA ligand presentation.

49 substantial disparity between HBZ and APH-2 transcript levels and protein stability, respectively.

50 main, as determined by measurement of target transcript levels and the flocculation phenotype charact

51 revealed an inverse correlation between PER2 transcript levels and the number of miscarriages in wome

52 RyPPDC transcript levels and the resulting production of 2PE ar

53 181b from CDCs into Mvarphi reduces PKCdelta transcript levels and underlies the cardioprotective eff

54 A allele of rs393152 on intra-cerebral MAPT transcript levels and volume loss within the entorhinal

55 ciates with DNA repair and hormone-regulated transcript levels and with an early recurrent prostate c

56 th bound loci, the effect of ARK1 binding on transcript levels, and evolutionary conservation of ARK1

57 decreased SOX9 protein expression and Col2a1 transcript levels, and increased apoptosis.

58 nt HIV-1 p24 levels, reduced CXCL10 and IL-6 transcript levels, and induced peroxisome proliferator-a

59 Transcript levels are a critical determinant of the prot

60 pts are purified by immunoprecipitation, and transcript levels are determined by reverse-transcriptio

61 PEPCK and G6Pase transcript levels are downregulated in hepatocytes from

62 A3, TCF7 (TCF-1), AHR, SOX4, RUNX2, and ZEB1 transcript levels are higher in CD56(bright) cells, whil

63 role of alternatively spliced MBSs affecting transcript levels are important for understanding plant

64 accessions, we were able to estimate whether transcript levels are mainly determined by genetic (i.e.

65 n-mediated bud inhibition, and increased IPT transcript levels are not needed for bud release followi

66 cdc25 transcript levels are regulated such that smaller cells

67 in 3D chromatin collude to influence target transcript levels as well as clinical risk.

68 n of NnCYP76B6 resulted in reduction of mRNA transcript levels as well as CPT content in comparison t

69 at the FRO2 locus leads to variation of FRO2 transcript levels, as well as ferric chelate reductase a

70 We previously reported SNP/transcript level associations with rs8070723/MAPT, rs242

71 ed upon iron deprivation and restores normal transcript levels at genes encoding mitochondrial protei

72 mperature treatments increased CONSTANS (CO) transcript levels at night.

73 Using quantitative PCR, we examined their transcript levels at seven stages of leaf development.

74 ffects of RP1-13D10.2 overexpression on LDLR transcript levels between hepatoma cells transfected wit

75 ve RT-PCR analyses showed no change in PD-L1 transcript levels between mock- and VZV-infected cells,

76 ription start site reduced the entire lncRNA transcript level by >90% with no effect on Cdkn1b transc

77 y plant genes can be facilitated by reducing transcript levels by hairpin RNA (hpRNA) mediated silenc

78 1 genes exhibited significant differences at transcript levels by microarray analysis were identified

79 potential of these results, we assessed the transcript levels (by quantitative PCR), DNA methylation

80 Furthermore, buds with high BRC1 transcript levels can be active.

81 nalysis of the data shows that a majority of transcript level changes in HD knock-in mice involve alt

82 gly supported fusions and fusions with large transcript level changes in the absence of multitumor re

83 ed that, on average, almost one-fifth of the transcript level changes induced by lncRNAs are dependen

84 6B6 showed a significant enhancement in mRNA transcript levels coincident with enhanced CPT accumulat

85 quamous cell carcinoma had the highest CXCR7 transcript levels compared with other lung cancer subtyp

86 tein-1, interleukin-1beta, and interleukin-8 transcripts levels compared with control.

87 To characterize the transcript level component of metabolic regulation, geno

88 leukemic variant of CTCL, and that high TOX transcript levels correlate with increased disease-speci

89 High cytokine transcript levels correlated with increased protein prod

90 Their transcript levels decreased significantly during senesce

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

92 nd determine whether these RNAs control CER3 transcript levels directly, we cloned additional genes i

93 However, increased transcript levels do not always translate into protein p

94 Transcript levels do not faithfully predict protein leve

95 at nuclear- and mitochondrial-encoded OXPHOS transcript levels do not increase concordantly.

96 crRNAs targeting the promoter region reduced transcript levels down to 8%.

97 ients achieved a 3-log reduction in BCR-ABL1 transcript levels during consolidation.

