ライフサイエンスコーパス: transcription of

1 sent in the human 4E-BP1 promoter to repress transcription of 4E-BP1.

2 HCFC2 was also necessary for the transcription of a large subset of other IRF2-dependent

3 bility involves infrequent, semi-coordinated transcription of a number of resistance markers at high

4 for an RUNX2-ER complex that stimulates the transcription of a set of genes, including most notably

5 at both Chd7 and Top2b are necessary for the transcription of a set of long neuronal genes in cerebel

6 bly and various biochemical reactions during transcription of a single-copy gene in vivo is the ideal

7 uently, the deacetylation of p53 reduces the transcription of a spectrum of its downstream target gen

8 mediator component is likely involved in the transcription of a subset of genes that promote papillae

9 tive to oxidative stress because of impaired transcription of a subset of stress genes whose expressi

10 strategies, like RNA-Seq, have revealed the transcription of a wide variety of long non-coding RNAs

11 ization and cAMP signals induce preferential transcription of activity-dependent genes containing pro

12 AP2 does not repress the transcription of AG in the inner two whorls, but instead

13 Thus, beta2AR is linked to transcription of alpha-synuclein and risk of PD in a lig

14 cription factor AP-1, which in turn enhances transcription of amyloid-beta precursor protein (APP) an

15 e numbers of a molecular species controlling transcription of an active promoter acts as a constant s

16 mechanism is the developmentally controlled transcription of an alternate NDC80 mRNA isoform, which

17 In Sinorhizobium meliloti, CuxR stimulates transcription of an EPS biosynthesis gene cluster at ele

18 reversible silencing of LTR promoter-driven transcription of an integrated provirus.

19 regulation raises the intriguing notion that transcription of an mRNA, despite carrying a canonical c

20 The BAC transgene drives cell-type-specific transcription of an out-of-frame mononucleotide repeat t

21 ase the phosphorylation of STAT5 and Akt and transcription of antiapoptotic mediator bcl-xL Several s

22 are essential RNA intermediates that license transcription of antisense genomic viral RNAs.

23 ranscription factors potentially controlling transcription of any given gene makes it often difficult

24 RpoN* reduced transcription of approximately 700 genes as determined b

25 ETO2-GLIS2 directly binds DNA to control transcription of associated genes by upregulation of exp

26 Insulin-mediated transcription of Atgl, the enzyme that mediates the rate

27 In two Spanish populations, we found active transcription of B-CAP-G, but it did not influence the e

28 Phytochromes mediate light-induced transcription of BICs to inactivate cryptochromes 548 II

29 is showed that (p)ppGpp positively regulates transcription of bifA, and negatively regulates transcri

30 We found that this AD is required for transcription of both chimeric reporter genes and authen

31 DLX1 and/or DLX2 activated the transcription of both Gad genes, and defects in Dlx func

32 letion of repair is expected to outweigh the transcription of broken templates.

33 taining cultures, BT0366 phosphorylation and transcription of BT0366-activated genes are inhibited an

34 BT0366 phosphorylation and transcription of BT0366-activated genes requires the con

35 earning induces differential CRTC1-dependent transcription of c-fos and the nuclear receptor subfamil

36 KII mRNA and a process that requires zygotic transcription of CaMKII mRNA.

37 KID region of CREB protein is central in the transcription of cAMP responsive genes, including those

38 4/ROS regulates hyaluronan synthesis and the transcription of CD44V6 via an effect upon AP-1 activity

39 f Zap1-mediated regulation whereby increased transcription of certain target genes results in reduced

40 Notch1 signal pathway regulates the transcription of certain types of miRNAs which further a

41 virus can override the silencing and promote transcription of chimeric proviral DNAs.

42 nstrated that mTORC1-S6K1 signaling controls transcription of CHK1 via Rb-E2F by upregulating cyclin

43 Cro is known to repress transcription of CI from pRM to prevent lysogeny.

44 Cdc15 also influences the complete transcription of clb2 gene and phosphorylates Ser-5 at t

45 (UsnRNA) and enhancer RNA (eRNA), and in the transcription of coding genes by RNA polymerase II.

46 r regulator ComR, that in turn activates the transcription of comS, encoding the XIP precursor, and o

47 Transcription of CPS1 is suppressed by LKB1 through AMPK

48 nal coactivators CBP and p300 to control the transcription of critical adaptive genes.

49 and H4K16 histone acetylation, facilitating transcription of CXCR4.

