ライフサイエンスコーパス: be silenced

1 In the presence of the target the probe is "silenced".

2 the metaphase plate, the checkpoint needs to be silenced.

3 nts and other repetitive sequences that must be silenced.

4 specific imprinting, the paternal UBE3A copy is silenced.

5 from birth as fetal gamma-globin expression is silenced.

6 e sexes, one of the X chromosomes in females is silenced.

7 anscriptional activation of p21 when the DDR is silenced.

8 work is activated and the antagonist network is silenced.

9 environment where the overall transcription is silenced.

10 ype is recapitulated in zebrafish when rasa3 is silenced.

11 reased significantly when miR-187 expression is silenced.

12 e downstream NF-kappaB inflammatory response is silenced.

13 replication defects and cell death when UBR5 is silenced.

14 cued in FABP4/aP2-null macrophages when UCP2 is silenced.

15 enzyme argininosuccinate synthetase 1 (ASS1) is silenced.

16 t results in APC/C reactivation when the SAC is silenced.

17 oxin A, in which immunogenic B-cell epitopes are silenced.

18 mutants and oncogenic cofactors when MEIS1/2 are silenced.

19 ic genes are expressed and nonvascular genes are silenced.

20 s machinery assembles, and resident elements are silenced.

21 AY1044 and in neurons in which S1P3 receptor was silenced.

22 aired in DCs in which the gene encoding TFEB was silenced.

23 but was trimethylated when MED25 expression was silenced.

24 AW 264.7 macrophage-like cells in which LRP1 was silenced.

25 ng confirmed in HepG2 cells where HINT2 mRNA was silenced.

26 plants in which the endogenous DNA ligase 1 was silenced.

27 s in which the hexose transporter gene LeHT1 was silenced.

28 wth, but displayed suppressed growth when PC was silenced.

29 n HuR was silenced but was enhanced when TTP was silenced.

30 C was nearly completely abolished when IL-32 was silenced.

31 3 did not bind to CGRE when c-myb expression was silenced.

32 or size was reduced when Ca(v)3.1 expression was silenced.

33 diminished in cells in which SKP2 expression was silenced.

34 clones in which the remaining wild-type TP53 was silenced.

35 ated THP-1 cells in which the P2X7R gene had been silenced.

36 th those cells in which GNA13 expression had been silenced.

37 hetized rats was observed when DVMN neurones were silenced.

38 rbcL was reduced when the PPR-encoding genes were silenced.

39 ) that have been shown to function as dimers were silenced.

40 saic flies in which subsets of Gr66a neurons were silenced.

41 ged after intratectal excitatory connections were silenced.

42 elementary motion detector neurons T4 and T5 were silenced.

43 ternal allele, with the maternal counterpart being silenced.

44 multaneously monitor the number of promoters being silenced.

45 rinted gene Cdkn1c, with the paternal allele being silenced.

46 by glutamate released from inner hair cells) is silenced [5, 6].

47 Plants in which IPUT1 was silenced accumulated IPC, the immediate precursor, a

48 e, but it is also associated with genes that are silenced after a burst of their expression.

49 -responsive olfactory sensory neurons (OSNs) are silenced after eclosion; thus, OSN activity is requi

50 ipt (XIST)-the master regulator of XCI-which are silenced after entry into meiosis.

51 The SAC is silenced after all the kinetochores establish proper

52 is suppression is abolished if DG expression is silenced, again demonstrating the central role of thi

53 When five of these genes were silenced, amebic strains with significant decreases

54 sms that determine how Polycomb target genes are silenced and how Polycomb silence is preserved throu

55 posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS

56 rein endogenous APH-1A and APH-1B expression was silenced and into which either the wild type APH-1B

57 midrib3 (caffeic acid O-methyltransferase), were silenced and characterized in the sweet corn line G

58 s (since if MSCI is achieved, Zfy genes will be silenced), and finally execute cells with MSCI failur

59 ources of new natural products, but how they are silenced, and how they may be rationally activated a

60 , however, fertility is restored, P elements are silenced, and P element piRNAs are produced de novo.

