1 ar dominance (ND) consists of the reversible
silencing of 35S/45S rDNA loci inherited from one of the
2 tivity and histone methylation-mediated gene
silencing of ABI5.
3 somiRs") were identified in infected plants;
silencing of AGO4 strongly changed miRNA accumulation dy
4 We further report that
silencing of AgRP neurons selectively blocks the effect
5 RNA interference-mediated
silencing of AgTRIO in A. gambiae resulted in a 60% redu
6 at, plays a central role, being critical for
silencing of all except a subset of weakly expressed gen
7 a library of short hairpin RNAs for targeted
silencing of all known epigenetic proteins and performed
8 Strikingly, deletion or epigenetic
silencing of an ERV-derived enhancer suppresses cell gro
9 Instead, our results suggest that
silencing of ANG activity may be beneficial for symptoma
10 Furthermore, we predict that the
silencing of anti-SWR interneurons can trigger SWRs.
11 Silencing of AP-1 subunits in primary myometrium cells l
12 to decipher mechanisms that drive epigenetic
silencing of AP-2gamma target genes are a critical area
13 in 2-expressing pyramidal neurons, or 200 ms
silencing of Archeorhodopsin T-expressing pyramidal neur
14 Using optogenetic
silencing of ArchT-expressing neurons in adult ferrets,
15 We found that
silencing of ataxia-telangiectasia mutated and RAD3-rela
16 Importantly, in vivo therapeutic
silencing of ATF4-FAM129A axis profoundly inhibited tumo
17 ion between this epigenetic modification and
silencing of Avr1b.
18 emphasized the risks of increased transgene
silencing of Bacillus thuringiensis (Bt) rice under elev
19 Chemogenetic
silencing of BLA shortens waiting times overall whereas
20 this new cellular adaptive mechanism, direct
silencing of BLM Na/K-ATPase in intestinal epithelial ce
21 Gene
silencing of Bmp4 or its downstream mediator Smad7, reve
22 exhibits strong dwarfism and cell death, and
silencing of both genes via RNA interference also leads
23 duced fusion of Petunia hybrida petals, with
silencing of both PhGATA19 and its close paralog causing
24 testinal defects were observed after genetic
silencing of Brd4 in mice(6), the platelet and gastroint
25 ptome with transcriptomes obtained following
silencing of broadly acting mRNA decay and repression fa
26 Silencing of c-SRC or treatment with the c-SRC inhibitor
27 Furthermore, gene
silencing of c3g partly rescued nephrocyte diaphragm def
28 D1/5 phosphorylation and gene expression and
silencing of CAV-1 and DNM2 diminishes LDL-mediated ALK-
29 ility of HBV RNA and HBcrAg as surrogates of
silencing of cccDNA, to characterise this dissociation,
30 s of CD97 correlate with poor prognosis, and
silencing of CD97 reduces disease aggressiveness in vivo
31 In contrast,
silencing of CDPK5 had no effect on egress.
32 Silencing of CDR1as or CDR1 significantly inhibited LUSC
33 We identified
silencing of cerebellar degeneration-related 1 antisense
34 s infected tissues, indicating near complete
silencing of CgCOM1 gene expression in the pathogen.
35 ted neural cells can trigger chromosome-wide
silencing of chromosome 21 in Down syndrome patient-deri
36 In vitro
silencing of ciliary genes in endothelial cells disrupts
37 Silencing of circFOXP1 dramatically impaired MSC differe
38 a myoblast-derived cell line with inducible
silencing of CK2alpha and carried out a comprehensive RN
39 Silencing of clathrin adaptor proteins (AP) AP-1A, AP-1B
40 Targeted
silencing of clathrin or the gamma1 subunit of clathrin
41 Selective chemogenetic
silencing of cocaine-activated OFC neurons or their term
42 Host mediated
silencing of COM1 gene of Colletotrichum gloeosporioides
43 itro, both overexpression of mutant COPA and
silencing of COPA induced STING-dependent IFN signaling.
44 re-related antigen (HBcrAg) as surrogates of
silencing of covalently closed circular DNA (cccDNA), to
45 Silencing of COX19 using an artificial miRNA did not cau
46 ns of the transcription factor in C. elegans
Silencing of CRH-1e-expressing neurons during training f
47 Silencing of CrzR in PTTH neurons increased pupal size,
48 These results indicate that the
silencing of CTLA-4 can potentiate the T cell priming ca
49 d demyelination, we demonstrate that genetic
silencing of CXCR2 on oligodendroglia did not affect cli
50 P2J2 in cardiac cells, we performed targeted
silencing of CYP2J2 expression in human adult ventricula
51 Genetic
silencing of DCC prodeath activity in a BRAF(V600E) mous
52 H3K27me3) is associated with transcriptional
silencing of developmentally important genes.
