ライフサイエンスコーパス: silencing of

1 with an increase in hepatic Factor VII gene silencing of 28% (rHSA/siRNA) compared to 4% (naked siRN

2 Uniparental silencing of 35S rRNA genes (rDNA), known as nucleolar d

3 l strategy for complete post-transcriptional silencing of a cytoplasmic mRNA.

4 These elements drive the translational silencing of a group of chemokine (CC/CXC) and chemokine

5 This study demonstrates that RNAi silencing of a member of the Bone Morphogenetic Protein

6 attention, yet the initiation of epigenetic silencing of a new transgene, virus, or transposable ele

7 hypermethylation was further correlated with silencing of a serial of testis determining genes, inclu

8 hat directly links junction integrity to the silencing of a set of mRNAs that critically affect epith

9 ion at goal locations to trigger optogenetic silencing of a subset of CA1 pyramidal neurons.

10 we hypothesize that the palindromes aid the silencing of active elements and influence transposition

11 Furthermore, silencing of ADAR2 in three EC cell lines resulted in a

12 Selective ablation or silencing of AgRP neurons causes anorexia [4, 5], wherea

13 Consistent with data in the murine context, silencing of AID in human bone marrow cells skews differ

14 teinase proteolysis in the NOTCH pathway, or silencing of alpha2beta1 integrin or JAG1, reduced the p

15 Silencing of alphaB-crystallin inhibited multiple fibrot

16 We describe the silencing of Alu monomers on the lineage leading to anth

17 Moreover, chemogenetic silencing of AmPir markedly reduced the stress hormone r

18 this key issue is addressed by RNAi-mediated silencing of an immune gene in a lepidopteran host Spodo

19 siRNA-based silencing of APCDD1 in 3T3-L1 preadipocytes markedly inc

20 Silencing of AqJAG revealed a wide range of defects in t

21 literature suggested that pretranscriptional silencing of AQP1 in salivary glands is mediated by meth

22 Polycomb silencing of Arabidopsis FLOWERING LOCUS C (FLC) acceler

23 ts (COOLAIR) in the cold-induced, epigenetic silencing of Arabidopsis FLOWERING LOCUS C (FLC), a regu

24 Conversely, silencing of ARHGAP21 enhanced Cdc42 activation and resc

25 in profile of the transgenic plants, whereas silencing of AtPyrP2 decreased accumulation of riboflavi

26 Taken together, our data suggest that silencing of AtRAP by AtlsiRNA-1 upon bacterial infectio

27 In particular, epigenetic silencing of BAMBI was identified as a hallmark of NSCLC

28 microRNAs in TEMC biology and indicates that silencing of both genes is necessary to increase the eff

29 silencing of DUSP1, silencing of ZFP36, nor silencing of both together prevented the repression of I

30 Gene silencing of BRD4, an important BET protein, and chromat

31 NURF was disabled by silencing of bromodomain PHD-finger containing transcrip

32 ding to suppression of c-Myc translation and silencing of c-Myc-dependent transcription.

33 elements, led to aggressive transposon-like silencing of canola-biased PUFA synthase transgenes.

34 Acute silencing of caspase-2 in cultured human cells recapitul

35 Lentiviral silencing of CBS in human breast cancer cells attenuated

36 nal centre (GC) formation through epigenetic silencing of CDKN1A and release of cell cycle checkpoint

37 sions precedes mesothelioma; this results in silencing of Cdkn2a (Ink4a/Arf) and loss of p16 and p19

38 Optogenetic silencing of CeAL CRF neurons during contextual fear acq

39 Silencing of CH-42, encoding a protein needed to make ch

40 tin-in males, but not in females, suggesting silencing of chromosomes in males.

41 The silencing of CK1alpha expression in NIFK-silenced cells

42 suppressed by small interfering RNA-mediated silencing of CK2alpha.

43 cancer cells formed larger mammospheres and silencing of CK5 using small hairpin RNA abolished this

44 This effect is recapitulated in vivo, where silencing of Cks1 and Cks2 decreases treslin phosphoryla

45 Simultaneous RNAi gene silencing of ClAQP1 and ClGlp1 significantly reduced wat

46 In vivo silencing of CLIP170 in C57BL/6 mice by CLIP170-specific

47 siRNA mediated silencing of Cofilin/ADF provokes striking nuclear defec

48 ample of EGFR deregulation in cancer through silencing of components of the nuclear import pathway.