61 here an rDNA array from one parental species is silenced, and that from the other parent is preferent

62 potential of HCT116 cells only when alpha1D was silenced, and blocking NCX1/3 increased cytosolic Ca

63 increased in vascular tumor cells where Akt3 was silenced, and the growth of these tumor cells was in

64 Larvae in which Odd neurons are silenced are less efficient at odor tracking than co

65 Latent HIV proviruses are silenced as the result of deacetylation and methylat

66 cell cycle inhibitor p57Kip2 (CDKN1C), which is silenced as a consequence of the recombination event.

67 cytoplasmic, and immediate-early (IE) genes were silenced as in primary CD34(+) cells.

68 ity: P-S6k levels are decreased when neurons are silenced, as well as after acute ethanol sedation.

69 f CYP27A1 expression in cells where its gene was silenced attenuated their growth in vitro and in tum

70 Our data suggest that ITCH could be silenced both in vitro and in vivo using nanoparticle

71 vels in Caco-2 cells were repressed when HuR was silenced but was enhanced when TTP was silenced.

72 significantly altered when individual PmTPCs are silenced, but the timing and shape of the cortical f

73 erentiation a subset of these enhancers must be silenced, but the mechanisms underlying enhancer sile

74 the upstream Hippo tumor suppressor pathway is silenced, but efforts to pharmacologically inhibit YA

75 In Neurospora crassa, unpaired genes are silenced by a mechanism called meiotic silencing by

76 trotransposons and endogenous viral elements are silenced by ADARs [adenosine deaminases acting on do

77 In bacteria, foreign nucleic acids are silenced by clustered, regularly interspaced, short

78 encing to identify key suppressor genes that are silenced by histone methylation in constitutively ac

79 gdala neurons activated by fear conditioning are silenced by local inhibitory interneurons after exti

80 es, potentially offensive autoreactive cells are silenced by mechanisms of immune tolerance, islet an

81 ly identified targets in non-hepatic tissues are silenced by miR-709 in hepatocytes, even though seve

82 ately one-third of medullary Tph2(+) neurons are silenced by postnatal (P) days 5 and 12, along with

83 scores of excess ribosomal RNA (rRNA) genes are silenced by repressive chromatin modifications.

84 emonstrate that it is enriched at genes that are silenced by RNAi-mediated TGS.

85 cripts is fine-tuned by AmrZ, all T6SS mRNAs are silenced by RsmA.

86 ioned at the loci HMR and HML, respectively, are silenced by Sir proteins recruited by proteins that

87 In the absence of beta-catenin, target genes are silenced by TCF-mediated recruitment of TLE/Groucho

88 These classes differ in whether the genes are silenced by the asRNA and whether the silencing is H

89 regulated horizontally acquired genes, which are silenced by the histone-like protein H-NS.

90 h horizontally acquired virulence genes that are silenced by the nucleoid-associated protein H-NS and

91 d migrate to the periphery, where they would be silenced by anergy.

92 hboring genes, the corresponding genes could be silenced by chance.

93 While previously known to be silenced by CHD4, the fetal globin genes are exposed

94 showed experimentally that these genes must be silenced by DNA methylation for cancer cell survival,

95 cipated, involving specificities expected to be silenced by mechanisms of tolerance; the regulatory a

96 However, Semaphorin repulsion can be silenced by other distinct cues and signaling cascade

97 C) gene, the expression of which is known to be silenced by prolonged exposure to winter-like tempera

98 fragments of once-functional genes that have been silenced by one or more nonsense, frameshift or mis

99 eratinocytes in which BPAG1-e expression had been silenced by stable expression of short hairpin RNA

100 How these genes are kept from being silenced by DNA methylation is not well understood

101 switches cardiac fetal gene expression from being silenced by HEY to being activated by BRG1.

102 AdDelta24.GFP), where initial Ad replication is silenced by a green fluorescent protein (GFP) transge

103 on the orientation, either MATa or MATalpha is silenced by centromeric chromatin.

104 a pivotal regulator of the Wnt pathway that is silenced by DNA hypermethylation in many colon cancer

105 that may represent cryptic information that is silenced by DNA methylation in the reference B73 geno

106 drivers of chemoresistance whose expression is silenced by DNA methylation that should be further ev

107 ression of miR-29a and -b, the Mir29b2c gene is silenced by DNA methylation.

108 abled homolog 2-interacting protein (DAB2IP) is silenced by EZH2-mediated H3K27 trimethylation of the

109 f this, we hypothesized that tosA expression is silenced by H-NS.

