1 podia were significantly decreased with APOE
knockdown.
2 and PLCbeta1, which were inhibited by STIM1
knockdown.
3 and the effects of YAP are blunted upon its
knockdown.
4 mice 1 week after adenovirus-mediated Acot1
knockdown.
5 as arrested at the G2 phase after FAM83H-AS1
knockdown.
6 expression of MYBL1 in tumor cells with OGT
knockdown.
7 ypes generated by MRN- and DRN-specific SERT
knockdown.
8 Gab2 overexpression but were rescued by Gab2
knockdown.
9 ato ORE1 as target gene for RNA interference
knockdown.
10 In human beta-cells, barr2
knockdown abolished glucose-induced insulin secretion.
11 uption of caveolae by MCD treatment or Cav-3
knockdown abolished the protection against H/R-induced m
12 STAMBP deubiquitinates NALP7 and STAMBP
knockdown abrogates LPS or Pam3CSK4-induced increases in
13 in the ventrolateral OFC and unilateral Bdnf
knockdown accompanied by lesions of the contralateral am
14 H19
knockdown activates SAHH, enabling DNA methyltransferase
15 KIT
knockdown also increased RAS/MAPK pathway activation in
16 Furthermore, laminin alpha2
knockdown also perturbed microtubule (MT) organization b
17 Moreover, KDM3A
knockdown also potently inhibited tumorigenic potentials
18 Intra-NAc GLT-1
knockdown also prevented ceftriaxone from attenuating re
19 STEAP1/4
knockdown also reduced the ability of keratinocytes to i
20 APOE
knockdown also resulted in increased cellular cholestero
21 The cathepsin B
knockdown and 24-h treatment with OA resulted in increas
22 or monoubiquitination at H2A Lys-119 as both
knockdown and deletion of USP7 results in decreased leve
23 engineer a Cas13 ortholog capable of robust
knockdown and demonstrated RNA editing by using catalyti
24 Overexpression of HBL1 repressed, whereas
knockdown and knockout of HBL1 increased, cardiomyocyte
25 ry role for TRAIL-R3/4 was revealed by shRNA
knockdown and mAb blockade, showing that these regulator
26 s transfer learning to incorporate CLIP-Seq,
knockdown and over expression experiments, which are inh
27 PARTICLE
knockdown and over-expression resulted in inverse change
28 Knockdown and overexpression lines of HER2 confirmed the
29 ur analysis showed that Pak1 overexpression,
knockdown and Pak1 knockout cell line models showed that
30 Genetic
knockdown and pharmacological inhibition in vascular smo
31 ers a novel chemical probe for selective VHL
knockdown,
and demonstrates the potential for a new moda
32 in PRL-induced transcription following HMGN2
knockdown,
and it does so by allowing increased STAT5 re
33 Furthermore using siRNA-induced in vivo
knockdown approach we demonstrated that beneficial effec
34 Using cell-based
knockdown approaches and microarray analyses we found th
35 Neuropharmacological and Homer2
knockdown approaches were also used in C57BL/6J mice to
36 Aptamer-mediated pull-down and gcgr
knockdown assay verified that GCGR was the target of apt
37 erentiation, phenocopying the effects of IYO
knockdown at the transcriptomic and developmental levels
38 ed Sp1-mediated Aqp5 activation, while HDAC3
knockdown augmented AQP5 protein expression.
39 Furthermore, EAF2
knockdown blocked androgen repression of LNCaP or C4-2 c
40 the ERK1/2 inhibitor UO126, or ERK1/2 siRNA
knockdown blocked the H2O2-induced shift of MLK3, while
41 JB12
knockdown by siRNA led to the induction of caspase proce
42 Thus, ASO-mediated DNM2
knockdown can efficiently correct muscle defects due to
43 We further found that lncRNA
knockdown can perturb complex transcriptional networks i
44 e of the CB1 receptor was explored using CB1-
knockdown (
CB1Kd) intestinal epithelial cells.