98 ntitative RT-PCR analyses identified reduced transcript levels during stamen development and pollen t

99 erences in expression units and gene- versus transcript-level estimation.

100 ted in other species to build a pipeline for transcript-level expression and alternative splicing ana

101 controlled genes also oscillates, but mature transcript levels follow three distinct patterns.

102 higher levels of ROS, the LEW rat had lower transcript levels for antioxidant enzymes (lactoperoxida

103 o achieve and maintain undetectable BCR-ABL1 transcript levels for at least 2 years remain disease-fr

104 Interestingly, substantial reduction in transcript levels for KV2.1 preceded down-regulation of

105 Transcript levels for myocardial infarction associated t

106 This identified altered transcript levels for oxidative phosphorylation and oxid

107 Transcript levels for pan-ErbB4, four ErbB4 splicing var

108 r and failing LVs revealed 0.64-fold reduced transcript levels for the mitochondrial-LD tether, peril

109 The suppression of CLU was verified at transcript level in different melanoma cell lines, and a

110 O2 signaling modules appear unchanged at the transcript level in guard cells from C3 and C4 species,

111 genes in the Slit-Robo pathway have altered transcript levels in a subset of mouse and human osteosa

112 n-pathway lipoxygenases and auxin-responsive transcript levels in border cells corresponded to differ

113 ighly expressed in TNN18 and TNG31; however, transcript levels in DBE and SBE were extremely low.

114 High resolution genetic mapping of transcript levels in HMDP, reveals both local and trans

115 0 mutations to SCZ susceptibility and to the transcript levels in human brain tissues.

116 extensive variation in glycophorin B (GYPB) transcript levels in individuals from Benin, suggesting

117 patients and pointed toward increased (ISG) transcript levels in IT patients, compared to subsequent

118 t among the three receptors) had the highest transcript levels in mature stage leaves, where PCD is n

119 Human specific ISG transcript levels in mouse liver increased significantly

120 AmERS1c had significantly higher transcript levels in NPCD compared to PCD cells.

121 19 was significantly associated with ANKRD55 transcript levels in PBMCs and CD4(+) T cells and, thus,

122 e receptor 1 [duffy blood group]) whose mRNA transcript levels in plasma exosomes significantly incre

123 Here, we compare transcript levels in primordia that will develop into ju

124 ause termination is associated with enhanced transcript levels in several positive elements stimulati

125 of the expression of the gene discloses high transcript levels in several tumor tissues, such as germ

126 By measuring transcript levels in single cells from early embryos, we

127 onal profiling of ebfG1-4 indicated elevated transcript levels in the biofilm-forming mutant compared

128 Notably, SLC5A11 transcript levels in the brain increase significantly wh

129 it mutants appear to result from low SlMYB12 transcript levels in the fruit skin.

130 ence QTLs contain KCNN2 and KCNN3, and Kcnn3 transcript levels in the nucleus accumbens (NAc) of gene

131 ssed in all tested bean tissues, with higher transcript levels in the root meristems and senesced nod

132 f SPL2 had reduced ASYMMETRIC LEAVES 2 (AS2) transcript levels in their siliques.

133 is associated with increased CD20 and IGF-1 transcript levels in tumors and IGF-1 expression in tumo

134 Changes in transcript levels in vts1Delta cells established the reg

135 Comparing transcript levels in wild-type and puf3 cells revealed t

136 significant differences in cytokine receptor transcript levels (including IL-22RA1 and IL-23R) in dis

137 In P. vittata gametophytes, PvPht1;3 transcript levels increased in response to phosphate (Pi

138 Specifically, jun-1 transcript levels increased in wild-type animals post ga

139 rexpression in Huh7 and HepG2 increased LDLR transcript levels, increased LDL uptake, and decreased m

140 min A provides one example, with protein and transcript levels increasing with collagen 1 and tissue

141 al CDFs (CDF1, CDF3, CDF5) and increasing FT transcript levels, indicating both cis and trans functio

142 R-V7 mRNA levels but did not affect total AR transcript levels, indicating that HSP90 inhibition disr

143 ls and membrane currents mirrored changes in transcript levels, indicating the targeted transcripts w

144 changes in transcription, demonstrating that transcript levels influence specific productivity.