110 GAD1 is a target gene that is silenced by H3K27me3.

111 he transcriptional activity of wild-type E2A is silenced by high levels of corepressors, such as the

112 SKIP gene (SPHKAP) expression is silenced by hypermethylation of its promoter in acute

113 s Polyposis Coli (APC) tumor suppressor gene is silenced by hypermethylation or mutated in up to 70%

114 The paternal allele of Ube3a is silenced by imprinting in neurons, and Angelman syndr

115 wer mitotic exit when the spindle checkpoint is silenced by inhibition of the checkpoint kinase, Mps1

116 In hepatocytes, EpCAM is silenced by polycomb repressive complex 2 (PRC2) and

117 Moreover, SDPR expression is silenced by promoter DNA methylation, and as such it

118 (type I) in which most viral gene expression is silenced by promoter DNA methylation.

119 effects of alkylating agents; however, MGMT is silenced by promoter hypermethylation during carcinog

120 ontaining a caspase recruitment domain (ASC) is silenced by promoter methylation in many types of tum

121 sgenesis to generate NOD mice in which IL-17 is silenced by RNA interference.

122 When vimentin expression is silenced by small hairpin RNA (shRNA) to reduce vimen

123 ld, and is robust to adaptation; however, it is silenced by surround inhibition and is contrast depen

124 ifferentiation, chromatin at their enhancers is silenced by the activity of the Lsd1-Mi2/NuRD complex

125 Transcription from these promoters is silenced by the histone-like nucleoid structuring (H-

126 n the activity of graft-derived interneurons was silenced by a designer drug while using donor hiPSC-

127 that PGC1alpha expression in melanoma cells was silenced by chromatin modifications that involve pro

128 date the gene functions, each candidate gene was silenced by injecting the target dsi-RNA to female C

129 MAP1LC3A-Variant1 gene expression was silenced by promoter methylation.

130 8) gene, key in the SL biosynthetic pathway, was silenced by RNA interference (RNAi).

131 When Alix was silenced by RNA interference, TnBVANK1 was no longer

132 When SAMHD1 was silenced by siRNA transfection the composition of th

133 ated a direct effect by YAP on TGM2 when YAP was silenced by small interfering RNA.

134 ells in which the endogenous SDC1 expression was silenced by specific siRNAs.

135 h4a, which is expressed in all Hcrt neurons, was silenced by the CRISPR-mediated gene inactivation sy

136 Finally, Hcp expression in K pneumoniae was silenced by the histone-like nucleoid structuring pr

137 Claudin-1 expression was silenced by transfection with short interfering RNA

138 inhibitory Drosophila allatostatin receptor were silenced by application of an insect peptide allato

139 yses focused on known targets of 6BIO, which were silenced by this compound.

140 tate stromal and epithelial cells, when ARSB was silenced, C4S, versican and versican promoter activi

141 n which a fraction of the pre-synaptic input is silenced can reproduce this reduction in variability,

142 Although most are silenced, certain TEs have been co-opted by the host

143 When cortical Htt function was silenced, cortical and striatal excitatory synapses

144 s in which the NR1 subunit of NMDA receptors was silenced demonstrated a decrease in calcium uptake.

145 ein endothelial cells in which the HPS6 gene was silenced displayed impaired PDI secretion and exocyt

146 s, those in which GmMAPK4 homologs (GmMPK4s) were silenced displayed strong phenotypes including stun

147 ch occurs when transcription of the FXN gene is silenced due to an excessive expansion of GAA repeats

148 because its autopolyubiquitination activity is silenced due to an intra-interaction between the C2 a

149 e also find that specific subtelomeric genes are silenced during adaptation to loss of mtDNA.

150 rabidopsis thaliana, rRNA gene subtypes that are silenced during development were recently mapped to

151 5S ribosomal RNA (rRNA) genes, many of which are silenced during development.

152 tions, we show that stem cell identity genes are silenced during differentiation by loss of their act

153 take and metabolism of less-preferred sugars are silenced during growth with preferred sugars.

154 which tumor-suppressor and DNA-repair genes are silenced during tumor initiation and progression, th

155 ed that RSV F is under selective pressure to be silenced during vector replication in vivo, but this

156 atin insulators protect erythroid genes from being silenced during erythropoiesis, and the disruption

157 However, snai2 expression is silenced during CNC migration, and its roles at later

158 n of crucial lytic cycle transactivators but is silenced during latency in hematopoietic progenitor c

159 Transcription is silenced during mitosis and reactivated at mitotic ex

160 define an epigenetic mechanism whereby EPAS1 is silenced during sarcoma progression.