45 p16-overexpressing and small hairpin RNA-
knockdown cells were generated, and the effect of p16 on
46 erol metabolism and the p53 pathway in CDK19
knockdown cells.
47 s at ER-PM junctions, were reduced in RASSF4-
knockdown cells.
48 sion in HT-29 xenografts initiated from NOX1
knockdown cells.
49 he deficits in invadopodium function in Vav2-
knockdown cells.
50 ugmentation of contractility, whereas NDPK-C
knockdown decreased cAMP levels.
51 SKP2
knockdown decreased EZH2 levels in human PCa cells throu
52 Vivo-morpholino-mediated WT1
knockdown decreased Kdr transcripts in cultured embryoni
53 ADORA2A
knockdown decreases hypoxia-induced glycolytic enzyme ex
54 tiation, while morpholino- and siRNA-induced
knockdown diminishes it.
55 Our results show that double
knockdown (
dKD) of ZO-1/ZO-2 elevates the apical epithel
56 Importantly, NCALD
knockdown effectively ameliorates SMA-associated patholo
57 Its
knockdown elicited mesenchymal-to-epithelial transition
58 dation and reduced PPARalpha activity, Acot1
knockdown enhanced hepatic oxidative stress and inflamma
59 iption factors and verify predicted links in
knockdown experiments.
60 HSPA1L
knockdown facilitated the interaction of GP78 and PrP(C)
61 erties resulted in an enhanced in vitro gene
knockdown for the acid-degradable cationic nanoparticles
62 genetically manipulated GSC depletion, E(z)
knockdown germ cells also fail to replenish lost GSCs.
63 linked N-acetylglucosamine transferase (OGT)
knockdown grew significantly slower than those formed fr
64 Knockdown had minimal effects on cell proliferation but
65 Mice with single-minded 1-mediated Glp1r
knockdown had reduced hypothalamic-pituitary-adrenal axi
66 ocytes of Zdhhc13-deficient mice and Zdhhc13-
knockdown Hep1-6 cells.
67 ned beetle species by combining systemic dsx
knockdown,
high-throughput sequencing of diverse tissues
68 Pkm-
knockdown immortalized mouse podocytes had higher levels
69 AT1R
knockdown impaired IL-1beta-induced IL-6 and IL-8 secret
70 Concordantly, PDK3
knockdown improved mitochondrial function, emphasizing t
71 We engineered an H3.3
knockdown in Arabidopsis thaliana and observed transcrip
72 In vitro studies using Gal-3
knockdown in cardiac fibroblasts demonstrated that Gal-3
73 Of note, SRC-2
knockdown in cardiomyocytes decreased VEGF expression an
74 ocortices and RNA sequencing following CLOCK
knockdown in differentiated human neurons in vitro.
75 In vitro, siRNA-mediated FABP4
knockdown in endothelial cells led to a marked increase
76 In vivo, targeting RAGE shRNA
knockdown in human and mouse breast cancer cells, decrea
77 NgBR
knockdown in human breast cancer cells reduces Ras membr
78 Consistent with the above, Crb3
knockdown in mammalian cells affects the dynamics of IFT
79 dependent on stimulation by FGF2, and Ptprb
knockdown in mammary epithelial cells resulted in a high
80 that E2f3a, but not E2f3b, overexpression or
knockdown in mouse NAc regulates cocaine-induced locomot
81 hat the modulation of heat-shock factor-1 by
knockdown in nCPCs or overexpression in aCPCs significan
82 Folr1
knockdown in neural plate cells only is necessary and su
83 imilar results were obtained following ACSL6
knockdown in rat myotubes, which was associated with a d
84 In this study, C1QBP
knockdown in RCC cell influenced expression of multiple
85 Local 5-HT2CR
knockdown in the BLA with stereotaxic injection of 5-HT2
86 MAGUK removal via RNAi-mediated
knockdown in the CA1 hippocampal region in immature anim
87 tion for loss of torsinA in rodents, torsinA
knockdown in the immature cerebellum failed to produce d
88 SERT
knockdown in the MRN or DRN produced anxiety-like behavi
89 induced apoptosis, and shRNA-mediated HOTAIR
knockdown in TRAIL-resistant PANC-1 cells sensitized the
90 d from an affected individual and ACTB siRNA
knockdown in wild-type fibroblasts showed altered cell s
91 Molecular pathways overrepresented after FLG
knockdown included inflammation, protease activity, cell
92 eptor death receptor 5 (DR5), whereas HOTAIR
knockdown increased DR5 expression.