53 l corepressor complex recently linked to the
silencing of developmentally regulated endogenous retrov
54 palmitoylation via 2-bromopalmitate, or the
silencing of DHHC3, activates antitumour immunity in vit
55 duction in fly Adar mutants is suppressed by
silencing of Dicer-2, which has a RNA helicase domain si
56 Small interfering RNA (siRNA)
silencing of DNMT3A expression in human macrophages caus
57 Silencing of DNMT3A in monocytes induced a paracrine pro
58 This translated into
silencing of dopaminergic midbrain neurons, reduced conn
59 epression of let-7 miRNAs and is mimicked by
silencing of downstream let-7 target HMGA2 or chemical i
60 cally directed deletion or acute optogenetic
silencing of DR(Sert) neurons dramatically increased the
61 Kidney-restricted
silencing of Drd1 in C57BL/6J mice increased blood press
62 and functional exhaustion through epigenetic
silencing of drivers of terminal differentiation.
63 feration and enhanced apoptosis, whereas RNA
silencing of Duxbl led to a decrease in apoptosis.
64 However,
silencing of DvABCB2 which is highly homologous to DvABC
65 Next, targeted "
silencing" of DYN+ neurons in the CeA was accomplished u
66 siRNA-
silencing of each RTC-proximal host factor demonstrated
67 an observation that was confirmed by genetic
silencing of EBP.
68 Consistent with being downstream of TOR,
silencing of EBP1 restrains, while overexpression promot
69 y, which was translated through HfQ mediated
silencing of EGFP by anti-EGFP synthetic small regulator
70 Silencing of eIF3e reduced the intracellular levels of t
71 Pharmacologic inhibition or genetic
silencing of either DHCR7 or DHCR24 had no impact on cel
72 ed ETO2, loss of ETO2 results in ineffective
silencing of embryonic/fetal globin gene expression, imp
73 ot formulations was also demonstrated by the
silencing of endogenous genes that encode two subunits o
74 g lysates from TIMAP-deficient mice and upon
silencing of endogenous TIMAP expression in ECs.
75 Silencing of endogenous UBR5 induced MYC protein express
76 We propose that PRC2-mediated
silencing of enhancers involved in cell differentiation
77 ting duct cells to see how overexpression or
silencing of epithelial sodium channel (ENaC) subunits a
78 d propose that the developmentally regulated
silencing of ESRRB triggers the selective inactivation o
79 ent data demonstrating widespread epigenetic
silencing of estrogen receptor in human osteosarcomas.
80 Silencing of exogenous DNA can make transgene expression
81 persistent shortcomings, but pH sensitivity,
silencing of expression and a limited concept of sensor
82 ion and genetic ablation of JNKs, as well as
silencing of expression of TRB3, did not restore insulin
83 Gene
silencing of Fbxl2 in skeletal myoblasts resulted in inc
84 perature-dependent repression and epigenetic
silencing of floral repressor FLOWERING LOCUS C (FLC).
85 odevelopmental disorder caused by epigenetic
silencing of FMR1 and loss of FMRP expression.
86 te immune sensor's involvement in epigenetic
silencing of foreign DNA.
87 a critical role for PTEN loss and epigenetic
silencing of FOXA1 in heterogeneous human disease and sh
88 Importantly, CRISPR-mediated
silencing of Foxp3 transcription, but not protein expres
89 Silencing of FPR3 in DCs and pretreatment with an antago
90 Silencing of galectin-3 induced significant reduction in
91 Selective
silencing of GC activity during specific temporal window
92 Optogenetic
silencing of GC allowed us to tease apart the contributi
93 Chemogenetic
silencing of GC impaired task performance.
94 They mediate epigenetic
silencing of gene expression in a wide range of developm
95 portant epigenetic mechanism responsible for
silencing of gene expression in animal development and c
96 hrin-dependent using chemical inhibitors and
silencing of gene expression.
97 family protein and implicated in epigenetic
silencing of gene expression.
98 ation and histone H1 mediate transcriptional
silencing of genes and transposable elements, but how th
99 In SBW25, CRISPRi-mediated
silencing of genes encoding the GacA/S two-component sys
100 ating small interfering RNA (siRNA), for the
silencing of genes in bone-marrow endothelial cells.