145 well established that precise control at the transcript level is a key genetic underpinning of lung b

146 els of triacylglycerol accumulation, and the transcript level is directly correlated to the level of

147 Gene expression studies showed that OsNHX1 transcript level is highly induced by salt and PEG-induc

148 evels of biogenesis-related genes from their transcript levels is causal for the changes occurring in

149 Tuning of target transcript levels is guided by the density of homologous

150 To study transcript levels, leaves were harvested throughout the

151 Our multi-level data, including transcript levels, metabolite levels, and gut microbiota

152 ery of HrcA binding and return to non-stress transcript levels occurred more slowly.

153 Glc could regulate the transcript level of 72% of BR-regulated genes at the who

154 Our results indicated that in rice, transcript level of OsamiR395 (Oryza sativa miR395) incr

155 Expression analysis indicated that the transcript level of PtD14a is generally more abundant th

156 ately 7,200 eQTL regulating the steady-state transcript levels of 5,300 genes.

157 native polyadenylation (APA) profiles and/or transcript levels of a subset of genes.

158 y drought treatment, constitutively elevated transcript levels of abscisic acid biosynthetic genes an

159 Transcript levels of ADAM17 were increased in blood samp

160 Based on RT-qPCR data, the transcript levels of amoA and hao decreased when exposed

161 rs of schizophrenia and comparison subjects, transcript levels of ARP2/3 complex signaling pathway we

162 rs of schizophrenia and comparison subjects, transcript levels of ARP2/3 complex signaling pathway we

163 Transcript levels of ARP2/3 complex subunits and of nucl

164 that in CK-depleted plants exposed to As(V), transcript levels of As(V)/phosphate-transporters were s

165 These data were compared with transcript levels of associated genes.

166 the soil seed bank, seeds exhibit increased transcript levels of ATM and ATR, with changes in dorman

167 Interestingly, the transcript levels of AtSUC2 and AtSWEET11 to AtSWEET15 w

168 The transcript levels of AtSWEET11 (for sugar will eventuall

169 d stress conditions and, thus, adjusting the transcript levels of CAT2.

170 ed CovR levels and a greater increase in the transcript levels of CovR-repressed genes than did CovS

171 had high levels of phosphorylated CovR, low transcript levels of CovR-repressed genes, and strikingl

172 Sse(A+) SpeB(A+) variants had transcript levels of CovRS-controlled virulence genes co

173 the uninfected LEW rat has inherently higher transcript levels of cytochrome enzymes (Cyp2d3, Cyp2d5,

174 The mRNA transcript levels of each gene were calculated.

175 nt in Tenera was associated with much higher transcript levels of EgWRI1, homolog of Arabidopsis thal

176 e dissected in greater detail the changes in transcript levels of elements of several signaling pathw

177 Microarray studies have shown elevated transcript levels of endothelial and natural killer (NK)

178 Transcript levels of ESR1 and HER2 genes were available

179 Finally, we show that relative transcript levels of FD-like and 14-3-3 genes vary among

180 posure resulted in a significant decrease in transcript levels of five aflatoxin genes and at least t

181 In the mutant, the transcript levels of genes for PSI structural and access

182 Transcript levels of genes involved in alternative pathw

183 We show that the transcript levels of genes within two metabolic clusters

184 Transcript levels of glutaminolytic factors were quantif

185 otocols for the quantitative analysis of the transcript levels of HTTexon1 in human tissue and applie

186 Transcript levels of IL-12p35, IL-12/23p40 and IL-23p19

187 Transcript levels of Kcnn3 in the NAc negatively correla

188 We show that HCV modulates the transcript levels of key enzymes of glutamine metabolism

189 truncatula hairy roots resulted in elevated transcript levels of known triterpene saponin biosynthet

190 hich was characterized by an increase in the transcript levels of M1 cytokines involved in leukocyte

191 id as the sole carbon source and had reduced transcript levels of major beta-oxidation genes.

192 erestingly, mutant cells also show increased transcript levels of mitochondrial DNA but not nuclear D

193 The transcript levels of most genes functioning in energy me

194 um after they have committed to meiosis, the transcript levels of most meiotically upregulated genes

195 multiple nucleopolyhedrovirus (AcMNPV), the transcript levels of most SNARE genes initially were upr

196 We also found that transcript levels of MSN2/MSN4 are increased in glucose-

197 Here, we found that protein and transcript levels of nescient helix loop helix 2 (NHLH2)

198 F-kappaB activation and a marked increase of transcript levels of NF-kappaB inhibitors, IkappaBalpha

199 was performed at several stages to determine transcript levels of PACAP and corresponding receptors.