50 vivo then slowly released to drive long-term transcription of cytokine-response genes.

51 The central transcription of cytokines and aromatase was measured, a

52 Here, we report that MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) th

53 s potentiated and have a faster and stronger transcription of defense genes and higher activities of

54 4 (BRD4) was previously shown to control the transcription of defined subsets of genes in various cel

55 Additionally, we observed an increase in transcription of dipeptidylpeptidase 4, as well as a pla

56 The epigenetic mechanisms that (dys)regulate transcription of Dlg4/PSD95, or other plasticity genes,

57 Transcription of DLL4 coincides with dynamic ERG-depende

58 tic cell identity tra-1, which represses the transcription of dmd-3 in hermaphrodite PHC.

59 Here we report the in vivo transcription of DNA containing dNaM and dTPT3 into mRNA

60 gatively affects its ability to activate the transcription of downstream genes and promote cell proli

61 modulate LTR enhancer function in activating transcription of downstream genes critical to cellular p

62 ng-range LTR enhancer function in activating transcription of downstream, cis-linked globin genes.

63 Moreover, Lxralpha could mediate the transcription of elovl4 directly or indirectly through r

64 and in vitro studies both indicated that the transcriptions of elovl5 and elovl4 elongases could be r

65 Transcription of enzymes within the liver responsible fo

66 Taken together, our results reveal that the transcription of essential genes controlled by T-box rib

67 rf2 was found to regulate the OA-NO2-induced transcription of ET-B in human and mouse endothelial cel

68 ting in enhanced ETS factor activity and the transcription of ETS family target genes related to spli

69 Transcription of expanded microsatellite repeats is asso

70 promotor of FAM83H and that MYC promotes the transcription of FAM83H, which was supported by the resu

71 entified the BSs and assessed the effects on transcription of FLOWERING LOCUS C (FLC) and PERPETUAL F

72 r, arising from a mutation that disrupts the transcription of Fragile X Mental Retardation Protein (F

73 s a transcriptional activator that regulates transcription of gamma-aminobutyric acid aminotransferas

74 ation into functional RNAs involves separate transcription of gene pieces, joining of precursor RNAs

75 expression analysis showed a lack of active transcription of genes associated with acute inflammator

76 ecreased chromatin accessibility and reduced transcription of genes associated with migration, invasi

77 JQ1 alters transcription of genes controlled by the host protein BA

78 reserves during the day, and is defective in transcription of genes crucial for utilization of carboh

79 SMAD6 knockdown also reduced transcription of genes encoding lipoprotein and choleste

80 CYCLE (CLK-CYC) heterodimers, which activate transcription of genes encoding the feedback repressors

81 Transcription of genes in the ddhD-wzz O-antigen gene cl

82 TFEB is a master regulator for transcription of genes involved in autophagy and lysosom

83 ant factor in tumorigenesis by promoting the transcription of genes involved in cancer development.

84 YTOCHROME B4-#3 (SOB3) to influence both the transcription of genes involved in cell elongation and h

85 n responders to hepatocyte death, increasing transcription of genes involved in myeloid cell recruitm

86 s to neural/stem progenitor cells to control transcription of genes involved in self-renewal and diff

87 neural stem cell populations to control the transcription of genes involved in self-renewal and diff

88 ions and regulatory factors that control the transcription of genes is an important, unsolved problem

89 with the chromatin remodeler dMi-2 prevents transcription of genes normally expressed only in somati

90 mediator component is likely involved in the transcription of genes promoting papillae deposition in

91 and are both functionally important for the transcription of genes regulated by these enhancers.

92 ne expression causing profound modulation of transcription of genes related to photosynthesis and oth

93 s as an anti-anti-sigma factor and regulates transcription of genes required for stress adaptation an

94 e manner to fine-tune the cell-type-specific transcription of genes that are critical for brain funct

95 cell adhesion, PKP2 is necessary to maintain transcription of genes that control intracellular calciu

96 IZR-1 ligand, and activated HIZR-1 increases transcription of genes that promote zinc efflux and stor

97 AG) endonuclease engage this DDR to modulate transcription of genes that regulate lymphocyte-specific

98 a hitherto unreported conserved mechanism of transcription of genes with methylated proximal promoter

99 response by facilitating the stress-induced transcription of genes.