93 HDAC3 binds to Sp1 and HDAC3
knockdown increased interaction of GATA6/Sp1, GATA6/p300
94 on of STAT6 in OVA-exposed mice, whereas Lyn
knockdown increased STAT6 and MUC5AC levels in 16HBE cel
95 n of Zonulin-1 and E-cadherin, whereas Nlrp3
knockdown increased the permeability of cholangiocyte mo
96 g the components of mTORC2 showed that Pdcd4
knockdown increased the protein but not mRNA level of st
97 nd that short hairpin RNA-mediated macroH2A1
knockdown induces acquisition of CSC-like features, incl
98 d, we tested whether NLRC3 overexpression or
knockdown influences NALP3 activity in human monocyte an
99 In keratinocytes, SIRT1
knockdown inhibited EMT, cell migration, and TGF-beta si
100 pecific TEs and TE-adjacent loci during PIWI
knockdown is suppressed when PIWI and PAF1 levels are bo
101 ased dendritic spine density, whereas Tomo-1
knockdown (
KD) decreased spine density.
102 Here, we show that PTEN
knockdown (
KD) impairs beta-Arrestin1 membrane localizat
103 In this study, we show that
knockdown (
KD) of all expressed members of the KDM5 fami
104 Lentiviral shRNA-mediated
knockdown (
KD) of PKCiota leads to decreased nuclear YAP
105 Pdcd4
knockdown/
knockout significantly increased the translati
106 e, we show that HDAC6 inhibition and genetic
knockdown lead to a strong decrease in human proplatelet
107 site transcriptomes from a conditional AP2-G
knockdown line and NF54 wild-type parasites at multiple
108 Knockdown lines of TpSAP1 and 3 displayed malformed valv
109 IDL6 overexpression and
knockdown lines respectively decrease and increase the A
110 sing pharmacological PKD inhibitors and PKD1-
knockdown macrophages revealed that PKD1 is indispensabl
111 sion of Keratin 10 (K10) resulting from Cdk5
knockdown may be responsible for an abnormal epidermal s
112 ed B cells (NF-kappaB) activation, and Znrf4
knockdown mice have reduced NOD2-induced tolerance and m
113 memory in NMDA receptor hypofunctioning NR1-
knockdown mice, and were essentially devoid of catalepsy
114 NOD2
knockdown((-/-)())
mice were rescued from the detrimenta
115 Furthermore, like stable Pin1
knockdown,
moderate overexpression of miR-140-5p not onl
116 Znrf4
knockdown monocytes have sustained nuclear factor kappa-
117 BCR
knockdown occludes OGD-induced Rac1 activation in hippoc
118 on of HoxA genes upon differentiation, while
knockdown of a long noncoding RNA overlapping E1 has no
119 - and/or P-receptors) inhibited motility but
knockdown of acr-16+acr-26 (M- and/or N-receptors) did n
120 Stable
knockdown of ACTN4 by shRNA in HPCs significantly reduce
121 apoptosis, we for the first time found that
knockdown of Akt1 and the NF-kappaB-activating kinase IK
122 Knockdown of aldolases activates AMPK even in cells with
123 H2.35 liver cells with shRNA
knockdown of ANLN formed tumors more slowly in FRG mice
124 Pharmacological inhibition or
knockdown of any one of the PI3KKs significantly decreas
125 Knockdown of AR with shRNAs and a new generation anti-an
126 or ARL15 were investigated using conditional
knockdown of Arl15 in murine 3T3-L1 (pre)adipocytes.