200 In this study, sequences and transcript levels of peanut CSD1 isoforms (AhCSD1-1, AhC

201 Transcript levels of PgUGT5b were higher than those of P

202 asured in polar bear adipose tissue, as were transcript levels of PPARG and the PPARG target gene fat

203 latelet-derived growth factor alpha and high transcript levels of Rars, Cxcl12, and stem cell factor

204 and altitudinal variations in messenger RNA transcript levels of ReCHSs correlating positively with

205 nts of GA3 and cytokinins due to upregulated transcript levels of several plastidic 2-C-methyl-d-eryt

206 liver within 24 h, accompanied by increased transcript levels of several proinflammatory cytokines a

207 ferentially expressed genes, among which the transcript levels of some of the heat shock protein gene

208 This coincided with increased transcript levels of some senescence-specific and pathog

209 heir differentiation, indicated by increased transcript levels of Sox9, Ihh, Col2a1, and Col10a1.

210 sistent with substantial upregulation of the transcript levels of specific pathogen-responsive genes.

211 -wide transcriptome profiling indicates that transcript levels of TEs are more likely regulated by JM

212 (AaTPS1) and correlated with an increase in transcript levels of the 2-C-methyl-D-erythritol 4-phosp

213 Presence of SAD1 led to an increase of the transcript levels of the auxin transporter PIN-FORMED1 i

214 y modulation of branching through increasing transcript levels of the auxin transporter PIN1 and dere

215 tension wood formation are all sensitive to transcript levels of the Class I KNOX homeodomain transc

216 nd found that, unlike the enzyme activities, transcript levels of the corresponding genes did not exh

217 and effect of this accumulation, we followed transcript levels of the cytokinin biosynthetic pathway

218 mulation, susceptibility to antibiotics, and transcript levels of the known vaginolysin, and sialidas

219 n, whereas ssGnih-2 treatment did not affect transcript levels of the main reproductive genes.

220 iRNA pathway components do not act to reduce transcript levels of the P-element transposon during P-M

221 y ZIKV, which was confirmed by analyzing the transcript levels of the proteins of inflammasome pathwa

222 rming a complete knockout in the full length transcript levels of the target genes as well as a reduc

223 vity determines stem wax load by controlling transcript levels of the wax-related gene CER3 Character

224 Methylfarnesoate suppresses transcript levels of the yolk precursor Vitellogenin bot

225 We have recently discovered that the transcript levels of TOX were significantly increased in

226 Furthermore, transcript levels of TPCs correlated negatively with p62

227 AOP2 expression can increase the transcript levels of two known regulators (MYB28 and MYB

228 Overexpression of MED15 or WRI1 increased transcript levels of WRI1 target genes involved in glyco

229 n of MED15 in the wri1 mutant also increased transcript levels of WRI1 target genes, suggesting that

230 or infected with Dengue virus revealed high transcripts levels of genes associated with lipid storag

231 reverse transcription-PCR revealed decreased transcript levels (P<0.04, n >/=5/group) for five other

232 modules revealing novel associations between transcript level patterns and biological processes.

233 netic hot spots regulating a large number of transcript level patterns relating to diverse biological

234 Important eQTL regulating transcript level patterns were related to leaf number an

235 is and affects the expression of genes whose transcript levels peak during mitosis.

236 aB4H, SaBIS, and phenylalanine ammonia lyase transcript levels preceded phytoalexin accumulation.

237 domain correlated most with esophageal gene transcript levels, predominantly with mast cell-specific

238 tailored output to facilitate comparison of transcript levels, PTESFinder will facilitate the discov

239 n be successfully applied to the problems of transcript-level quantification from RNA-seq reads and t

240 gnificantly correlated with intrarenal GDF15 transcript levels (r=0.54, P=0.01).

241 At transcript level, RBP - RNA interaction data for the yea

242 entified modules were shown to have a higher transcript level relationship (i.e. connectivity) in tre

243 is not mediated by abnormal telomerase gene transcript levels relative to those of endogenous genes.

244 eiosis II, termed protected transcripts, the transcript levels remain stable even after nutrients are

245 demonstrated that, during sporulation, codY transcript levels remained high in SM101 but rapidly dec

246 tatistical model that provides unprecedented transcript-level resolution.