49 Furthermore, silencing of CXCL12 in TGFbeta-unresponsive MSCs restore

50 Overexpression and gene silencing of CypA verified osteogenic and anti-osteoclas

51 aintenance of heterochromatin needed for the silencing of developmental genes in the adult heart.

52 ell cycle transitions, as well as epigenetic silencing of developmental transcription factor genes bo

53 ion of proximal homeobox gene expression and silencing of distal-associated genes, whereas limb trunc

54 e the activation of target cell programs and silencing of donor cell programs.

55 induced increased expression of Duox-1, and silencing of Doux-1 improved the rate of cell wound repa

56 We confirm that genetic silencing of Drp1 increases mitochondrial proton leak in

57 d heat, and this modulation was abolished by silencing of dry-air receptors.

58 erms of repression by dexamethasone, neither silencing of DUSP1, silencing of ZFP36, nor silencing of

59 esiRNA silencing of each component suggest that Smad3 and EZH2

60 Silencing of EDEM1, EDEM2, and ERManI strongly increases

61 Herein, we report that silencing of Egr-1 in the hippocampus by shRNA reduces t

62 Silencing of eIF2Bbeta in a TuMV-susceptible mustard pla

63 Under the silencing of either PAP1 or PAP2, the level of snoRNAs i

64 was suppressed most frequently by epigenetic silencing of either STING or the cyclic GMP-AMP synthase

65 Silencing of Elavl4 and Nova2 increased beta cell apopto

66 ced expression of IL-6 and TNF-alpha whereas silencing of endogenous CLIP170 potentiated the levels o

67 responses, and this effect was reproduced by silencing of endogenous Lyn expression.

68 rotein (KRAB-ZFP) family linked primarily to silencing of endogenous retroelements, as a direct repre

69 Complete silencing of enhancer function, however, required evolut

70 effects of miR-519d overexpression, whereas silencing of EphA4 phenocopied the effect of miR-519d.

71 Reduction of JH levels via silencing of ETH signaling genes impairs short-term cour

72 In this report, we show that silencing of EWS-FLI1 with either siRNA or small-molecul

73 Finally, optogenetic silencing of existing DGCs during novel environmental ex

74 RNA silencing of four of these glutaredoxin genes (AtGRXS3/4

75 Crucially, resembling paclitaxel treatment, silencing of FOXM1 and KIF20A similarly promotes abnorma

76 dhesion, axon guidance, and gliogenesis upon silencing of FoxO6 We then show that FoxO6 binds to DAF-

77 Further, the silencing of functional HvCERK1 gene in the resistant ge

78 Silencing of GCN4 in Nicotiana benthamiana and Arabidops

79 Aberrant silencing of genes by DNA methylation contributes to can

80 Thus, we concluded that epigenetic silencing of genes involved in angiogenesis is a hallmar

81 C-CIMP was furthermore characterized by silencing of genes related to vasculature development.

82 genome stability and the cell type-specific silencing of genes.

83 lence of Xcm avrb6 deletion strains, whereas silencing of GhSWEET10 compromises cotton susceptibility

84 Silencing of GLS1 expression, in the presence of Gln, ab

85 Expression of PsAvh23 or silencing of GmADA2/GmGCN5 resulted in misregulation of

86 RNA-mediated silencing of GPD2 revealed that the multidomain enzyme w

87 Silencing of GPR31 expression partially mislocalized KRA

88 monstrate that the acute, cell type-specific silencing of HA neurons during wakefulness is sufficient

89 TMNv HA neurons in vivo We found that acute silencing of HA neurons during wakefulness promotes slow

90 fficient to relieve the post-transcriptional silencing of HAC1 mRNA, yet the precise mechanism by whi

91 Silencing of HBEGF in vivo resulted in tumor regression

92 ncing of transposons and repeats, as well as silencing of heterochromatic transposons.

93 ells with the HIF-1alpha inhibitor PX-478 or silencing of HIF-1alpha (small interfering HIF-1alpha) a

94 Silencing of HIF-1alpha in NG108 cells leads to a signif

95 harmacological inhibition as well as genetic silencing of histone deacetylase 6 (HDAC6) increase alph

96 tion of LDH, dsRNA uptake in plant cells and silencing of homologous RNA on topical application.

97 Silencing of HSulf-1 in OV202 and TOV2223 cells (ovarian

98 AC, PARPi monotherapy combined with targeted silencing of HuR significantly reduced tumor growth comp

99 wth, and upregulated RAS/MAPK signaling with silencing of hypermethylated genes, which normally inhib

100 ctivation was responsible for mediating gene silencing of IL-27p28 and EBV-induced gene 3.