127 METHODS AND
Knockdown of ATF6 in cardiac myocytes subjected to I/R i
128 Interestingly,
knockdown of ATGL, the best-known molecular target of AB
129 SiRNA
knockdown of autophagy initiator beclin-1 enhanced Mtb s
130 Small interfering RNA
knockdown of beta2-microglobulin reduced the expression
131 ock-out of individual ZDHHCs, siRNA-mediated
knockdown of both ZDHHC3 and ZDHHC7 in ZDHHC20 knock-out
132 able suppression on Ca(2+) entry with double
knockdown of both.
133 Knockdown of C3 and CFB expression inhibited migration a
134 Knockdown of cadherin-10 reduces excitatory but increase
135 The
knockdown of CD73 expression in cultured IECs resulted i
136 Overexpression of betaTrCP2 or the
knockdown of Cdc25A remedies the high mitotic index and
137 Short hairpin RNA
knockdown of Chrna7 in the DG enhanced baseline aggressi
138 via regulation of a subset of oncogenes, and
knockdown of circCCDC66 inhibited tumor growth and cance
139 A transient
knockdown of CRABP2 was established in human NF1-associa
140 (Gja1 (adipoq) KO) and by overexpression and
knockdown of Cx43 in cultured adipocytes.
141 ch was again attenuated by either AMD3100 or
knockdown of CXCR4 or CXCR7.
142 Knockdown of cytoplasmic nucleoside kinases reduced mtDN
143 Knockdown of Drp1 in D1-MSNs blocks drug seeking after c
144 how here that chemical inhibition or genetic
knockdown of DYRK1A interferes with neural specification
145 th CRISPR-mediated gene activation and shRNA
knockdown of DYRK1A, we show here that chemical inhibiti
146 Knockdown of each of these E3 ligases enhances LT stabil
147 RNAi
knockdown of either Cbx3 or Med26 inhibits neural differ
148 Knockdown of either SERPINB3 or SERPINB4 mRNA (both P <
149 Knockdown of either TUBB3 or UNC5C blocked netrin-1-prom
150 ximal region of the GC during repulsion, and
knockdown of either UNC5C or TUBB3 abolished the netrin-
151 Finally, we show that
knockdown of EmMBD2/3 expression disrupts normal cellula
152 Further, siRNA
knockdown of endogenous GATAD2B significantly reduced P4
153 virus-based gene therapy combining complete
knockdown of endogenous PABPN1 and its replacement by a
154 Knockdown of EphB2 disrupted the separation of the VZ/SV
155 Moreover,
knockdown of FABP4 increases survival in Hoxa9/Meis1-dri
156 Furthermore,
knockdown of FEN1 resulted in G1/S or G2/M phase cell cy
157 Additionally,
knockdown of FEN1 significantly attenuated homologous DN
158 We show that
knockdown of folate receptor 1 (Folr1; also known as FRa
159 Knockdown of FOXO4 but not FOXO1 expression decreased pr
160 expression of mutant htt On the other hand,
knockdown of Foxp1 promotes death in otherwise healthy n
161 n of GAPDH1 structure-function relationships
Knockdown of GAPDH1 expression and catalytic site disrup
162 primary CD3+ T cells, showing that specific
knockdown of GIMAP6 led to enhancement of phorbol 12-myr
163 rug resistance gene 2 knockout), the hepatic
knockdown of GnRH decreased IBDM and liver fibrosis.
164 Knockdown of GP130 or IL-2Rgamma induced cell death in s
165 e behavior while intra-BLA administration or
knockdown of GPR171 in the BLA reduces anxiety-like beha
166 _1, as well as following lentiviral-mediated
knockdown of GPR171 in the BLA.