247 Coordinated transcript level responses to silicon starvation are pro

248 Analysis of transcript levels revealed differential expression of IL

249 ogy, but decreases inflammation-related gene transcript levels selectively late in disease progressio

250 nic lines and the line with the highest PhlD transcript level showed the most accumulation of PG.

251 ine self-administration increased BNST PACAP transcript levels similar to what we have previously rep

252 the knockout mice, reconstitution of Ormdl3 transcript levels specifically in the bronchial epitheli

253 ying thousands of genetic variants affecting transcript levels (strength) or the distribution of TSSs

254 nd a linear relationship between H3K36ac and transcript levels, suggesting that H3K36ac is a binary i

255 Investigation of the effect on marker gene transcript levels suggests that the Xoc diterpenoid affe

256 transcripts tended to increase, whereas GABA transcript levels tended to decrease, from caudal to ros

257 Intradermal infections had higher var gene transcript levels than intravenous infections and a sign

258 cular, SCLC cell lines possessed greater BIM transcript levels than most other solid tumors and are a

259 Finally, at the transcript level, the CCA1-ox strain adopted a global pa

260 eat expansion to upregulate normal variant 1 transcript levels, the defective vesicle trafficking and

261 ouchless phenotypes to downregulated sorbs3 transcript levels, this work re-attributes the phenotype

262 activation, whereas the other maintains high transcript levels throughout stimulation.

263 We sought to estimate the contribution of transcript levels to these two orthogonal sources of var

264 machine learning model accurately predicted transcript levels using binding sites of 20+ regulators.

265 copersicum) to identify the genetic basis of transcript level variation.

266 , read alignment, quantification of gene and transcript levels, visualization, differential gene expr

267 nal gene silencing (PTGS) in regulating CER3 transcript levels, we investigated two additional suppre

268 Through laser-capture microscopy, transcript levels were also determined in cells undergoi

269 RNMT transcript levels were also most abundant in roots, in c

270 Importantly, lower CYP27A1 transcript levels were associated with shorter disease-f

271 Transcript levels were decreased by small interfering RN

272 In contrast, GAL and GALR3 transcript levels were decreased, GALR1 was increased, a

273 The var gene transcript levels were determined in early and late post

274 Median AID transcript levels were higher in lymph node material com

275 Both metabolite and transcript levels were higher in skin than in flesh and

276 antly atrial expression, and atrial K(2P)3.1 transcript levels were highest among functional K(2P) ch

277 ACKR3 transcript levels were highest in lung squamous cell car

278 SAD1 transcript levels were highly up-regulated during biotro

279 SAMHD1 transcript levels were IFN responsive, increasing during

280 oid- and triterpenoid-related metabolite and transcript levels were increased dramatically.

281 In cold, COR gene transcript levels were increased in flc and pep1-1 mutan

282 nder different stress conditions showed that transcript levels were increased with dehydration, sodiu

283 (fold changes) of histone modifications and transcript levels were much better correlated than absol

284 Profound shifts in transcript levels were observed for genes encoding known

285 ith the fire blight bacterium, highest MdB4H transcript levels were observed in the transition zone.

286 Among the findings, circulating IGF2BP2 transcript levels were positively associated with fastin

287 FLOWERING LOCUS T (FT) transcript levels were reduced at dusk, but increased at

288 SERCA2A mRNA transcript levels were reduced in HCM regardless of geno

289 Higher AID full-length transcript levels were significantly associated (P < 0.0

290 similar, we could show that allele-specific transcript levels were significantly higher for the nove

291 AmERS1a transcript levels were significantly lower in window sta

292 Scn5a transcript levels were similar in Scn2b null and wild-ty

293 evels from microarray data, at both gene and transcript level, which has not previously been possible

294 ion studies and methods for examining global transcript levels, which gave rise to the field of "inte

295 d protein-coding transcript of an RBP at the transcript level while intensity of the CLIP signal, num

296 associated with their target transcripts at transcript level while ~95% of the studied RBPs were als

297 direct characterization by correlating their transcript levels with alkamide accumulation patterns in

298 d to compensate for a potential imbalance in transcript levels with male cells, which contain a singl

299 pression resulted in inverse changes in WWOX transcripts levels with siRNA interference eliminating P

300 methylation and copy number integration with transcript levels yielded an assessment of their relativ