100 nodeficiency virus type 1 (HIV-1) is reverse transcription of genomic RNA to DNA, a process that is p

101 inates the Hedgehog signaling to enhance the transcription of glycolysis activators HK2 and PFKFB3.

102 radient is established in response to graded transcription of glycolytic enzymes downstream of fibrob

103 ap1p and the Hap2/3/4/5p complex and induced transcription of HAP4 and genes required for the tricarb

104 We found that heme induces transcription of HAP4, the transcriptional activation su

105 es was decreased, amplifying glucose-induced transcription of hepatic Dpp4 In older mice, hepatic tri

106 host protein Naf1 inhibited HIV-1 LTR-driven transcription of HIV genes and contributed to the mainte

107 sease in part by controlling tissue-specific transcription of host genes.

108 tone methyltransferases is known to activate transcription of Hox genes in other contexts, we found t

109 opment, the telomeric TAD controls the early transcription of Hoxd genes in forearm cells, whereas th

110 Deletion of mcrA upregulates transcription of hundreds of genes including many that a

111 histone S/T phosphorylation and changes the transcription of hundreds of genes.

112 3 and BR signaling converge to influence the transcription of hypocotyl growth-promoting SAUR19 subfa

113 LPS, sickness-like behaviors increased, the transcription of IL-1beta was higher in both sexes, and

114 , CLIC1 or CLIC4 siRNA transfection impaired transcription of IL-1beta, ASC speck formation, and secr

115 tion of AT1R through losartan modulated mRNA transcription of IL-6 and IL-8 in HPLF but not in HGF.

116 65 subunit, which subsequently modulates the transcription of IL-8.

117 Photoreceptor-specific transcription of individual genes collectively constitut

118 osome placement and repositioning can direct transcription of individual genes; however, the precise

119 f CKO mouse hippocampus identified increased transcription of inflammation-related genes linked to mi

120 regulated with highly increased or decreased transcription of inflammatory genes and consistently dep

121 to act as a coactivator of NF-kappaB for the transcription of inflammatory genes in innate immune cel

122 , which is essential for the replication and transcription of influenza virus RNA.

123 ts with the Ino2p-Ino4p complex, attenuating transcription of INO1 A strain devoid of Scs2p (scs2Delt

124 ) that nuclear FAK regulates Runx1-dependent transcription of insulin-like growth factor binding prot

125 ered hippocampal clock function and elevated transcription of Insulin-like Growth Factor2 (Igf2).

126 Consistently, transcription of interferon-stimulated genes (eg, OAS1,

127 NLRX1 had a minimal effect on the transcription of IRF1 mediated by the transcription fact

128 element-binding protein 1 (SREBP1)-directed transcription of its direct targets including the BCAT2

129 following low dose irradiation and regulates transcription of its neighbouring gene - Methionine aden

130 he DNA-binding activity of NF-kappaB and the transcription of its target genes in a dose-dependent ma

131 me- and transcriptome-wide analysis revealed transcription of key C-1 capture and additional energy c

132 Thereby, the transcription of key endothelial genes such as SOX18, SM

133 ERV-9 human endogenous retrovirus activated transcription of key erythroid genes and modulated ex vi

134 at chromatin for histone acetylation and the transcription of key neuronal genes.

135 JMJD2B induction attenuates the transcription of key p53 transcriptional targets includi

136 t the (p)ppGpp/CodY network does not promote transcription of known metal transporters.

137 In somatic cells, transcription of L1 elements is repressed by distinct mo

138 nscription of bifA, and negatively regulates transcription of lapA and the lapBC, and lapE operons, e

139 Amt-87 that can significantly reactivate the transcription of latent HIV provirses and act synergisti

140 d lngS mutants were considerably affected in transcription of lngA pilin gene.

141 s further revealed reductions in the nascent transcription of long genes and uncovered widespread pos

142 altered chromatin landscape and the enhanced transcription of low-expressed genes.

143 idence that mechanisms governing the initial transcription of lytic genes are distinct from those of

144 macological inhibition of EGFR increases the transcription of lytic IE1/IE2 mRNA while curbing the ex

145 duced muscle fiber atrophy and increased the transcription of MAFbx and TRIM63.

146 response to zinc deficiency, Zap1 activates transcription of many genes and consequently increases a

147 timulation of memory cells revealed enhanced transcription of "memory-primed" genes compared with nai

148 These observations suggest that transcription of microsatellite repeat-containing RNAs i

149 In turn this regulates transcription of milk protein genes.

150 Transcription of MIR122 is inhibited by GRHL2, which is

151 erse the first nucleosome, thereby promoting transcription of most genes.