167 Knockdown of GRP78 reversed the attenuating effect of EC
168 ly, genetic or shRNA-mediated conditional KO/
knockdown of GSK3beta reduced inhibitory phosphorylation
169 Knockdown of H1 rescues the decrease in PRL-induced tran
170 eatment of HCC cells with HDAC inhibitors or
knockdown of HDAC1 and/or HDAC2 restored FBP1 expression
171 Additionally,
knockdown of hgrs-1 had little to no effect on SNX-1 and
172 Here, we show that
knockdown of Hop in the germ line nurse cells (GLKD) of
173 Overexpression, but not
knockdown of HRS, promoted hyperubiquitination of CLR un
174 A siRNA
knockdown of HSP70-1 suppressed angiogenic responses and
175 SiRNA
knockdown of integrin beta3 and inhibition of Akt activi
176 The mechanistic study indicates that
knockdown of IRE1alpha repressed the expression of beta-
177 ctivation increased Irf5 expression, whereas
knockdown of Irf5 blunted CB1R-induced secretion of infl
178 RNAi analysis revealed that
knockdown of isoatp4056 expression had no effect on A. p
179 shRNA-mediated
knockdown of isoform 2 in BRAFi resistant cells restored
180 Consistently,
knockdown of KANK1 in neurofibroma cells promoted cell g
181 1 appears reduced in T2D islets, and further
knockdown of KCNB1 does not inhibit Kv current in T2D be
182 Here, using siRNA-mediated
knockdown of KIF20B in a human cell line and fixed and l
183 We find that
knockdown of KPNA4 reduces cell migration in multiple PC
184 impact viral replication, while in contrast,
knockdown of Ku80 and inhibition of the DNA-PK enzyme, w
185 Knockdown of Kv2.1 expression reduces secretory granule
186 s within the dorsal root ganglion (DRG), and
knockdown of Kv4.3 selectively induces mechanical hypers
187 ShRNA
knockdown of La in HEK 293 T cells increased Sendai viru
188 Finally, we showed that the
knockdown of LAMB1 or K19 in subcutaneous xenograft mous
189 Chronic
knockdown of LH GLP-1R induced by intraparenchymal deliv
190 Finally,
knockdown of liver CES1 in mice markedly increased the s
191 Finally, siRNA
knockdown of LRRC8C+LRRC8D strongly inhibited the releas
192 Knockdown of LY6E in human peripheral blood mononuclear,
193 We show that
knockdown of mcircRasGEF1B results in altered expression
194 Knockdown of MDA-9/Syntenin sensitizes GBM cells to radi
195 Knockdown of MDC1 or abrogation of Plk1 phosphorylation
196 nt results were observed with spatiotemporal
knockdown of miR-8 and luciferase assays.
197 An siRNA-mediated
knockdown of Mule or TRIM26 leads to stabilisation of NE
198 Knockdown of Myc, but not the mutant p53, significantly
199 Acute
knockdown of Myt1l in the developing mouse brain mimicke
200 Overexpression or RNAi-mediated
knockdown of neuroligins, respectively, causes a dramati
201 hibition of calcineurin by cyclosporine A or
knockdown of NFATc4 using small interfering RNA suppress
202 RT-10 meditated growth inhibition for CCA as
knockdown of NGAL decreased Ki-67 expression in SNU308 c
203 Targeted
knockdown of Notch3 expression by transient siRNA transf
204 and extra-terminal domain inhibitor JQ1, or
knockdown of overlapping long noncoding RNAs (lncRNAs) b
205 Either genetic
knockdown of p62 or inhibition of NF-kappaB sensitized t
206 SH-SY5Y cells with a stable
knockdown of Parkin or SLP-2, as well as induced pluripo
207 Knockdown of phb2 partially reversed beneficial effects
208 hila models of Huntington's disease, genetic
knockdown of PIP4K ameliorated neuronal dysfunction and
209 We show that
knockdown of PLK1, PLK3, and PLK4, as well as inhibition
210 Significantly,
knockdown of PRMT5 in AR-positive LNCaP cells completely
211 Knockdown of PRMT5 or inhibition of PRMT5 by a specific
212 ow for the first time that overexpression or
knockdown of RanBP9 directly enhances and reduces tau le
213 Hsc70 inhibitors, whereas overexpression or
knockdown of RanBP9 significantly diminishes the anti-ta
214 Knockdown of RhopH2 expression in cycle one leads to a d
215 Knockdown of RIMA causes delayed onset of cell different
216 In mice,
knockdown of RTN3 expression eliminated cooling-induced
217 Knockdown of several Trailblazer genes shows significant
218 Knockdown of Shrm4 in rat severely impairs GABABR activi
219 Taken together, these results indicate that
knockdown of Sin3A directly alters the expression of met
220 Knockdown of Sirt1 in endothelial cells, and conditional
221 Antisense
knockdown of slincR results in an increase in sox9b expr
222 Knockdown of SOX2 in hiPSCs led to decreased HBL1 expres
223 Knockdown of Spry2 resulted in reduced expression of Ser
224 Knockdown of STN NMDA receptors, which also suppresses p
225 Mutation or
knockdown of TAR3 (tyrRII, CG16766) had no effect.