161 CIITA and MHC class II expression is silenced during the differentiation of B cells to pla

162 h bivalent histone modifications; one allele was silenced during differentiation.

163 Two genes studied in detail, MAL and OLIG2, were silenced during transformation, initially through e

164 genes proximal to the X-inactivation center are silenced earlier than distal genes, while lowly expr

165 thogen Vibrio cholerae to show that VacJ/Yrb is silenced early during mammalian infection, which stim

166 The canonical Wnt signaling can be silenced either through beta-catenin-mediated ubiquit

167 essed, while coamplified passenger genes may be silenced epigenetically.

168 ovide novel evidence that miR-34a expression is silenced epigenetically by EZH2 and DNA methylation,

169 triguingly, RCC precursor cells where Jade-1 was silenced exhibited an increased capacity for AKT-dep

170 When these neurons are silenced, exploratory laterality increases, with mor

171 When RhoG expression is silenced, FA are more stable and live longer, resulti

172 virulent strains of Vibrio parahaemolyticus are silenced for the vibrio archetypal pathway of quorum

173 Importantly, KIF1Bbeta and DRP1 are silenced in 1p36 hemizygous-deleted neuroblastomas,

174 Concordantly, these genes are silenced in castration-resistant prostate cancer ren

175 s of DIRAS3 imprinting, DIRAS3 and GNG12-AS1 are silenced in cis and the remaining GNG12-AS1 transcri

176 Transposable elements (TEs) are silenced in germ cells by a mechanism in which PIWI

177 essors of acute myeloid leukemia (AML); they are silenced in human AML, and abrogation of both genes

178 HERVs are silenced in most normal tissues, up-regulated in ste

179 ease in ROS and OCR were DUOX 1 and 2, which are silenced in pancreatic ductal adenocarcinoma, but up

180 that Sir3 and Sir4 associate with genes that are silenced in the absence of H3K4 methylation.

181 ably, when epidermal Stat3, Skints, or DETCs are silenced in young skin, re-epithelialization followi

182 e first time that the pH regulator NHE-1 can be silenced in a human cancer and also suggest that pH d

183 ant missing link in how microRNAs (miRs) can be silenced in chronic lymphocytic leukemia (CLL):histon

184 (termed Cxcr2-CKO mice) allows for Cxcr2 to be silenced in oligodendrocytes in adult mice following

185 Subsequently, Foxd3 needs to be silenced in primed pluripotent cells to allow re-acti

186 ng silencing in B. oleracea, but has already been silenced in B. rapa.

187 -head antisense transcript, both transcripts being silenced in colon primary tumors concomitant with

188 e mismatch repair gene MutL homolog 1 (MLH1) is silenced in a clinically important subgroup of sporad

189 Finally, we provide evidence that YAP is silenced in a subset of highly aggressive and undiffe

190 negative regulator of PI3K-AKT signaling and is silenced in approximately 30% of CRC.

191 urons, the paternally inherited UBE3A allele is silenced in cis by a long non-coding RNA called UBE3A

192 We show that Notch signaling is silenced in human AML samples, as well as in AML-init

193 the hormone receptor status, its expression is silenced in human primary breast tumor tissues, breas

194 Our results demonstrate that C/EBPalpha is silenced in human SCC and loss of C/EBPalpha confers

195 at the portal of entry into the body and yet is silenced in latently infected neurons, and (c) the me

196 he 28S rRNA gene, we show that X-linked rDNA is silenced in males.