101 RNAi-mediated gene silencing of il17a in fibrotic mice arrested the progres

102 1B-induced IRF1 protein expression at 4-6 h, silencing of IL1B plus dexamethasone-induced DUSP1 signi

103 Here we show that silencing of INPP4B blocks activation of Akt and serum-

104 recordings in vivo combined with optogenetic silencing of interneurons to investigate how dendritic e

105 lect role of BRD4S-BRG1 complexes in genomic silencing of invasive retroelements.

106 In mice, optogenetic silencing of IPN neurons increases salience of and inter

107 Importantly, silencing of KDM3A, KLF2 or IRF4 both decreases MM cell

108 Here, we demonstrate that gene silencing of KIND1 decreased keratinocyte proliferation

109 d the highest efficiency in siRNA uptake and silencing of kinesin spindle protein at peptide:siRNA w/

110 Remarkably, silencing of KSRP decreased cell proliferation, reversed

111 Consistently, silencing of let-7 in the eye increased laser-induced CN

112 We demonstrate that premature silencing of LINE-1 elements decreases chromatin accessi

113 ency is characterized mainly by a reversible silencing of LTR promoter-driven transcription of an int

114 increased tumor biodistribution, and greater silencing of luciferase compared to our previously-optim

115 Inducible silencing of LZK caused near-complete loss of colony-for

116 Furthermore, silencing of major histocompatibility complex class II r

117 s (CXCL1, CXCL2, CCL3, CCL4, IL6, and CSF3), silencing of major inflammatory intracellular signaling

118 Silencing of Malat1 also significantly aggravated OGD-in

119 Silencing of Malat1 by Malat1 GapmeR significantly incre

120 CRISPR/Cas9-mediated deletion or silencing of MANTIS with small interfering RNAs or Gapme

121 We propose that the silencing of many TEs in Arabidopsis is controlled by th

122 ally significant is the stable and heritable silencing of master regulators that would specify altern

123 t that could be phenocopied by RNAi-mediated silencing of MCL1.

124 Genetic silencing of mdig reduced activity of the major downstre

125 Additionally, silencing of MED15 resulted in reduced fatty acid conten

126 GapmeR-mediated silencing of Meg3 in CFs resulted in the downregulation

127 Silencing of METTL14 promotes terminal myeloid different

128 Most importantly, in vivo silencing of miR-125b by systemic delivery of locked nuc

129 In contrast, silencing of miR-155 expression with its inhibitor in th

130 Similarly, silencing of miR-21 or STAT3 and forced expression of PD

131 mmatory cytokines is reduced by ex vivo gene-silencing of miR-34a.

132 A knockout, an antagonist, or a local silencing of MKP-1 attenuates depressive-like behaviors,

133 In contrast, silencing of multiple bacterial flagellin-induced CRKs r

134 us, temporally controlled, and cell-specific silencing of multiple genes or pathways.

135 tructural phenotypes through allele-specific silencing of mutant keratin genes.

136 thermore, we discovered that miR858-mediated silencing of MYB83 is tightly regulated through a feedba

137 We specifically demonstrate the presence and silencing of MYC, JUN, and SOX2 mRNAs by miR-24 and miR-

138 s running bouts, that selective chemogenetic silencing of natural GAD65LH cell activity depresses vol

139 bBSK1 blocked BR-induced TMV resistance, and silencing of NbBES1/BZR1 blocked Bikinin-reduced TMV res

140 Silencing of NbBRI1 and NbBSK1 blocked BR-induced TMV re

141 Silencing of ND75, a subunit of the mitochondrial respir

142 models of DCIS, we found that RNAi-mediated silencing of NEMO increased tumor invasion and progressi

143 e results suggest that selective optogenetic silencing of nociceptive bladder afferents may represent

144 Virus-induced gene silencing of NOG1 compromised nonhost resistance in N. b

145 lung fibroblasts with genetic deficiency (or silencing) of Nox4.