101 a and is associated with DNA methylation and
silencing of genes involved in tumor suppression.
102 EZH2 expression results in the
silencing of genes that suppress tumor formation and met
103 This process includes
silencing of genes to erase original tissue memory and p
104 ould be important specifically for heritable
silencing of genes which are flagged as 'foreign', such
105 th a spreading surfactant resulted in strong
silencing of GFP transgenes in both species.
106 Silencing of Glo1, selectively increasing MG, activated
107 Strikingly,
silencing of glomerulus-selective OSNs extends the CP fo
108 various outcomes could also be attenuated by
silencing of glutathione S-transferase P1 (GSTP1), a med
109 Overexpression and RNA interference
silencing of GmMYB29A2 increased and decreased expressio
110 Silencing of Gprasp1 or Gprasp2 increased the survival,
111 We showed that the
silencing of GRASLND resulted in lower accumulation of c
112 n urothelial carcinoma of the bladder (UCB),
silencing of GULP1 facilitated the nuclear accumulation
113 Silencing of GULP1 was associated with GULP1 promoter hy
114 Silencing of H. schachtii ACC by RNAi induced similar ph
115 This mechanism involves the
silencing of H3K27me3 writers, activity of H3K27me3 eras
116 cognizes' H3K27me3 specifically and enforces
silencing of H3K27me3-demarcated genes in mammalian cell
117 Consistently,
silencing of HDAC3 expression with siRNA largely recapit
118 treatment or small interfering RNA-mediated
silencing of HDAC4 also suppressed expression of those p
119 ts for compounding hypermethylation and gene
silencing of hemizygous tumor suppressor genes (TSG), we
120 anscription and may partly mediate IFN-alpha
silencing of hepadnaviral cccDNA transcription.
121 Depletion of the microbiota or
silencing of hepatic ACSS2, which generates acetyl-CoA f
122 t gene expression and to faithfully maintain
silencing of heterochromatin.
123 Silencing of HIAR abrogated the pro-angiogenic and pro-m
124 Here, we demonstrate that specific
silencing of high-molecular-weight MAP2 in vivo abolishe
125 Silencing of histone deacetylase 8 led to the inhibition
126 Silencing of HK-2 prevented increased glucose metabolism
127 Down-regulation or epigenetic
silencing of HML-2 env resulted in dissociation of the s
128 ation and suppressive functions; conversely,
silencing of HOTAIRM1 or HOXA1 expression in MDSCs from
129 Mir142 loss-of-function counteracts aberrant
silencing of Hoxa cluster genes by IDH2(R140Q).
130 works are active in human heart disease, and
silencing of hub genes limits fibroblast activation.
131 In mice, di-siRNAs induced the potent
silencing of huntingtin, the causative gene in Huntingto
132 Silencing of ICMT led to significant reduction of TAZ pr
133 Silencing of IDH2 in prostate cancer cells impaired oxid
134 Interestingly,
silencing of IL-17B or IL-17RB led to significant suppre
135 atment ameliorated Th17-induced EAU, whereas
silencing of IL-24 in Th17 cells enhanced disease.
136 ge induces L13a/GAIT-dependent translational
silencing of inflammatory genes in response to HFD as an
137 f the corticospinal pathway, as chemogenetic
silencing of injured corticospinal neurons transiently a
138 Stable
silencing of Intraflagellar Transport 88 (Ift88) or Kine
139 Mutation of IR52a and optogenetic
silencing of IR52a+ neurons decrease levels of male sexu
140 sive chromatin conformation resulting in the
silencing of IRF8 expression in a celltype-specific mann
141 We claim that a selective
silencing of IRF8 in inflammatory leukocytes (such as Ly
142 n vitro and in vivo using nanoparticles, and
silencing of ITCH sensitizes the tumour cells to irradia
143 Silencing of JMJD2B prevented the EndMT-induced reductio
144 Silencing of JMJD2B reduced TGF-beta2-induced expression
145 Small interfering RNA (siRNA)-mediated
silencing of KLF2 in RAW 264.7 cells could restore the a
146 IFI16-dependent epigenetic modifications and
silencing of KSHV lytic genes.