152 Retroduplications come from reverse transcription of mRNAs and their insertion back into the

153 epigenetic status of D-loop on the mtDNA and transcription of mtDNA-encoded genes.

154 Transcription of myo18b is restricted to fast-twitch myo

155 We find that transcription of nearly all mRNAs is strongly dependent

156 diator complex is required for the regulated transcription of nearly all RNA polymerase II-dependent

157 injury and treatment with PEDF + DHA induced transcription of neuropeptide y (npy), small proline-ric

158 Transcriptional analysis showed increased transcription of nirK and nirS genes during nitrate flux

159 e Notch receptor (NICD), which regulates the transcription of Notch-responsive genes.

160 Nrf2 in the cytosol, thereby repressing the transcription of Nrf2-dependent antioxidative genes.

161 s to positive feedback on the Nrf2-dependent transcription of oncogenes.

162 e that intragenic enhancers not only enhance transcription of one or more genes from a distance but a

163 ted in written corpora, or in the equivalent transcription of oral corpora.

164 However, FMRP regulates the transcription of other proteins and participates in an u

165 RNAs is more sensitive to perturbation than transcription of other RNAs, indicating potentially viab

166 uccessive germ cell subtypes reveals dynamic transcription of over 4000 genes during human spermatoge

167 lyses revealed that FOXP1 directly represses transcription of p16INK4A.

168 ) increased AQP5 expression and Sp1-mediated transcription of p358P/E.

169 increases levels of p53, and results in the transcription of p53 target genes, induction of the tumo

170 identify regulatory factors that control the transcription of P5CS1, Y1H screens were performed with

171 ikely that the mutations directly affect the transcription of PBX1 target genes to impact embryonic d

172 otes the activation of SREBP2 and subsequent transcription of PCSK9.

173 d that cellular externalization, rather than transcription of Pfn1, is affected by the perturbations

174 l recessive early-onset PD, and controls the transcription of PGC-1alpha, a master regulator of mitoc

175 protein levels, MgtC enables normal temporal transcription of PhoP-activated genes.

176 engineering resistant crops through ectopic transcription of plants' own defence genes, such as the

177 nome not currently annotated suggests active transcription of previously unannotated genomic loci dur

178 and endogenous hG9a augmented p53-dependent transcription of pro-apoptotic genes, including Bax and

179 PGE2 has been shown to increase the transcription of pro-IL-1beta.

180 Fibrogenic signals drive transcription of procollagen I, which enters the endopla

181 ally reversed TNF-alpha and IL-1beta induced transcription of proinflammatory cytokines in the primar

182 d histone-packaged promoters and reduces the transcription of proinflammatory genes (IL-6, CCL-2, and

183 Transcription of protein-coding and noncoding DNA occurs

184 by regulatory programs that orchestrate the transcription of protein-coding and noncoding genes.

185 The historical focus on transcription of protein-coding genes has left the roles

186 I (Pol II) C-terminal domain (CTD) regulates transcription of protein-coding mRNAs and noncoding RNAs

187 CTD function in transcription of protein-coding RNAs has been studied ex

188 rates of urea-derived N and the abundance or transcription of putative Thaumarchaeota ureC genes.

189 on of the flavonoids to P. aeruginosa alters transcription of quorum sensing-controlled target promot

190 skeletal muscle by directly controlling the transcription of RAB20 and TXNIP These results hint towa

191 ate decision is executed, the suppression of transcription of ribosomal genes and upregulation of lin

192 the C-box retain the ability to inhibit the transcription of RNA pol III targets, reduce lipid bioge

193 prising ELL, Ice1, Ice2, and ZC3H8, promotes transcription of RNAPII-specific spliceosomal snRNA and

194 nding protein (TBP) was found to function in transcription of RP genes in Drosophila.

195 tes with the core promoter region, activates transcription of RP genes.

196 ominant catalytic subunit of PRC1, activates transcription of Sall4, which codes for a transcription

197 component BZR1, further indicating that the transcription of SAUR19 subfamily members are influenced

198 DnaA activates transcription of sda, and Sda inhibits histidine protein

199 Foxc1/c2 directly activates the transcription of Sema3c in the OFT, whereas, a hypomorph

200 ly response, which encompasses the transient transcription of several genes belonging to the AP-1 tra

201 re, in vivo experiments demonstrate that the transcription of several genes is affected by the lack o

202 We noted that GCs increase the transcription of several key regulators of glucose metab

203 ssion analysis revealed that SMCR8 regulates transcription of several other autophagy genes including

204 regulates the RNA polymerase III-associated transcription of small non-coding RNAs.