146 In vitro, silencing of Nox5 in human mesangial cells was associate

147 RNAi-mediated silencing of NR4A1 decreased expression of PAX3-FOXO1A a

148 Silencing of NRF2 using siRNA diminished the protective

149 ccRCC harboring epigenetic silencing of NSD1 displayed a specific genome-wide methy

150 4-deficient lung fibroblasts is inhibited by silencing of nuclear factor erythroid-derived 2-like 2 (

151 I channels by BTP2 and diethylstilbestrol or silencing of ORAI expression impairs albumin uptake.

152 Silencing of orthologues of these candidate genes enhanc

153 e orthologous ZmSHR1 gene to avoid potential silencing of OsSHR2, stomatal cell files were observed b

154 These results and the observation that silencing of other ribosomal stalk proteins partially re

155 ade of OXT receptors as well as chemogenetic silencing of OXT neurons within the PVN prevented the ef

156 In end-stage mesothelioma, silencing of p16/Ink4a is sustained and deletion of p19/

157 Small interfering RNA-mediated silencing of parathyroid hormone 2 receptor (PTH2R), the

158 tion in microglial cells was associated with silencing of particular viral genes.

159 o play a key role in transmitting epigenetic silencing of PcG targets by linking PRC1 to formation of

160 Silencing of PECAM-1 or key ER stress genes abrogated SS

161 Finally, silencing of PFKFB4-induced apoptosis in p53-deficient c

162 with piRNA-binding protein Piwi and mediates silencing of phenotypic variations.

163 RNA interference-mediated silencing of pixr, or immunity against PIXR in mice, imp

164 l activity of PKR appears to be complete, as silencing of PKR expression has no impact on viral propa

165 Genetic silencing of PLD4, either globally or conditionally in p

166 ssion of TRPM2 mutant channel (C1008-->A) or silencing of poly ADP-ribose polymerase in ECs of mice p

167 RNAi-mediated silencing of POU5F1 reduced KANSL2 levels, linking these

168 ference model within the Orf50 region, where silencing of previously expressed isoforms by transcript

169 Previously, we have shown that silencing of PRMT5 expression in differentiated GBM cell

170 cell potential through selective epigenetic silencing of pro-memory genes in effector T cells.

171 In RPE19 cells, silencing of PrP(C) decreases ferritin while over-expres

172 Overexpression of miR-124 or siRNA silencing of PTPB1 restored normal proliferation and gly

173 In contrast to permanent silencing of PV neurons, transient inhibition of GABA re

174 ased overexpression and CRISPR/Cas9-mediated silencing of Qki5, we identified regulated expression of

175 Silencing of Rab5 shifts receptor-triggered secretion fr

176 Upon silencing of Rad51, a protein critical for HDR, Wwox-def

177 Finally, we show that epigenetic silencing of RAD51C and BRCA1 by promoter methylation is

178 induce marked dephosphorylation of MEK/ERK, silencing of RAF-MEK-ERK pathway transcriptional output,

179 found in a subset of glioblastoma (GBM) and silencing of RanBP6 promoted glioma growth in vivo.

180 Dual small interfering RNA (siRNA) silencing of RARalpha and RARgamma reversed RA blockade

181 RNAi-mediated silencing of RASSF1A induced epithelial-to-mesenchymal t

182 Nova2 increased beta cell apoptosis, whereas silencing of Rbfox1 and Rbfox2 increased insulin content

183 essive heterochromatin structure and loss of silencing of reporter genes in constitutive heterochroma

184 PAF1 knockdown enhances PIWI silencing of reporters when piRNAs target the transcript

185 ing subtelomeric chromatin to the NE and the silencing of resident genes.

186 rmine the mechanism for activation-dependent silencing of Rgs10 expression in microglia.

187 ating that HDAC enzymes are required for LPS silencing of Rgs10 Furthermore, we used chromatin immuno

188 Notably, silencing of RNA sensors RIG-I or MDA5 abrogated DC matu

189 Silencing of RNA5SP141 strongly dampened the antiviral r

190 Inhibition or silencing of ROCK1 was sufficient to rescue keratinocyte

191 mpensating for MSCI-mediated transcriptional silencing of Rpl10.

192 were observed after transient shRNA-mediated silencing of Rps19, but not several other tested ribosom

193 ed Arabidopsis more susceptible, whereas RNA silencing of RTP1 led to enhanced resistance to P. paras

194 diated heterochromatin formation, epigenetic silencing of S-phase genes and permanent cell cycle arre

195 Partial silencing of S100A4 suppressed migratory capabilities of

196 ly mutated in GCB DLBCL; the transcriptional silencing of S1PR2 by FOXP1 represents an alternative me

197 The silencing of SALL4 in cancer cells decreased the express

198 Silencing of SAP augmented and overexpression blocked PD

199 gestation, H3K27me3-induced transcriptional silencing of select gene targets ensured uterine quiesce

200 siRNA targeted to tumor cells for effective silencing of selected proteins.