147 Silencing of LAMR abrogated these effects.
148 epended on top-down feedback as chemogenetic
silencing of lateral OFC neurons disrupted reversal lear
149 REM sleep-specific optogenetic
silencing of LH(vgat) cells induced a reorganization of
150 CDR1as depletion results from epigenetic
silencing of LINC00632, its originating long non-coding
151 Silencing of LTR retrotransposons is dependent on downst
152 Deletion of CAF-1 p150 subunit impairs the
silencing of many genes including Oct4, Sox2 and Nanog a
153 ously been implicated in the transcriptional
silencing of many retroviruses by binding to DNA sequenc
154 In vivo
silencing of Mcl and Mincle or blockade of their endogen
155 The
silencing of MCL and Mincle resulted in TNF-alpha secret
156 Silencing of MeAPL3 in cassava through stable transgenic
157 In vitro experiments confirmed that
silencing of MGL decreases prostaglandin E(2) accumulati
158 Lentivirus-mediated
silencing of MIA3 (melanoma inhibitory activity protein
159 ted in cholestatic mouse models, and in vivo
silencing of miR-210 ameliorated BA-induced liver pathol
160 Silencing of MMP7 and MMP9 abolished increased migration
161 al culture (268 ug/l), as authenticated from
silencing of molecular expression of the Taxol-rate limi
162 heterochromatic domains yet dispensable for
silencing of most transposable elements; H1 depletion af
163 Silencing of mPFC NPY1R+ neurons overall, and specifical
164 bining a number of approaches, including the
silencing of MRGPRX2, we now report that MRGPRX2 is inde
165 Furthermore, the
silencing of MUC5AC in human pancreatic cancer cells red
166 genetic editing and simultaneous epigenetic
silencing of multiple ERVs, we demonstrate that ERV dere
167 We also explored, whether cardiac specific
silencing of MYOCD expression could ameliorate the cardi
168 Silencing of MYOCD in RAL rats by a cardiac homing pepti
169 synchronized down-state featuring prolonged
silencing of neural activity in all layers of many corti
170 We also show that epigenetic
silencing of new Ty1/copia copies can affect their impac
171 Silencing of Nicotiana benthamiana NbGPAT6a increased le
172 hroughout the genome and promotes epigenetic
silencing of nicotinic acid phosphoribosyltransferase (N
173 ion transcription factors Isl1 and Tbx18 and
silencing of Nkx2.5.
174 Silencing of NM23-M1 in mouse bone marrow-derived macrop
175 The
silencing of NRF2 resulted in a constant activation of A
176 Since
silencing of NRSF is known to initiate neural differenti
177 Importantly,
silencing of OMA1 expression increased oxidant-induced c
178 in human chordoma cells promotes epigenetic
silencing of oncogenic TBXT, alters gene networks critic
179 Complete
silencing of one allele was also observed irrespective o
180 Partial
silencing of one of these, the HANABA TARANU (HAN)-like
181 netic phenomena that involve transcriptional
silencing of one parental allele.
182 oding RNA Xist mediates chromosome-wide gene
silencing of one X Chromosome in female mammals to equal
183 Double
silencing of OsVOZ1 and OsVOZ2 in the Piz-t background d
184 Silencing of other claudins had no such effects, and re-
185 Silencing of p300/CBP-associated factor (PCAF), which ac
186 t either pharmacological inhibition or siRNA
silencing of p38 impaired caffeine-induced Ca(2+) releas
187 contrast, although there is transcriptional
silencing of P4HA3 in a subset of melanomas, the collage
188 Both reactivation of telomerase and
silencing of p53 rescued hepatocyte formation in telomer
189 Genetic
silencing of PAG-USV neurons rendered males unable to pr
190 s a target in PDAC models using both genetic
silencing of PARG and established small-molecule PARG in
191 In vivo,
silencing of PARG significantly decreased tumor growth.
192 RNAi-mediated transient and stable
silencing of PDC1 expression in melon showed that this g
193 RNAi mediated
silencing of pectin degrading enzyme of R. solani gives
194 Silencing of pericyte-derived Ptn rendered neurons vulne
195 Genetic
silencing of Pik3ca in KrasG12D/Trp53R172H-driven pancre
196 ute HRDE-1 that maintains trans-generational
silencing of piRNA targets.
197 pressive chromatin marks and transcriptional
silencing of piRNA targets.
198 e the secondary endo-siRNAs required for the
silencing of piRNA targets.