205 Thus, monitoring endogenous transcription of SNCA is of utmost importance to underst

206 The poly(A)-independent termination of transcription of snoRNAs, however, remained unaffected i

207 irectly or indirectly through regulating the transcription of srebp-1.

208 n-mediated epigenetic changes that stimulate transcription of stem cell genes, including ALDH1A1 and

209 ufC and sufD (sufD*), resulting in decreased transcription of sufSUB Consistent with the transcriptio

210 polysulfide, activating sigma(54) -dependent transcription of sulfide-oxidizing genes for sulfide rem

211 ation, sustained MYCN activity maintains the transcription of "switch" genes that are rate-limiting f

212 y in Huntington's disease, in which abnormal transcription of synaptic genes and metabolic disturbanc

213 ive p53-and correlates with the induction of transcription of target genes such as CDKN1a.

214 S-domain transcription factors, activate the transcription of target genes to specify the identity of

215 ging epigenetic enzyme that mainly represses transcription of target genes via symmetric dimethylatio

216 specific gene expression by facilitating the transcription of target genes.

217 tor coactivator-1 (SRC-1), to facilitate the transcription of targeted genes.

218 which was crucial for YAP activation and the transcription of TEA domain (TEAD) family members.

219 Transcription of telomere repeats can initiate at subtel

220 in mammals, telomere dysfunction induces the transcription of telomeric DDRNAs (tDDRNAs) and their lo

221 se phenotypes could be rescued by the forced transcription of TERRA independent of CTCF binding.

222 , a genome-wide approach was used to examine transcription of the 43,673 genes annotated in the Xenop

223 At the molecular level, transcription of the adherens junction protein E-cadheri

224 induces AhR translocation to the nucleus and transcription of the AhR target gene Cyp1a1, showing tha

225 BC) and hydrogenase (HydABCD) as well as the transcription of the alternative respiratory acceptor co

226 cer cell growth by epigenetically activating transcription of the androgen receptor (AR) in prostate

227 clear exclusion in DCs, leading to decreased transcription of the autophagy component microtubule-ass

228 auxin gene regulatory network (GRN) through transcription of the Aux/IAA genes.

229 at cryptochromes mediate light activation of transcription of the BIC genes, by suppressing the activ

230 nctions in biofilm development by activating transcription of the biofilm matrix exopolysaccharide an

231 Here we show that reverse transcription of the Bordetella phage DGR is primed by a

232 TBX2 acted in trans by promoting transcription of the canonical WNT (WNT3A) promoter.

233 Transcription of the CCC1 gene is largely regulated by t

234 MAPK signaling pathways that stimulate gene transcription of the common alpha-subunit (Cga) and the

235 CSR is preceded by inducible germline (GL) transcription of the constant genes and is controlled by

236 ith the s-LNv molecular clocks by regulating transcription of the core clock gene period (per).

237 e CPD area, substantially reversed defective transcription of the CPD L gene and substantially restor

238 We found that RANKL represses the transcription of the E3 ubiquitin ligase RNF146 through

239 pidermal growth factors (EGFs) by repressing transcription of the EGF maturation factor rhomboid.

240 t dual-functionality by also down-regulating transcription of the entire chromosomal locus encoding t

241 for > 94% of all transcripts, with increased transcription of the entire locus driving Flt1 upregulat

242 C-lobe of CaM abrogated estrogen-stimulated transcription of the estrogen responsive genes pS2 and p

243 The mechanisms contributing to enhanced transcription of the gene coding for PKCbetaII, PRKCB, i

244 1,25D stimulated transcription of the gene encoding PD-L1 in epithelial a

245 We show here for KSHV that transcription of the gene encoding RTA is complex and le

246 that the liaS mutation significantly altered transcription of the genes encoding pilus in the presenc

247 me that a virus induces widespread antisense transcription of the host cell genome.

248 ble hTNF cytokine, but surprisingly not with transcription of the hTNF transgene.

249 Several DREB/CBF TFs directly promote transcription of the IAA5 and IAA19 genes in response to

250 in human fibroblasts by directly activating transcription of the INSIG-2 gene.