226 However, deletion of both genes, or
knockdown of TAR3 on a TAR2 mutant background, eliminate
227 In the current study, we showed that
knockdown of taurine up-regulated gene 1 (TUG1) induces
228 Knockdown of TGF-beta1 expression in the tumor cells neg
229 on of dominant-negative (DN) forms of NSF or
knockdown of the expression of NSF, the key regulator of
230 Using a targeted
knockdown of the GLP-1 receptor in the single-minded 1 n
231 In contrast,
knockdown of the H3K27 demethylase ubiquitously transcri
232 ISC/EB-specific
knockdown of the mitophagy-related genes Pink1 or Parkin
233 Using antisense
knockdown of the n1-src microexon, we have studied neuro
234 leukemia cell line K562 in response to shRNA
knockdown of the RNA editing enzyme ADAR1.
235 Interestingly,
knockdown of the RNA surveillance nuclease, Xrn1, and me
236 This was validated through shRNA-mediated
knockdown of the target protein, HNF1beta, in five high-
237 Knockdown of these proteins substantially increases HA e
238 The
knockdown of TIM-1 expression significantly reduced HCV
239 expression in monocytes exposed to HCV, and
knockdown of TLR7 partially attenuated this expression,
240 Furthermore,
knockdown of TLR8 completely attenuated collagen express
241 Additionally,
knockdown of TMEM20 in miR-150-deficient naive CD8(+) T
242 Conversely,
knockdown of transformer in chromosomal females eliminat
243 acrophage activation, whereas siRNA-mediated
knockdown of TRIM59 enhanced LPS-induced macrophage acti
244 omain 5 (TTC5), a p53 co-factor, and genetic
knockdown of TRIP13 in murine inner medullary collecting
245 We also show that
knockdown of TrkB or Bdnf in this brain region does not
246 We show that
knockdown of TrkB, but not Bdnf, in the DRN results in l
247 Single
knockdown of TRPC6 and TRPC1 resulted in a comparable su
248 n anesthetized rats with and without in vivo
knockdown of TRPC6 in kidneys.
249 Knockdown of TRPP3 repressed the expression of the brown
250 hable drug targets with different functions:
Knockdown of unc-38+unc-29 (L- and/or P-receptors) inhib
251 enhances epithelial barrier integrity, while
knockdown of USP48 attenuates TNF-alpha/JNK pathway and
252 Knockdown of YTHDF2 enhanced lytic replication by impedi
253 Moreover, RNAi-mediated
knockdown of YY1 in GC cells significantly decreased ATP
254 Knockdown of ZEB1 resulted in more profound reduction of
255 Knockdown of ZNF148 results in reduced TERT expression,
256 al and genetic approaches including specific
knockdowns of genes of interest from primary CD34(+) hem
257 oduction that was blocked by sigma1-receptor
knockdown or Akt inhibition.