197 ASS1 is silenced in many human malignancies therefore, these

198 In contrast, telomerase activity is silenced in most adult somatic cells.

199 as AML data set reveals that GLI3 expression is silenced in most AML patient samples, and the GLI3 lo

200 rder, fragile X mental retardation 1 (FMR1), is silenced in most cases by a CGG-repeat expansion muta

201 lude that cross-talk between PTEN and PHLPPs is silenced in normal prostate cells but activated in TG

202 We found that NHE-1 on 1p is silenced in oligodendrogliomas secondary to IDH-assoc

203 is established, viral lytic gene expression is silenced in part by a cellular intrinsic defense cons

204 effects of the chemokine gene CXCL12, which is silenced in PDAC tumors, yet is sufficient to suppres

205 T6SS activity is silenced in plasmid-containing, antibiotic-resistant

206 However, why SKIP activity is silenced in primary AML cells is unclear.

207 GR expression is silenced in prostate cancer by a combination of AR bi

208 We conclude that LTF mRNA expression is silenced in prostate tumorigenesis via hypermethylati

209 of Ccl1, a gene required for M2bM survival, is silenced in the MLNs of 7 Gy GIARS mice because of Ga

210 ng view of development is that transcription is silenced in the oocyte until early divisions in the e

211 is expressed in normal cells, but expression is silenced in tumor cells by epigenetic mechanisms.

212 tivities, but it harbors microRNA 152, which is silenced in tumor cells concurrently with COPZ2 and a

213 Mitogen-induced Skp2 expression is silenced in vascular smooth muscle cells (VSMC) isola

214 ssed in microglia at high levels, expression is silenced in vitro following activation of TLR4 recept

215 Indeed, when CXCR7 was silenced in breast cancer cells, their metastatic ab

216 lizing antibody or when uPAR gene expression was silenced in cells used to prepare CM, the activity o

217 First, the PLD2 gene was silenced in highly metastatic, aggressive breast can

218 DJ-1 was silenced in human CD34(+)-derived MCs and in the LAD

219 Complimentary studies in which Plexin C1 was silenced in human melanocytes were performed.

220 STAT3 was silenced in LAD2 and primary human mast cells to stu

221 PP2A was silenced in lung epithelial cells treated with A1AT

222 Rictor, the functional component of mTORC2, was silenced in Madin-Darby canine kidney cell cysts gro

223 e while opposite results were seen when Bmi1 was silenced in Panc-1 cells.

224 When VAMP2-dependent exocytosis was silenced in single axons, oligodendrocytes preferent

225 ol biosynthesis in ProCESA7:miRNA CCR1 lines was silenced in the lignifying cells themselves, but not

226 tumors or metastases in mice when BRCA1-IRIS was silenced in them.

227 loid cells in vivo Strikingly, although IRF8 was silenced in tumor-induced MDSCs, iNOS expression was

228 When RNase 7 was silenced in vitro, the percentage of UPEC binding or

229 DAC preferentially regulated genes that were silenced in cancer and that were methylated at thei

230 l transduction pathways while TLR4 and MyD88 were silenced in IEC18 cells using shRNA.

231 Orai1 and Kindlin-3 genes were silenced in neutrophil-like HL-60 cells to assess t

232 p14 and p16, targets of p53, were silenced in our cell system and did not seem to pla

233 hese effects are reversed when E7 expression is silenced, indicating that this pathway may have progn

234 rs occurred independently of ESR1 when GATA3 was silenced, indicating that GATA3, when present on the

235 ts were abrogated when SOCS3 gene expression was silenced, indicating that SEA-mediated signaling inh

236 r, mating terminated normally when these PNs were silenced, indicating that SSFT is not required for

237 When NaCDPK4 and NaCDPK5 were silenced individually, neither stunted growth nor h

238 mouse models in which endogenous cohesin can be silenced inducibly.

239 onditions, and our understanding of how they are silenced is in its infancy.

240 l silencing, but what identifies the loci to be silenced is unclear.

241 in which both X chromosomes are active, Rsx is silenced, linking Rsx expression to X-chromosome inac

242 Cs in which gene expression of Akt1 and XIAP was silenced lost their protection and demonstrated incr

243 he PWS-SRO in oocytes so that paternal genes are silenced on the future maternal allele.

244 ablishes a structural framework for why cGAS is silenced on chromatinized self-DNA.

245 ached kinetochores; moreover, the checkpoint is silenced only after the final kinetochore-spindle att

246 Plants in which the PIP1 subfamily was silenced only in the BS (SCARECROW:microRNA plants)

247 GABAergic interneuronal types are silenced or fire during these events, but the mechan

248 tor, Ir40a, and flies in which these neurons are silenced or Ir40a is knocked down lose avoidance to

249 All var genes are silenced or transcribed at low levels in blood stage

250 not observed when olfactory receptor neurons are silenced or when other sensory organs are severed, s

251 structural variants are also more likely to be silenced or dysregulated.