251 ombination is key to coordinately regulating transcription of the majority of RP genes in Drosophila.

252 screen to isolate mutations that upregulate transcription of the non-ribosomal peptide synthetase ge

253 p21(Waf1/Cip1) Consistently, Foxp1 activates transcription of the p21(Waf1/Cip1) gene promoter, and o

254 FN in these cells, which primed an increased transcription of the p35 subunit of IL-12p70 during infe

255 Transcription of the paternal genome was highly restrict

256 to bind GC-rich promoter regions to elevate transcription of the PAX3-FOXO1A gene.

257 rainbow enhancers activate RGB cone-specific transcription of the ponli and crb2b genes.

258 well as CHLP, which is not due to defective transcription of the POR and CHLP genes but to the postt

259 lysine-4 histone H3 modification to activate transcription of the pro-tumorigenic TNF-NF-kappaB gene

260 aling pathway as it promotes the neighboring transcription of the protein-coding gene SLC3A2 in cis b

261 and DNA targeting relies on the directional transcription of the protospacer in vivo.

262 We propose that the transcription of the relatively flexible single-stranded

263 nificantly reduced or no ability to activate transcription of the reporter gene CDKN1A, and in situ s

264 Furthermore, IGSF1 stimulates transcription of the thyrotropin-releasing hormone recep

265 Unexpectedly, Pol II transcription of the transgene was required for efficien

266 oRNA and epigenetic regulators that controls transcription of the tumour suppressor E-cadherin in epi

267 n-3 LC-PUFA suppressed transcription of the two elongase genes, as well as sreb

268 (HIF-1alpha) stabilization and decreased the transcription of the two most abundant PDK isoforms, PDK

269 etrieval of the information requires in vivo transcription of the unnatural base pair into mRNA and t

270 h HIV-1 uncoating has been linked to reverse transcription of the viral genome in target cells, the m

271 inhibited biofilm formation by altering the transcription of the vps genes involved in biofilm matri

272 Transcription of the Zap1-responsive genes RTC4 and RAD2

273 te the transcription or lead to read-through transcription of their downstream genes.

274 1 rs3212924 and XPC rs2229090 might regulate transcription of their genes, which is consistent with t

275 ore genes from a distance but also fine-tune transcription of their host gene through transcription i

276 sed among mice injected at ZT2; furthermore, transcription of these enzymes correlated with splenic p

277 Transcription of these ERVs is, however, tightly regulat

278 Importantly, HDAC3 promotes the basal transcription of these genes independently of adrenergic

279 enhancer activity and for correct endogenous transcription of these genes.

280 nsistently showed higher activity to promote transcription of these target genes relative to wild-typ

281 nt signalling plays an important role in the transcription of this cytokine.

282 s selected for expression in the oocyst, and transcription of this gene increases dramatically in the

283 Instead, transcription of this isoform represses the canonical ND

284 Transcription of this var gene during parasite developme

285 chromatin dynamics, we observed the cryptic transcription of thousands of treatment-induced non-anno

286 (BRC1) binds to and positively regulates the transcription of three related Homeodomain leucine zippe

287 rom the requirement for MntR to activate the transcription of two genes encoding cation diffusion fac

288 We targeted transcription of two types of SfAV-1a genes; first, 44 c

289 Also, there was an increase in the transcription of type I IFN-stimulated genes that correl

290 IFI16 has also been shown to regulate transcription of type I IFNs during HSV infection.

291 ective signaling of STING, thus blunting the transcription of type I IFNs.

292 IL-1 signaling, we noted an increase in the transcription of type I interferon (IFN)-stimulated gene

293 lation of PGC-1alpha and is required for the transcription of Ucp1, Ppargc1a (encoding PGC-1alpha), a

294 M15 as a chromatin factor that modulates the transcription of upstream regulators of WNT and MAPK-ERK

295 In El Tor biotype vibrios, transcription of vieSAB is repressed by the quorum sensi

296 iate early transcripts, we visualized active transcription of viral genomes in naturally infected cel

297 a circular, histone-associated episome, and transcription of viral lytic cycle genes is largely supp

298 ed by the PB1 polymerase subunit to initiate transcription of viral proteins.

299 Tbeta4 co-operative binding promotes optimal transcription of Wt1 as the master regulator of embryoni

300 l in which DnaA and Rok cooperate to repress transcription of yxaJ, the yybNM operon and the sunA-bdb