199 we identified a functional role of Nup93 in
silencing of Polycomb target genes and in spatial foldin
200 Silencing of PrP(C) in primary human TM cells induces ag
201 Ptch1 locus, which correlated with premature
silencing of Ptch1 These cells also had decreased expres
202 Genetic
silencing of PTX3 in invasive melanoma cells dramaticall
203 Silencing of Rab9 or Rab11 GTPases, which are involved i
204 dditional, dominant repressive mechanism for
silencing of repetitive major satellite sequences.
205 of ATRX, a chromatin remodeler with roles in
silencing of repetitive regions of the genome and in rec
206 Functionally,
silencing of REX1 potentiated the tumor-initiating and m
207 Targeted
silencing of ROBO4 or mutant ROBO4 expression in endothe
208 Small-molecule inhibition of RON or siRNA
silencing of RON significantly reduced OPN-induced migra
209 Silencing of S100A10, ANXA2, SPT6, or KDM6A expression b
210 between transcription of essential genes and
silencing of selfish DNA.
211 Our results presented herein show that
silencing of SEMA7A decreases tumor growth in a model of
212 Importantly,
silencing of SH3YL1 in primary human CD4 cells demonstra
213 ene sid-1, suggesting that transgenerational
silencing of sid-1 underlies inherited defects in RNAi.
214 Virus-induced gene
silencing of SlFAD2-7 in spr2 results in significant inc
215 In vivo, nephrocyte-specific gene
silencing of sns or c3g compromised nephrocyte filtratio
216 rtitioning solely to non-raft domains, while
silencing of SNX19 impaired D(1) R function in RPTCs.
217 Kidney-restricted
silencing of Snx19 resulted in hypertension in C57BL/6J
218 Small interfering RNA-mediated
silencing of SOCS1 and SOCS3 in macrophage and T cells,
219 Vivo morpholino-mediated
silencing of SOCS1 and SOCS3 resulted in protective cyto
220 Silencing of SPANXB1 reduced migration, invasion and rea
221 d RNA molecules can efficiently trigger RNAi
silencing of specific genes, but their therapeutic use h
222 thods for neural circuit manipulation allows
silencing of specific hyperactive neural circuits.
223 ure models of human OCCC, we find that shRNA
silencing of SPINK1 sensitizes tumor cells to anoikis an
224 Silencing of SRSF3, RBM22, PTBP1 and RBM3 decreased aggr
225 tone hyper-acetylation, and Sirtuin-mediated
silencing of starvation-induced subtelomeric domains.
226 stone-deacetylation mediated transcriptional
silencing of STM.
227 Silencing of SUB1 mRNA expression did not affect parasit
228 aneous activity guides the strengthening and
silencing of synapses which underlies tonotopic map refi
229 Inhibition or
silencing of TAK1 prevented expression of Rorgammat and
230 27 (H3K27) methylation to mediate epigenetic
silencing of target genes.
231 transcriptome analyses revealed that genetic
silencing of TBK1 increased expression of proteins and g
232 xoglycosidase treatment and after RNAi-based
silencing of TbSTT3A, the oligosaccharyltransferase that
233 As a consequence, the
silencing of TEs was impaired, causing in particular you
234 enomenon, whose ancestral role is epigenetic
silencing of TEs.
235 noncoding RNAs implicated in the epigenetic
silencing of TEs.
236 In vivo
silencing of TET3 in GSC-enriched tumors reduces 5hmC ac
237 GFBR2 kinase activity, small interfering RNA
silencing of Tgfbr2 expression, or inhibition of SMAD3 a
238 0.0009, and 0.02, respectively), whereas RNA
silencing of the AR-RGN top key driver, PQBP1 (polygluta
239 Thus, we propose that the heritable
silencing of the Cd4 gene in CD8(+) T cells exploits coo
240 Because
silencing of the copper transporter ATP7A also reduced c
241 Genetic
silencing of the descending neurons shows that oviposito
242 ng development prevented CpG methylation and
silencing of the Dlk1-Dio3 locus, thereby increasing miR
243 Overexpression or
silencing of the ENaC gamma-subunit was associated with
244 Previously, we discovered that
silencing of the fetal gamma-globin gene requires the er
245 The full mutation results in transcriptional
silencing of the Fmr1 gene and loss of fragile X mental
246 neurodegenerative disease caused by partial
silencing of the FXN gene.