201 as shown by agonist treatment and transient silencing of sensory neurons.

202 er in tumor-induced MDSCs, and inhibition or silencing of SETD1B diminished iNOS expression in tumor-

203 alling pathway is repressed by Myt1l through silencing of several members, including Hes1.

204 ssential role in the meiotic progression and silencing of sex chromosomes in the male germline, which

205 RNAi-mediated silencing of SLC13A5 expression in two human hepatoma ce

206 In vivo silencing of SLFN11 was associated with marked depositio

207 RNA interference-mediated silencing of SlGGB1 resulted in smaller seeds, higher nu

208 ase-2 (SHP-2), and SHP-2 down-regulation via silencing of small interfering RNA in endothelial cells

209 Silencing of SOCS1 protein with shRNAi lentivirus (shR-S

210 ntified as a target gene of miR-199a-3p, and silencing of SOCS7 promoted STAT3 activation.

211 Silencing of Sox102F led to misorientated and disorganiz

212 Silencing of SOX5 in human SH-SY5Y neuroblastoma cells r

213 pment involves the successive activation and silencing of specific gene expression programs and is dr

214 e used to treat disease caused by epigenetic silencing of specific loci.

215 IF1alpha and HIF2alpha protein levels due to silencing of Spry2 also up-regulated HIFalpha target gen

216 Consistently, silencing of Stat3 in tumors reduced Jab1/Csn5 expressio

217 -early gene expression and produced a robust silencing of STN neurons as measured using whole-cell re

218 This frequency-dependent mobilization or silencing of sub-pools in the RRP in terminals of granul

219 ted ubiquitylation of pol II is required for silencing of subtelomeric gene transcription.

220 (6)-methyladenine correlates with epigenetic silencing of such LINE-1 transposons, together with thei

221 Our results show that both blocking and silencing of SVIP lead to significant reduction in VTV f

222 Additionally, we show that silencing of SVIP reduces VLDL secretion, suggesting a p

223 Silencing of TaADF4 resulted in enhanced susceptibility

224 n of TNF by priming chromatin to prevent the silencing of target genes of the transcription factor NF

225 Silencing of TEAD phenocopies loss of YAP1, implicating

226 Gene silencing of TET2 obviously diminished NaCl-induced Tfh

227 mice, the exposure to HFD induces epigenetic silencing of the Ankrd26 gene, which contributes to the

228 We show that genetic silencing of the CcO complex by shRNA expression and los

229 However, silencing of the CCR gene results in considerable flux c

230 s not easily explained by imprecision in the silencing of the cones.

231 show that loss of JMJ24 results in increased silencing of the DNA transposon AtMu1c, while overexpres

232 Here we show that silencing of the EGF-related factor amphiregulin (AREG)

233 In vivo silencing of the FETUA gene in BALB/c mice results in a

234 COLDAIR, associates with Polycomb to mediate silencing of the floral repressor FLOWERING LOCUS C (FLC

235 FMR1 expression and significantly delayed re-silencing of the FMR1 gene in AZA-treated FXS cells.

236 Unexpectedly, silencing of the heterochromatic HML and HMR loci was no

237 integrative analysis, we discovered frequent silencing of the histone H3 K36 methyltransferase NSD1 a

238 Silencing of the HLA class-I APM is due to histone deace

239 Here, we show that CRISPR-Cas9-mediated silencing of the HuR locus increases the relative sensit

240 ed/inactivated with aging and identified the silencing of the IL7R gene and the IL-7 signaling pathwa

241 treatment or knockdown of hnRNP E1 relieves silencing of the inhibin betaA transcript, resulting in

242 rments proved to be decisive in vivo because silencing of the INSR attenuated clinical symptoms in an

243 Here we show that in rats, genetic silencing of the largest population of brainstem vagal p

244 Mechanistically, silencing of the let-7 target HMGA2 gene mimics the phen

245 Finally, the selective chemogenetic silencing of the LH-to-LHb pathway impairs aversion-driv

246 In addition, we found that epigenetic silencing of the miR-200 family microRNAs affects ZEB2 e

247 xpression is correlated with transcriptional silencing of the MLV promoter through the deposition of

248 ulted in potent, dose-dependent, and durable silencing of the mRNA encoding glycolate oxidase and inc

249 g leads to heterochromatinization and stable silencing of the NCoR gene, suggesting that NCoR loss ca

250 Silencing of the neuron increases sucrose feeding; optog

251 In vitro silencing of the novel AKT3 variant resulted in signific

252 by which learning reverses microRNA-mediated silencing of the novel plasticity protein ACVR1C via tra

253 ng this signal with morpholino technology or silencing of the polyadenylation factor CPSF1 caused a s

254 Our results suggest that silencing of the RPC5L in N. benthamiana disrupted not o

255 uired for improved load-bearing capacity and silencing of the spindle assembly checkpoint.