252 analysis of liver in which miR-192/-194 had been silenced or overexpressed, respectively, and tested

253 tissues in which SOX30 was unmethylated, but was silenced or downregulated in lung cancer cell lines

254 tric, because cis-regulators on the X cannot be silenced (otherwise there would be no expression in f

255 When these interneurons were silenced, persistence increased and males copulated

256 These genes are silenced, predominantly by hypermethylation and less

257 Clr4, indicated that the relocalized region was silenced redundantly by heterochromatin and another

258 fection of host macrophages in which Il6 had been silenced resulted in increased expression of interf

259 Cells in which GPR81 was silenced showed a dramatic decrease in growth and me

260 Memory formation was prevented when mPFC was silenced specifically during the interval separating

261 er (QC) cells, expression of the marker gene was silenced specifically in the QC cells without affect

262 eriments showed that the colocalized alleles were silenced, suggesting a common repression mechanism.

263 BCs recruit more inputs when their neighbors are silenced than either active or silenced BCs with equ

264 lated males sleep less, and when MS1 neurons are silenced, the normal male sleep suppression in femal

265 receptacles, where the expression of FaEOBII was silenced, the expression of cinnamyl alcohol dehydro

266 When galectin-3 was silenced, the increases in Sp1 binding to the Wnt9A

267 We observed that when PHD3 is silenced, there is a significant decrease in TNF-alph

268 y attenuated in macrophages in which mPGES-1 was silenced, thereby identifying mPGES-1 as a therapeut

269 Many tumor suppressor genes (TSGs) are silenced through synergistic layers of epigenetic re

270 Vs) containing long terminal repeats (LTRs), are silenced through trimethylation of histone H3 on lys

271 ls, it is plausible that CXCR4 signaling can be silenced through a physical heterodimeric association

272 ion of the posterior selector gene engrailed is silenced through an autoregulatory silencing mechanis

273 ISG15 expression was silenced through transfection with small interferenc

274 senescence, and we propose that they have to be silenced, through miR172c-induced AP2-1 cleavage, in

275 y genes, such as Sonic hedgehog (Shh), which is silenced throughout Schwann cell development before i

276 s bipolar competence in Otx2+ cells and must be silenced to allow bipolar cell generation.

277 Prior to differentiation, Oct4 must be silenced to allow for the development of the three ge

278 erfusion injury (IRI) or graft rejection may be silenced to improve organ quality after transplantati

279 arge fraction of eukaryotic genomes and must be silenced to protect genome integrity.

280 it is poorly understood how this checkpoint is silenced to allow anaphase onset.

281 mes properly attached, its checkpoint signal is silenced to allow progression into anaphase.

282 ch the tumor-suppressor candidate gene TUSC4 was silenced to gain insights into its function.

283 findings suggest that Myc transcription can be silenced using an RNA interference (RNAi)-based strat

284 RAW/LR5 macrophages in which Hck expression was silenced using RNA-mediated interference (Hck shRNA)

285 For this, HMGB1 was silenced using small interfering RNA, whereas contro

286 To examine this hypothesis, AQP genes were silenced using artificial microRNAs that were expre

287 The endogenous Ig loci were silenced using designer zinc finger nucleases.

288 imental results, where the selected proteins were silenced using specific siRNAs and the viability of

289 xin receptors in mouse and human macrophages were silenced using targeted siRNAs or blocked with spec

290 ntain either GFP or mCherry epitope tags can be silenced via multigenerational RNAe, whereas a transg

291 ing in lesions where LTF mRNA has presumably been silenced via CpG island methylation.

292 anscribed; some showed indications of having been silenced via pseudogenization.

293 therefore, hypothesized that LTF expression is silenced via CpG island hypermethylation in the early

294 sarcoma-associated herpesvirus (KSHV) genes is silenced via repressive histone marks on their promot

295 Isoflavonoid biosynthesis was silenced via RNA interference of isoflavone synthase

296 be restored when hemizygous transgenes that were silenced via multigenerational RNAe become homozygo

297 In cells where KAP1 was silenced, we identified multiple downregulated genes

298 When tagged CA1 cells were silenced, we found that memory retrieval was impair

299 sitive breast cancer cell line, when SLC6A14 is silenced with shRNA.

300 The phytoene desaturase gene was silenced with a transient hairpin RNA expression, re