247 2) that mediates coordinated transcriptional
silencing of the MHC-I antigen processing pathway (MHC-I
248 In vitro, genetic
silencing of the Npr2 abolished protective effects of C-
249 ibition of PI(3,5)P(2) synthesis, or genetic
silencing of the PI(3,5)P(2)-regulated lysosomal Ca(2+)-
250 Our data indicate that Whsc1 links
silencing of the pluripotency regulatory network with ac
251 improve glucose tolerance in obese mice, 2)
silencing of the Pnpla2 in interscapular BAT causes a br
252 Silencing of the PttCLE47 gene expression affected later
253 developmental capacity through RNAi-mediated
silencing of the QS signaling machinery ("inducible mono
254 NA methylation in CG and CHG contexts in the
silencing of the S-genome rDNA loci was revealed.
255 are independent of V1 and are abolished upon
silencing of the SC.
256 n but can also be associated with epigenetic
silencing of the SDHC gene.
257 nversely, inhibition of trans-endocytosis by
silencing of the small GTPase TC21 or expression of a do
258 We find that initial
silencing of the somatic program proceeds indistinguisha
259 a previously uncharacterized HOAP function:
silencing of the specialized telomeric retrotransposons
260 Silencing of the spindle assembly checkpoint involves tw
261 Silencing of the TFEB and TFE3 genes, alone or in combin
262 data demonstrates extensive epigenetic gene
silencing of the transcription factor PRDM16 in renal ca
263 precision that were reversed by chemogenetic
silencing of the transplanted neurons and a long-lasting
264 adverse prognosis associated with epigenetic
silencing of the tumour suppressor RASSF1A is due to inc
265 As potential mechanisms involved in the
silencing of the two miR-15/16 loci, we identified a gen
266 aimed at the transcriptional and epigenetic
silencing of the viral reservoir to block reactivation f
267 functional cure aimed at the transcriptional
silencing of the viral reservoir.
268 Silencing of the WRKY25/22 orthologous genes in Nicotian
269 countermeasures that prevent the epigenetic
silencing of their genes during lytic replication, and t
270 Silencing of these neurons attenuates the anorexia cause
271 ucose concentration, whereas DREADD-mediated
silencing of these neurons was without effect.
272 Here we show that targeted optogenetic
silencing of these signals, performed selectively during
273 ed a genetic loss of miR-15a and miR-15b and
silencing of these two loci by methylation.
274 Silencing of this enzyme suppresses melanoma invasion an
275 Silencing of this intronic circular RNA in pancreatic is
276 Optogenetic
silencing of this sparse ABN activity during REM sleep a
277 culture models revealed that siRNA-mediated
silencing of TMPRSS13 expression decreases proliferation
278 role in transgene expression regulation and
silencing of transgenic crops.
279 Silencing of transposable elements (TEs) is established
280 Panx and are required for co-transcriptional
silencing of transposons in somatic and germline cells o
281 Chemogenetic
silencing of TRPV1-expressing afferents or rostral ventr
282 revealed enhanced intratumoral necrosis upon
silencing of tumor cell Angpt2 expression in the absence
283 altered PRMT5 expression to transcriptional
silencing of tumor-suppressing miRNAs in lymphoma cells
284 estore epigenetic aberrations that result in
silencing of tumor-suppressor genes, oncogene addictions
285 We demonstrated that genetic
silencing of TWIST1 or treatment with the TWIST1 inhibit
286 Additionally, virus-induced gene
silencing of two trichomes preferentially expressed cand
287 ed) ascospores, suggesting efficient meiotic
silencing of unpaired FgAMA1.
288 3 were studied by determining the effects of
silencing of USP7 and USP10.
289 Chemogenetic
silencing of USV-responsive neurons in TeA impairs audit
290 Accordingly, pharmacogenetic
silencing of V1 SST(+) interneurons fully blocked oxytoc
291 Optogenetic
silencing of ventral hippocampal (VH) terminals in the P
292 uption of local PL firing during optogenetic
silencing of VH-PL suggest that the VH continuously upda
293 e anti-Rac1-GTP antibody, which is lost upon
silencing of vimentin expression.
294 gical tau in neuronal cells, whereas genetic
silencing of VPS35 results in its accumulation.
295 shown to be a positive regulator of HR since
silencing of VuPOB1 expression in transgenic B301 roots
296 n corroboration with the over-expression and
silencing of WsMYC2 suggested its positive influence on
297 by DLC1-deficient endothelial cells, as the
silencing of YAP prevents this loss.
298 1, that is essential for the methylation and
silencing of young transposable elements.
299 proliferation in vitro and in vivo, whereas
silencing of ZFP36L1 enhanced tumor cell growth.
300 Silencing of ZNF529 in human hepatoma cells results in u