258 We also found that Rap1B
knockdown or an EPAC antagonist increases endothelial pe
259 Moreover, TAK1
knockdown or JNK pathway inhibition induced the expressi
260 eatic and ovarian cancer cells with ST6Gal-I
knockdown or overexpression, we determined that alpha2-6
261 ricular dysfunction in vivo, whereas genetic
knockdown or pharmacological blockade of microRNA-146a b
262 Interestingly, DDR2
knockdown or pharmacological inhibition of DDR2 also inh
263 ute suppression of RNF145 via shRNA-mediated
knockdown,
or chronic inactivation of RNF145 by genetic
264 Vitamin D receptor (VDR)
knockdown partly abolished MART-10-induced inhibition of
265 oved the alveolar bone and PDL damage of the
knockdown phenotype, which are thus shown to be partiall
266 ELENA1
knockdown plants show decreased expression of PATHOGENES
267 KIBRA
knockdown podocytes were also protected against protamin
268 report that silencing the INSR in inducible
knockdown rats impairs selective T cell functions but no
269 Finally, Glp1r
knockdown reduced anxiety-like behavior, implicating PVN
270 Importantly, we found that tau
knockdown reduced axon outgrowth and growth cone turning
271 ride-stimulated human THP1 monocytes, ARID5B
knockdown reduced expression of genes involved in athero
272 CD44
knockdown reduced NF-kappaB nuclear translocation and do
273 In particular, ARF
knockdown reduced non-nuclear localization of YAP which
274 Despite increased FA oxidation, Acot1
knockdown reduced the expression of peroxisome prolifera
275 Consistent with this, CTCF
knockdown reduced the Ser2P but increased Ser5P modified
276 trolled by the host protein BACH1, and BACH1
knockdown reduces BZLF1 expression.
277 Rac3
knockdown reduces matrix degradation by invadopodia, whe
278 Indeed, RIMA
knockdown reduces the nuclear levels of IYO and prevents
279 Despite an apparent limited role of
knockdown resistance in An. funestus, it is necessary to
280 LGR4-deficient breast cancer cells, and LGR4
knockdown resulted in increased E-cadherin and decreased
281 r Wilms tumor 1 (WT1) binding sites, and WT1
knockdown resulted in reduced SHMT1 transcription in ova
282 CXCR7
knockdown resulted in the inhibition of IL6-induced prol
283 Conditional gene
knockdown reveals that inhibition of ROCKII promotes the
284 Myoferlin
knockdown significantly decreased IL-6-mediated tumor ce
285 However, the IPO5
knockdown significantly decreased the intracellular leve
286 e first time, to our knowledge, that lipin-1
knockdown significantly inhibits tumor growth in vivo us
287 red neuronal cells, we found that SRC-1 gene
knockdown specifically in the NTS significantly diminish
288 A
knockdown strain of ssp1 exhibited reduced production of
289 DJ-1
knockdown substantially reduced mediator release, as wel
290 effects of FTO KO anti-correlate with METTL3
knockdown suggesting the involvement of m6A.
291 ides both innate immunity and efficient gene-
knockdown tools in many eukaryotic species, but curiousl
292 PIK3R1
knockdown transforms human mammary epithelial cells, and
293 in ASM cells from severe asthmatics and PP5
knockdown using siRNA restored fluticasone repressive ac
294 expression, which was reduced in CVB3 S100A8
knockdown versus scrambled siRNA CVB3 cells.
295 ation of guide strands correlating with gene
knockdown,
we employed a peptide-nucleic acid (PNA) hybr
296 Using retroviral shRNA
knockdown,
we have demonstrated that these JAK inhibitor
297 f several of the genes downregulated by JAK2
knockdown,
we questioned whether TFEB is regulated by JA
298 SN-deficient mice (knockout/heterozygous and
knockdown)
were subjected to targeted lung delivery of E
299 HDAC4
knockdown with or without an HDAC inhibitor significantl
300 Bilateral Bdnf
knockdown within the ventrolateral OFC and unilateral Bd