256 Inhibition of Mule phosphorylation by silencing of the Spleen Tyrosine Kinase (Syk) prevents i

257 is essential for facilitating the downstream silencing of the targeted mRNA.

258 Overexpression of miR302 effected silencing of the TGFbeta type II receptor and facilitate

259 l phenotype observed following RNAi-mediated silencing of the Trypanosoma brucei SODA ortholog sugges

260 Here, we show that the optogenetic silencing of the VH prevented the recall of contextual f

261 Silencing of the virus sensor, RIGI, or overexpression o

262 sability and autism spectrum disorder due to silencing of the X-linked, fragile-X mental retardation-

263 trafficking genes ARF4, COPB1, and USO1, and silencing of these genes attenuated the metastatic pheno

264 se effects were ablated with selective siRNA silencing of these proteins.

265 Our results demonstrate that epigenetic silencing of these SiM-miRNAs can result in increased AR

266 Genetic silencing of these TRCs abolished water-evoked responses

267 argely by FGF5 activation of FGFR2, as siRNA silencing of this ligand or receptor, respectively, inhi

268 Transcriptional gene silencing of this regulatory element repressed TERT expr

269 mice, we examined the effects of optogenetic silencing of TMNv HA neurons in vivo We found that acute

270 Consistent with this model, silencing of TNFalpha and MEKK4 dramatically reduces cys

271 ivity and subsequently refined by epigenetic silencing of transcripts associated with memory lymphocy

272 role in the recognition and transcriptional silencing of transposable elements (TEs), consistent wit

273 iction pathway and illustrate how epigenetic silencing of transposable elements rewires host gene exp

274 t and is associated with the transcriptional silencing of transposable elements.

275 ecture, DNA repair and genome stability, and silencing of transposon and gene expression.

276 coordinate RNA-directed DNA methylation for silencing of transposons and a subset of genes.

277 ms in gene body DNA methylation, euchromatic silencing of transposons and repeats, as well as silenci

278 We show that silencing of transposons in the pericentromeric heteroch

279 ciate with PiwiL2, a protein involved in the silencing of transposons.

280 Silencing of TREK-1 in mice prevents the previously demo

281 In primary haematopoietic cell cultures, silencing of TRIB3 facilitated megakaryocyte differentia

282 In the haematopoietic cell line UT7/mpl, silencing of TRIB3 increased basal and thrombopoietin-st

283 Secondly, silencing of TRIM14 expression significantly enhanced tu

284 Silencing of TTP in endometriotic and endometrial epithe

285 se with CXCR4 mutations show transcriptional silencing of tumor suppressors associated with acquisiti

286 It combines RNAi-mediated silencing of two endogenous proteins with the expression

287 Silencing of UBB reduces cellular UBB levels and results

288 Furthermore, shRNA-mediated silencing of USP14 or UCHL5 in Ewing sarcoma cells produ

289 or of host defenses consisting of RNAi-based silencing of viral genes.

290 HIV-1 latency is characterized by reversible silencing of viral transcription driven by the long term

291 Silencing of VPS13C was associated with lower mitochondr

292 Furthermore, acute silencing of VT3(Lbx1) neurons attenuated pre-establishe

293 l changes observed following transcriptional silencing of wag31 in M. tuberculosis.

294 zyme Q10 (CoQ10) biosynthesis gene Coq2, the silencing of which disrupted slit diaphragm morphology.

295 oncoding RNA (lncRNA) is thought to catalyze silencing of X-linked genes in cis during X-chromosome i

296 Silencing of XPO1 by either shRNA or selinexor significa

297 levels, after small interfering RNA-mediated silencing of YAP in Sk-Hep1, SNU182, HepG2, or pancreati

298 Silencing of young adult-born neurons also produced chan

299 y dexamethasone, neither silencing of DUSP1, silencing of ZFP36, nor silencing of both together preve

300 Lentivirus-mediated silencing of ZSCAN21 increased significantly SNCA promot